• 文献标题:   Enhancement of the electrocatalytic activity for the oxygen reduction reaction of boron-doped reduced graphene oxide via ultrasonic treatment
  • 文献类型:   Article
  • 作  者:   TAFOYA JPV, DOSZCZECZKO S, TITIRICI MM, SOBRIDO ABJ
  • 作者关键词:   borondoped carbon, oxygen reduction reaction, polymer electrolyte membrane fuel nbsp, cell, ultrasonication, reduced graphene oxide, electrocatalyst
  • 出版物名称:   INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
  • ISSN:   0360-3199 EI 1879-3487
  • 通讯作者地址:  
  • 被引频次:   7
  • DOI:   10.1016/j.ijhydene.2021.11.127 EA JAN 2022
  • 出版年:   2022

▎ 摘  要

Commercial polymer electrolyte membrane fuel cells have relied on scares Platinum to catalyse the kinetically sluggish oxygen reduction reaction occurring at their anodes. Over the last decade organic materials, frequently based on graphitic structures have been demonstrated as promising alternative electrocatalysts to the noble metals. Researchers typically utilize ultrasonic treatment as part of the synthesis procedure to achieve homogeneous dispersion of graphitic carbon prior to. Herein we investigate the implications of the structural and compositional changes induced by the ultrasonication treatment on boron-doped reduced graphene oxide for oxygen reduction reaction. It is shown that ultrasonication pre-treatment prior to the boron doping and reduction of graphene oxide via hydrothermal process step leads to the increase of both substitutional B and electrocatalytic surface area, with associated reduction of average pore size diameter, leading to a significant improvement in the oxygen reduction reaction performance, with respect to the non-ultrasonicated material. It is proposed that the higher degree of substitutional doping of boron is a result of formation of the additional epoxy functionalities on graphitic planes, which act as a doping site for boric acid. (c) 2021 The Author(s). Published by Elsevier Ltd on behalf of Hydrogen Energy Publications LLC. This is an open access article under the CC BY license (http://creativecommons.org/ licenses/by/4.0/).