TY - JOUR
T1 - Importance of Cobalt-Doping for the Preparation of Hollow CuBr/Co@CuO Nanocorals on Copper Foils with Enhanced Electrocatalytic Activity and Stability for Oxygen Evolution Reaction
AU - Wu, Chien Wei
AU - Unnikrishnan, Binesh
AU - Periasamy, Arun Prakash
AU - Chen, I. Wen Peter
AU - Tseng, Yu Ting
AU - Yang, Ya Yun
AU - Lin, Wei Jan
AU - Huang, Chih Ching
AU - Chang, Huan Tsung
N1 - Funding Information:
This study was supported by the Ministry of Science and Technology of Taiwan under the contracts 107-2113-M-002-015-MY3, 107-2113-M-019-004-MY3, and 108-2638-M-002-001-MY2. Yu-Ting Tseng is grateful to the Ministry of Science and Technology of Taiwan for a postdoctoral fellowship under the contract number NS108-2811-M-002 -589. We are grateful for the assistance of C.-Y. Lin from the Instrument Center of National Taiwan University (NTU) for TEM measurements. Thanks to C.-Y. Chien and M.-J. Huang from Instrument Center (National Taiwan University) for assistance in situ TEM experiments. Thanks to Nan Ya Plastics for kindly providing copper foils for our experiments. We thank W.-M. Huang and C.-H. Hsiao for assistance in Raman measurements. The Autolab instrument was supported by Prof. C.-J. Yu from the Department of Applied Physics and Chemistry of National Taipei University.
Publisher Copyright:
Copyright © 2020 American Chemical Society.
PY - 2020/7/6
Y1 - 2020/7/6
N2 - In this work, we demonstrate a simple electrochemical approach to convert copper foil into a cost-effective and stable cobalt-doped hollow-structured CuBr@CuO electrocatalyst with high surface porosity for oxygen evolution reaction (OER). First, a thin layer of surface copper atoms of the foil was converted to γ-CuBr nanocorals (NCs) by dissolution and in situ deposition in a bromide medium. Then, the CuBr NCs were doped with Co utilizing the high ionic mobility of Cu+ in the γ-CuBr structure through cation exchange and dissolution reactions. During the Co-doping process, the surface γ-CuBr was converted to Cu2O, leading to the formation of CuBr/Co@Cu2O NCs. CuBr/Co@Cu2O NCs were then converted to CuBr/Co@CuO hollow NCs (h-NCs), with high surface roughness and high stability by three linear sweep voltammetry (LSV) scans in O2-saturated KOH solution (0.1 M) over a potential range of 1.2-1.7 V (vs RHE). The h-NC was not formed without Co-doping of γ-CuBr. The as-formed CuBr/Co@CuO h-NCs exhibit an overpotential of 270 mV with a current density of 10 mA cm-2 and a Tafel slope of 66 mV dec-1 for OER as a result of having high electrochemically active surface area and synergistic catalytic Co and CuBr@CuO nanostructures.
AB - In this work, we demonstrate a simple electrochemical approach to convert copper foil into a cost-effective and stable cobalt-doped hollow-structured CuBr@CuO electrocatalyst with high surface porosity for oxygen evolution reaction (OER). First, a thin layer of surface copper atoms of the foil was converted to γ-CuBr nanocorals (NCs) by dissolution and in situ deposition in a bromide medium. Then, the CuBr NCs were doped with Co utilizing the high ionic mobility of Cu+ in the γ-CuBr structure through cation exchange and dissolution reactions. During the Co-doping process, the surface γ-CuBr was converted to Cu2O, leading to the formation of CuBr/Co@Cu2O NCs. CuBr/Co@Cu2O NCs were then converted to CuBr/Co@CuO hollow NCs (h-NCs), with high surface roughness and high stability by three linear sweep voltammetry (LSV) scans in O2-saturated KOH solution (0.1 M) over a potential range of 1.2-1.7 V (vs RHE). The h-NC was not formed without Co-doping of γ-CuBr. The as-formed CuBr/Co@CuO h-NCs exhibit an overpotential of 270 mV with a current density of 10 mA cm-2 and a Tafel slope of 66 mV dec-1 for OER as a result of having high electrochemically active surface area and synergistic catalytic Co and CuBr@CuO nanostructures.
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U2 - 10.1021/acssuschemeng.0c02309
DO - 10.1021/acssuschemeng.0c02309
M3 - Article
AN - SCOPUS:85088898779
SN - 2168-0485
VL - 8
SP - 9794
EP - 9802
JO - ACS Sustainable Chemistry and Engineering
JF - ACS Sustainable Chemistry and Engineering
IS - 26
ER -