Molybdenum-leaching induced rapid surface reconstruction of amorphous/crystalline heterostructured trimetal oxides pre-catalyst for efficient water splitting and Zn-air batteries

被引:37
|
作者
Zeng, Kai [1 ,2 ]
Li, Yibing [2 ]
Tian, Meng [1 ]
Wei, Chaohui [1 ]
Yan, Jin [1 ]
Rummeli, Mark H. [1 ,3 ,4 ]
Strasser, Peter [5 ]
Yang, Ruizhi [1 ]
机构
[1] Soochow Univ, Soochow Inst Energy & Mat Innovat, Coll Energy, Suzhou 215006, Peoples R China
[2] Southwest Jiaotong Univ, Inst Smart City & Intelligent Transportat, Chengdu 610032, Peoples R China
[3] Polish Acad Sci, Ctr Polymer & Carbon Mat, M Curie Sklodowskiej 34, PL-41819 Zabrze, Poland
[4] VSB Tech Univ Ostrava, Inst Environm Technol, Listopadu 15, Ostrava 70833, Czech Republic
[5] Tech Univ Berlin, Dept Chem, Chem Engn Div, D-10623 Berlin, Germany
基金
中国国家自然科学基金;
关键词
Multi-metal oxides; Amorphous/crystalline heterostructure; Surface reconstruction; Water electrolysis; Zn-air batteries; TRANSITION-METAL-OXIDES; OXYGEN; ELECTROCATALYSTS; NANOSHEETS;
D O I
10.1016/j.ensm.2023.102806
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
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 cellvoltage 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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页数:9
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