“One Stone, Two Birds”: Multi-Element Doping Induced Crystallinity Modulation for Large Current Density Oxygen Evolution Reaction

IF 18.5 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY Advanced Functional Materials Pub Date : 2025-01-23 DOI:10.1002/adfm.202422889
Yuhang Yuan, Yifan Yang, Guanglei Liu, Mingwei Chang, Zhu Liu, Kaichun Gao, Hongbang Zheng, Mingxin Ye, Jianfeng Shen
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Abstract

Oxygen evolution reaction (OER) plays a critical role in water splitting, which can directly determine the energy consumption of hydrogen production. However, the poor stability of catalysts at large current density inhibits their industrial application. Therefore, the development of efficient catalysts with industry-relevant activities still faces great challenges. Herein, a one-step corrosion strategy is reported for the preparation of multi-element low-crystal transition metal hydroxide (denoted as NiFeCrMnCo-c). Density functional theory calculation indicates that multi-element doping strategy improves the conductivity of the catalyst and reduces the energy barrier in the catalytic process. Only 259 and 303 mV overpotentials are required to achieve the anodic current densities of 100 and 1000 mA cm−2 respectively, and it can work at the anodic current density of 50 and 1000 mA cm−2 for 300 h without apparent attenuation. Furthermore, when it is self-assembled as an anion exchange membrane electrolyzer, it requires only 1.72 V at 1000 mA cm−2 for industrial water splitting and operates stably for 100 h at 60 °C, which can meet the requirements of industrial hydrogen production. The design of the OER catalysts with simple preparation, high activity, and high current density provides a new perspective for practical industrial water splitting.

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“一石两鸟”:多元素掺杂诱导大电流密度析氧反应的结晶度调制
析氧反应(OER)在水裂解过程中起着至关重要的作用,它直接决定了制氢过程的能耗。然而,催化剂在大电流密度下稳定性差,阻碍了其工业应用。因此,开发具有工业相关活性的高效催化剂仍然面临着很大的挑战。本文报道了制备多元素低晶过渡金属氢氧化物(表示为NiFeCrMnCo-c)的一步腐蚀策略。密度泛函理论计算表明,多元素掺杂策略提高了催化剂的导电性,降低了催化过程中的能垒。阳极电流密度分别为100 mA和1000 mA cm - 2,只需要259 mV和303 mV过电位就可以实现,并且可以在50和1000 mA cm - 2的阳极电流密度下工作300 h而无明显衰减。此外,当它自组装为阴离子交换膜电解槽时,在1000 mA cm - 2下仅需要1.72 V用于工业水分解,并且在60℃下稳定运行100 h,可以满足工业制氢的要求。制备简单、活性高、电流密度大的OER催化剂的设计为实际工业水裂解提供了新的前景。
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来源期刊
Advanced Functional Materials
Advanced Functional Materials 工程技术-材料科学:综合
CiteScore
29.50
自引率
4.20%
发文量
2086
审稿时长
2.1 months
期刊介绍: Firmly established as a top-tier materials science journal, Advanced Functional Materials reports breakthrough research in all aspects of materials science, including nanotechnology, chemistry, physics, and biology every week. Advanced Functional Materials is known for its rapid and fair peer review, quality content, and high impact, making it the first choice of the international materials science community.
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