| 1. |
- Guo, Xuewen, et al.
(författare)
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Understanding the effect of N2200 on performance of J71 : ITIC bulk heterojunction in ternary non-fullerene solar cells
- 2019
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Ingår i: Organic electronics. - : Elsevier. - 1566-1199 .- 1878-5530. ; 71, s. 65-71
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Tidskriftsartikel (refereegranskat)abstract
- None-fullerene solar cells with ternary architecture have attracted much attention because it is an effective approach for boosting the device power conversion efficiency. Here, the crystalline polymer N2200 as the third component is integrated into J71: ITIC bulk heterojunction. A series of characterizations indicate that N2200 could increase photo-harvesting, balanced hole and electron mobilities, enhanced exciton dissociation, and suppressed charge recombination, which result in the comprehensive improvement of open circuit voltage, short circuit current and fill factor in the device. Moreover, after introduction of N2200, the morphology of the ternary active layer is optimized, and the film crystallinity is improved. This work demonstrates that adding a small quantity of high crystallization acceptor into non-fullerene donor: acceptor mixture is a promising strategy toward developing high-performance organic solar cells.
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| 2. |
- Jiang, Sheng, et al.
(författare)
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Constructing Chromium Multioxide Hole-Selective Heterojunction for High-Performance Perovskite Solar Cells
- 2022
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Ingår i: Advanced Science. - : Wiley. - 2198-3844. ; 9:30
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Tidskriftsartikel (refereegranskat)abstract
- Perovskite solar cells (PSCs) suffer from significant nonradiative recombination at perovskite/charge transport layer heterojunction, seriously limiting their power conversion efficiencies. Herein, solution-processed chromium multioxide (CrOx) is judiciously selected to construct a MAPbI(3)/CrOx/Spiro-OMeTAD hole-selective heterojunction. It is demonstrated that the inserted CrOx not only effectively reduces defect sites via redox shuttle at perovskite contact, but also decreases valence band maximum (VBM)-HOMO offset between perovskite and Spiro-OMeTAD. This will diminish thermionic losses for collecting holes and thus promote charge transport across the heterojunction, suppressing both defect-assisted recombination and interface carrier recombination. As a result, a remarkable improvement of 21.21% efficiency with excellent device stability is achieved compared to 18.46% of the control device, which is among the highest efficiencies for polycrystalline MAPbI(3) based n-i-p planar PSCs reported to date. These findings of this work provide new insights into novel charge-selective heterojunctions for further enhancing efficiency and stability of PSCs.
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| 3. |
- Jiang, Sheng, et al.
(författare)
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In Situ Reconstruction of Hole-Selective Perovskite Heterojunction with Graded Energetics Toward Highly Efficient and Stable Solar Cells
- 2023
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Ingår i: Advanced Energy Materials. - : WILEY-V C H VERLAG GMBH. - 1614-6832 .- 1614-6840. ; 13:27
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Tidskriftsartikel (refereegranskat)abstract
- Perovskite solar cells (PSCs) have demonstrated a high power conversion efficiency, however, the large energy loss due to non-radiative recombination is the main challenge for further performance enhancement. Here, a surface treatment strategy is developed by heat-induced decomposition of a thin interlayer 2,7-Naphthaleneditriflate (NAP) to in situ reconstruct perovskite energetics. It is verified that the reconstructed perovskite surface energetics match better with the upper hole transport layer compared to the intrinsic condition. Spontaneous generation of n/n(-) homojunctions between the perovskite film bulk and the surface region promotes hole extraction, enhancing built-in electric field, and thus significantly suppresses charge recombination at such perovskite hole-selective heterojunctions. Moreover, the surface decomposed fluorine-rich complexes passivate the defects and improve the crystallinity of the perovskite film. These advantages are confirmed by a remarkably improved efficiency from 20.52% for the control device to 23.37% for the treated one with excellent stability. The work provides a promising approach of in situ reconstructing perovskite surface and interface for the design of highly efficient and stable PSCs.
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| 4. |
- Xiao, Wei, et al.
