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CeO2改性V-NiFeP双功能催化剂的制备及其电解海水性能研究

蔡奇1,张令杰1,赵芳2,杨阳2,于静1   

  1. 1. 哈尔滨工程大学材料科学与化学工程学院
    2. 华能伊春热电有限公司
  • 收稿日期:2025-07-19 修回日期:2025-09-04 网络首发:2025-09-10 发布日期:2025-09-10
  • 通讯作者: 于静 E-mail:jing.yu@hrbeu.edu.cn
  • 基金资助:
    中央高校基本科研业务费(批准号:3072025YC1007)资助

Preparation of CeO2-modified V-NiFeP bifunctional catalyst and its electrolytic performance of seawater

CAI Qi1, ZHANG Lingjie1, ZHAO Fang2, YANG Yang2, YU Jing1   

  1. 1. College of Materials Science and Chemical EngineeringHarbin Engineering University 2. Huaneng Yichun Thermal Power Co., Ltd,

  • Received:2025-07-19 Revised:2025-09-04 Online First:2025-09-10 Published:2025-09-10
  • Contact: Jing YU E-mail:jing.yu@hrbeu.edu.cn
  • Supported by:
    Supported by the Fundamental Research Funds of the Central University, China(No. 3072025YC1007)

摘要: 本文通过水热法、磷化处理、元素掺杂以及电沉积方法在泡沫镍基底上原位生长了CeO2修饰的钒掺杂多孔镍铁磷化物纳米片催化剂电极(V-NiFeP@CeO2),V掺杂增加了活性位点的数量,磷化可调节电子结构,CeO2与V-NiFeP发生界面相互作用,有利于电子转移和反应物吸附,从而提高了催化活性。对制备的双功能催化剂在碱性溶液和碱性海水溶液中的析氢和析氧性能进行研究,全水解电化学测试结果表明,催化剂在碱性溶液和碱性海水溶液中100 mA·cm-2电流密度下所需的电池电压仅为1.83和1.85 V,并在10 mA·cm-2电流密度下稳定运行27 h无电压衰减,表现出优异的电催化性能和长期耐久性。

关键词: 过渡金属磷化物, 二氧化铈, 电解海水, 析氢反应, 析氧反应

Abstract: In this paper, CeO2-modified vanadium-doped porous nickel-iron phosphide nanosheet catalyst electrodes (V-NiFeP@CeO2) were in-situ grown on nickel foam substrates through hydrothermal method, phosphating treatment, element doping and electrodeposition. V doping increased the number of active sites, and phosphorization could adjust the electronic structure. The interface interaction between CeO2 and V-NiFeP was conducive to electron transfer and reactant adsorption, thereby enhancing the catalytic activity. The hydrogen evolution and oxygen evolution performance of the prepared bifunctional catalyst in alkaline solution and alkaline seawater solution were studied. The results of full water electrolysis tests showed that the required cell voltage of the catalyst at a current density of 100 mA·cm-2 in alkaline solution and alkaline seawater solution was only 1.83 and 1.85 V, respectively, along with stable operation for 27 h at a current density of 10 mA·cm-2 without voltage decay. The results exhibit V-NiFeP@CeO2 has excellent electrocatalytic performance and long-term durability.

Key words: Transition metal phosphides, CeO2, Electrolysis of seawater, Hydrogen evolution reaction, Oxygen evolution reaction

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