材料科学
钙钛矿(结构)
堆积
结晶度
单层
分子间力
氧化镍
纳米技术
氧化物
光伏系统
镍
光电子学
分子
钙钛矿太阳能电池
化学工程
聚合物
平面的
化学物理
非阻塞I/O
作者
Changli Wu,Yanchun Guo,Xuefeng Xia,Fang Xu,Qixin Wan,Qianying Lin,Yanfeng Chen,Wenyan Nie,Qiu Xiong,Xia Yang,Zhihua Xiong,Tianxiang Zhao
标识
DOI:10.1021/acsami.6c15364
摘要
Self-assembled molecules (SAMs) have emerged as an efficient strategy for addressing buried nickel oxide (NiOX) interface defects in inverted perovskite solar cells (PSCs). Nevertheless, conventional carbazole-based SAMs suffer from weak intermolecular interactions, leading to film aggregation that hinders the formation of dense and uniform SAMs, which in turn causes discontinuities in the contact between NiOX and the perovskite film, thereby inducing interfacial defects and nonradiative recombination. Herein, 1-(2-carboxyethyl)-2,3,3-trimethyl-3H-indol-1-ium (CTI) was combined with 2PACz to prepare co-SAMs for modifying the NiOX substrate. Benefiting from the complementary charge distribution of the conjugated moieties in CTI and (2-(9H-carbazol-9-yl)ethyl)phosphonic acid (2PACz), the intermolecular π-π stacking interactions are significantly strengthened, thereby enabling the preparation of uniform and dense co-SAMs. The resulting embedded interface is in close contact with the perovskite film, which substantially elevates the crystallinity of the perovskite film and reduces defect density. Consequently, inverted devices based on the optimized 2PACz+CTI not only achieved an impressive photoconversion efficiency of 25.12% but also demonstrated excellent long-term storage stability under high-temperature and humid conditions.
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