| 1. |
- Wang, Zhongqiang, et al.
(författare)
-
Realizing 18.03% efficiency and good junction characteristics in organic solar cells via hydrogen-bonding interaction between glucose and ZnO electron transport layers
- 2022
-
Ingår i: Journal of Materials Chemistry A. - : Royal Society of Chemistry (RSC). - 2050-7488 .- 2050-7496. ; 11:4, s. 1810-1816
-
Tidskriftsartikel (refereegranskat)abstract
- Electron transport layers (ETLs) with excellent electron extraction capability are essential for realizing high efficiency in organic solar cells (OSCs). A sol-gel-processed ZnO ETL is widely used in OSCs due to its high mobility and suitable work function. However, the existence of defects usually results in low photovoltaic performance during the operation of OSCs. In this work, glucose (Gl) was used to passivate free OH traps via hydrogen-bonding interaction and formed ZnO/Gl ETLs with ZnO, which exhibited improved electron extraction capability and reduced trap defect density. Thus, a champion efficiency of 18.03% was obtained in a PM6:Y6 light absorber-based cell, which is >11% higher than that of the reference cell (16.15%) with a pristine ZnO ETL. Impressive enhancements by >11% were also observed in different fullerene and non-fullerene light absorber-based cells relative to that of the reference cell. This study demonstrates a new strategy to design ETLs for realizing high efficiency in OSCs.
|
|
| 2. |
- Hu, Tianyu, et al.
(författare)
-
Steric hindrance induced low exciton binding energy enables low-driving-force organic solar cells
- 2024
-
Ingår i: Aggregate. - 2692-4560 .- 2766-8541. ; In Press
-
Tidskriftsartikel (refereegranskat)abstract
- Exciton binding energy (Eb) has been regarded as a critical parameter in charge separation during photovoltaic conversion. Minimizing the Eb of the photovoltaic materials can facilitate the exciton dissociation in low-driving force organic solar cells (OSCs) and thus improve the power conversion efficiency (PCE); nevertheless, diminishing the Eb with deliberate design principles remains a significant challenge. Herein, bulky side chain as steric hindrance structure was inserted into Y-series acceptors to minimize the Eb by modulating the intra- and intermolecular interaction. Theoretical and experimental results indicate that steric hindrance-induced optimal intra- and intermolecular interaction can enhance molecular polarizability, promote electronic orbital overlap between molecules, and facilitate delocalized charge transfer pathways, thereby resulting in a low Eb. The conspicuously reduced Eb obtained in Y-ChC5 with pinpoint steric hindrance modulation can minimize the detrimental effects on exciton dissociation in low-driving-force OSCs, achieving a remarkable PCE of 19.1% with over 95% internal quantum efficiency. Our study provides a new molecular design rationale to reduce the Eb.
|
|
| 3. |
- Li, Wei, et al.
(författare)
-
One-Step Synthesis of Precursor Oligomers for Organic Photovoltaics: A Comparative Study between Polymers and Small Molecules
- 2015
-
Ingår i: ACS Applied Materials and Interfaces. - : American Chemical Society (ACS). - 1944-8244 .- 1944-8252. ; 7:49, s. 27106-27114
-
Tidskriftsartikel (refereegranskat)abstract
- Two series of oligomers TQ and rhodanine end-capped TQ-DR were synthesized using a facile one-step method. Their optical, electrical, and thermal properties and photovoltaic performances were systematically investigated and compared. The TQ series of oligomers were found to be amorphous, whereas the TQ-DR series are semicrystalline. For the TQ oligomers, the results obtained in solar cells show that as the chain length of the oligomers increases, an increase in power conversion efficiency (PCE) is obtained. However, when introducing 3-ethylrhodanine into the TQ oligomers as end groups, the PCE of the TQ-DR series of oligomers decreases as the chain length increases. Moreover, the TQ-DR series of oligomers give much higher performances compared to the original amorphous TQ series of oligomers owing to the improved extinction coefficient (epsilon) and crystallinity afforded by the rhodanine. In particular, the highly crystalline oligomer TQ5-DR, which has the shortest conjugation length shows a high hole mobility of 0.034 cm(2) V-1 s(-1) and a high PCE of 3.14%, which is the highest efficiency out of all of the six oligomers. The structure-property correlations for all of the oligomers and the TQ1 polymer demonstrate that structural control of enhanced intermolecular interactions and crystallinity is a key for small molecules/oligomers to achieve high mobilities, which is an essential requirement for use in OPVs.
|
|
| 4. |
- Shi, Furong, et al.
(författare)
-
A Nitroxide Radical Conjugated Polymer as an Additive to Reduce Nonradiative Energy Loss in Organic Solar Cells
- 2023
-
Ingår i: Advanced Materials. - : Wiley. - 0935-9648 .- 1521-4095. ; 35:23
-
Tidskriftsartikel (refereegranskat)abstract
- Nonfullerene-acceptor-based organic solar cells (NFA-OSCs) are now set off to the 20% power conversion efficiency milestone. To achieve this, minimizing all loss channels, including nonradiative photovoltage losses, seems a necessity. Nonradiative recombination, to a great extent, is known to be an inherent material property due to vibrationally induced decay of charge-transfer (CT) states or their back electron transfer to the triplet excitons. Herein, it is shown that the use of a new conjugated nitroxide radical polymer with 2,2,6,6-tetramethyl piperidine-1-oxyl side groups (GDTA) as an additive results in an improvement of the photovoltaic performance of NFA-OSCs based on different active layer materials. Upon the addition of GDTA, the open-circuit voltage (VOC), fill factor (FF), and short-circuit current density (JSC) improve simultaneously. This approach is applied to several material systems including state-of-the-art donor/acceptor pairs showing improvement from 15.8% to 17.6% (in the case of PM6:Y6) and from 17.5% to 18.3% (for PM6:BTP-eC9). Then, the possible reasons behind the observed improvements are discussed. The results point toward the suppression of the CT state to triplet excitons loss channel. This work presents a facile, promising, and generic approach to further improve the performance of NFA-OSCs.
|
|
| 5. |
- Tang, Shi, et al.
(författare)
-
Aggregation-Induced Emission by Molecular Design: A Route to High-Performance Light-Emitting Electrochemical Cells
- 2023
-
Ingår i: Angewandte Chemie - International Edition. - : Wiley. - 1433-7851 .- 1521-3773. ; 62:23
-
Tidskriftsartikel (refereegranskat)abstract
- The emission efficiency of organic semiconductors (OSCs) often suffers from aggregation caused quenching (ACQ). An elegant solution is aggregation-induced emission (AIE), which constitutes the design of the OSC so that its morphology inhibits quenching π–π interactions and non-radiative motional deactivation. The light-emitting electrochemical cell (LEC) can be sustainably fabricated, but its function depends on motion of bulky ions in proximity of the OSC. It is therefore questionable whether the AIE morphology can be retained during LEC operation. Here, we synthesize two structurally similar OSCs, which are distinguished by that 1 features ACQ while 2 delivers AIE. Interestingly, we find that the AIE-LEC significantly outperforms the ACQ-LEC. We rationalize our finding by showing that the AIE morphology remains intact during LEC operation, and that it can feature appropriately sized free-volume voids for facile ion transport and suppressed non-radiative excitonic deactivation.
|
|
| 6. |
- Wang, Chuanfei, et al.
(författare)
-
Low Band Gap Polymer Solar Cells With Minimal Voltage Losses
- 2016
-
Ingår i: Advanced Energy Materials. - : Wiley. - 1614-6832 .- 1614-6840. ; 6:18
-
Tidskriftsartikel (refereegranskat)abstract
- One of the factors limiting the performance of organic solar cells (OSCs) is their large energy losses (E loss) in the conversion from photons to electrons, typically believed to be around 0.6 eV and often higher than those of inorganic solar cells. In this work, a novel low band gap polymer PIDTT-TID with a optical gap of 1.49 eV is synthesized and used as the donor combined with PC71BM in solar cells. These solar cells attain a good power conversion efficiency of 6.7% with a high open-circuit voltage of 1.0 V, leading to the E loss as low as 0.49 eV. A systematic study indicates that the driving force in this donor and acceptor system is sufficient for charge generation with the low E loss. This work pushes the minimal E loss of OSCs down to 0.49 eV, approaching the values of some inorganic and hybrid solar cells. It indicates the potential for further enhancement of the performance of OSCs by improving their V oc since the E loss can be minimized.
|
|
| 7. |
- Wang, Chuanfei, et al.
(författare)
-
Ternary organic solar cells with enhanced open circuit voltage
- 2017
-
Ingår i: Nano Energy. - : Elsevier BV. - 2211-2855 .- 2211-3282. ; 37, s. 24-31
-
Tidskriftsartikel (refereegranskat)abstract
- By introducing a non-fullerene small molecule acceptor as a third component to typical polymer donor: fullerene acceptor binary solar cells, we demonstrate that the short circuit current density (Jsc), open circuit voltage (Voc), power conversion efficiency (PCE) and thermal stability can be enhanced simultaneously. The different surface energy of each component causes most of the non-fullerene acceptor molecules to self-organize at the polymer/fullerene interface, while the appropriately selected oxidation/reduction potential of the non-fullerene acceptor enables the resulting ternary junction to work through a cascade mechanism. The cascade ternary junction enhances charge generation through complementary absorption between the non-fullerene and fullerene acceptors and aids the efficient charge extraction from fullerene domains. The bimolecular recombination in the ternary blend layer is reduced as the ternary cascade junction increases the separation of holes and electrons during charge transportation and the trap assistant recombination induced by integer charge transfer (ICT) state potentially reduced due to the smaller pinning energy of inserted non-fullerene acceptor, leading to an unprecedented increase in the open circuit voltage beyond the binary reference values.
|
|
| 8. |
- Zhang, Bingke, et al.
