CIESC Journal ›› 2025, Vol. 76 ›› Issue (10): 5141-5149.DOI: 10.11949/0438-1157.20250209

• Catalysis, kinetics and reactors • Previous Articles     Next Articles

Preparation of cobalt-iron hydrogen phosphite bifunctional water electrolysis catalyst by one-step electrodeposition

Kun ZHANG1(), Tieshan ZOU1,2, Haifeng ZHANG1, Xiaotong HAN2(), Yanxiong FANG3()   

  1. 1.School of Chemical Engineering, Northeast Electric Power University, Jilin 132012, Jilin, China
    2.School of Chemistry and Chemical Engineering, Chongqing University, Chongqing 401331, China
    3.School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou 510006, Guangdong, China
  • Received:2025-03-04 Revised:2025-03-21 Online:2025-11-25 Published:2025-10-25
  • Contact: Xiaotong HAN, Yanxiong FANG

一步电沉积法制备钴铁亚磷酸氢盐双功能电解水催化剂

张坤1(), 邹铁山1,2, 张海丰1, 韩晓彤2(), 方岩雄3()   

  1. 1.东北电力大学化学工程学院,吉林 吉林 132012
    2.重庆大学化学化工学院,重庆 401331
    3.广东工业大学 轻工化工学院,广东 广州 510006
  • 通讯作者: 韩晓彤,方岩雄
  • 作者简介:张坤(1991—),男,博士,讲师,zhangkun@neepu.edu.cn
  • 基金资助:
    国家自然科学基金项目(22208035);重庆市自然科学基金项目(2024NSCQ-MSX1402)

Abstract:

Electrolysis of water to produce hydrogen has the advantages of being green and efficient, but is limited by the slow kinetics and high cost of precious metal catalysts, and it is urgent to develop efficient and stable non-precious metal catalysts. An Fe-doped cobalt hydrogen phosphite [Fe-Co(H2PO2)2] catalyst is synthesized via a one-step electrodeposition method on a nickel foam substrate. Structural analyses reveal that Fe-Co(H2PO2)2 adopts a self-supported microspherical architecture with an amorphous nature, significantly increasing the exposure of electrochemically active sites. Moreover, Fe-doping effectively modulates the electronic structure of Co(H2PO2)2, enhancing charge transfer efficiency and accelerating electrocatalytic reaction kinetics. The electrochemical test results show that the overpotentials of hydrogen and oxygen evolution of Fe-Co(H2PO2)2 at a current density of 10 mA·cm-2 are 24 mV and 220 mV, respectively, and it can work stably for 40 h at 50 mA·cm-2, showing excellent bifunctional electrocatalytic activity and good stability, and has broad application prospects in the field of water electrolysis and hydrogen production.

Key words: electrochemistry, catalysis, water electrolysis, hydrogen production, bifunctional catalyst, doping engineering

摘要:

电解水制氢具有绿色高效的优势,但受限于动力学缓慢及贵金属催化剂成本高,亟需开发高效稳定的非贵金属催化剂。以泡沫镍为基底,采用一步电沉积法制备Fe掺杂Co(H2PO2)2催化剂[Fe-Co(H2PO2)2]。研究表明,该催化剂形成三维自支撑微球结构,并呈现无定形特征,从而显著提高电化学活性位点的暴露度。此外,Fe掺杂有效调控Co(H2PO2)2的电子结构,增强电荷传输能力,加速催化反应动力学。电化学测试结果显示,Fe-Co(H2PO2)2在10 mA·cm-2电流密度下的析氢和析氧过电位分别为24 mV和220 mV,并可在50 mA·cm-2下稳定工作40 h,展现出优异的双功能电催化活性和良好的稳定性,在电解水制氢领域具有广阔的应用前景。

关键词: 电化学, 催化, 电解水, 制氢, 双功能催化剂, 掺杂工程

CLC Number: