| 1. |
- Li, Yongxi, et al.
(författare)
-
A fused-ring based electron acceptor for efficient non-fullerene polymer solar cells with small HOMO offset
- 2016
-
Ingår i: NANO ENERGY. - : ELSEVIER SCIENCE BV. - 2211-2855. ; 27, s. 430-438
-
Tidskriftsartikel (refereegranskat)abstract
- A non-fullerene electron acceptor bearing a novel backbone with fused 10-heterocyclic ring (in-dacenodithiopheno-indacenodiselenophene), denoted by IDTIDSe-IC is developed for fullerene free polymer solar cells. IDTIDSe-IC exhibits a low band gap (E-g=1.52 eV) and strong absorption in the 600850 nm region. Combining with a large band gap polymer J51 (E-g=1.91 eV) as donor, broad absorption coverage from 300 nm to 800 nm is obtained due to complementary absorption of J51 and IDTIDSe-IC, which enables a high PCE of 8.02% with a V-oc of 0.91 V, a J(SC) of 15.16 mA/cm(2) and a FF of 58.0% in the corresponding PSCs. Moreover, the EQE of 50-65% is achieved in the absorption range of IDTIDSe-IC with only about 0.1 eV HOMO difference between J51 and IDTIDSe-IC. (C) 2016 Elsevier Ltd. All rights reserved.
|
|
| 2. |
- Chen, Youchun, et al.
(författare)
-
Insights into the working mechanism of cathode interlayers in polymer solar cells via [(C8H17)(4)N](4)[SiW12O40]
- 2016
-
Ingår i: Journal of Materials Chemistry A. - : ROYAL SOC CHEMISTRY. - 2050-7488 .- 2050-7496. ; 4:48, s. 19189-19196
-
Tidskriftsartikel (refereegranskat)abstract
- A low-cost (amp;lt;$1 per g), high-yield (amp;gt;90%), alcohol soluble surfactant-encapsulated polyoxometalate complex [(C8H17)(4)N](4)[SiW12O40] has been synthesized and utilized as a cathode interlayer (CIL) in polymer solar cells (PSCs). A power conversion efficiency of 10.1% can be obtained for PSCs based on PTB7-Th (poly[[2,6-4,8-di(5-ethylhexylthienyl) benzo[1,2-b;3,3-b]-dithiophene][3-fluoro-2[(2-ethylhexyl) carbonyl] thieno [3,4-b]-thiophenediyl]]):PC71BM ([6,6]-phenyl C71-butyric acidmethyl ester) due to the incorporation of [(C8H17)(4)N](4)[SiW12O40]. Combined measurements of current density-voltage characteristics, transient photocurrent, charge carrier mobility and capacitance-voltage characteristics demonstrate that [(C8H17)(4)N](4)[SiW12O40] can effectively increase the built-in potential, charge carrier density and mobility and accelerate the charge carrier extraction in PSCs. Most importantly, the mechanism of using [(C8H17)(4)N](4)[SiW12O40] as the CIL is further brought to light by X-ray photoemission spectroscopy (XPS) and ultraviolet photoemission spectroscopy (UPS) of the metal/ [(C8H17)(4)N](4)[SiW12O40] interface. The findings suggest that [(C8H17)(4)N](4)[SiW12O40] not only decreased the work function of the metal cathodes but also was n-doped upon contact with the metals, which provide insights into the working mechanism of the CILs simultaneously improving the open circuit voltage, short circuit current and fill factor in the PSCs.
|
|
| 3. |
- Feng, Guitao, et al.