(författare)
-
Facile Synthesis of Organic–Inorganic Hybrid Heterojunctions of Glycolated Conjugated Polymer-TiO 2−X for Efficient Photocatalytic Hydrogen Evolution
- 2024
-
Ingår i: Small. - 1613-6810 .- 1613-6829. ; In Press
-
Tidskriftsartikel (refereegranskat)abstract
- The utilization of the organic–inorganic hybrid photocatalysts for water splitting has gained significant attention due to their ability to combine the advantages of both materials and generate synergistic effects. However, they are still far from practical application due to the limited understanding of the interactions between these two components and the complexity of their preparation process. Herein, a facial approach by combining a glycolated conjugated polymer with a TiO2−X mesoporous sphere to prepare high-efficiency hybrid photocatalysts is presented. The functionalization of conjugated polymers with hydrophilic oligo (ethylene glycol) side chains can not only facilitate the dispersion of conjugated polymers in water but also promote the interaction with TiO2−X forming stable heterojunction nanoparticles. An apparent quantum yield of 53.3% at 365 nm and a hydrogen evolution rate of 35.7 mmol h−1 g−1 is achieved by the photocatalyst in the presence of Pt co-catalyst. Advanced photophysical studies based on femtosecond transient absorption spectroscopy and in situ, XPS analyses reveal the charge transfer mechanism at type II heterojunction interfaces. This work shows the promising prospect of glycolated polymers in the construction of hybrid heterojunctions for photocatalytic hydrogen production and offers a deep understanding of high photocatalytic performance by such heterojunction photocatalysts.
|
|
| 9. |
- Cai, C. S., et al.
(författare)
-
Polymer solar cells spray coated with non-halogenated solvents
- 2017
-
Ingår i: Solar Energy Materials and Solar Cells. - : Elsevier BV. - 0927-0248. ; 161, s. 52-61
-
Tidskriftsartikel (refereegranskat)abstract
- Using spray-coating technique, we successfully fabricated conventional ITO-based and inverted ITO-free polymer solar cells (PSCs) based on a conjugated polymer poly[2,3-bis-(3-octyloxyphenyl) quinoxaline-5,8-diyl-alt-thiophene-2,5-diyl] (TQ1) as the donor and [6,6]-phenyl-C61-butyric acid methyl ester (PC61BM) or [6,6] -phenyl-C71-butyric acid methyl ester (PC71BM) as the acceptor. Environment-friendly non-halogenated solvents were used to process the active layers. The influence of substrate temperatures and processing solvents on the photovoltaic performance of the ITO-based TQ1:PC61BM PSCs was systemically investigated. A higher substrate temperature can accelerate the solvent evaporating rate and afford a micro-textured rougher surface, which efficiently reduced light reflectance and enhanced absorption. Furthermore, finer phase separation was observed when using this high substrate temperature, which led to enhanced photocurrent due to the reduced bimolecular recombination. The device performance of spray-processed PSCs using the non-halogenated solvent mixtures was comparable to that of spray-processed PSCs using the halogenated o-dichlorobenzene (oDCB), which demonstrates that the non-halogenated solvents are very promising in spray-processed PSCs. This work sheds new light on developing efficient roll-to-roll compatible spray-coated PSCs with environment-friendly solvents.
|
|
| 10. |
- Chen, W., et al.
(författare)
-
Enhanced efficiency of polymer solar cells by improving molecular aggregation and broadening the absorption spectra
- 2019
-
Ingår i: Dyes and Pigments. - : Elsevier BV. - 0143-7208 .- 1873-3743. ; 166, s. 42-48
-
Tidskriftsartikel (refereegranskat)abstract
- Alkylthio-substituted thiophene-based benzo[1,2-b:4,5-b’]dithiophene (BDT) was used to construct PBDTS-DTBT, a medium band gap donor-acceptor (D-A) polymer with 5,6-difluoro-4,7-bis[4-(2-octyldodecyl)thiophene-2-yl]benzo[c] [1,2,5]thiadiazole (DTBT). The incorporation of sulfur atoms into the side chains not only lowered the highest occupied molecular orbital (HOMO) energy level but also improved molecular aggregation and thus afforded lower band gap (1.68 eV) with full width at half maximum (FWHM) of 170 nm in comparison to that of the analogous polymer (PBDT-DTBT) without sulfur atoms in side chains. Therefore, the bulk heterojunction polymer solar cells based on PBDTS-DTBT with 2% diiodooctane (DIO) as processing additive showed a high power conversion efficiency (PCE) of 9.73% with high open-circuit voltage (V OC , 0.93 V), large short-circuit current density (J SC , 14.23 mA/cm 2 ) and high fill factor (FF, 0.735).
|
|
| 11. |
- Chen, W., et al.
(författare)
-
Revealing the Position Effect of an Alkylthio Side Chain in Phenyl-Substituted Benzodithiophene-Based Donor Polymers on the Photovoltaic Performance of Non-Fullerene Organic Solar Cells
- 2019
-
Ingår i: ACS Applied Materials & Interfaces. - : American Chemical Society (ACS). - 1944-8252 .- 1944-8244. ; 11:36, s. 33173-33178
-
Tidskriftsartikel (refereegranskat)abstract
- In this work, position effects of an alkylthio side chain were investigated by designing and synthesizing two copolymers based on a phenyl-substituted benzo[1,2-b:4,5-b′]dithiophene (BDTP) and difluorobenzotriazole (FTAZ). The polymer based on the meta-position-alkylthiolated BDTP, named m-PBDTPS-FTAZ, showed a relatively broader bandgap (2.00 vs 1.96 eV) and lower highest occupied molecular orbital (HOMO) energy level (-5.40 vs-5.32 eV) than its para-positioned structural isomeric analogue polymer (named p-PBDTPS-FTAZ), that is, m- A nd p-PBDTPS-FTAZ with the side chain structured as ethylhexyl-in the phenyl unit and hexyldecyl-in the FTAZ moiety. When blended with ITIC, m-PBDTPS-FTAZ showed a comparable crystallinity but more uniform morphology compared to that of p-PBDTPS-FTAZ. A high power conversion efficiency of 13.16% was achieved for m-PBDTPS-FTAZ:ITIC devices with a high open circuit voltage (VOC) of 0.95 V, which is higher than that of p-PBDTPS-FTAZ:ITIC devices (10.86%) with a VOC of 0.89 V. Therefore, m-BDTPS could be an effective donor unit to construct high-efficiency polymers due to its effectively decreased HOMO energy level of polymers while still maintaining good molecular stacking.
|
|
| 12. |
- Dang, D. F., et al.
(författare)
-
Manipulating backbone structure with various conjugated spacers to enhance photovoltaic performance of D-A-type two-dimensional copolymerse
- 2014
-
Ingår i: Organic Electronics: physics, materials, applications. - : Elsevier BV. - 1566-1199. ; 15:11, s. 2876-2884
-
Tidskriftsartikel (refereegranskat)abstract
- A class of low band-gap two-dimensional conjugated polymers of PBDTT-FQ PBDTT-TQ PBDTT-BTQ and PBDTT-TTQ was designed and synthesized, which contains the same di(alkylthiophene)-substituted benzo[1,2-b:4,5-b']dithiophene (BDTT) and 6,7-difluoro-quinoxaline (Q) units, as well as various conjugated spacers of furan, thiophene, bithiophene and thieno[3,2-b]thiophene in the main chain. Significant effect of the varied spacers between the BDTT and Q units on the thermal, optical, electrochemical and photovoltaic properties was investigated and observed for these two-dimensional copolymers in the polymer solar cells. The maximum power conversion efficiency of 5.9% with a short circuit current of 13.7 mA/cm(2) and a fill factor of 0.56 was obtained for the PBDTT-TQ with thiophene spacer in the bulk hetero-junction PSCs using [6,6]-phenyl-C-71-butyric acid methyl ester as acceptor.
|
|
| 13. |
- Du, Siying, et al.
(författare)
-
Nonfullerene acceptors from thieno[3,2-b]thiophene-fused naphthalene donor core with six-member-ring connection for efficient organic solar cells
- 2021
-
Ingår i: Dyes and Pigments. - : Elsevier BV. - 0143-7208 .- 1873-3743. ; 185
-
Tidskriftsartikel (refereegranskat)abstract
- Comprehensive design ideas on the fused-ring donor-core in state-of-the-art acceptor-donor-acceptor (A-D-A) nonfullerene acceptors (NFAs) are still of great importance for regulating the electron push-pull effect for the sake of optimal light-harvesting, frontier molecular orbital levels, and finally their photovoltaic properties. Herein, thieno[3,2-b]thiophenes were fused in bay-area of naphthalene via six-member-ring connection, resulting in the formation of dihydropyrenobisthieno[3,2-b]thiophene based octacyclic ladder-type donor core, which was flanked by two 1,1-dicyanomethylene-3-indanone (IC) acceptor motifs with and without 5,6-diflourination, namely PTT-IC and PTT-2FIC, respectively, as novel efficient A-D-A fused-ring electron acceptors (FREAs). Compared with PTT-IC, fluorinated PTT-2FIC possesses narrower optical bandgap of 1.48 eV, better π-π stacking, and its PBDB-T:PTT-2FIC blend film exhibited better morphology, and better hole and electron mobility. As a result, nonfullerene solar cells using PBDB-T:PTT-2FIC as the active layer achieved a decent PCE of 10.40%, with an open-circuit voltage (VOC) of 0.87 V, a fill factor (FF) of 0.65, and a much higher short-circuit current (JSC) of 18.26 mA/cm2. Meanwhile, the PBDB-T:PTT-IC cells delivered a lower JSC of 12.58 mA/cm2 but a higher VOC of 0.99 V, thus resulting in a PCE of 7.39% due to its wider optical bandgap of 1.58 eV and higher LUMO energy level. These results demonstrated that NFAs based on fused-ring donor core from fusing thieno[3,2-b]thiophenes with naphthalene via six-member-ring connection are promising for organic photovoltaic applications.
|
|
| 14. |
- Fan, Qunping, et al.
