N掺杂MoP基核壳纳米棒的制备及其电催化析氢性能

Preparation of N-doped MoP-based core-shell nanorods and their electrocatalytic performance in hydrogen evolution

  • 摘要: 通过气-固反应方式对三氧化钼-乙二胺有机无机杂化材料(MoO3/EDA)进行原位磷化,利用空间限域效应合成了N掺杂的MoP基核壳纳米棒(N-MoP/NC-8)电化学析氢催化剂。表征结果显示,N-MoP/NC-8由N掺杂碳层包覆的N掺杂钼(MoP)组成,引入的电负性原子调节了活性相电子结构,同时碳层与MoP之间的复合限制了MoP内部团聚,产生较大的孔体积和比表面积,在双重调控下N-MoP/NC-8催化剂表现出较好的析氢性能(在0.5 mol/L H2SO4溶液中,10 mA/cm2电流密度下的过电位为92 mV,Tafel斜率为68 mV/dec),且稳定性超过20 h。

     

    Abstract: N-doped MoP-based core-shell nanorods (N-MoP/NC-8) were synthesized by in-situ phosphorization of molybdenum trioxide-ethylenediamine organic-inorganic hybrid material (MoO3/EDA) via a gas-solid reaction; their electrocatalytic performance in hydrogen evolution was investigated. The results indicate that N-MoP/NC-8 is composed of N-doped molybdenum phosphide (MoP) coated by N-doped carbon layer. The introduced electronegative atom can regulate the electronic structure of the active phase, whilst the combination of carbon layer and MoP can inhibit the internal agglomeration of MoP, resulting in large pore volume and surface area. Owing to such a dual effect, the N-MoP/NC-8 catalyst shows excellent performance in electrocatalytic hydrogen evolution and great charge transfer ability; the overpotential is 92 mV at 10 mA/cm2 current density in 0.5 mol/L H2SO4 solution, with a Tafel slope of 68 mV/dec and a durability of above 20 h.

     

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