化学
堆积
小提琴手
分子间力
半导体
电子转移
电导率
结晶学
晶体结构
晶体工程
光化学
化学物理
分子
超分子化学
光电子学
物理化学
有机化学
物理
作者
Peng-Hao Wang,Bin‐Wen Liu,Guoqiang Wang,Cai Sun
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2022-10-20
卷期号:61 (43): 17196-17201
被引量:18
标识
DOI:10.1021/acs.inorgchem.2c02760
摘要
Semiconductor conductivities depend largely on the crystal structures and the associated electronic structures. If the electronic structures can be switched reversibly in the same crystal structure, then a drastic conductivity change may be controllable. The effect of electron transfer (ET) on semiconductor conductivity remained elusive so far. In this work, a series of two pillared inorganicorganic hybrid photochromic semiconductors (PSCs), [(CQ)Pb3X6(H2O)]·2H2O [X = Cl (1) and Br (2), CQ = N-4,4′-bipyridiniopropionate (viologen)], with II-stacking viologen π-aggregates, are constructed by a bottom-up self-assembly strategy through inorganic skeleton-directed intercalation and intermolecular noncovalent interaction. The conductivities are abnormally “invariant” after photoinduced ET, breaking the convention that the generation of radicals favors conductivity. The abnormally “invariant” conductivities are mainly derived from approximate electronic couplings before and after ET between II-stacking viologen π-aggregates.
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