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Facile Synthesis of 3d Transition-Metal-Doped α-Co(OH)2 Nanomaterials in Water–Methanol Mediated with Ammonia for Oxygen Evolution Reaction
Author(s) -
Bo Cao,
Chunhua Luo,
Jie Lao,
Hanqing Chen,
Ruijuan Qi,
Hechun Lin,
Hui Peng
Publication year - 2019
Publication title -
acs omega
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.779
H-Index - 40
ISSN - 2470-1343
DOI - 10.1021/acsomega.9b02504
Subject(s) - overpotential , oxygen evolution , electrocatalyst , catalysis , chronoamperometry , materials science , nanomaterials , transition metal , cobalt , inorganic chemistry , methanol , chemical engineering , nanoparticle , water splitting , faraday efficiency , nanotechnology , chemistry , electrochemistry , photocatalysis , electrode , organic chemistry , cyclic voltammetry , engineering
Layered cobalt hydroxides are cost-efficient electrocatalysts for oxygen evolution reaction (OER) in the field of energy conversion. Herein, we developed a facile synthesis method of 3d transition-metal-doped α-Co(OH) 2 nanomaterials mediated with ammonia in water-methanol at room temperature. The doping of Cu 2+ and Ni 2+ leads to flower-like nanostructures similar to pure α-Co(OH) 2 , whereas the doping of Fe 2+ produces nanoparticles with more than 2 times larger surface area in comparison with the Cu 2+ - and Ni 2+ -doped nanoflowers. The obtained dispersion with the addition of Nafion can be used directly as an electrocatalyst for OER with excellent catalytic activity, especially that the overpotential of Fe 2+ doped is as low as 290 mV at 10 mA cm -2 and the turnover frequency is improved by 3 times as compared with that of α-Co(OH) 2 . Furthermore, the catalyst can be loaded onto foam nickel, which presents excellent durability with the current density unchanged under continuous chronoamperometry reaction for as long as 12 h and almost quantitative faradaic efficiency. The superior electrocatalytic properties combined with the simple synthesis without the tedious purification procedure is very promising for OER.

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