Tailoring Phase Alignment and Interfaces via Polyelectrolyte Anchoring Enables Large-Area 2D Perovskite Solar Cells
- Authors
- Han, Chenxu; Wang, Yao; Yuan, Jiabei; Sun, Jianguo; Zhang, Xuliang; Cazorla, Claudio; Wu, Xianxin; Wu, Ziang; Shi, Junwei; Guo, Junjun; Huang, Hehe; Hu, Long; Liu, Xinfeng; Woo, Han Young; Yuan, Jianyu; Ma, Wanli
- Issue Date
- 5-9월-2022
- Publisher
- WILEY-V C H VERLAG GMBH
- Keywords
- 2D Perovskites; Polyelectrolytes; Ruddelsden-Popper Phase; Solar Cells
- Citation
- ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, v.61, no.36
- Indexed
- SCIE
SCOPUS
- Journal Title
- ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Volume
- 61
- Number
- 36
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/145761
- DOI
- 10.1002/anie.202205111
- ISSN
- 1433-7851
- Abstract
- Ruddlesden-Popper phase 2D perovskite solar cells (PSCs) exhibit improved lifetime while still facing challenges such as phase alignment and up-scaling to module-level devices. Herein, polyelectrolytes are explored to tackle this issue. The contact between perovskite and hole-transport layer (HTL) is important for decreasing interfacial non-radiative recombination and scalable fabrication of uniform 2D perovskite films. Through exploring compatible butylamine cations, we first demonstrate poly(3-(4-carboxybutyl)thiophene-2,5-diyl)-butylamine (P3CT-BA) as an efficient HTL for 2D PSCs due to its great hydrophilicity, relatively high hole mobility and uniform surface. More importantly, the tailored P3CT-BA has an anchoring effect and acts as the buried passivator for 2D perovskites. Consequently, a best efficiency approaching 18 % was achieved and we further first report large-area (2x3 cm(2), 5x5 cm(2)) 2D perovskite minimodules with an impressive efficiency of 14.81 % and 11.13 %, respectively.
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