State Key Laboratory of Heavy Oil Processing, Key Laboratory of Catalysis, China University of Petroleum (East China) , 66 West Changjiang Road, Qingdao, Shandong 266580, China.
ACS Appl Mater Interfaces. 2016 Jun 8;8(22):13890-901. doi: 10.1021/acsami.6b02023. Epub 2016 May 27.
The enhancement of catalytic performance of cobalt phosphide-based catalysts for the hydrogen evolution reaction (HER) is still challenging. In this work, the doping effect of some transition metal (M = Fe, Ni, Cu) on the electrocatalytic performance of the M-Co2P/NCNTs (NCNTs, nitrogen-doped carbon nanotubes) hybrid catalysts for the HER was studied systematically. The M-Co2P/NCNTs hybrid catalysts were synthesized via a simple in situ thermal decomposition process. A series of techniques, including X-ray diffraction, X-ray photoelectron spectroscopy, inductively coupled plasma-optical emission spectrometry, transmission electron microscopy, and N2 sorption were used to characterize the as-synthesized M-Co2P/NCNTs hybrid catalysts. Electrochemical measurements showed the catalytic performance according to the following order of Fe-Co2P/NCNTs > Ni-Co2P/NCNTs > Cu-Co2P/NCNTs, which can be ascribed to the difference of structure, morphology, and electronic property after doping. The doping of Fe atoms promote the growth of the [111] crystal plane, resulting in a large specific area and exposing more catalytic active sites. Meanwhile, the Fe(δ+) has the highest positive charge among all the M-Co2P/NCNTs hybrid catalysts after doping. All these changes can be used to contribute the highest electrocatalytic activity of the Fe-Co2P/NCNTs hybrid catalyst for HER. Furthermore, an optimal HER electrocatalytic activity was obtained by adjusting the doping ratio of Fe atoms. Our current research indicates that the doping of metal is also an important strategy to improve the electrocatalytic activity for the HER.
在提高基于磷化钴的催化剂在析氢反应(HER)中的催化性能方面仍然具有挑战性。在这项工作中,系统研究了一些过渡金属(M=Fe、Ni、Cu)掺杂对 M-Co2P/NCNTs(NCNTs,氮掺杂碳纳米管)混合催化剂析氢性能的影响。M-Co2P/NCNTs 混合催化剂通过简单的原位热分解过程合成。采用一系列技术,包括 X 射线衍射、X 射线光电子能谱、电感耦合等离子体-光学发射光谱、透射电子显微镜和氮气吸附对所合成的 M-Co2P/NCNTs 混合催化剂进行了表征。电化学测量结果表明,根据以下顺序显示出催化性能:Fe-Co2P/NCNTs>Ni-Co2P/NCNTs>Cu-Co2P/NCNTs,这可以归因于掺杂后结构、形态和电子性质的差异。掺杂 Fe 原子促进了[111]晶面的生长,从而获得了较大的比表面积并暴露出更多的催化活性位点。同时,在所有 M-Co2P/NCNTs 混合催化剂中,掺杂后的 Fe(δ+)具有最高的正电荷。所有这些变化都有助于提高 Fe-Co2P/NCNTs 混合催化剂在 HER 中的电催化活性。此外,通过调整 Fe 原子的掺杂比例,可以获得最佳的 HER 电催化活性。我们目前的研究表明,金属掺杂也是提高析氢反应电催化活性的重要策略。