(författare)
-
10.13% Efficiency All-Polymer Solar Cells Enabled by Improving the Optical Absorption of Polymer Acceptors
- 2020
-
Ingår i: Solar RRL. - : Wiley. - 2367-198X. ; 4:6
-
Tidskriftsartikel (refereegranskat)abstract
- The limited light absorption capacity for most polymer acceptors hinders the improvement of the power conversion efficiency (PCE) of all-polymer solar cells (all-PSCs). Herein, by simultaneously increasing the conjugation of the acceptor unit and enhancing the electron-donating ability of the donor unit, a novel narrow-bandgap polymer acceptor PF3-DTCO based on an A–D–A-structured acceptor unit ITIC16 and a carbon–oxygen (C–O)-bridged donor unit DTCO is developed. The extended conjugation of the acceptor units from IDIC16 to ITIC16 results in a red-shifted absorption spectrum and improved absorption coefficient without significant reduction of the lowest unoccupied molecular orbital energy level. Moreover, in addition to further broadening the absorption spectrum by the enhanced intramolecular charge transfer effect, the introduction of C–O bridges into the donor unit improves the absorption coefficient and electron mobility, as well as optimizes the morphology and molecular order of active layers. As a result, the PF3-DTCO achieves a higher PCE of 10.13% with a higher short-circuit current density (Jsc) of 15.75 mA cm−2 in all-PSCs compared with its original polymer acceptor PF2-DTC (PCE = 8.95% and Jsc = 13.82 mA cm−2). Herein, a promising method is provided to construct high-performance polymer acceptors with excellent optical absorption for efficient all-PSCs.
|
|
| 15. |
- Genene, Zewdneh, 1983, et al.
(författare)
-
A comparative study of the photovoltaic performances of terpolymers and ternary systems
- 2017
-
Ingår i: RSC Advances. - : Royal Society of Chemistry (RSC). - 2046-2069. ; 7:29, s. 17959-17967
-
Tidskriftsartikel (refereegranskat)abstract
- Random terpolymers were synthesized from the electron-rich unit thiophene as the donor and two electron-deficient units with complementary absorption as the acceptor. Polymer solar cells (PSCs) fabricated from these terpolymers were compared with those fabricated from the ternary blends of two alternating polymers to explore the best strategy for extending the light absorption range. The two approaches showed similar open-circuit voltages (Voc) but different short-circuit current densities (Jsc). The terpolymer strategy broadened the light absorption range and provided a high power conversion efficiency (PCE) of 5.8%. This is due to a high Jsc and high hole mobility. The device fabricated from the ternary blend exhibited a lower PCE (3.5%) compared to those fabricated from the terpolymers and alternating polymer blends due to the morphological incompatibility of the donor polymers. Our results illustrate the potential of the terpolymer systems as a promising strategy to effectively increase the light absorption and thereby performance of PSCs by combining two morphologically incompatible polymers.
|
|
| 16. |
|
|
| 17. |
- Guo, Pengzhi, et al.
(författare)
-
Twisted Alkylthiothien-2-yl Flanks and Extended Conjugation Length Synergistically Enhanced Photovoltaic Performance by Boosting Dielectric Constant and Carriers Kinetic Characteristics
- 2021
-
Ingår i: Macromolecular Chemistry and Physics. - : Wiley. - 1022-1352 .- 1521-3935. ; 222:12
-
Tidskriftsartikel (refereegranskat)abstract
- Alternating conjugated polymers (CPs), derived from 2-ethylhexylthiothiophen-2-yl (TS) or 2-ethylhexylthiophen-2-yl (T) flanked dithieno[3,2-d:3,2-d ']benzo[1,2-b:4,5-b ']dithiophene (DTBDT) and diketopyrrolo-pyrrole (DPP) termed as PDTBDT-TS-DPP and PDTBDT-T-DPP, are prepared and characterized. It is found that the PDTBDT-TS-DPP not only exhibits slightly deepening the highest occupied molecular orbital energy levels, and similar absorption, etc., but also presents higher dielectric constant (epsilon(r)) of 6.7 at 1 kHz in contrast to 3.2 for PDTBDT-T-DPP, which are even higher than those of 4.3 and 3.0 for PBDT-TS-DPP/PBDT-T-DPP generated from TS and T flanked benzo[1,2-b:4,5-bMODIFIER LETTER PRIME]dithiophene and DPP. Beyond that, the power conversion efficiency of 8.17% for the inverted photovoltaic devices from DPP-based CPs, is achieved from PDTBDT-TS-DPP. The alkylthio side chains are used in the DTBDT of the larger twisting angles of TS flanks and longer conjugation length, synergistically contribute to the highest dipole moments, and then lead to the enhancement of epsilon(r), thus devoted the modification exciton dissociation and charge carriers kinetic characteristics. To the authors' knowledge, it is the first time to report that epsilon(r) of the CPs is connected with the twisting angle of flanks and conjugation length of the building blocks, besides the use of functional side chains and atoms.
|
|
| 18. |
- Hou, Lintao, et al.
(författare)
-
Lateral Phase Separation Gradients in Spin-Coated Thin Films of High-Performance Polymer: Fullerene Photovoltaic Blends
- 2011
-
Ingår i: Advanced Functional Materials. - : Wiley. - 1616-3028 .- 1616-301X. ; 21:16, s. 3169-3175
-
Tidskriftsartikel (refereegranskat)abstract
- In this study, it is demonstrated that a finer nanostructure produced under a rapid rate of solvent removal significantly improves charge separation in a high-performance polymer: fullerene bulk-heterojunction blend. During spin-coating, variations in solvent evaporation rate give rise to lateral phase separation gradients with the degree of coarseness decreasing away from the center of rotation. As a result, across spin-coated thin films the photocurrent at the first interference maximum varies as much as 25%, which is much larger than any optical effect. This is investigated by combining information on the surface morphology of the active layer imaged by atomic force microscopy, the 3D nanostructure imaged by electron tomography, film formation during the spin coating process imaged by optical interference and photocurrent generation distribution in devices imaged by a scanning light pulse technique. The observation that the nanostructure of organic photovoltaic blends can strongly vary across spin-coated thin films will aid the design of solvent mixtures suitable for high molecular-weight polymers and of coating techniques amenable to large area processing.
|
|
| 19. |
- James, David, 1987, et al.
(författare)
-
High-Performance Hole Transport and Quasi-Balanced Ambipolar OFETs Based on D–A–A Thieno-benzo-isoindigo Polymers
- 2016
-
Ingår i: Advanced Electronic Materials. - : Wiley. - 2199-160X. ; 2:4
-
Tidskriftsartikel (refereegranskat)abstract
- Two new conjugated polymers are synthesized based on a novel donor–acceptor–acceptor (D–A–A) design strategy with the intention of attaining lower lowest unoccupied molecular obital levels compared to the normally used D–A strategy. By coupling two thieno-benzo-isoindigo units together via the phenyl position to give a new symmetric benzene-coupled di-thieno-benzo-isoindigo (BdiTBI) monomer as an A–A acceptor and thiophene (T) or bithiophene (2T) as a donor, two new polymers PT-BdiTBI and P2T-BdiTBI are synthesized via Stille coupling. The two polymers are tested in top gate and top contact field effect transistors, which exhibit balanced ambipolar charge transport properties with poly(methyl methacrylate) as dielectric and a high hole mobility up to 1.1 cm2 V–1 s–1 with poly(trifluoroethylene) as dielectric. The polymer films are investigated using atomic force microscopy, which shows fibrous features due to their high crystallinity as indicated by grazing incidence wide-angle X-ray scattering. The theoretical calculations agree well with the experimental data on the energy levels. It is demonstrated that the D–A–A strategy is very effective for designing low band gap polymers for organic electronic applications.
|
|
| 20. |
- Li, Zhaojun, 1989, et al.
(författare)
-
High-performance all-polymer solar cells based on fluorinated naphthalene diimide acceptor polymers with fine-tuned crystallinity and enhanced dielectric constants
- 2018
-
Ingår i: Nano Energy. - : Elsevier BV. - 2211-2855. ; 45, s. 368-379
-
Tidskriftsartikel (refereegranskat)abstract
- Growing interests have been devoted to the synthesis of polymer acceptors as alternatives to fullerene derivatives to realize high-performance and stable all-polymer solar cells (all-PSCs). So far, one of the key factors that limit the performance of all-PSCs is low photocurrent density (normally < 14 mA/cm 2 ). One potential solution is to improve the dielectric constants (ε r ) of polyme r :polymer blends, which tend to reduce the binding energy of excitons, thus boosting the exciton dissociation efficiencies. Nevertheless, the correlation between ε r and photovoltaic performance has been rarely investigated for all-PSCs. In this work, five fluorinated naphthalene diimide (NDI)-based acceptor polymers, with different content of fluorine were synthesized. The incorporation of fluorine increased the ε r of the acceptor polymers and blend films, which improved the charge generation and overall photocurrent of the all-PSCs. As a result, the PTB7-Th:PNDI-FT10 all-PSC attained a high power conversion efficiency (PCE) of 7.3% with a photocurrent density of 14.7 mA/cm 2 , which surpassed the values reported for the all-PSC based on the non-fluorinated acceptor PNDI-T10. Interestingly, similarly high photovoltaic performance was maintained regardless of a large variation of donor:acceptor ratios, which revealed the good morphological tolerance and the potential for robust production capability of all-PSCs.
|
|
| 21. |
- Liu, Lihui, 1985, et al.
