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Please use this identifier to cite or link to this item:
https://tkuir.lib.tku.edu.tw/dspace/handle/987654321/128519
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| Title: | Dual bulk and surface passivation of 3D perovskite solar cells using zwitterionic molecules |
| Authors: | Tseng, Kai-Wei;Chen, Guan-Lin;Chen, Po-Yuan;Hsieh, Hsiao-Chi;Wang, Leeyih |
| Date: | 2025-08 |
| Issue Date: | 2026-03-04 12:05:31 (UTC+8) |
| Publisher: | Elsevier |
| Abstract: | Defect passivation plays a pivotal role in perovskite solar cells (PSCs), effectively mitigating non-radiative recombination and significantly enhancing their photovoltaic performance and stability. Herein, the zwitterionic molecule cocamidopropyl betaine (CAPB) was introduced into 3D triple-cation lead mixed-halide (CsFAMA) perovskite films, enabling dual bulk and surface passivation. The quaternary ammonium group in CAPB established electrostatic interactions with iodine ions in PbI2, while its carboxylate and amide C=O groups coordinated with Pb2+ ions, effectively suppressing non-radiative recombination. Devices incorporating CAPB achieved a notable maximum power conversion efficiency (PCE) of 21.47 % and demonstrated exceptional humidity resistance, retaining 98 % of their initial PCE after 4,080 h under 25 °C and 50 % relative humidity. Additionally, hydrogen bonds formed between the carboxylate C=O, amide C=O, and N-H groups in CAPB and the N-H groups of amines effectively mitigated amine volatilization at elevated temperatures. As a result, CAPB-based devices maintained 93 % and 80 % of their original PCE after 1,872 h at 65 °C and 85 °C, respectively. The successful integration of CAPB for dual bulk and surface passivation underscores its significant potential in advancing photovoltaic technologies. |
| Relation: | 52, p.101933 |
| DOI: | 10.1016/j.mtener.2025.101933 |
| Appears in Collections: | [Graduate Institute & Department of Chemical and Materials Engineering] Journal Article
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