Precise Control of Crystallization and Phase-Transition with Green Anti-Solvent in Wide-Bandgap Perovskite Solar Cells with Open-Circuit Voltage Exceeding 1.25 V
- Authors
- Zhang, Xinpeng; Li, Xiangyu; Tao, Lei; Zhang, Zemin; Ling, Hao; Fu, Xue; Wang, Shibo; Ko, Min Jae; Luo, Jingshan; Chen, Jiangzhao; Li, Yuelong
- Issue Date
- Jun-2023
- Publisher
- WILEY-V C H VERLAG GMBH
- Keywords
- crystal growth; green chemistry; high-quality perovskite films; perovskite; solar cells
- Citation
- SMALL, v.19, no.22, pp.1 - 9
- Indexed
- SCIE
SCOPUS
- Journal Title
- SMALL
- Volume
- 19
- Number
- 22
- Start Page
- 1
- End Page
- 9
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/186055
- DOI
- 10.1002/smll.202208289
- ISSN
- 1613-6810
- Abstract
- Wide-bandgap perovskite solar cells (PSCs) have attracted a lot of attention due to their application in tandem solar cells. However, the open-circuit voltage (V-OC) of wide-bandgap PSCs is dramatically limited by high defect density existing at the interface and bulk of the perovskite film. Here, an anti-solvent optimized adduct to control perovskite crystallization strategy that reduces nonradiative recombination and minimizes V-OC deficit is proposed. Specifically, an organic solvent with similar dipole moment, isopropanol (IPA) is added into ethyl acetate (EA) anti-solvent, which is beneficial to form PbI2 adducts with better crystalline orientation and direct formation of alpha-phase perovskite. As a result, EA-IPA (7-1) based 1.67 eV PSCs deliver a power conversion efficiency of 20.06% and a V-OC of 1.255 V, which is one of the remarkable values for wide-bandgap around 1.67 eV. The findings provide an effective strategy for controlling crystallization to reduce defect density in PSCs.
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