吡啶
光电流
卤化物
金属
化学
光电效应
结晶学
谱线
金属卤化物
可见光谱
材料科学
光电子学
无机化学
有机化学
天文
物理
作者
Bo Zhang,Jun Li,Lianzhi Li,Xiao‐Chen Ren,Ming Pang,Yongfu Shao
标识
DOI:10.1021/acs.cgd.1c00634
摘要
By utilizing in situ-formed MCP ligands (HMCP+ = 1-methyl-4-(carboxyl)pyridinium) as decoration agents, two new iodoplumbate hybrids, namely, [Pb(MCP)2I]PbI3 (1) and Cs2[Pb(MCP)4]Pb3I10 (2), have been solvothermally prepared and structurally characterized. Compound 1 features the typical one-dimensional (1D) [PbI3]nn– anions, while compound 2 exhibits two-dimensional (2D) [Pb3I10]n4n– slabs perforated with large parallelogram-shaped windows. The intriguing structural characteristic of compounds 1 and 2 is that they contain unique chain-like cations of [Pb(MCP)2I]+ and [Pb(MCP)4]2+, respectively. Interestingly, upon alternate visible-light and full spectrum light irradiation, compounds 1 and 2 show stable and rapid photoelectric switching properties, whose photocurrent densities are comparable or larger than those of many metal halide hybrids. Additionally, their optical properties, Hirshfeld surface analyses, X-ray photoelectron spectra, as well as the theoretical band structures and density of states have also been studied.
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