• 文献标题:   The supporting of Co-2(OH)PO4 onto N, P Co-Doped graphene via an in-situ hydrothermal assembly synthesis for efficient oxygen reduction reaction
  • 文献类型:   Article
  • 作  者:   MA XX, HE XQ
  • 作者关键词:   conpg, nitrogen, phosphate codoped graphene, oxygen reduction reaction, synergistic coupling
  • 出版物名称:   INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
  • ISSN:   0360-3199 EI 1879-3487
  • 通讯作者地址:   Changchun Univ Sci Technol
  • 被引频次:   0
  • DOI:   10.1016/j.ijhydene.2017.11.139
  • 出版年:   2018

▎ 摘  要

Developing efficient and durable non-noble catalysts toward oxygen reduction reaction (ORR) is an ongoing challenge. Herein, a highly efficient ORR catalyst (Co-NPG) is explored by assembling Co-2(OH)PO4 on conductive nitrogen, phosphate co-doped graphene (NPG) via an in-situ hydrothermal process. The graphene oxide matrix ammoniated by ethylenediamine not only constructs stable building blocks for hosting active sites, but also induces strong interaction between assembled cobalt-based nanoparticles. Morphology characterizations demonstrate the formation of the bulk-like structure with rough surface for the hybrid. Electrochemical measurements confirm this designed catalyst displays more efficient ORR performance than the un-ammoniated graphene oxide based one, and even comparable to that of 20 wt% Pt/C under the identical experimental conditions. The high ORR activity of the hybrid originates from the joint effects of the four aspects: first, the ammoniated graphene oxide tends to induce stronger NPs interaction than graphene oxide due to polarization, causing higher electronic conductivity and resulting in orientated growth; second, the N and P co-doping effects modulate the electronic structure of graphene, exposing more defects; third, the hybrid employs a high specific BET surface area and mesoporous characteristics, which afford quick mass transport during the ORR process; last, the synergistic coupling between the formed Co-2(OH)PO4 and NPG plays a critical role. (C) 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.