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水相暗环境中少层黑磷的氧化

Water-Catalyzed Oxidation of Few-Layer Black Phosphorous in a Dark Environment.

机构信息

Department of Physics, National University of Singapore, Singapore, 117542, Singapore.

Center for advanced 2D materials, National University of Singapore, Singapore, 117546, Singapore.

出版信息

Angew Chem Int Ed Engl. 2017 Jul 24;56(31):9131-9135. doi: 10.1002/anie.201705012. Epub 2017 Jun 30.

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.

摘要

黑磷(BP)具有厚度依赖的直接带隙和双极性输运特性等半导体性质,在电子和光电子器件中具有巨大的应用潜力。然而,BP 在空气中的稳定性差严重限制了其实际应用。为了开发有效的保护 BP 的方案,揭示各种环境下的降解机制至关重要。迄今为止,人们普遍认为 BP 在光照下通过光诱导氧化降解。在此,我们报告了一种通过黑暗中 BP 水催化氧化的新降解途径。当氧气与 BP 表面上高度极化的水分子共吸附时,水的极化效应可以显著降低氧气的能级(即增强电子亲合性),从而促进 BP 中的电子从 BP 转移到氧气,即使在黑暗环境中也能引发 BP 的氧化。这种新的降解机制为基于黑磷的器件中合适的保护方案的开发奠定了重要基础。

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