材料科学
析氧
过电位
催化作用
化学工程
无定形固体
分解水
电解水
X射线光电子能谱
电催化剂
电解
无机化学
电极
电化学
光催化
物理化学
化学
工程类
电解质
生物化学
有机化学
作者
Kai Zeng,Yibing Li,Meng Tian,Chaohui Wei,Jin Yan,Mark H. Rümmeli,Peter Strasser,Ruizhi Yang
标识
DOI:10.1016/j.ensm.2023.102806
摘要
Crystalline and amorphous structure can entitle a catalyst with high stability and activity, respectively. Oxygen evolution reaction (OER) catalysts, which widely used in water electrolysis and rechargeable Zn-air batteries, often undergo a surface phase reconstruction process and generate amorphous active phases under applied anodic potential. Although widely known, few studies and strategies have been reported to rationally tune OER pre-catalysts for enhanced reaction kinetics. Herein, we report a trimetallic oxides (a/c-NiFeMoOx) OER per-catalyst with rationally tunable amorphous/crystalline heterostructure degrees by a precise-tuning component strategy. The best a/c-NiFeMoOx electrode exhibits an OER overpotential merely of 256 mV and a small cell-voltage of 1.52 V to reach 10 mA cm–2 for water electrolysis, respectively. It is find that Mo leaching with tailored amorphous/crystalline heterostructure via the rational tuned degree of amorphousness promotes a rapid surface reconstruction of the a/c-NiFeMoOx pre-catalyst to form (oxy)hydroxide active species, whilst operando Raman, ex-situ X-ray photoelectron spectroscopy and density functional theory (DFT) analysis show the ample oxygen vacancies generated by phase transition significantly accelerates the deprotonation of OH* and lower the O* ➝ OOH* free energy for a fast oxygen evolution kinetics. Additionally, the practical application of a/c-NiFeMoOx cathode in rechargeable Zn-air battery delivers a robust long-term cycling (over 840 cycles).
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