(författare)
-
“Double-Cable” Conjugated Polymers with Linear Backbone toward High Quantum Efficiencies in Single-Component Polymer Solar Cells
- 2017
-
Ingår i: Journal of the American Chemical Society. - : AMER CHEMICAL SOC. - 0002-7863 .- 1520-5126. ; 139:51, s. 18647-18656
-
Tidskriftsartikel (refereegranskat)abstract
- A series of "double-cable" conjugated polymers were developed for application in efficient single-component polymer solar cells, in which high quantum efficiencies could be achieved due to the optimized nanophase separation between donor and acceptor parts. The new double-cable polymers contain electron-donating poly(benzodithiophene) (BDT) as linear conjugated backbone for hole transport and pendant electron-deficient perylene bisimide (PBI) units for electron transport, connected via a dodecyl linker. Sulfur and fluorine substituents were introduced to tune the energy levels and crystallinity of the conjugated polymers. The double-cable polymers adopt a "face-on" orientation in which the conjugated BDT backbone and the pendant PBI units have a preferential pi-pi stacking direction perpendicular to the substrate, favorable for interchain charge transport normal to the plane. The linear conjugated backbone acts as a scaffold for the crystallization of the PBI groups, to provide a double-cable nanophase separation of donor and acceptor phases. The optimized nanophase separation enables efficient exciton dissociation as well as charge transport as evidenced from the high-up to 80%-internal quantum efficiency for photon-to-electron conversion. In single-component organic solar cells, the double-cable polymers provide power conversion efficiency up to 4.18%. This is one of the highest performances in single-component organic solar cells. The nanophase-separated design can likely be used to achieve high-performance single-component organic solar cells.
|
|
| 4. |
- Pan, W. W., et al.
(författare)
-
Optical properties and band bending of InGaAs/GaAsBi/InGaAs type-II quantum well grown by gas source molecular beam epitaxy
- 2016
-
Ingår i: Journal of Applied Physics. - : AIP Publishing. - 0021-8979 .- 1089-7550. ; 120:10
-
Tidskriftsartikel (refereegranskat)abstract
- Photoluminescence (PL) properties of In0.2Ga0.8As/GaAs0.96Bi0.04/In0.2Ga0.8As quantum well (QW) grown on GaAs substrates by gas source molecular beam epitaxy were studied by varying excitation power and temperature, respectively. The type-II transition energy shifts from 1.149 eV to 1.192 eV when increasing the excitation power from 10 mW to 150 mW at 4.5 K, which was ascribed to the band-bending effect. On the other hand, the type-II PL quenches quickly along with fast redshift with the increasing temperature due to the relaxation of the band bending caused by the thermal excitation process. An 8 band k.p model was used to analyze the electronic properties and the band-bending effect in the type-II QW. The calculated subband levels and transition energy fit well with the experiment results, and two thermal activation energies of 8.7 meV and 50 meV, respectively, are deduced. Published by AIP Publishing.
|
|
| 5. |
- Qian, Deping, et al.
(författare)
-
Design rules for minimizing voltage losses in high-efficiency organic solar cells
- 2018
-
Ingår i: Nature Materials. - : NATURE PUBLISHING GROUP. - 1476-1122 .- 1476-4660. ; 17:8, s. 703-
-
Tidskriftsartikel (refereegranskat)abstract
- The open-circuit voltage of organic solar cells is usually lower than the values achieved in inorganic or perovskite photovoltaic devices with comparable bandgaps. Energy losses during charge separation at the donor-acceptor interface and non-radiative recombination are among the main causes of such voltage losses. Here we combine spectroscopic and quantum-chemistry approaches to identify key rules for minimizing voltage losses: (1) a low energy offset between donor and acceptor molecular states and (2) high photoluminescence yield of the low-gap material in the blend. Following these rules, we present a range of existing and new donor-acceptor systems that combine efficient photocurrent generation with electroluminescence yield up to 0.03%, leading to non-radiative voltage losses as small as 0.21 V. This study provides a rationale to explain and further improve the performance of recently demonstrated high-open-circuit-voltage organic solar cells.
|
|
| 6. |
- Xu, Bo, et al.