(författare)
-
Substrate-dependent resistance decrease of graphene by ultraviolet-ozone charge doping
- 2016
-
Ingår i: RSC Advances. - : Royal Society of Chemistry (RSC). - 2046-2069. ; 6:67, s. 62091-62098
-
Tidskriftsartikel (refereegranskat)abstract
- Large sheet resistance is the critical problem of graphene for application in electronic and optoelectronic devices as transparent electrodes. Ultraviolet/ozone (UVO) treatment is a convenient, highly effective, vacuum process and post-clean free method. This paper reveals that the effect of UVO treatment on the resistance of graphene is substrate dependent, which means that the band gap and photogenerated charge carriers of the substrates under UV illumination play a key role in the doping effect. The resistance of graphene can be decreased by as much as 80% on F8BT, GaN and PTFE substrates, by 70% on PMMA substrate, and by 50% on paraffin and glass substrates. Large band gap substrates (>hν) will induce a p-doping effect, while small band gap substrates (
|
|
| 22. |
- Liu, Shungang, et al.
(författare)
-
The role of connectivity in significant bandgap narrowing for fused-pyrene based non-fullerene acceptors toward high-efficiency organic solar cells
- 2020
-
Ingår i: Journal of Materials Chemistry A. - : Royal Society of Chemistry (RSC). - 2050-7488 .- 2050-7496. ; 8:12, s. 5995-6003
-
Tidskriftsartikel (refereegranskat)abstract
- Great attention has been paid to developing low bandgap non-fullerene acceptors (NFAs) for matching wide bandgap donor polymers to increase the photocurrent and therefore the power conversion efficiencies (PCEs) of NFA organic solar cells, while pyrene-core based acceptor-donor-acceptor (A-D-A) NFAs have been mainly reported via the 2,9-position connection due to their bisthieno[3′,2′-b']thienyl[a,h]pyrene fused via a five-membered ring bridge at the ortho-position of pyrene as the representative one named FPIC5, which has prohibited further narrowing their energy gap. Herein, an acceptor FPIC6 was exploited by creating the 1,8-position connection through fusing as bisthieno[3′,2′-b′]thienyl[f-g,m-n]pyrene linked at the bay-position via a six-membered bridge, with enhanced push-pull characteristics within such A-D-A structure. As a structural isomer of FPIC5, FPIC6 exhibited a much lower bandgap of 1.42 eV (1.63 eV for FPIC5). Therefore, the photocurrent and PCE of PTB7-Th:FPIC6 cells were improved to 21.50 mA cm-2 and 11.55%, respectively, due to the balanced mobilities, better photoluminescence quenching efficiency and optimized morphology, which are both ∼40% better than those of PTB7-Th:FPIC5 cells. Our results clearly proved that a pyrene fused core with 1,8-position connection with electron-withdrawing end groups instead of 2,9-position connection is an efficient molecular design strategy to narrow the optical bandgap and improve the photovoltaic performance of NFA based OSCs.
|
|
| 23. |
- Liu, Yi, et al.
(författare)
-
Effect of fluorine atoms on optoelectronic, aggregation and dielectric constants of 2,1,3-benzothiadiazole-based alternating conjugated polymers
- 2021
-
Ingår i: Dyes and Pigments. - : Elsevier BV. - 0143-7208 .- 1873-3743. ; 193
-
Tidskriftsartikel (refereegranskat)abstract
- Three 2,1,3-benzothiadiazole-based conjugated copolymers named PBDT-0F-BTs, PBDT-2F-BTs and PBDT-6F-FBTs, which were derived from 4,8-bis(4,5-dioctylthiophen-2-yl)benzo[1,2-b:4,5-b′]dithiophene and (3,4′-bis(2-hexyl- decyl)-2,2′-dithiophene-5-yl) substituted 2,1,3-benzothiadiazole and/or 5,6-difluoro- 2,1,3-benzothiadiazole derivatives with 2,2′-dithiophene and/or 3,3′-difluoro- 2,2′-dithiophene as π-linkers, were prepared and characterized. The copolymers PBDT-0F-BTs, PBDT-2F-BTs and PBDT-6F-FBTs exhibited the highest occupied molecular orbital (HOMO) and lowest unoccupied orbital (LUMO) energy levels of −5.38 eV/−3.57 eV, −5.45 eV/−3.65 eV and −5.55 eV/−3.78 eV, with the light response from 300 nm to 720–750 nm, alongside with the similar aggregation, except that the charge transporting mobilities were successively increased, and the dielectric constants were gradually improved from 3.3 to 4.8 to 5.9 at 1 KHz, while the fluorine atoms in the each repeat unit of polymers were varied from 0 to 2 and then up to 6, respectively. Beyond that, it has also been found that the power conversion efficiencies and exciton dissociation probability (P(E,T)) of the bulk heterojunction organic photovoltaic cells (BHJ-OPVs) from the blend films of polymers paired with Y6 (2,2'-((2Z,2'Z)-((12,13-bis(2-ethylhexyl)-3,9-diundecyl12,13-dihydro[1,2,5]thia- diazolo[3,4-e]thieno[2'',3'':4',5']thieno[2',3':4,5]pyrrolo[3,2-g]thieno[2',3':4,5]thieno[3,2-b]indole-2,10-diyl)bis(methanylylidene))bis(5,6-difluoro-3-oxo-2,3-dihydro-1H-ind-ene-2,1-diylidene))dimalononitrile), were varied from 7.83% and 85.9%, to 9.22% and 90.2% and then up to 12.34% and 91.4%. The results indicated that the continuous insertion of the fluorine atoms into the repeat units of the conjugated polymers would result in the consecutively deepening the HOMO energy levels, increase dielectric constants and charge mobilities, thus devote to the enhancement of the P(E,T) and the performance of the BHJ-OPVs.
|
|
| 24. |
- Ma, Ruijie, et al.
(författare)
-
All-polymer solar cells with over 16% efficiency and enhanced stability enabled by compatible solvent and polymer additives
- 2022
-
Ingår i: Aggregate. - : Wiley. - 2692-4560 .- 2766-8541. ; 3:3
-
Tidskriftsartikel (refereegranskat)abstract
- Considering the robust and stable nature of the active layers, advancing the power conversion efficiency (PCE) has long been the priority for all-polymer solar cells (all-PSCs). Despite the recent surge of PCE, the photovoltaic parameters of the state-of-the-art all-PSC still lag those of the polymer:small molecule-based devices. To compete with the counterparts, judicious modulation of the morphology and thus the device electrical properties are needed. It is difficult to improve all the parameters concurrently for the all-PSCs with advanced efficiency, and one increase is typically accompanied by the drop of the other(s). In this work, with the aids of the solvent additive (1-chloronaphthalene) and the n-type polymer additive (N2200), we can fine-tune the morphology of the active layer and demonstrate a 16.04% efficient all-PSC based on the PM6:PY-IT active layer. The grazing incidence wide-angle X-ray scattering measurements show that the shape of the crystallites can be altered, and the reshaped crystallites lead to enhanced and more balanced charge transport, reduced recombination, and suppressed energy loss, which lead to concurrently improved and device efficiency and stability.
|
|
| 25. |
- Mone, Mariza, 1992, et al.
(författare)
-
Near-Infrared Emission by Tuned Aggregation of a Porphyrin Compound in a Host–Guest Light-Emitting Electrochemical Cell
- 2021
-
Ingår i: Advanced Optical Materials. - : Wiley. - 2195-1071 .- 2162-7568. ; 9:6
-
Tidskriftsartikel (refereegranskat)abstract
- The synthesis of 5,10,15,20-tetrakis((5,10-bis((2-hexyldecyl)oxy)dithieno[3,2-c:3′,2′-h][1,5]naphthyridin-2-yl)ethynyl)porphyrin zinc(II) (Por4NT), a near-infrared (NIR) emitting compound, comprising a zinc porphyrin core linked with triple bonds through its meso positions to four 5,10-bis((2-hexyldecyl)oxy)dithieno[3,2-c:3′,2′-h][1,5]naphthyridine (NT) arms is reported. Por4NT featured high solubility in common non-polar solvents, which is ideal for easy processing through solution techniques, and high photoluminescence (PL) efficiency of ≈30% in dilute toluene solution. It also exhibited a strong tendency for aggregation because of its flat conformation, and this aggregation resulted in a strong redshifted emission and a drop in PL efficiency. A well-matched PBDTSi-BDD-Py “host” terpolymer is therefore designed, which is capable of mitigating the aggregation of the Por4NT “guest”. An optimized blend of the host, guest, and an ionic-liquid electrolyte is utilized as the active material in a light-emitting electrochemical cell (LEC), which delivered strong NIR radiance of 134 µW cm-2 with a long wavelength maximum at 810 nm at a low drive voltage of 5.0 V. The attainment of the strong NIR emission from the host–guest LEC is attributed to a tuned aggregation of the Por4NT emitter, which resulted in the desired aggregation-induced redshift of the emission at a reasonably retained efficiency.
|
|
| 26. |
- Mone, Mariza, 1992, et al.
