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人工晶体学报 ›› 2023, Vol. 52 ›› Issue (9): 1691-1697.

• 研究论文 • 上一篇    下一篇

高效Mo-Ni5P4双功能电催化剂的制备及其电解水性能研究

高鹏, 张艳平, 王敏, 余婉菲, 李建保   

  1. 海南大学材料科学与工程学院, 南海海洋资源利用国家重点实验室,海口 570228
  • 收稿日期:2023-03-14 出版日期:2023-09-15 发布日期:2023-09-19
  • 通信作者: 李建保,博士,教授。E-mail:ljb-555@163.com
  • 作者简介:高 鹏(1998—),男,河南省人,硕士研究生。E-mail:1445967346@qq.com
  • 基金资助:
    国家自然科学基金(52172086);海南省自然科学基金(522MS038)

Preparation and Electrolytic Water Performance of an Economically Efficient Mo-Ni5P4 Bifunctional Electrocatalyst

GAO Peng, ZHANG Yanping, WANG Min, YU Wanfei, LI Jianbao   

  1. State Key Laboratory of Marine Resource Utilization in South China Sea, School of Materials Science and Engineering, Hainan University, Haikou 570228, China
  • Received:2023-03-14 Online:2023-09-15 Published:2023-09-19

摘要: 电催化制氢通过析氢反应(HER)和析氧反应(OER)同时产生氢气(H2)和氧气(O2),是一种高效且环境友好的产氢方式。但现阶段商业化的高效催化剂价格昂贵且储量较少,限制了电解水技术的大规模应用。因此,开发低成本、高稳定和环境友好的高效电催化剂,特别是基于非贵金属材料的磷化物电催化剂,成为近期研究热点。本研究通过水热和相对较低的磷化温度成功制备出了具有镂空纳米花结构的Mo掺杂Ni5P4催化剂。通过X射线衍射(XRD)、扫描电子显微镜(SEM)和透射电子显微镜(TEM)对Mo-Ni5P4催化剂进行了表征,并研究了Mo-Ni5P4材料的电化学性能。研究发现,所合成的催化剂凭借掺杂对电子结构的改变,以及多孔纳米片的大表面积优势,提高了HER水解离步骤的速率。在碱性电解液中,Mo负载下的Ni5P4仅需116 mV的析氢过电位就可实现10 mA·cm-2的电流密度,同时析氧过电位只需255 mV。在双电极配置中仅需1.608 V的电池电压,持续测试27 h后,催化剂仍显示出良好的稳定性。

关键词: Ni5P4, Mo, 掺杂, 电催化析氢, 电催化析氧, 电催化全解水

Abstract: Electrocatalytic hydrogen production, to produce hydrogen (H2) and oxygen (O2) at the same time through hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), which is considered as an efficient and environmentally friendly way to produce hydrogen. However, the high-efficiency catalysts for commercialization are expensive and have limited reserves, which limit the large-scale application of electrolytic water technology. Therefore, the development of efficient electrocatalysts with low cost, high stability and environmental friendliness, especially phosphides based on non-precious metal materials, is very challenging and much desired. Here, Mo-doped Ni5P4 catalysts with hollow nanoflower structure were successfully prepared by hydrothermal and relatively low phosphorylation temperature. The microstructure of Mo-Ni5P4 catalysts was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM), and the electrochemical properties of Mo-Ni5P4 materials were investigated. The results show that, catalysts synthesized in this work promote the rate of the HER water dissociation step, taking advantage of the Mo and Ni5P4 hollow structures change and the large surface area of the porous nanosheets. In alkaline electrolytes, Ni5P4 under Mo loading requires only 116 mV of hydrogen evolution overpotential to achieve a current density of 10 mA·cm-2, while only 255 mV of oxygen evolution overpotential is required. In a two-electrode configuration, a battery voltage of only 1.608 V is required. The catalyst still shows good stability after 27 h of continuous testing.

Key words: Ni5P4, Mo, doping, electrocatalytic hydrogen evolution, electrocatalytic oxygen evolution, overall water splitting

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