Amorphous CoFe(OH)x hollow hierarchical structure: an efficient and durable electrocatalyst for oxygen evolution reaction. Issue 1 (11th December 2019)

• Record Type: Journal Article
• Authors: Yue, Xiaoyang; Ke, Wentao; Xie, Minghua; Shen, Xiaoping; Yan, Zhenyu; Ji, Zhenyuan; Zhu, Guoxing; Xu, Keqiang; Zhou, Hu
• Is Part Of: Catalysis science & technology. Volume 10:Issue 1(2020)
• Page Start: 215
• Page End: 221
• Publication Date: 2019-12-11
• Subjects: Catalysis -- Periodicals; 541.395
• DOI: 10.1039/c9cy02092f
• Languages: English
• ISSNs: 2044-4753

Abstract

Abstract : Amorphous CoFe(OH) x hollow hierarchical microspheres are fabricated by using a polyhedral Cu2 O template. CoFe(OH) x shows excellent OER activity and long-term durability due to its unique hollow hierarchical structure and composition. Abstract : Developing novel earth-abundant electrocatalysts with highly efficient and durable activity for the oxygen evolution reaction (OER) is in great demand in the clean hydrogen production. Herein, an amorphous mixed cobalt–iron hydroxide (CoFe(OH) x ) with a uniform hollow hierarchical structure is exploited and applied in the OER. The amorphous structure can supply abundant defects and reaction sites, and the hollow hierarchical microspheres with numerous vertically grown nanosheets on the shell can provide sufficient contact between electrolyte and active species, thus exposing abundant accessible active sites for electrocatalysis. As a result, the as-prepared CoFe(OH) x exhibits a superior electrocatalytic OER activity in alkaline medium with a low overpotential of 293 mV at a current density of 10 mA cm −2 and a small Tafel slope of 67.4 mV dec −1 . CoFe(OH) x also shows significantly enhanced OER activity compared to Co(OH)2 owing to its optimized electronic structure and conductivity tuned by the introduction of Fe. The turnover frequency of CoFe(OH) x (55.7 × 10 −3 s −1 ) is 8.8 times larger than that of Co(OH)2 (6.3 × 10 −3 s −1 ). This work paves a way for rational design of hollow structured bimetal hydroxides with enhanced electrocatalytic performance.