(författare)
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Exploring Red, Green, and Blue Light-Activated Degradation of Perovskite Films and Solar Cells for Near Space Applications
- 2020
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Ingår i: Solar RRL. - : Wiley-VCH Verlagsgesellschaft. - 2367-198X. ; 4:3
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Tidskriftsartikel (refereegranskat)abstract
- Hybrid perovskite solar cells with a high specific power have great potential to become promising power sources mounted on spacecrafts in space applications. However, there is a lack of study on their photostability as light absorbers in those conditions. Herein, the stability of the perovskite films and solar cells under red, green, and blue (RGB) light illumination in medium vacuum that belongs to near space is explored. The perovskite active layers exhibit different degradations from morphological, chemical, and structural points of view. This is attributed to the strong coupling between photoexcited carriers and the crystal lattice and the diversity of RGB light absorption in the perovskite films. Device characterizations reveal that the efficiency loss of perovskite solar cells results from not only perovskite degradation, but also the photoexcited carriers reducing the energy barrier of ion migration and accelerating the migration to generate more deep-level trap defects. Moreover, comparative devices suggest that the well encapsulation can weaken the effect of vacuum on stability.
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| 5. |
- Xiong, Shaobing, et al.
(författare)
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Additive-Induced Synergies of Defect Passivation and Energetic Modification toward Highly Efficient Perovskite Solar Cells
- 2021
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Ingår i: Advanced Energy Materials. - : WILEY-V C H VERLAG GMBH. - 1614-6832 .- 1614-6840. ; 11:29
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Tidskriftsartikel (refereegranskat)abstract
- Defect passivation via additive and energetic modification via interface engineering are two effective strategies for achieving high-performance perovskite solar cells (PSCs). Here, the synergies of pentafluorophenyl acrylate when used as additive, in which it not only passivates surface defect states but also simultaneously modifies the energetics at the perovskite/Spiro-OMeTAD interface to promote charge transport, are shown. The additive-induced synergy effect significantly suppresses both defect-assisted recombination and interface carrier recombination, resulting in a device efficiency of 22.42% and an open-circuit voltage of 1.193 V with excellent device stability. The two photovoltaic parameters are among the highest values for polycrystalline CsFormamidinium/Methylammonium (FAMA)/FAMA based n-i-p structural PSCs using low-cost silver electrodes reported to date. The findings provide a promising approach by choosing the dual functional additive to enhance efficiency and stability of PSCs.
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| 6. |
- Xiong, Shaobing, et al.
(författare)
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Defect passivation by nontoxic biomaterial yields 21% efficiency perovskite solar cells
- 2021
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Ingår i: Journal of Energy Challenges and Mechanics. - : ELSEVIER. - 2056-9386. ; 55, s. 265-271
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Tidskriftsartikel (refereegranskat)abstract
- Defect passivation is one of the most important strategies to boost both the efficiency and stability of perovskite solar cells (PSCs). Here, nontoxic and sustainable forest-based biomaterial, betulin, is first introduced into perovskites. The experiments and calculations reveal that betulin can effectively passivate the uncoordinated lead ions in perovskites via sharing the lone pair electrons of hydroxyl group, promoting charge transport. As a result, the power conversion efficiencies of the p-i-n planar PSCs remarkably increase from 19.14% to 21.15%, with the improvement of other parameters. The hydrogen bonds of betulin lock methylamine and halogen ions along the grain boundaries and on the film surface and thus suppress ion migration, further stabilizing perovskite crystal structures. These positive effects enable the PSCs to maintain 90% of the initial efficiency after 30 days in ambient air with 60%+/- 5% relative humidity, 75% after 300 h aging at 85 degrees C, and 55% after 250 h light soaking, respectively. This work opens a new pathway for using nontoxic and low-cost biomaterials from forest to make highly efficient and stable PSCs. (C) 2020 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by ELSEVIER B.V. and Science Press. All rights reserved.
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| 7. |
- Xiong, Shaobing, et al.
(författare)
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Defect-Passivation Using Organic Dyes for Enhanced Efficiency and Stability of Perovskite Solar Cells
- 2020
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Ingår i: Solar RRL. - : WILEY-V C H VERLAG GMBH. - 2367-198X. ; 4:5
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Tidskriftsartikel (refereegranskat)abstract
- Perovskite solar cells are a highly competitive candidate for next-generation photovoltaic technology. Defects in the perovskite grain boundaries and on the film surfaces however have significant impacts on both the device efficiency and environmental stability. Herein, a strategy using organic dyes as additives to passivate the defect states and produce more n-type perovskite films, thereby improving charge transport and decreasing charge recombination, is reported. Based on this strategy, the power conversion efficiency of the perovskite solar cell is significantly increased from 18.13% to 20.18% with a negligible hysteresis. Furthermore, the rich hydrogen bonds and carbonyl structures in the organic dye can significantly enhance device stability both in terms of humidity and thermal stress. The results present a promising pathway using abundant and colorful organic dyes as additives to achieve high-performance perovskite solar cells.
