超亲水性
析氧
分解水
电极
电解
制氢
催化作用
材料科学
双功能
化学工程
电解水
可再生能源
贵金属
纳米技术
润湿
金属
化学
电化学
冶金
电解质
电气工程
工程类
复合材料
光催化
物理化学
生物化学
作者
Seulgi Jeong,Ungsoo Kim,Sang Jin Lee,Yihan Zhang,Eunbin Son,Kyoung Jin Choi,Young‐Kyu Han,Jeong Min Baik,Hyesung Park
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-02-29
卷期号:18 (10): 7558-7569
被引量:15
标识
DOI:10.1021/acsnano.3c12533
摘要
Water electrolysis is emerging as a promising renewable-energy technology for the green production of hydrogen, which is a representative and reliable clean energy source. From economical and industrial perspectives, the development of earth-abundant non-noble metal-based and bifunctional catalysts, which can simultaneously exhibit high catalytic activities and stabilities for both the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER), is critical; however, to date, these types of catalysts have not been constructed, particularly, for high-current-density water electrolysis at the industrial level. This study developed a heterostructured zero-dimensional (0D)–one-dimensional (1D) PrBa0.5Sr0.5Co1.5Fe0.5O5+δ (PBSCF)-Ni3S2 as a self-supported catalytic electrode via interface and morphology engineering. This unique heterodimensional nanostructure of the PBSCF-Ni3S2 system demonstrates superaerophobic/superhydrophilic features and maximizes the exposure of the highly active heterointerface, endowing the PBSCF-Ni3S2 electrode with outstanding electrocatalytic performances in both HER and OER and exceptional operational stability during the overall water electrolysis at high current densities (500 h at 500 mA cm–2). This study provides important insights into the development of catalytic electrodes for efficient and stable large-scale hydrogen production systems.
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