| 1. |
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| 2. |
- Almora, Osbel, et al.
(författare)
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Device Performance of Emerging Photovoltaic Materials (Version 1)
- 2020
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Ingår i: Advanced Energy Materials. - : Wiley. - 1614-6832 .- 1614-6840. ; 11:11
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Tidskriftsartikel (refereegranskat)abstract
- Emerging photovoltaics (PVs) focus on a variety of applications complementing large scale electricity generation. Organic, dye-sensitized, and some perovskite solar cells are considered in building integration, greenhouses, wearable, and indoor applications, thereby motivating research on flexible, transparent, semitransparent, and multi-junction PVs. Nevertheless, it can be very time consuming to find or develop an up-to-date overview of the state-of-the-art performance for these systems and applications. Two important resources for recording research cells efficiencies are the National Renewable Energy Laboratory chart and the efficiency tables compiled biannually by Martin Green and colleagues. Both publications provide an effective coverage over the established technologies, bridging research and industry. An alternative approach is proposed here summarizing the best reports in the diverse research subjects for emerging PVs. Best performance parameters are provided as a function of the photovoltaic bandgap energy for each technology and application, and are put into perspective using, e.g., the Shockley–Queisser limit. In all cases, the reported data correspond to published and/or properly described certified results, with enough details provided for prospective data reproduction. Additionally, the stability test energy yield is included as an analysis parameter among state-of-the-art emerging PVs.
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| 3. |
- Benavides, Cindy Montenegro, et al.
(författare)
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High-Performance Organic Photodetectors from a High-Bandgap Indacenodithiophene-Based π-Conjugated Donor-Acceptor Polymer
- 2018
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Ingår i: ACS Applied Materials & Interfaces. - : American Chemical Society (ACS). - 1944-8252 .- 1944-8244. ; 10:15, s. 12937-12946
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Tidskriftsartikel (refereegranskat)abstract
- A conjugated donor-acceptor polymer, poly[4,4,9,9-tetrakis(4-hexylphenyl)-4,9-dihydro-s-indaceno[1,2-b:5,6-b′]dithiophene-2,7-diyl-alt-5-(2-ethylhexyl)-4H-thieno[3,4-c] pyrrole-4,6(5H)-dione-1,3-diyl] (PIDT-TPD), is blended with the fullerene derivative [6,6] phenyl-C61-butyric acid methyl ester (PC 61 BM) for the fabrication of thin and solution-processed organic photodetectors (OPDs). Systematic screening of the concentration ratio of the blend and the molecular weight of the polymer is performed to optimize the active layer morphology and the OPD performance. The device comprising a medium molecular weight polymer (27.0 kg/mol) in a PIDT-TPD:PC 61 BM 1:1 ratio exhibits an external quantum efficiency of 52% at 610 nm, a dark current density of 1 nA/cm 2 , a detectivity of 1.44 × 10 13 Jones, and a maximum 3 dB cutoff frequency of 100 kHz at -5 V bias. These results are remarkable among the state-of-the-art red photodetectors based on conjugated polymers. As such, this work presents a functional organic active material for high-speed OPDs with a linear photoresponse at different light intensities.
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| 4. |
- Chen, Haiwei, et al.
(författare)
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Extending the environmental lifetime of unpackaged perovskite solar cells through interfacial design
- 2016
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Ingår i: Journal of Materials Chemistry A. - : Royal Society of Chemistry (RSC). - 2050-7488 .- 2050-7496. ; 4:30, s. 11604-11610
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Tidskriftsartikel (refereegranskat)abstract
- Solution-processed oxo-functionalized graphene (oxo-G1) is employed to substitute hydrophilic PEDOT:PSS as an anode interfacial layer for perovskite solar cells. The resulting devices exhibit a reasonably high power conversion efficiency (PCE) of 15.2% in the planar inverted architecture with oxo-G1 as a hole transporting material (HTM), and most importantly, deploy the full open-circuit voltage (Voc) of up to 1.1 V. Moreover, oxo-G1 effectively slows down the ingress of water vapor into the device stack resulting in significantly enhanced environmental stability of unpackaged cells under illumination with 80% of the initial PCE being reached after 500 h. Without encapsulation, ∼60% of the initial PCE is retained after ∼1000 h of light soaking under 0.5 sun and ambient conditions maintaining the temperature beneath 30 °C. Moreover, the unsealed perovskite device retains 92% of its initial PCE after about 1900 h under ambient conditions and in the dark. Our results underpin that controlling water diffusion into perovskite cells through advanced interface engineering is a crucial step towards prolonged environmental stability.