(författare)
-
Star-Shaped Diketopyrrolopyrrole-Zinc Porphyrin that Delivers 900 nm Emission in Light-Emitting Electrochemical Cells
- 2019
-
Ingår i: Chemistry of Materials. - : American Chemical Society (ACS). - 0897-4756 .- 1520-5002. ; 31:23, s. 9721-9728
-
Tidskriftsartikel (refereegranskat)abstract
- The development and application of a deep near-infrared (NIR) emitting star-shaped diketopyrrolopyrrole–Zn-porphyrin compound, ZnP(TDPP)4, is reported. The structure, conjugation, and planarity of the porphyrin compound were carefully tuned by molecular design, which resulted in a low-energy photoluminescence peak at 872 nm. The ZnP(TDPP)4 compound was employed as the emissive guest in light-emitting electrochemical cells (LECs), which also comprised the conjugated polymer poly[1,3-bis(2-ethylhexyl)-5-(5-(6-methyl-4,8-bis(5-(tributylsilyl)thiophen-2-yl)benzo[1,2-b:4,5-b′]dithiophen-2-yl)thiophen-2-yl)-7-(5-methylthiophen-2-yl)-4H,8H-benzo[1,2-c:4,5-c′]dithiophene-4,8-dione] (PBDTSi-BDD) as the majority host, an ionic liquid as the electrolyte, and two air-stabile electrodes. These systematically optimized host–guest LECs featured a peak electroluminescence at 900 nm, which was delivered at a significant radiance of 36 μW/cm2 and at a low drive voltage of 3.8 V. It is notable that this is the most redshifted NIR emission attained from an LEC device to date, and as such, this work introduces Zn porphyrins as a sustainable and tunable option for emerging emissive NIR applications.
|
|
| 27. |
- Shahid, Bilal, et al.
(författare)
-
Low-bandgap polymers with quinoid unit as π bridge for high-performance solar cells
- 2020
-
Ingår i: Journal of Energy Chemistry. - : Elsevier BV. - 2095-4956. ; 40:2020, s. 180-187
-
Tidskriftsartikel (refereegranskat)abstract
- To construct efficient low band gap polymers, increasing the Quinone structure of the polymer backbone could be one desirable strategy. In this work, two D–Q–A–Q polymers P1 and P2 were designed and synthesized with thiophenopyrrole diketone (TPD) and benzothiadiazole (BT) unit as the core and ester linked thieno[3,4-b]thiophene (TT) segment as π-bridging, and the main focus is to make a comparative analysis of different cores in the influence of the optical, electrochemical, photochemical and morphological properties. Compared with the reported PBDTT EH –TBTT HD−i , P1 exhibited the decreased HOMO energy level of −5.38 eV and lower bandgap of 1.48 eV. Furthermore, when replaced with BT core, P2 showed a red-shifted absorption profile of polymer but with up-shifted HOMO energy level. When fabricated the photovoltaic devices in conventional structure, just as expected, the introduction of ester substituent made an obvious increase of V OC from 0.63 to 0.74 V for P1. Besides, due to the deep HOMO energy level, higher hole mobility and excellent phase separation with PC 71 BM, a superior photovoltaic performance (PCE = 7.13%) was obtained with a short-circuit current density (J SC ) of 14.9 mA/cm 2 , significantly higher than that of P2 (PCE = 2.23%). Generally, this study highlights that the strategy of inserting quinoid moieties into D–A polymers could be optional in LBG-polymers design and presents the importance and comparison of potentially competent core groups.
|
|
| 28. |
- Shen, W. F., et al.
(författare)
-
High-performance ternary polymer solar cells from a structurally similar polymer alloy
- 2017
-
Ingår i: Journal of Materials Chemistry A. - : Royal Society of Chemistry (RSC). - 2050-7488 .- 2050-7496. ; 5:24, s. 12400-12406
-
Tidskriftsartikel (refereegranskat)abstract
- High-efficiency ternary polymer solar cells (PSCs) are fabricated by using two donor polymers (PBDTTPD and PBDTTT-C-T) with similar polymer backbones and complementary absorption and PC71BM as the acceptor. A high power conversion efficiency (PCE) of 9.3% is achieved with a high short-circuit current density (J(sc)) of 17.2 mA cm(-2). The enhanced J(sc) and PCEs are mainly attributed to the broadened photoresponse of the ternary blend. Good miscibility of the two donor polymers is found due to the similar polymer main chains, leading to the desired morphology between the donors and PC71BM in the ternary blends. The trend of open-circuit voltage (V-oc) variations indicates the formation of a polymer alloy in this ternary blend. Our work demonstrates that using two donor polymers with similar backbone structures is a rational strategy for realizing high-performance ternary PSCs.
|
|
| 29. |
- Su, Wenyan, et al.
(författare)
-
13.4 % Efficiency from All-Small-Molecule Organic Solar Cells Based on a Crystalline Donor with Chlorine and Trialkylsilyl Substitutions
- 2021
-
Ingår i: ChemSusChem. - : Wiley. - 1864-5631 .- 1864-564X. ; 14:17, s. 3535-3543
-
Tidskriftsartikel (refereegranskat)abstract
- How to simultaneously achieve both high open-circuit voltage (Voc) and high short-circuit current density (Jsc) is a big challenge for realising high power conversion efficiency (PCE) in all-small-molecule organic solar cells (all-SM OSCs). Herein, a novel small molecule (SM)-donor, namely FYSM−SiCl, with trialkylsilyl and chlorine substitutions was designed and synthesized. Compared to the original SM-donor FYSM−H, FYSM−Si with trialkylsilyl substitution showed a decreased crystallinity and lower highest occupied molecular orbital (HOMO) level, while FYSM−SiCl had an improved crystallinity, more ordered packing arrangement, significantly lower HOMO level, and predominant “face-on” orientation. Matched with a SM-acceptor Y6, the FYSM−SiCl-based all-SM OSCs exhibited both high Voc of 0.85 V and high Jsc of 23.7 mA cm−2, which is rare for all-SM OSCs and could be attributed to the low HOMO level of FYSM−SiCl donor and the delicate balance between high crystallinity and suitable blend morphology. As a result, FYSM−SiCl achieved a high PCE of 13.4 % in all-SM OSCs, which was much higher than those of the FYSM−H- (10.9 %) and FYSM−Si-based devices (12.2 %). This work demonstrated a promising method for the design of efficient SM-donors by a side-chain engineering strategy via the introduction of trialkylsilyl and chlorine substitutions.
|
|
| 30. |
- Su, Wenyan, et al.
(författare)
-
Nonconjugated Terpolymer Acceptors with Two Different Fused-Ring Electron-Deficient Building Blocks for Efficient All-Polymer Solar Cells
- 2021
-
Ingår i: ACS Applied Materials and Interfaces. - : American Chemical Society (ACS). - 1944-8244 .- 1944-8252. ; 13:5, s. 6442-6449
-
Tidskriftsartikel (refereegranskat)abstract
- The ternary polymerization strategy of incorporating different donor and acceptor units forming terpolymers as photovoltaic materials has been proven advantageous in improving power conversion efficiencies (PCEs) of polymer solar cells (PSCs). Herein, a series of low band gap nonconjugated terpolymer acceptors based on two different fused-ring electron-deficient building blocks (IDIC16 and ITIC) with adjustable photoelectric properties were developed. As the third component, ITIC building blocks with a larger pi-conjugation structure, shorter solubilizing side chains, and red-shifted absorption spectrum were incorporated into an IDIC16-based nonconjugated copolymer acceptor PF1-TS4, which built up the terpolymers with two conjugated building blocks linked by flexible thioalkyl chain-thiophene segments. With the increasing ITIC content, terpolymers show gradually broadened absorption spectra and slightly down-shifted lowest unoccupied molecular orbital levels. The active layer based on terpolymer PF1-TS4-60 with a 60% ITIC unit presents more balanced hole and electron mobilities, higher photoluminescence quenching efficiency, and improved morphology compared to those based on PF1-TS4. In all-polymer solar cells (all-PSCs), PF1-TS4-60, matched with a wide band gap polymer donor PM6, achieved a similar open-circuit voltage (V-oc) of 0.99 V, a dramatically increased short-circuit current density (J(sc)) of 15.30 mA cm(-2), and fill factor (FF) of 61.4% compared to PF1-TS4 = 0.99 V, J(sc) = 11.21 mA cm(-2), and FF = 55.6%). As a result, the PF1-TS4-60-based all-PSCs achieved a PCE of 9.31%, which is similar to 50% higher than the PF1-TS4-based ones (6.17%). The results demonstrate a promising approach to develop high-performance nonconjugated terpolymer acceptors for efficient all-PSCs by means of ternary polymerization using two different A-D-A-structured fused-ring electron-deficient building blocks.
|
|
| 31. |
- Sun, Fengbo, et al.
(författare)
-
1,5-Diiodocycloctane: a cyclane solvent additive that can extend the exciton diffusion length in thick film organic solar cells
- 2024
-
Ingår i: Energy and Environmental Sciences. - 1754-5692 .- 1754-5706. ; 17:5, s. 1916-1930
-
Tidskriftsartikel (refereegranskat)abstract
- The short exciton diffusion length associated with most state-of-the-art organic semiconductors used in organic solar cells (OSCs) imposes severe limits on the exciton transport in the larger donor/acceptor domains and the exciton dissociation at the interface, which hinder further improvements in the power conversion efficiencies (PCE) of the thick-film devices. In this study, a new cyclane, 1,5-diiodocycloctane (DICO), was employed as a solvent additive to effectively extend the exciton LD within the bulk-heterojunction blend, which can function with the multiple photovoltaic materials system. Due to the great enhancement of molecular stacking and exclusively large domain sizes of photovoltaic materials with the assistance of the DICO additive, the trap density in devices is significantly reduced, thereby nearly doubling the LD in the thick film OSCs. Notably, the DICO-processed PM6/L8-BO-based OSC showed high thickness tolerance for the bulk-heterojunction (BHJ) layer, delivering a high PCE of 19.1% in the case of a 110 nm thick film and still maintaining an excellent PCE of 17.2% in the case of a 300 nm thick film. Crucially, a noticeably increased stability of the multiple materials system was observed in the DICO-processed OSCs. These findings enrich the additive family with new cyclane systems to extend the exciton LD in thick film OSCs with high performance.
|
|
| 32. |
- Tang, Shi, et al.
