无机材料学报

• 研究论文 •    

钽掺杂低铱催化剂:构筑及其酸性氧析出性能研究

叶星辰1,2, 王现英1, 王绍岩1   

  1. 1.中国科学院 上海硅酸盐研究所,上海 200050;
    2.中国科学院大学 材料科学与光电工程中心, 北京 100049
  • 收稿日期:2026-04-15 修回日期:2026-05-29
  • 作者简介:叶星辰(2001-), 男, 硕士研究生. E-mail: yexingchen23@mails.ucas.ac.cn
  • 基金资助:
    上海自然科学基金(25ZR1402538); 上海碳中和项目 (21DZ1207901, 23DZ1200603)

Tantalum Doped IrO2 Catalyst: Construction and Its Acidic Oxygen Evolution Performance

YE Xingchen1,2, WANG Xianying1, WANG Shaoyan1   

  1. 1. Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050, China;
    2. Center of Materials Science and Optoelectronics Engineering, University of Chinese Academy of Sciences, Beijing 100049, China
  • Received:2026-04-15 Revised:2026-05-29
  • About author:YE Xingchen (2001-), male, Master candidate. E-mail: yexingchen23@mails.ucas.ac.cn
  • Supported by:
    Natural Science Foundation of Shanghai (25ZR1402538); Shanghai Carbon Neutralization Project (21DZ1207901, 23DZ1200603).

摘要: 开发兼具高活性、高稳定性与低铱载量的阳极催化剂是推动质子交换膜电解水制氢技术规模化应用的关键。因此,本研究提出了一种通过改良的Adams熔融法在二氧化铱中掺杂高价态钽(Ta)以构建丰富氧空位(OV)的Ta-IrO2催化剂的策略。掺杂Ta5+为Ta-IrO2催化剂引入了较高的氧空位浓度,有效改善了催化活性,使其在酸性析氧反应中表现出优异的电催化性能,在10 mA·cm-2电流密度下过电位(仅为196 mV)低于商用IrO2 (289 mV),塔菲尔斜率(47.13 mV·dec-1)较小,展现出更快的反应动力学,并且其具有高的质量活性(1.6 V, 2187 mA·mgIr-1)。其次,生成的Ta-O键有效稳定了催化中心,使Ta-IrO2催化剂在10 mA·cm-2下可稳定运行450 h,显示出良好的耐久性。此外,Ta-IrO2催化剂中铱的载量0.13 mgIr cm-2,达到了在显著降低贵金属用量的同时提升性能的目标。本研究为通过高价金属掺杂工程化设计高性能、低铱载量的析氧反应催化剂提供了有效的方案。

关键词: 二氧化铱, 氧空位, 钽掺杂, 析氧反应(OER), 铱载量

Abstract: The development of anode catalysts that combine high activity, high stability, and low iridium loading is key to advancing the large-scale application of proton exchange membrane water electrolysis for hydrogen production. Therefore, this study proposes a strategy to construct Ta-IrO2 catalysts rich in oxygen vacancies (OV) by doping high-valent tantalum (Ta) into iridium dioxide using a modified Adams fusion method. Doping of Ta5+ introduced a high concentration of oxygen vacancies into the Ta-IrO2 catalyst, effectively enhancing its catalytic activity. This enabled the catalyst to exhibit excellent electrocatalytic performance in the acidic oxygen evolution reaction, with an overpotential of only 196 mV at a current density of 10 mA·cm-2, which is lower than that of commercial IrO2 (289 mV), and a lower Tafel slope (47.13 mV·dec-1), indicating faster reaction kinetics, and a high mass activity (1.6 V, 2187 mA·mgIr-1). Furthermore, the formed Ta-O bonds effectively stabilize the catalytic sites, enabling the Ta-IrO2 catalyst to operate stably for 450 h at 10 mA·cm-2, demonstrating excellent durability. Additionally, the iridium loading of 0.13 mgIr·cm-2 in the Ta-IrO2 catalyst validates the objective of enhancing performance while significantly reducing the amount of precious metal used. This study provides an effective strategy for the engineered design of high-performance, low-Ir-loading oxygen evolution reaction catalysts through the doping of high-valent metals.

Key words: iridium dioxide, oxygen vacancies, tantalum doping, oxygen evolution reaction (OER), Ir loading

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