Activating the hydrogen evolution reaction in low-dimensional carbon by partial hydrogenation: Role of the hybrid sp2-sp3 orbital interface

Hanqing Yin , Aijun Du
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引用次数: 2

Abstract

Developing highly efficient catalyst for the hydrogen evolution reaction (HER) and understanding their mechanism is crucial for establishing the hydrogen economy. Carbon-based materials are particularly attractive as HER catalysts because of their abundance and morphological variety. Herein, using density functional theory (DFT) calculations, we propose for the first time a virtual interface consisting of sp2 and sp3 orbitals of carbon, for activating the intrinsically inert low-dimensional carbon toward the HER. This hybrid orbital interface is generated by pre-adsorbed hydrogen introduced by the partial hydrogenation of these low-dimensional carbon materials (C60, carbon nanotubes and graphene). The pre-adsorbed hydrogen can activate adjacent carbon atoms to become active sites for the HER. The best performance among these sites is comparable to that of the commercial Pt/C catalyst. Given that the partial hydrogenation of low-dimensional carbon has been experimentally realized, our work provides a simple yet novel concept for HER catalyst design.

通过部分氢化激活低维碳中的析氢反应:杂化sp2-sp3轨道界面的作用
开发用于析氢反应(HER)的高效催化剂并了解其机理对于建立氢经济性至关重要。碳基材料作为HER催化剂特别有吸引力,因为它们的丰富性和形态多样性。在此,使用密度泛函理论(DFT)计算,我们首次提出了一个由碳的sp2和sp3轨道组成的虚拟界面,用于向HER激活本质惰性的低维碳。这种杂化轨道界面是由这些低维碳材料(C60、碳纳米管和石墨烯)的部分氢化引入的预吸附氢产生的。预吸附的氢可以活化相邻的碳原子成为HER的活性位点。这些位点中的最佳性能与商业Pt/C催化剂的性能相当。鉴于低维碳的部分加氢已经在实验中实现,我们的工作为HER催化剂的设计提供了一个简单而新颖的概念。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
3.90
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