Optimizing electronic state in Sr2Co2O5-x with ferromagnetic state by improving oxygen vacancies for oxygen evolution reaction

被引：7

作者：

Zhang, Qian ^{[1
]}

Sun, Maosong ^{[2
]}

Zhu, Jie ^{[1
]}

Yang, Sudong ^{[1
]}

Chen, Lin ^{[1
]}

Yang, Xulin ^{[3
]}

Wang, Pan ^{[3
]}

Li, Kui ^{[3
]}

Zhao, Peng ^{[1
]}

机构：

[1] Chengdu Univ, Inst Adv Study, Chengdu 610106, Peoples R China

[2] Guangxi Univ, Res Ctr Optoelect Mat & Devices, Sch Phys Sci Technol, Nanning 530004, Peoples R China

[3] Chengdu Univ, Sch Mech Engn, Chengdu 610106, Peoples R China

来源：

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY | 2022年 / 47卷 / 44期

关键词：

Oxygen vacancies; Ferromagnetic state; Eg electrons; Oxygen evolution reaction; PEROVSKITE ELECTROCATALYST; CONDUCTIVITY; NANOSHEETS; COBALTITE; COOOH; OXIDE;

D O I：

10.1016/j.ijhydene.2022.04.095

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：

The eg occupancy in perovskite oxides plays a crucial role for the oxygen electrocatalysis. Herein, we demonstrated a new method to optimize the eg filling and electronic-state of Co ions in Sr2Co2O5-x (SCO) via altering concentrations of oxygen vacancies using the CaH2 as reductant in an evacuated asymptotic to 10(-2) Pa) pyrex tube. As the oxygen vacancies concentration increased, the eg electron filling of SCO was optimized and its conductivity was greatly improved. Notably, the electronic state of SCO changed from antiferromagnetic (AFM) to ferromagnetic (FM) state. Moreover, the SCO exhibited a remarkable activity toward oxygen evolution reaction (OER), with a low overpotential of 320 mV and a tafel slope of 65 mV dec(-1), which is superior to most well-known perovskite oxides catalysts. The theoretical calculations demonstrated that oxygen vacancies could reduce the energy barrier of OER process. This work not only establishes a clear relationship among oxygen vacancies, eg filling, magnetic behavior and OER performance, but also provides a new method for designing highly activity efficient catalysts for OER. (C) 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

引用

页码：19027 / 19037

页数：11

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