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- 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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| 3. |
- Yang, Jianming, et al.
(författare)
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Energetics and Energy Loss in 2D Ruddlesden-Popper Perovskite Solar Cells
- 2020
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Ingår i: Advanced Energy Materials. - : WILEY-V C H VERLAG GMBH. - 1614-6832 .- 1614-6840. ; 10:23
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Tidskriftsartikel (refereegranskat)abstract
- 2D Ruddlesden-Popper perovskites (RPPs) are emerging as potential challengers to their 3D counterpart due to superior stability and competitive efficiency. However, the fundamental questions on energetics of the 2D RPPs are not well understood. Here, the energetics at (PEA)(2)(MA)(n)-1PbnI3n+1/[6,6]-phenyl-C61-butyric acid methyl ester (PCBM) interfaces with varying n values of 1, 3, 5, 40, and infinity are systematically investigated. It is found that n-n junctions form at the 2D RPP interfaces (n = 3, 5, and 40), instead of p-n junctions in the pure 2D and 3D scenarios (n = 1 and infinity). The potential gradient across phenethylammonium iodide ligands that significantly decreases surface work function, promotes separation of the photogenerated charge carriers with electron transferring from perovskite crystal to ligand at the interface, reducing charge recombination, which contributes to the smallest energy loss and the highest open-circuit voltage (V-oc) in the perovskite solar cells (PSCs) based on the 2D RPP (n = 5)/PCBM. The mechanism is further verified by inserting a thin 2D RPP capping layer between pure 3D perovskite and PCBM in PSCs, causing the V-oc to evidently increase by 94 mV. Capacitance-voltage measurements with Mott-Schottky analysis demonstrate that such V-oc improvement is attributed to the enhanced potential at the interface.
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