黑磷
降级(电信)
氧气
催化作用
材料科学
析氧
化学工程
双极扩散
电子转移
极化(电化学)
图层(电子)
光化学
化学物理
化学
电子
光电子学
纳米技术
电化学
计算机科学
电极
物理
电信
物理化学
生物化学
有机化学
工程类
量子力学
作者
Zehua Hu,Qiang Li,Bo Lei,Qionghua Zhou,Du Xiang,Zhiyang Lyu,Fang Hu,Junyong Wang,Yinjuan Ren,Rui Guo,Goki Eda,Li Wang,Cheng Han,Jinlan Wang,Wei Chen
标识
DOI:10.1002/anie.201705012
摘要
Abstract Black phosphorus (BP) shows great potential in electronic and optoelectronic devices owing to its semiconducting properties, such as thickness‐dependent direct bandgap and ambipolar transport characteristics. However, the poor stability of BP in air seriously limits its practical applications. To develop effective schemes to protect BP, it is crucial to reveal the degradation mechanism under various environments. To date, it is generally accepted that BP degrades in air via light‐induced oxidation. Herein, we report a new degradation channel via water‐catalyzed oxidation of BP in the dark. When oxygen co‐adsorbs with highly polarized water molecules on BP surface, the polarization effect of water can significantly lower the energy levels of oxygen (i.e. enhanced electron affinity), thereby facilitating the electron transfer from BP to oxygen to trigger the BP oxidation even in the dark environment. This new degradation mechanism lays important foundation for the development of proper protecting schemes in black phosphorus‐based devices.
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