(författare)
-
On the Design of Host-Guest Light-Emitting Electrochemical Cells : Should the Guest be Physically Blended or Chemically Incorporated into the Host for Efficient Emission?
- 2019
-
Ingår i: Advanced Optical Materials. - : Wiley-VCH Verlagsgesellschaft. - 2162-7568 .- 2195-1071. ; 7:18
-
Tidskriftsartikel (refereegranskat)abstract
- It has recently been demonstrated that light-emitting electrochemical cells (LECs) can be designed to deliver strong emission with high efficiency when the charge transport is effectuated by a majority host and the emission is executed by a minority guest. A relevant question is then: should the guest be physically blended with or chemically incorporated into the host? A systematic study is presented that establishes that for near-infrared-(NIR-) emitting LECs based on poly(indacenodithieno[3,2-b]thiophene) (PIDTT) as the host and 4,7-bis(4,4-bis(2-ethylhexyl)-4H-silolo[3,2-b:4,5-b ']dithiophen-2-yl)benzo[c][1,2,5]-thiadiazole (SBS) as the guest the chemical-incorporation approach is preferable. The host-to-guest energy transfer in LEC devices is highly efficient at a low guest concentration of 0.5%, whereas guest aggregation and ion redistribution during device operation severly inhibits this transfer in the physical-blend devices. The chemical-incorporation approach also results in a redshifted emission with a somewhat lowered photoluminescence quantum yield, but the LEC performance is nevertheless very good. Specifically, an NIR-LEC device comprising a guest-dilute (0.5 molar%) PIDTT-SBS copolymer delivers highly stabile operation at a high radiance of 263 mu W cm(-2) (peak wavelength = 725 nm) and with an external quantum efficiency of 0.214%, which is close to the theoretical limit for this particular emitter and device geometry.
|
|
| 33. |
- Tang, Wei, et al.
(författare)
-
17.25% high efficiency ternary solar cells with increased open-circuit voltage using a high HOMO level small molecule guest donor in a PM6:Y6 blend
- 2021
-
Ingår i: Journal of Materials Chemistry A. - : Royal Society of Chemistry (RSC). - 2050-7496 .- 2050-7488. ; 9:36, s. 20493-20501
-
Tidskriftsartikel (refereegranskat)abstract
- A small molecule donor TiC12 with an asymmetric thieno[3,2-c]isochromene unit is incorporated into the PM6:Y6 system as the third component for constructing ternary organic solar cells (OSCs). It was found that TiC12 played an outstanding role in improvement of open-circuit voltage (V-oc), short-circuit current (J(sc)) and fill factor (FF) for the OSCs. The effects of TiC12 on the absorption, exciton dissociation, charge extraction, bimolecular recombination and morphology of the active layer are analyzed in detail. The synergetic improvement of J(sc), V-oc and FF parameters is realized to generate an advanced power conversion efficiency (PCE) of 17.25% in the optimized PM6 : TiC12 : Y6 (0.9 : 0.1 : 1.2) ternary device. Furthermore, the V-oc is increased in proportion to the added amount of TiC12 in the ternary devices due to reduced disorder and nonradiative energy loss, although the guest donor TiC12 exhibited a higher HOMO level than PM6. This study provides an effective and innovative approach to elevate V-oc and thus PCE for ternary OSCs by introducing a guest small molecule donor with a higher HOMO level and better miscibility with the acceptor.
|
|
| 34. |
- Vithanage, Dimali, et al.
(författare)
-
Charge carrier dynamics of polymer: Fullerene blends: From geminate to non-geminate recombination
- 2014
-
Ingår i: Advanced Energy Materials. - : Wiley. - 1614-6840 .- 1614-6832. ; 4:8
-
Tidskriftsartikel (refereegranskat)abstract
- The charge carrier dynamics of a new polymer-fullerene blend are examined on the femtosecond to the millisecond time scale. The full time range is globally fitted using a chemical reaction rate model that includes all key processes, charge generation, energy transfer, charge separation, and recombination, over the full 12 orders of magnitude in time and a factor of 33 in light intensity. Particular attention is paid to the charge recombination processes and it is found that they are highly material specific. Comparison of the dynamics to those of a previously studied polymer:fullerene blend reveals that while for one blend the recombination dynamics are mainly controlled by geminate recombination, the charge recombination in the presently studied polymer:fullerene blend are entirely controlled by non-geminate electron-hole recombination. Carrier density dependence of the non-geminate recombination rate is analyzed and a correlated disorder model of site energies is proposed to explain the observed dependency. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
|
|
| 35. |
- Wang, Chuanfei, 1986-, et al.
(författare)
-
Ternary Organic Solar Cells with Minimum Voltage Losses
- 2017
-
Ingår i: Advanced Energy Materials. - : Wiley. - 1614-6832 .- 1614-6840. ; 7:21
-
Tidskriftsartikel (refereegranskat)abstract
- A new strategy for designing ternary solar cells is reported in this paper. A low-bandgap polymer named PTB7-Th and a high-bandgap polymer named PBDTTS-FTAZ sharing the same bulk ionization potential and interface positive integer charge transfer energy while featuring complementary absorption spectra are selected. They are used to fabricate efficient ternary solar cells, where the hole can be transported freely between the two donor polymers and collected by the electrode as in one broadband low bandgap polymer. Furthermore, the fullerene acceptor is chosen so that the energy of the positive integer charge transfer state of the two donor polymers is equal to the energy of negative integer charge transfer state of the fullerene, enabling enhanced dissociation of all polymer donor and fullerene acceptor excitons and suppressed bimolecular and trap assistant recombination. The two donor polymers feature good miscibility and energy transfer from high-bandgap polymer of PBDTTS-FTAZ to low-bandgap polymer of PTB7-Th, which contribute to enhanced performance of the ternary solar cell.
|
|
| 36. |
- Wang, Ergang, 1981, et al.
(författare)
-
An Easily Synthesized Blue Polymer for High-Performance Polymer Solar Cells
- 2010
-
Ingår i: ADVANCED MATERIALS. - : John Wiley and Sons, Ltd. - 0935-9648 .- 1521-4095. ; 22:46, s. 5240-5244
-
Tidskriftsartikel (refereegranskat)abstract
- High performance solar cells fabricated from an easily synthesized donor-acceptor polymer show maximum power point up to 6.0 mW cm(-2), with an open-circuit voltage of 0.89 V, short-circuit current density of 10.5 mA cm(-2) and fill factor of 0.64, making this polymer a particularly promising candidate for high-efficiency low-cost polymer solar cells.
|
|
| 37. |
- Wang, Ergang, 1981, et al.
(författare)
-
Side-Chain Architectures of 2,7-Carbazole and Quinoxaline-Based Polymers for Efficient Polymer Solar Cells
- 2011
-
Ingår i: Macromolecules. - : American Chemical Society (ACS). - 1520-5835 .- 0024-9297. ; 44:7, s. 2067-2073
-
Tidskriftsartikel (refereegranskat)abstract
- Three polymers bearing a common carbazole thiophene quinoxaline thiophene backbone, but different side chains, were designed and synthesized in order to investigate the effect of side chains on their photovoltaic performance. Their photophysical, electrochemical, and photovoltaic properties were investigated and compared. The polymer EWC3, with the largest amount of side chains, showed the highest power conversion efficiency of 3.7% with an open-circuit voltage (V-oc) of 0.92 V. The atomic force microscopy images of the active layers of the devices showed that the morphology was highly influenced by the choice of the solvent and processing additive. It is worth noting that polymer solar cells (PSCs) fabricated from EWC3, with branched side chains on the carbazole units, gave a much higher V-oc than the devices made from EWC1, which bears the same electron-deficient segment as EWC3 but straight side chains on carbazole units. This study offered a useful and important guideline for designing 2,7-carbazole-based polymers for high-performance PSCs.
|
|
| 38. |
- Wang, Ergang, 1981, et al.
(författare)
-
Small Band Gap Polymers Synthesized via a Modified Nitration of 4,7-Dibromo-2,1,3-benzothiadiazole
- 2010
-
Ingår i: Organic Letters. - : American Chemical Society (ACS). - 1523-7052 .- 1523-7060. ; 12:20, s. 4470-4473
-
Tidskriftsartikel (refereegranskat)abstract
- The nitration of 4,7-dibromo-2,1,3-benzothiadiazole was modified by using CF3SO3H and HNO3 as the nitrating agent, and the related yield was improved greatly. On the basis of this improvement, two new small band gap polymers, P1TPQ and P3TPQ, were developed. Bulk heterojunction solar cells based on P3TPO and [6,6]-phenyl-C-71-butyric acid methyl ester exhibit interesting results with a power conversion efficiency of 21% and photoresponse up to 1.1 mu m
|
|
| 39. |
- Wang, Yufei, et al.