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| 5. |
- Hu, Wei, et al.
(författare)
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Axisymmetric and Asymmetric Naphthalene-Bisthienothiophene Based Nonfullerene Acceptors: On Constitutional Isomerization and Photovoltaic Performance
- 2020
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Ingår i: ACS Applied Energy Materials. - : American Chemical Society (ACS). - 2574-0962. ; 3:6, s. 5734-5744
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Tidskriftsartikel (refereegranskat)abstract
- Two pairs of constitutional isomers of fused-octacyclic nonfullerene acceptors (NFAs) based on a naphthalene-bisthienothiophene core with or without fluorination at the ending groups have been developed. Compared with the axisymmetric NFAs N66-IC and N66-2FIC with two six-member-ring bridges, their asymmetric constitutional isomers N65-IC and N65-2FIC both with one six-member-ring bridge and one five-member-ring bridge exhibit remarkable red-shifted absorption, higher crystallinity, and slightly down-shifted LUMO energy levels. Organic solar cells based on PBDB-T-2F:N65-2FIC achieved a promising power conversion efficiency of 10.19%, which is three times higher than that of its counterpart PBDB-T-2F:N66-2FIC cell (3.46%). While being blended with PBDB-T as the donor material, the asymmetric acceptor analogue N65-IC based solar cell pronounces a PCE of 9.03%, being significantly improved from that of 5.45% for the PBDB-T:N66-IC based cell, which is in consistency with the results from those cells from their both fluorinated donor and acceptor counterparts. Design rules on either both fluorinated, both nonfluorinated, or cross-combined donor/acceptors for device fabrication has been explored. In addition, PBDB-T-2F:N65-2FIC possesses very promising device stability with 85% of its initial PCE after an exposure time of 1500 h under one sun illumination, which is meaningful for their future commercial devices.
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| 6. |
- Liu, Shungang, et al.
(författare)
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The role of connectivity in significant bandgap narrowing for fused-pyrene based non-fullerene acceptors toward high-efficiency organic solar cells
- 2020
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Ingår i: Journal of Materials Chemistry A. - : Royal Society of Chemistry (RSC). - 2050-7488 .- 2050-7496. ; 8:12, s. 5995-6003
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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.
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| 7. |
- Liu, Yanfeng, 1992-
(författare)
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Studying Morphology Formation and Charge Separation in Organic Solar Cells
- 2021
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- We are currently living in the era of automation and artificial intelligence, which requires more energy than ever before. Meanwhile, the reduction of carbon footprint is needed for keeping the environment sustainable. Exploring green energy is crucial. Solar power is one of the green energy sources. The apparatus that converts solar energy to electricity is a solar cell. Organic solar cells (OSCs), employing organic materials absorbing solar radiation and converting to electricity have got extensive attention in the last decades due to their unique advantages like lightweight, semi-transparency, and potential industrialization. In most cases, an OSC composes of two different organic semiconductors as electron donor and acceptor to form a photoactive layer with a bulk heterojunction (BHJ) structure, and sandwiched between the electron and hole transport layers and then two electrodes. The morphology of the BHJ plays a crucial role in the device's performance, and it is a result of a complicated interplay between donor, acceptor, and solvent during the film drying from a solution. Thus, in-situ monitoring the film drying during solvent evaporation could deepen understanding of the mechanism of the morphology formation. A versatile multiple spectroscopic setup is assembled for this purpose, which can record laser scattering, steady-state photoluminescence (PL), time-resolved photoluminescence (TRPL), and white-light absorption during film formation. By comparing the drying dynamics of three different blend systems with their corresponding pristine films, we find that the blend film formation and its final morphology are more dominated by the component with a higher molecular weight. Different PL and