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原位制备水氧化铁基薄膜电极研究

徐昕a,b, 廖芳杰a,b, 佟振合a,b, 吴骊珠a,b,*   

  1. a中国科学院理化技术研究所 光化学转换与功能材料重点实验室 中国科学院-香港大学新材料合成和检测联合实验室 新基石科学实验室 北京 100190;
    b中国科学院大学 未来技术学院 北京 100049
  • 投稿日期:2026-06-08
  • 作者简介:“纪念兰州大学化学学科创建80周年”专辑
  • 基金资助:
    国家重点研发计划(No. 2022YFA1502900 and 2022YFA0911900)、国家自然科学基金(No. 22588101 and 92356309)和新基石科学基金会资助项目.

In-situ Preparation of Iron-based Film Electrode for Water Oxidation

Xu Xina,b, Liao Fang-jiea,b, Tung Chen-hoa,b, Wu Li-zhua,b,*   

  1. aKey Laboratory of Supramolecular Photochemistry and HKU-CAS Joint Laboratory on New Materials, New Cornerstone Science Laboratory, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing 100190;
    bSchool of Future Technology, University of Chinese Academy of Sciences, Beijing 100049
  • Received:2026-06-08
  • Contact: *E-mail: lzwu@mail.ipc.ac.cn
  • Supported by:
    National Key R&D Program of China (No. 2022YFA1502900 and 2022YFA0911900), the National Natural Science Foundation of China (No. 22588101 and 92356309), the Strategic Priority Research Program of the Chinese Academy of Science (No. XDB0960000), and New Cornerstone Science Foundation.

The depletion of petroleum reserves and imminent environmental problems has promoted the pursuit of clean and sustainable energy. Electrocatalytic water splitting to produce hydrogen represents a critical strategy in the field of new energy development. Water oxidation reaction is regarded as the bottleneck restricting the process due to the high energy demanding and slow kinetics process. Development of efficient and stable anode electrodes to enhance the efficiency of water splitting is essential. Here, Fe-based film electrode was in-situ prepared by electrodeposition directly from complex [Fe(bpy-pma)] (bpy-pma=N1-(2-([2,2'-bipyridin]-6-yl)propan-2-yl)-N2-methyloxalamide) in BBS (pH=9.0). The morphology, composition, structure and catalytic activity of the catalytic film were characterized using scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), X-ray photoelectron spectroscopy (XPS) and electrochemical measurements. The results indicate that the surface of the Fe-cat electrode is covered with cubic Fe2O3 nanoparticles. Inductively coupled plasma (ICP) measurements showed that 1.8 μg cm-2 of Fe was deposited on the Fe-cat electrode. The catalytic film exhibits an overpotential of 540 mV at 1 mA cm-2 current density and a Tafel slop of 85 mV dec-1 for water oxidation in carbonate/bicarbonate solution (pH=9.75). A stable current density of 7.3 mA cm-2 over 10 h was observed during controlled potential electrocatalysis (CPE) with an applied potential of 1.3 V. No current attenuation occurred in the longer-term CPE for 24 h. The electrolysis products, H2 and O2, were detected using gas chromatography (GC), yielding a calculated Faradaic efficiency of 99%. During the electrodeposition process, the slow dissociation of ligands effectively suppresses Fe(OH)3 precipitation, yielding ultrathin nanomembranes with uniform density. Compared with FeCl3 as a precursor, ligand coordination not only markedly modulates the film morphology but also greatly enhances the iron loading and electrocatalytic activity. This strategy overcame the problems of poor quality, low efficiency and poor stability of film electrode caused by the precipitation of iron ions under neutral to alkaline conditions.

Key words: water oxidation, electrocatalysis, electrodeposition, catalytic film, high stability