无定形固体
X射线光电子能谱
半导体
单独一对
电子
结晶学
材料科学
聚乙烯吡咯烷酮
结合能
路易斯酸
化学物理
化学
分子
原子物理学
物理
有机化学
光电子学
核磁共振
高分子化学
量子力学
催化作用
作者
Junli Wang,Ying Feng,Tingting Wang,Yajie Qiao,Kangmin Chen
出处
期刊:ChemNanoMat
[Wiley]
日期:2018-08-07
卷期号:4 (11): 1160-1167
被引量:5
标识
DOI:10.1002/cnma.201800303
摘要
Abstract The bonded or nonbonded interactions at the interface of ligands and surface atoms are a core issue in engineering the surface chemistry and (photo)electronic properties of semiconductor colloidal solids. Herein, we demonstrate the interfacial Lewis acid‐base N→Sb nonbonded interaction: N atoms in polyvinylpyrrolidone (PVP) molecules acting as an electron donor to enhance the photoconductivity and ‐responsivity of PVP‐capped Sb 2 S 3 amorphous semiconductor colloids. The electron donation effect of PVP N atoms in the N→Sb interaction is backed by the upper shift of N 1s binding energy in the X‐ray photoelectron spectra (XPS) and the relevant literature. The repulsion of lone pair electrons (LPEs) of N atoms is thought to make 5 s 2 LPEs of Sb atoms retract from Sb nuclei with an increased orbital volume, giving rise to high probability for the overlap and coupling of 5 s 2 LPEs among neighboring Sb atoms on the surface of Sb 2 S 3 amorphous colloids. Such a spatially and energetically matched electron‐electron coupling greatly contributes to the photoelectronic performance enhancement of amorphous Sb 2 S 3 . We believe that the electron coupling and improved (photo)electronics can be generalized in many semiconductors containing n s 2 LPE metal cations by the surface/interface Lewis acid‐base interactions with suitable ligands.
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