4.7 Article

Biomass-derived self-supported porous carbon membrane embedded with Co nanoparticles as an advanced electrocatalyst for efficient and robust hydrogen evolution reaction

Journal

RENEWABLE ENERGY
Volume 155, Issue -, Pages 447-455

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.renene.2020.03.164

Keywords

Biomass; Porous carbon membrane; Co nanoparticles; Self-supported electrode; H-2 evolution reaction

Funding

  1. Natural Science Foundation of Ningxia Province [2018AAC02011, 2019AAC03113]
  2. National Natural Science Foundation of China [21763001]
  3. West Light Foundation of the Chinese Academy of Sciences [XAB2018AW13]
  4. Fundamental Research Funds for the Central Universities, North Minzu University [2019XYZHG07]
  5. Foundation of Training Program for Yong and Middle-aged Talents of State Ethnic Affairs Commission of China
  6. Support Project of Youth Science and Technology Talent of Ningxia Province
  7. Foundation of Key Laboratory of Electrochemical Energy Conversion Technology and Application

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Powderous transition metal-based electrocatalysts have been widely studied for hydrogen evolution reaction (HER), but their practical application still remains challenging due to the tedious slurry-based electrode assembly process and unavoidable stability decay at high current density. Herein, a self-supported H-2 evolution cathode based on pomelo peel (PP)-derived porous carbon (PPDC) membrane with embedded Co nanoparticles (Co@PPDC) is developed by direct carbonization of Co-adsorbed PP (Co2+ -PP). Benefiting from the large surface areas, the abundant open and interconnected pores, the highly graphitic PPDC membrane, and the highly dispersed Co nanoparticles, the self-supported Co@PPDC electrode demonstrates superior electrocatalytic performance for HER in 1.0 M KOH solution, with overpotentials of 154 and 264 mV at current densities of 10 and 100 mA cm(-2) , respectively. In addition, owing to the good structural integrity, the Co@PPDC electrode exhibits an excellent cycling stability for 2000 cycles and a stable current density of similar to 100 mA cm(-2) at a constant overpotential of 265 mV over 12 h with a nearly 100% Faradaic efficiency (FE) and H-2 production rate of 1.56 mmol h(-1) . Therefore, this work provides a versatile and effective strategy for development of high-performance self-supported electrodes at low cost for large-scale H-2 production from electrochemical water splitting. (C) 2020 Elsevier Ltd. All rights reserved.

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