4.7 Article

Biomass-derived porous carbon supported Co-CoO yolk-shell nanoparticles as enhanced multifunctional electrocatalysts

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 44, Issue 13, Pages 6525-6534

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2019.01.155

Keywords

Biomass-derived carbon; Yolk-shell; Co-CoO; Oxygen reduction reaction; Water splitting

Funding

  1. National Natural Science Foundation of China [21822801, 21576008, 91634116]
  2. PetroChina Innovation Foundation [2016D-5007-0505]

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Developing highly efficient, durable and low-cost electrocatalysts for oxygen reduction reaction (ORR), oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) in energy conversion and storage is still required, urgent and challenging. Herein, a novel structure of biomass-derived nitrogen-doped porous carbon supported yolk-shell Co-CoO nanoparticles (yolk-shell Co-CoO/BC) was successfully prepared via a facile impregnation strategy. The pyrolysis temperature and heating rate of Co2+/BC composite are two key factors in the formation of the yolk-shell structure. The synthesized yolk-shell Co-CoO/BC exhibits excellent electrochemical activity and stability as multifunctional electrocatalysts. The yolk-shell Co-CoO/C with a positive onset potential (0.91 V vs. RHE) and half-wave potential (0.82 V vs. RHE) exhibits an effective 4-electron transfer path and excellent methanol tolerance in alkaline electrolyte for ORR. Moreover, a low cell potential (eta(10) = 1.77 V vs. RHE at the current density of 10 mA cm(-2)) for overall water splitting can be reached. The synergistic catalytic effects between BC support and yolk-shell Co-CoO nanoparticles should be responsible for the excellent performance for ORR, OER and HER. This work opens up a way to the facile fabrication of carbon supported yolk-shell nano structures with high-performance in electrocatalytic applications for ORR, OER and HER. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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