| Literature DB >> 28627084 |
Zehua Hu1,2, Qiang Li3, Bo Lei1,2, Qionghua Zhou3, Du Xiang2,4, Zhiyang Lyu4, Fang Hu5, Junyong Wang1,2, Yinjuan Ren4, Rui Guo4, Eda Goki1,2, Li Wang6, Cheng Han2,4,7, Jinlan Wang3,8, Wei Chen9,1,2,4.
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.Entities:
Keywords: black phosphorus; degradation; density functional calculations; surface chemistry; water-catalyzed oxidation
Year: 2017 PMID: 28627084 DOI: 10.1002/anie.201705012
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336