(författare)
-
Integrated Design of Organic Hole Transport Materials for Efficient Solid-State Dye-Sensitized Solar Cells
- 2015
-
Ingår i: Advanced Energy Materials. - : Wiley. - 1614-6832 .- 1614-6840. ; 5:3
-
Tidskriftsartikel (refereegranskat)abstract
- A series of triphenylamine-based small molecule organic hole transport materials (HTMs) with low crystallinity and high hole mobility are systematically investigated in solid-state dye-sensitized solar cells (ssDSCs). By using the organic dye LEG4 as a photosensitizer, devices with X3 and X35 as the HTMs exhibit desirable power conversion efficiencies (PCEs) of 5.8% and 5.5%, respectively. These values are slightly higher than the PCE of 5.4% obtained by using the state-of-the-art HTM Spiro-OMeTAD. Meanwhile, transient photovoltage decay measurement is used to gain insight into the complex influences of the HTMs on the performance of devices. The results demonstrate that smaller HTMs induce faster electron recombination in the devices and suggest that the size of a HTM plays a crucial role in device performance, which is reported for the first time.
|
|
| 7. |
- Zheng, Wenhao, et al.
(författare)
-
Dual Function of UV/Ozone Plasma-Treated Polymer in Polymer/Metal Hybrid Electrodes and Semitransparent Polymer Solar Cells
- 2017
-
Ingår i: ACS Applied Materials and Interfaces. - : AMER CHEMICAL SOC. - 1944-8244 .- 1944-8252. ; 9:51, s. 44656-44666
-
Tidskriftsartikel (refereegranskat)abstract
- In this work, high-performance inverted indium tin oxide (ITO)-free semitransparent polymer solar cells are comprehensively investigated using a novel polymer/metal hybrid transparent electrode. The electrical and optical characteristics of hybrid electrodes are significantly enhanced by introducing UV/ozone plasma treatment on the polymer poly[(9,9-bis(3-(N,N-dimethylamino)propyl)-2,7-fluorene)-alt-2,7-(9,9-dioctylfluorene)] (PFN), which is functioned as both a seed layer for ultrathin Ag metal electrode and an optical spacer for transparent devices. The optimized sheet resistance of PFN/Ag (12 nm) hybrid electrode is only half of the commercial ITO (9.4 vs 20.0 Omega sq(-1)) and the high wavelength-dependent reflectance of hybrid electrode helps to increase the ITO-free device short-circuit current density. Furthermore, the interface property between PFN and ultrathin Ag is analyzed in detail and the optical field distribution is calculated for comparison. A high power conversion efficiency of 5.02%, which is increased by 35% compared to that of the ITO-based device, is achieved in the ITO-free semitransparent device in conjunction with an excellent average visible transmittance above 28% that is higher than the benchmark of 25% for power-generating window, indicating its great potential in building integrated photovoltaic systems in the future. Furthermore, the strategy is successfully developed for other polymer systems, suggesting the universal applicability for plastic electronics.
|
|
| 8. |
- Bai, Sai, et al.
(författare)
-
Electrophoretic deposited oxide thin films as charge transporting interlayers for solution-processed optoelectronic devices: the case of ZnO nanocrystals
- 2015
-
Ingår i: RSC Advances. - : Royal Society of Chemistry. - 2046-2069. ; 5:11, s. 8216-8222
-
Tidskriftsartikel (refereegranskat)abstract
- A promising fabrication method of electron transporting interlayers for solution-processed optoelectronic devices by electrophoretic deposition (EPD) of colloidal zinc oxide (ZnO) nanocrystals was demonstrated. A low voltage of 3-5 V and a short deposition time of 40 s at room temperature were found to be sufficient to generate dense and uniform ZnO thin films. The EPD ZnO nanocrystal films were applied as ETLs for inverted organic solar cell and polymer light emitting diodes (PLEDs). By optimizing the EPD processing of ZnO nanocrystal electron transporting layers (ETLs), inverted organic solar cells based on [3,4-b]-thiophene/benzodithiophene (PTB7): [6-6]-phenyl-C71-butyric acid methyl ester (PC71BM) and poly(3-hexylthiophene) (P3HT): [6-6]-phenyl-C-61-butyric acid methyl ester (PC61BM) with an average PCE of 8.4% and 4.0% were fabricated. In combination with the PLEDs and flexible devices results, we conclude that the EPD processed ZnOnanocrystal thin films can serve as high quality ETLs for solution-processed optoelectronic devices.
|
|
| 9. |
- Bai, Sai, et al.
