Dion–Jacobson-Phase 2D Sn-Based Perovskite Comprising a High Dipole Moment of π-Conjugated Short-Chain Organic Spacers for High-Performance Solar Cell Applications

材料科学 钙钛矿(结构) 能量转换效率 相(物质) 结晶 共轭体系 化学工程 纳米技术 光电子学 结晶学 有机化学 化学 复合材料 聚合物 工程类
作者
Jie Qian,Yawen Li,Yifan Shen,Xiangqing Zhao,Chong Wu,Hao Gu,Zhipeng Zhang,Yanfeng Chen,Bo Cai,Junmin Xia,Wei Shen,Kun Cao,Lihui Liu,Lijun Zhang,Gang Cheng,Shufen Chen,Guichuan Xing,Wei Huang
出处
期刊:ACS Nano [American Chemical Society]
卷期号:18 (23): 15055-15066 被引量:1
标识
DOI:10.1021/acsnano.4c02076
摘要

The stability issue of Sn-based perovskite solar cells (PSCs) is expected to be resolved by involving a two-dimensional (2D) layered structure. However, Sn-based 2D PSCs, especially Dion–Jacobson (DJ)-phase ones with potentially good stability, have rarely been reported. Herein, superior DJ-phase Sn 2D perovskites with 3-aminobenzylamine (3ABA2+) or 4-aminobenzylamine (4ABA2+) π-conjugated short-chain ligands are reported to fabricate efficient 2D lead-free PSCs. Notably, the high dipole moment of the 3ABAI2 organic spacer is approved to possess faster charge transfer for forming (3ABA)FA4Sn5I16 2D perovskite with an extremely low exciton binding energy (only 84 meV). In combination with a diacetate partial substitution and methylamine iodide/bromide (MAI/MABr) post-treatment strategy to delay crystallization and improve compactness and coverage of the perovskite film, a record power conversion efficiency (PCE) of 6.81% and stability of 840 h (less than 5% degradation in a N2 atmosphere for unencapsulated devices) are acquired in eventual (3ABA)FA4Sn5I16 2D PSCs, which are among the highest PCE and the longest stability of Sn-based 2D PSCs reported to date. Our work provides a prospective molecule design and film preparation strategy of 2D Sn perovskites toward nontoxic high-performance tin-based PSCs, which pushes the almost stagnant research forward.
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