二甲胺
相(物质)
化学物理
化学计量学
材料科学
响应度
范德瓦尔斯力
量子阱
同种类的
动能
化学
量子
凝聚态物理
结晶
纳米技术
光电子学
分解
超晶格
基质(水族馆)
光电探测器
光致发光
载流子
光激发
超顺磁性
上部结构
载流子寿命
杂质
作者
Jianbo Wu,Siliang Hu,Yi Shen,Qiuxiao Yin,Yuxuan Zhang,Haifan Li,Nan Wang,Mengxue Chen,Yingjun Xia,Dongchang He,Chun-Yuen Wong,Zhengxun Lai,Johnny C. Ho
标识
DOI:10.1021/acsenergylett.6c01347
摘要
Quasi-two-dimensional (quasi-2D) Dion−Jacobson (DJ) perovskites feature bidentate diammonium cations that eliminate van der Waals gaps, providing efficient carrier transport and structural stability. However, aggressive coordination between these spacers and the inorganic framework during crystallization causes disordered quantum well (QW) distributions, severely hindering carrier transport. Herein, we present a competitive coordination-directed phase evolution strategy to achieve phase-pure quasi-2D DJ perovskites with uniform QWs. By introducing dimethylamine as a competitive ligand, Pb 2+ species are effectively captured during the initial wet-film stage, preventing the formation of undesired high-n phases. During subsequent annealing, the controlled release of Pb 2+ species enables stoichiometric reactions with pre-existing low-n phases, resulting in targeted phase-pure DJ perovskites. With the elimination of phase boundaries and a homogeneous energy landscape, our photodetectors demonstrate an impressive on/off ratio of 2.2 × 10 5, high responsivity of 4.32 A W −1, and enhanced stability, establishing a robust kinetic modulation approach for high-performance optoelectronics.
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