TRPL quenching profiles between fullerene- and non-fullerene-based systems provide hints about different donor-acceptor interactions. Moreover, with the help of TRPL, the relative change of quantum yield during film formation can be calculated. Besides, this setup is also proved suitable for studying mechanisms behind device optimization processes, like the usage of solvent additives. One of the unique features of OSCs based on non-fullerene acceptors is the highly efficient hole transfer from the acceptor to the donor, sometimes even under zero or negative energetic offsets. However, in these cases the mechanism of hole transfer has not been fully understood. By studying hole transfer at the donor:acceptor interface in different material systems and device configurations, we highlight the role of electric field on the charge separation of OSCs when energetic offsets are not enough. To achieve better device performance, engineering the photoelectric properties of interfacial layers is equally essential. A good interfacial layer can facilitate carrier extraction and reduce carrier recombination. We demonstrate that adding MXenes into the PEDOT:PSS can increase the conductivity of this composite hole transport layer, without sacrificing its optical transparency and work function.
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| 8. |
- Murto, Petri Henrik, 1984, et al.
(författare)
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High performance all-polymer photodetector comprising a donor-Acceptor-Acceptor structured indacenodithiophene-bithieno[3,4-c] pyrroletetrone copolymer
- 2018
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Ingår i: ACS Macro Letters. - : American Chemical Society (ACS). - 2161-1653. ; 7:4, s. 395-400
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Tidskriftsartikel (refereegranskat)abstract
- The synthesis of an acceptor polymer PIDT-2TPD, comprising indacenodithiophene (IDT) as the electron-rich unit and an interconnected bithieno[3,4-c]pyrrole-4,4′,6,6′-Tetrone (2TPD) as the electron-deficient unit, and its application for all-polymer photodetectors is reported. The optical, electrochemical, charge transport, and device properties of a blend of poly(3-hexylthiophene) and PIDT-2TPD are studied. The blend shows strong complementary absorption and balanced electron and hole mobility, which are desired properties for a photoactive layer. The device exhibits dark current density in the order of 10 -5 mA/cm 2 , external quantum efficiency broadly above 30%, and nearly planar detectivity over the entire visible spectral range (maximum of 1.1 × 10 12 Jones at 610 nm) under-5 V bias. These results indicate that PIDT-2TPD is a highly functional new type of acceptor and further motivate the use of 2TPD as a building block for other n-Type materials.
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| 9. |
- Wachsmuth, Josua, et al.
(författare)
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Overcoming Moisture-Induced Degradation in Organic Solar Cells
- 2023
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Ingår i: Advanced Engineering Materials. - : John Wiley & Sons. - 1438-1656 .- 1527-2648. ; , s. 1-7
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Tidskriftsartikel (refereegranskat)abstract
- Unencapsulated organic solar cells are prone to severe performance losses in the presence of moisture. Accelerated damp heat (85 °C/85% RH) studies are presented and it is shown that the hygroscopic hole-transporting PEDOT:PSS layer is the origin of device failure in the case of prototypical inverted solar cells. Complementary measurements unveil that under these conditions a decreased PEDOT:PSS work function along with areas of reduced electrical contact between active layer and hole-transport layer are the main factors for device degradation rather than a chemical reaction of water with the active layer. Replacements for PEDOT:PSS are explored and it is found that tungsten oxide (WO3) or phosphomolybdic acid (PMA)—materials that can be processed from benign solvents at room temperature—yields comparable performance as PEDOT:PSS and enhances the resilience of solar cells under damp heat. The stability trend follows the order PEDOT:PSS << WO3 < PMA, with PEDOT:PSS-based devices failing after few minutes, while PMA-based devices remain nearly pristine over several hours. PMA is thus proposed as a robust, solution-processable hole extraction layer that can act as a one to one replacement of PEDOT:PSS to achieve organic solar cells with significantly improved longevity.
