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Atomically dispersed Fe-O4-C sites as efficient electrocatalysts for electrosynthesis of hydrogen peroxide.
Cao, Liuyue; Wang, Hongrui; Cheng, Ningyan; Zhang, Lei; Shi, Meiqing; Zhang, Bin-Wei.
Afiliação
  • Cao L; School of Chemistry and Chemical Engineering, Chongqing University, Chongqing 400044, China. binwei@cqu.edu.cn.
  • Wang H; School of Chemical Engineering, University of New South Wales, 2 High Street, Kensington, Sydney, NSW, 2052, Australia.
  • Cheng N; School of Chemistry and Chemical Engineering, Chongqing University, Chongqing 400044, China. binwei@cqu.edu.cn.
  • Zhang L; Key Laboratory of Structure and Functional Regulation of Hybrid Materials of Ministry of Education, Institutes of Physical Science and Information Technology, Anhui University, Hefei 230601, Anhui, China. ningyancheng@ahu.edu.cn.
  • Shi M; Centre for Clean Environment and Energy, Gold Coast Campus, Griffith University, Gold Coast, Queensland, 4222, Australia.
  • Zhang BW; School of Metallurgy and Environment, Central South University, Changsha, Hunan 410083, China. shimeiqing0925@126.com.
Chem Commun (Camb) ; 59(81): 12148-12151, 2023 Oct 10.
Article em En | MEDLINE | ID: mdl-37740332
ABSTRACT
The electrochemical reduction of oxygen via the 2e pathway is an environmentally friendly approach to the electrosynthesis of H2O2. Nevertheless, its sluggish kinetics and limited selectivity hinder its practical application. Herein, single Fe atoms anchored on graphene oxide (SA Fe/GO) with Fe-O4-C sites are developed as an efficient electrocatalyst for the electro-synthesis of H2O2. These Fe-O4-C site active centres could efficiently enhance the activity and selectivity towards 2e electrochemical oxygen reduction in an alkaline environment. The newly-developed SA Fe/GO electrocatalyst demonstrates exceptional electrochemical performance, exhibiting impressive activity with an onset potential of 0.90 and H2O2 production of 0.60 mg cm-2 h-1 at 0.4 V. Remarkably, it achieves a remarkable H2O2 selectivity of over 95.5%.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article