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| 8. |
- Xiong, Shaobing, et al.
(författare)
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Direct Observation on p- to n-Type Transformation of Perovskite Surface Region during Defect Passivation Driving High Photovoltaic Efficiency
- 2021
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Ingår i: Joule. - : CELL PRESS. - 2542-4351. ; 5:2, s. 467-480
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Tidskriftsartikel (refereegranskat)abstract
- Perovskite solar cells (PSCs) suffer from significant nonradiative recombination, limiting their power conversion efficiencies. Here, for the first time, we directly observe a complete transformation of perovskite MAPbI(3) surface region energetics from p- to n-type during defect passivation caused by natural additive capsaicin, attributed to the spontaneous formation of a p-n homojunction in perovskite active layer. We demonstrate that the p-n homojunction locates at similar to 100 nm below perovskite surface. The energetics transformation and defect passivation promote charge transport in bulk perovskite layer and at perovskite/PCBM interface, suppressing both defect-assisted recombination and interface carrier recombination. As a result, an efficiency of 21.88% and a fill factor of 83.81% with excellent device stability are achieved, both values are the highest records for polycrystalline MAPbI(3) based p-i-n PSCs reported to date. The proposed new concept of synergetic defect passivation and energetic modification via additive provides a huge potential for further improvement of PSC performance.
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| 9. |
- Xiong, Shaobing, et al.
(författare)
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Engineering of the Back Contact between PCBM and Metal Electrode for Planar Perovskite Solar Cells with Enhanced Efficiency and Stability
- 2019
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Ingår i: Advanced Optical Materials. - : WILEY-V C H VERLAG GMBH. - 2162-7568 .- 2195-1071. ; 7:19
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Tidskriftsartikel (refereegranskat)abstract
- The cathode interface plays a critical role in achieving high-performance fullerene/perovskite planar solar cells. Herein, the simple molecule Isatin and its derivatives are introduced at the back contact [6,6]-phenyl-C61-butyric acid methyl ester (PCBM)/Al as a cathode modification interlayer. It is revealed that the Isatin interlayers facilitate electron transport/extraction and suppress electron recombination, attributed to the formation of negative dipole potential steps and the passivation of the interfacial trap density. The average power conversion efficiencies of the resulting devices are significantly improved by 11% from 17.68% to 19.74%, with an enhancement in all device parameters including short-circuit current, open-circuit voltage, and fill factor. The hysteresis index is found to disappear. In addition, such interlayer enhances device stability under ambient conditions compared to the control devices due to suppression of moisture-induced degradation of the perovskite films. These findings provide a comprehensive understanding of the engineering of the back contact between PCBM and the metal electrode to improve efficiency and stability of perovskite solar cells.
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| 10. |
- Xiong, Shaobing, et al.
(författare)
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Revealing buried heterointerface energetics towards highly efficient perovskite solar cells
- 2023
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Ingår i: Nano Energy. - : ELSEVIER. - 2211-2855 .- 2211-3282. ; 109
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Tidskriftsartikel (refereegranskat)abstract
- The heterointerfaces of charge-selective contacts are crucial in determining efficiency and stability of perovskite optoelectronic devices, where the fundamental knowledge of the buried heterointerface between perovskite and bottom charge transport layer is less well understood compared to the top interface. Herein, we systematically investigate the energetics at the perovskite/SnO2 buried heterointerface for an n-i-p perovskite solar cell (PSC) and the perovskite/PEDOT:PSS buried heterointerface for a p-i-n one, respectively. In contrast to previous cognitions, we discover a perovskite transition phase at the buried interface region that originates from the chemical bonding interaction with the bottom charge transport layer. The transition phase causes an energy level barrier and induces defects, impeding charge transport across the heterointerface. These detrimental effects trigger significant nonradiative recombination and limit the attainable device photovoltage. We then develop the energetic models that describe such buried heterointerfaces. Moreover, we further test the proposed model -derived mechanisms via inserting a thin polyvinyl alcohol layer into the buried heterointerfaces of the de-vices. We demonstrate that chemical interactions and formation of the perovskite transition phase at the buried heterointerface thereby are fully restrained, leading to a diminished electron extraction barrier and improved charge transport. As a result, significant increases in open-circuit voltage and fill factor of the devices are ach-ieved. These results will help guide future efforts on developing suitable buried heterointerfaces for superior performance of perovskite optoelectronics.
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