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| 10. |
- Yu, Jianwei, 1992-
(författare)
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The Influence of Energy Levels on Voltage Losses and Charge Generation in Organic Solar Cells
- 2022
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Organic solar cells (OSCs) are a next-generation photovoltaic technology that convert solar energy to electrical energy. They have attracted great attention due to their advantages of low cost, ease of synthesis, light weight, mechanical flexibility, and roll-to-roll processability. In the past decades, owing to the development of the materials, device optimization and the understanding of the working mechanism, the power conversion efficiency (PCE) has been boosted to ~19%. However, the efficiency of the OSCs is still not comparable to the conventional inorganic solar cells and emerging perovskite solar cells due to the large open-circuit voltage loss (Vloss). In addition, it is also important to obtain efficient charge generation while reducing the Vloss. Thus, understanding the loss mechanisms in the OSCs is significant for achieving further improvement.In this thesis, a novel small-molecule donor named ZR1 was used to fabricate all-small-molecule OSCs (SM-OSCs), which shows efficient charge separation and transport with the optimized hierarchical morphologies, obtaining a breakthrough efficiency of 13.34% with a low Vloss (0.54 eV) in SM-OSCs. In this system, the energy offsets between the donor and acceptor (ΔHOMO or ΔLUMO) play an important role in the open-circuit voltage (VOC) of the OSCs. According to the optoelectronic reciprocity introduced in this thesis, the sub-gap absorption and emission by charge transfer (CT) states lead to large radiative and non-radiative recombination losses. The results show that the decreased HOMO offsets between donor and acceptor can effectively reduce both radiative and non-radiative recombination losses from the CT states, resulting in a suppressed Vloss.In addition to the SM-OSCs, we also study the Vloss and charge generation in the all-polymer OSCs (all- PSCs). A series of polymer acceptors were designed and applied in all-PSCs. In this work, all devices with negligible LUMO offsets show high VOCs of 1.02-1.15 V and good short-circuit currents (JSCs) of 8.87-15.16 mA cm−2 as well as small Vlosss. This study reveals that the small Vloss and the effective charge generation can also be realized simultaneously in all-PSCs with small energy offsets.Next, we found that introducing a third component can also reduce Vloss. In this work, we start with the fundamental photophysical processes which determine the VOCs of the devices and provide a universal approach framework well explaining the VOC of ternary OSCs (TOSCs) in different situations. By combining experimental investigations with theoretical simulations, we highlight the significant influence of the thermal population arising from the guest component-related CT states and local excited (LE)states on the non-radiative recombination losses in TOSCs. Firmly based on our new understanding, we provide design rules for enhancing the VOC in TOSCs: 1) high emission yield for the guest binary system; close charge-transfer energies between two binary systems; 2) high miscibility of the guest component with the low-optical-gap component in the host binary blends.In the all-PSCs work we did before, we find the small Vloss and the effective charge generation can be achieved simultaneously with small energy offsets, which can be also observed in other non-fullerene based OSCs. It was found that some of non-fullerene acceptors based OSCs can realize an efficient charge generation and a suppressed charge recombination process with small energy offsets (< 0.3 eV) between the donor and the acceptor, leading to a low Vloss, a high JSC, and a high fill factor (FF) simultaneously. Here, we investigate a series of OSCs blends with different HOMO offsets between donor and in a large range of ~ 0 to 0.50 eV. Along with decreasing HOMO offsets, the blends show reduced Vlosss. For the JSC and the FF, we observe a maximum value at an optimal energetic offset around 0.2-0.3 eV and the optimal energetic offset appears at different values for different non-fullerene acceptors. Through the analysis of the ultrafast transient absorption, we find inefficient charge generation when the HOMO offset is close to zero, which attributed to the back transfer of a hole from the donor to the acceptor. The affected charge generation at the small HOMO offsets is probably the main reason for the deceased JSC and FF. This study demonstrates the existence of optimal energy offsets for achieving high-performance OSCs.
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