(författare)
-
Acidochromic organic photovoltaic integrated device
- 2023
-
Ingår i: Chemical Engineering Journal. - : Elsevier BV. - 1385-8947. ; 452
-
Tidskriftsartikel (refereegranskat)abstract
- Tremendous efforts have been devoted to boosting the power conversion efficiency (PCE) of organic solar cells (OSCs) via the introduction of cathode interlayers (CILs). However, CIL materials have limited diversity and the development of multifunctional devices is largely neglected. Herein, an acidochromic organic photovoltaic integrated device is firstly proposed by introducing an acid-sensitive stimulating-reaction organic molecule as both the CIL of OSCs and the sensor of monitoring environmental acidity. The oxazolidine unit of acidochromic molecule can form a ring-opening structure after acid treatment, resulting in the remarkable color change with the direct reflection of pH value of ecological environment. The additive-free PM6:Y6 OSCs using the acidochromic molecule as the CIL achieve an excellent PCE of above 15.29 %, which is 47 % higher than that of the control device. The PCE can even maintain above 92 % after treating CIL with various strong acids (pH = 1). Moreover, the color of acidified films and the degraded performance of acidified OSCs can be easily restored by alkaline treatment. The successful application of CIL in other highly efficient photovoltaic systems proves its good universality. This work triggers the promising application of acidochromic molecules in solar cells as CIL with the additional function of recognition of acid environment.
|
|
| 40. |
- Wang, Zhongqiang, et al.
(författare)
-
Mixed solvents for reproducible photovoltaic bulk heterojunctions
- 2011
-
Ingår i: Journal of Photonics for Energy. - : SPIE-Intl Soc Optical Eng. - 1947-7988. ; 1:1 (Special Section on Organic Photovoltaics), s. 011122-
-
Tidskriftsartikel (refereegranskat)abstract
- Most efficient polymer solar cells are usually fabricated from toxic organic solvents, such as chloroform, chlorobenzene, or dichlorobenzene (ODCB). Here, we demonstrate a power conversion efficiency of 4.5% in solar cells with a new blue polymer poly[2,3-bis-(3-octyloxyphenyl)quinoxaline-5,8-diyl-alt-thiophene-2,5-diyl] (TQ1) mixed with PC71BM and processed from mixed solvents of toluene and ODCB in a ratio of 9:1. Decreasing the content of ODCB makes device processing more compatible with the environment for large scale production, with 10% reduction of photocurrent compared to devices from pure ODCB under optimized conditions. In addition, less variation of photocurrent is obtained in solar cells processed from mixed solvents than from pure ODCB due to varying nanostructure in the blends, which is also critical for production.
|
|
| 41. |
- Wang, Zongtao, et al.
(författare)
-
Shamrock-shaped non-fullerene acceptors enable high-efficiency and high-voltage organic photovoltaics
- 2024
-
Ingår i: Energy and Environmental Sciences. - 1754-5692 .- 1754-5706. ; 17:11, s. 3868-3877
-
Tidskriftsartikel (refereegranskat)abstract
- Minimizing energy loss to increase open-circuit voltage (VOC) is an essential topic to further improve the power conversion efficiency (PCE) in organic photovoltaics (OPVs). Though various molecular strategies have been developed, simultaneously achieving a VOC beyond 1.0 V and maintaining a high PCE above 15% is a huge challenge. Herein, with A-DA ' D-A type banana-shaped nonfullerene acceptor (NFA) Y6 as a benchmark, we creatively design acenaphtho[1,2-b]quinoxaline imide (AQI) as a large A ' unit and synthesize two shamrock-shaped NFAs AQI2 and AQI4, which contain different numbers of fluorine atoms on terminal groups. NFAs containing the AQI units could realize enhanced luminescence, decreased Stoke's shift, and minimized energy loss in OPVs. The conjugation extension in the longitudinal direction affords enlarged dipole moments, resulting in efficient hole transfer and long polaron lifetime. Consequently, the D18:AQI2-based devices obtained a PCE of 16.48% with an impressive VOC of 1.00 V, and the D18:AQI4-based devices achieved a higher PCE of 18.02% with a VOC of 0.95 V. A high PCE of 16.48% with a VOC of 1.0 V has been realized for the first time. Our work introduces an effective molecular design strategy and demonstrates that shamrock-shaped NFAs can be a class of promising materials for high-performance OPVs with high voltage. We developed two shamrock-shaped NFAs, AQI2 and AQI4. D18:AQI2 achieved a PCE of 16.48% with a VOC of 1.00 V, and D18:AQI4 achieved a higher PCE of 18.02% with a VOC of 0.95 V due to decreased energy loss and efficient photon utilization.
|
|
| 42. |
- Wu, Jingnan, et al.
(författare)
-
Carboxylate substituted pyrazine: A simple and low-cost building block for novel wide bandgap polymer donor enables 15.3% efficiency in organic solar cells
- 2021
-
Ingår i: Nano Energy. - : Elsevier BV. - 2211-2855. ; 82
-
Tidskriftsartikel (refereegranskat)abstract
- In addition to high power conversion efficiency (PCE) and good stability, the low-cost of photovoltaic materials is also very important for the practical application of organic solar cells (OSCs). Herein, we synthesized a carboxylate substituted pyrazine-based electron-deficient building block (DTCPz) with a simple structure and low synthetic cost, and then developed a novel wide bandgap polymer donor PFBCPZ. Due to the synergistic electron-withdrawing effects of the fluorination in donor unit (BDT-TF) and esterification and C=N double-bond in DTCPz unit, PFBCPZ shows a deeper HOMO level of −5.60 eV, a strong intermolecular π-π interaction, good crystallinity and stacking, and high hole-mobility of 2.11 × 10−3 cm2 V−1 s−1. Matched with a low bandgap acceptor IT-4F, excellent charge transfer, weak recombination, and small non-radiative energy loss in OSCs was achieved, resulting in an impressive fill factor of 0.785 and a high open-circuit voltage of 0.92 V. As a result, a PCE of up to 15.3% is obtained in OSCs, which is the highest value in the IT-4F-based binary OSCs so far and indicates that low-cost DTCPz with a simple structure is a promising building block to construct high-performance polymer donors for application in efficient OSCs.
|
|
| 43. |
- Xia, Yuxin, et al.
(författare)
-
Inverted all-polymer solar cells based on a quinoxaline-thiophene/naphthalene-diimide polymer blend improved by annealing
- 2016
-
Ingår i: Journal of Materials Chemistry A. - : Royal Society of Chemistry (RSC). - 2050-7488 .- 2050-7496. ; 4:10, s. 3835-3843
-
Tidskriftsartikel (refereegranskat)abstract
- We have investigated the effect of thermal annealing on the photovoltaic parameters of all-polymer solar cells based on a quinoxaline-thiophene donor polymer (TQ1) and a naphthalene diimide acceptor polymer (N2200). The annealed devices show a doubled power conversion efficiency compared to nonannealed devices, due to the higher short-circuit current (J(sc)) and fill factor (FF), but with a lower open circuit voltage (V-oc). On the basis of the morphology-mobility examination by several scanning force microscopy techniques, and by grazing-incidence wide-angle X-ray scattering, we conclude that better charge transport is achieved by higher order and better interconnected networks of the bulk heterojunction in the annealed active layers. The annealing improves charge transport and extends the conjugation length of the polymers, which do help in charge generation and meanwhile reduce recombination. Photoluminescence, electroluminescence, and light intensity dependence measurements reveal how this morphological change affects charge generation and recombination. As a result, the J(sc) and FF are significantly improved. However, the smaller band gap and the higher HOMO level of TQ1 upon annealing causes a lower V-oc. The blend of an amorphous polymer TQ1, and a semi-crystalline polymer N2200, can thus be modified by thermal annealing to double the power conversion efficiency.
|
|
| 44. |
- Xia, Y. X., et al.
(författare)
-
Pyramid shape of polymer solar cells: a simple solution to triple efficiency
- 2013
-
Ingår i: Journal of Physics D: Applied Physics. - : IOP Publishing. - 1361-6463 .- 0022-3727. ; 46:30
-
Tidskriftsartikel (refereegranskat)abstract
- Pyramid-shaped polymer solar cells fabricated on flexible substrates were investigated. Effective light trapping can be realized due to light reflection in all 360 degrees directions, and 100% space utilization is achieved when assembled into arrays. The power conversion efficiency is enhanced by 200% ([60] PCBM as the acceptor) and 260% ([70] PCBM as the acceptor) with a dihedral angle of 30 degrees between the opposite sides of the pyramid compared with a planar device, and a high V-oc of 3.5 V in series connection is obtained. Considering the material utilization, an angle of 90 degrees for pyramid-shaped polymer solar cells is proposed. Pyramid-shaped polymer solar cells are particularly suitable for installation on roof of vehicles and houses, which have limited surface area.
|
|
| 45. |
- Xiang, Jiale, et al.
(författare)
-
In situ monitoring drying process to disclose the correlation between the molecular weights of a polymer acceptor with a flexible spacer and the performance of all-polymer solar cells
- 2024
-
Ingår i: Journal of Materials Chemistry C. - 2050-7526 .- 2050-7534. ; In Press
-
Tidskriftsartikel (refereegranskat)abstract
- Molecular weight (Mn) and conjugation of polymers can profoundly influence the performance of all-polymer solar cells (all-PSCs) via nanostructures of bulk heterojunctions (BHJs). To study the correlation between Mn and the performance of all-PSCs based on an acceptor with a flexible conjugation-break spacer (FCBS), three batches of acceptors, named PYTS, were synthesized with different number-average Mn from 9, 13 to 19 kDa. Blends with a polymer donor PBDB-T, the all-PSCs based on PYTS with Mn of 9 kDa and 19 kDa, exhibit power conversion efficiencies (PCEs) of 5.99% and 9.43%, respectively, primarily due to the increased short-circuit current density (Jsc) from 13.02 to 18.73 mA cm−2. To disclose the impact of Mn on device performance, dynamics of mixed PBDB-T:PYTS solutions to solid BHJs is studied by monitoring the drying process with home-made in situ multifunctional spectroscopy, which demonstrates that PYTS with Mn of 19 kDa has a longer drying time than the PYTS with Mn of 9 kDa. Prolonged drying of the BHJs with higher Mn PYTS facilitates more tightly packed structures with higher crystallinity. A systematic investigation on the nanostructures of BHJs, charge generation, transport and recombination is carried out with grazing-incidence wide-angle X-ray scattering (GIWAXS), transient absorption spectroscopy (TAS) and characterization of all-PSCs. The results indicate that increased crystallinity in the BHJs benefits exciton dissociation, electron transport, prolonged carrier lifetimes, and decreased non-geminate recombination rate constants in the corresponding devices. Combining the in situ study of drying and the investigation on films and devices provides us a comprehensive understanding of the interplay between Mn, the drying process, the nanostructures of BHJs and device performance. This work not only emphasizes the essential role of Mn in governing the device performance, but also exhibits recorded film formation through the in situ spectroscopy, enabling us to manipulate the nanostructure of BHJs by optimizing Mn of polymers and processing parameters.
|
|
| 46. |
- Xing, Xing, et al.
