催化作用
石墨烯
磷化物
电催化剂
活动站点
吸附
材料科学
活动层
化学工程
氢
纳米技术
化学
兴奋剂
碳纤维
无机化学
物理化学
图层(电子)
复合材料
电化学
有机化学
光电子学
工程类
复合数
薄膜晶体管
电极
作者
Meng-Ting Lin,Ruihu Lu,Wen Luo,Nuo Xu,Yan Zhao,Liqiang Mai
标识
DOI:10.1021/acsaem.1c00121
摘要
Systematic research on potential active sites, in particular, the intrinsic mechanism between the nitrogen-doped carbon (NC) and transition metal phosphides (TMPs) is of great significance to boost the development of hydrogen evolution reaction (HER) catalysts. In this work, we designed a reliable scheme to verify the interaction of a molybdenum phosphide/NC (MoP/NC) catalyst derived from theoretical calculations. According to our screening calculations of 19 feasible active sites on MoP/NC, interface engineering of MoP/NC was proved to provide an electronic transfer from the Mo layer to the graphene layer, thereby activating N-doped graphene serve as active sites. Furthermore, the sp2 or sp3 H-adsorption patterns could effectively adjust the adsorption strength, which promotes the HER catalytic activity. Meanwhile, to confirm the calculated results, an ultrathin N-doped carbon-coated MoP globular material (MoP/NC) was constructed, whose catalytic performance greatly surpasses that of the MoP material in both acid and alkaline media. These findings deepen the understanding of the intrinsic mechanism of functional carbon-incorporated TMPs and provide scientific guidance for the interface design of an efficient HER electrocatalyst.
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