(författare)
-
Ethanedithiol Treatment of Solution-Processed ZnO Thin Films: Controlling the Intragap States of Electron Transporting Interlayers for Efficient and Stable Inverted Organic Photovoltaics
- 2015
-
Ingår i: Advanced Energy Materials. - : Wiley-VCH Verlag. - 1614-6832 .- 1614-6840. ; 5:5, s. 1401606-
-
Tidskriftsartikel (refereegranskat)abstract
- The surface defects of solution-processed ZnO films lead to various intragap states. When the solution-processed ZnO films are used as electron transport interlayers (ETLs) in inverted organic solar cells, the intragap states act as interfacial recombination centers for photogenerated charges and thereby degrade the device performance. Here, a simple passivation method based on ethanedithiol (EDT) treatment is demonstrated, which effectively removes the surface defects of the ZnO nanocrystal films by forming zinc ethanedithiolates. The passivation by EDT treatment modulates the intragap states of the ZnO films and introduces a new intragap band. When the EDT-treated ZnO nanocrystal films are used as ETLs in inverted organic solar cells, both the power conversion efficiency and stability of the devices are improved. The control studies show that the solar cells with EDT-treated ZnO films exhibit reduced charge recombination rates and enhanced charge extraction properties. These features are consistent with the fact that the modulation of the intragap states results in reduction of interfacial recombination as well as the improved charge selectivity and electron transport properties of the ETLs. It is further demonstrated that the EDT treatment-based passivation method can be extended to ZnO films deposited from sol-gel precursors.
|
|
| 10. |
- Gedefaw, Desta Antenehe, 1971, et al.
(författare)
-
An alternating copolymer of fluorene donor and quinoxaline acceptor versus a terpolymer consisting of fluorene, quinoxaline and benzothiadiazole building units: synthesis and characterization
- 2016
-
Ingår i: Polymer Bulletin. - : Springer Science and Business Media LLC. - 0170-0839 .- 1436-2449. ; 73:4, s. 1167-1183
-
Tidskriftsartikel (refereegranskat)abstract
- An alternating polyfluorene copolymer based on fluorene donor and quinoxaline acceptor (P1) and an alternating terpolymer (P2) with fluorene (50 %) donor and quinoxaline (25 %) and benzothiadiazole (25 %) acceptor units were designed and synthesized for use as photoactive materials in solar cells. The presence of benzothiadiazole unit in P2 increased the optical absorption coverage in the range of 350-600 nm, which is an interesting property and a big potential for achieving improved photovoltaic performances with judicious optimization of the devices. Solar cells were fabricated from 1:4 blends of polymers-PCBM[70] using o-dichlorobenzene (o-DCB) as processing solvent, and P1 showed a power conversion efficiency (PCE) of 3.18 %, with a short-circuit current density (J (SC)) of 7.78 mA/cm(2), an open-circuit voltage (V (OC)) of 0.82 V, and a fill factor (FF) of 50 % while P2 showed an overall PCE of 2.14 % with corresponding J (SC) of 5.97 mA/cm(2), V (OC) of 0.84 V and FF of 42 %. In general, P2 gave lower J (SC) and FF presumably due to the fine domain sizes of the polymer-PCBM[70] blend as seen from the atomic force microscopy (AFM) image which might have affected the charge carrier transport. Alternating (P1) and ternary (P2) conjugated polymers were designed, synthesized and used for fabrication of photovoltaic devices.
|
|