(författare)
-
The trade-off between electrochromic stability and contrast of a thiophene-Quinoxaline copolymer
- 2017
-
Ingår i: Electrochimica Acta. - : Elsevier BV. - 0013-4686 .- 1873-3859. ; 253, s. 530-535
-
Tidskriftsartikel (refereegranskat)abstract
- The stability of organic electrochromic devices is a crucial issue for their applications. However, until now the degradation mechanism of electrochromic materials are still not fully understood especially for electrochromic conjugated polymers (ECPs). To improve device stability, intensive investigation on the degradation mechanism of ECPs is urgently needed. Here we report our study on the electrochromic degradation in a thiophene-quinoxaline copolymer: poly [2,3-bis-(3-octyloxyphenyl) quinoxaline-5,8diyl- alt-thiophene-2,5-diyl] (TQ1). The results of X-ray photoelectron spectroscopy (XPS), ultraviolet photoelectron spectra (UPS) and UV-vis transmission spectra reveal that there are three main factors during the electrochromic degradation of TQ1. The first one is anion (ClO4-) irreversibly deep trapped, while the second is peroxidation of the thiophene group in TQ1. Both factors reduce the conductivity and electrochromism of TQ1. The third is structural relaxation resulting lager conjugated system of TQ1 molecules in film, which is gradually developed during 400 cycling of CV at a narrow potential range (01 V). When a potential range 0-0.7 V is applied, all three factors are prohibited, no electrochromism degradation is observed anymore, although the contrast becomes smaller. Our investigation systematically discloses the degradation mechanism during the electrochemistry processing of a ECP (TQ1), demonstrating the significance of trade-off between the electrochromic stability and contrast of the ECP.
|
|
| 47. |
- Xu, Husen, et al.
(författare)
-
Synergistically boosting performances of organic solar cells from dithieno[3,2-b]benzo[1,2-b;4,5-b′]dithiophene-based copolymers via side chain engineering and radical polymer additives
- 2024
-
Ingår i: Journal of Materials Chemistry C. - 2050-7526 .- 2050-7534. ; 12:10, s. 3644-3653
-
Tidskriftsartikel (refereegranskat)abstract
- As a notable analogue of benzo[1,2-b:4,5-b′]dithiophene (BDT), dithieno[2,3-d:2′,3′-d′]benzo[1,2-b:4,5-b′]dithiophene (DTBDT) is expected to be a more promising building block for polymer photovoltaic donor materials due to its larger coplanar core and extended conjugation length as well as a similar electron donor ability to BDT. However, the performance of organic solar cells (OSCs) from DTBDT-based copolymers is much lower than that of OSCs from BDT-based copolymers, which is attributed to the higher voltage loss of the OSCs from DTBDT-based polymers as compared to that from BDT-based polymers. In this study, approaches such as increasing the donor (D) and acceptor (A) spacing by lengthening the side chains of the polymer donors and use of radical conjugated polymer additives are synergistically employed in OSCs from 2-alkyl-3-chlorothiophene flanked DTBDT-alt-1,3-bis(thiophen-2-yl)-5,7-bis(2-ethylhexyl)-4H,8H-benzo[1,2-c:4,5-c′]dithiophene-4,8-dione (BDD) polymers paired with Y6. Compared to the OSCs from the DTBDT-alt-BDD polymer with 2-ethylhexyl side chains (PBDT-Cl) paired with Y6, the power conversion efficiencies (PCEs) of the counterpart OSCs from the DTBDT-alt-BDD polymer with 2-butyloctyl side chains (PDBT-Cl-BO) increased from 12.67% to 14.58%, with a remarkable improvement of the open circuit voltage (VOC). The reduction of non-radiative energy loss of the OSCs from PBDT-Cl-BO:Y6, ascribed to the increase of the DA spacing by lengthening the side chains, is supported through detailed studies such as Fourier-transform photocurrent spectroscopy external quantum efficiency (FTPS-EQE), electroluminescence (EL), electroluminescence external quantum efficiency (EQEEL), and molecular dynamics simulations (MD). Afterwards, the PCEs of the OSCs from the blends of PDBT-Cl-BO:Y6 were further improved from 14.58% to 15.93% with a notable improvement of short circuit densities (JSCs) and fill factors (FFs), along with a small improvement in VOC upon the addition of the radical conjugated polymer GDTA as an additive. For comparison, the PCEs of the OSCs from the blends of PDBT-Cl:Y6 remained almost unchanged upon the addition of GDTA. This work suggests a wise strategy to synergistically utilize side-chain engineering and radical conjugated polymer additives to reduce the non-radiative energy loss, thus improving the performance of OSCs from DTBDT-based polymer donors.
|
|
| 48. |
- Xu, Xiaofeng, 1984, et al.
(författare)
-
Pyrrolo[3,4-g]quinoxaline-6,8-dione-based conjugated copolymers for bulk heterojunction solar cells with high photovoltages
- 2015
-
Ingår i: Polymer Chemistry. - : ROYAL SOC CHEMISTRY. - 1759-9954 .- 1759-9962. ; 6:25, s. 4624-4633
-
Tidskriftsartikel (refereegranskat)abstract
- A new electron-deficient building block 5,9-di(thiophen-2-yl)-6H-pyrrolo[3,4-g]quinoxaline-6,8(7H)-dione (PQD) was synthesized via functionalizing the 6- and 7-positions of quinoxaline (Qx) with a dicarboxylic imide moiety. Side chain substitution on the PQD unit leads to good solubility which enables very high molecular weight copolymers to be attained. The fusion of two strong electron-withdrawing groups (Qx and dicarboxylic imide) makes the PQD unit a stronger electron-deficient moiety than if the unit had just one electron-withdrawing group, thus enhancing the intramolecular charge transfer between electron-rich and deficient units of the copolymer. Four PQD-based polymers were synthesized which feature deep-lying highest occupied molecular orbital (HOMO) levels and bathochromic absorption spectra when compared to PBDT-Qx and PBDT-TPD analogues. The copolymers incorporated with benzo[1,2-b:4,5-b]dithiophene (BDT) units show that the 1D and 2D structural variations of the side groups on the BDT unit are correlated with the device performance. As a result, the corresponding solar cells (ITO/PEDOT:PSS/polymer: PC71BM/LiF/Al) based on the four copolymers feature very high open-circuit voltages (V-oc) of around 1.0 V. The copolymer PBDT-PQD1 attains the best power conversion efficiency of 4.9%, owing to its relatively high absorption intensity and suitable film morphology. The structure-property correlation demonstrates that the new PQD unit is a promising electron-deficient building block for efficient photovoltaic materials with high V-oc.
|
|
| 49. |
|
|
| 50. |
- Zhuang, Wenliu, 1979, et al.
(författare)
-
Synthesis and Electronic Properties of Diketopyrrolopyrrole-Based Polymers with and without Ring-Fusion
- 2021
-
Ingår i: Macromolecules. - : American Chemical Society (ACS). - 0024-9297 .- 1520-5835. ; 54:2, s. 970-980
-
Tidskriftsartikel (refereegranskat)abstract
- Diketopyrrolopyrroles (DPP) have been recognized as a promising acceptor unit for construction of semiconducting donor-acceptor (D-A) polymers, which are typically flanked by spacers such as thiophene rings via a carbon-carbon single bond formation. It may suffer from a decrease in the coplanarity of the molecules especially when bulky side chains are installed. In this work, the two N atoms in the DPP unit are further fused with C-3 of the two flanking thiophene rings, yielding a p-expanded, very planar fused-ring building block (DPPFu). A novel DPPFu-based D-A copolymer (PBDTT-DPPFu) was successfully synthesized, consisting of a benzo[1,2-b:4,5-b]dithiophene (BDTT) unit as a donor and a DPPFu unit as an acceptor. For comparison, the unfused DPP-based counterpart PBDTT-DPP was also synthesized. Two dodecyl alkyl chains were attached to thiophene rings of DPP moieties to ensure good solubility of the DPPFu-based polymer. The influence of the ring-fusion effect on their structure, photophysical properties, electronic properties, molecular packing, and charge transport properties is investigated. Ring-fusion enhances the intermolecular interactions of PBDTT-DPPFu polymer chains as indicated by density functional theory calculation and analysis of electrostatic potential and van der Waals potential and results in significantly improved molecular packing for both the in-plane and out-of-plane directions as suggested by X-ray measurements. Finally, we correlate the molecular packing to the device performance by fabricating field-effect transistors based on these two polymers. The charge carrier mobility of the ring-fused polymer PBDTT-DPPFu is significantly higher as compared to the PBDTT-DPP polymer without ring-fusion, although PBDTT-DPPFu exhibited a much lower number-average molecular weight of 17 kDa as compared to PBDTT-DPP with a molecular weight of 108 kDa. The results from our comparative study provide a robust way to increase the interchain interaction by ring-fusion-promoted coplanarity.
|
|
