Self-supported hierarchical CuOx@Co3O4 heterostructures as efficient bifunctional electrocatalysts for water splitting

The preparation of low-cost and efficient bifunctional catalysts towards water splitting is essential for the production of clean H2 energy. Herein, a hierarchical Co3O4-decorated CuO–Cu2O nanorod core–shell structure was in situ grown on a Cu foam (denoted as CuOx@Co3O4 NRs/CF) and investigated as...

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Published inJournal of materials chemistry. A, Materials for energy and sustainability Vol. 6; no. 29; pp. 14431 - 14439
Main Authors Zhou, Qianqian, Ting-Ting, Li, Qian, Jinjie, Hu, Yue, Guo, Fenya, Yue-Qing, Zheng
Format Journal Article
LanguageEnglish
Published Cambridge Royal Society of Chemistry 2018
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Abstract The preparation of low-cost and efficient bifunctional catalysts towards water splitting is essential for the production of clean H2 energy. Herein, a hierarchical Co3O4-decorated CuO–Cu2O nanorod core–shell structure was in situ grown on a Cu foam (denoted as CuOx@Co3O4 NRs/CF) and investigated as a bifunctional catalyst for both the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) in alkaline solution. Benefiting from its large electrochemical surface area and the synergetic effects between the CuOx core and Co3O4 shell, CuOx@Co3O4 NRs/CF exhibited considerable catalytic activity, which resulted in a small overpotential of 240 mV for the OER and 242 mV for the HER at a current density of 50 mA cm−2, along with low Tafel slopes of 46 and 61 mV dec−1, respectively. Remarkably, CuOx@Co3O4 NRs/CF could continuously produce O2 or H2 for at least 24 h with negligible decline in catalytic activity, and it gave rise to high faradaic efficiencies of 99.7% and 96.4% for the OER and HER, respectively. The electrochemical performance of CuOx@Co3O4 NRs/CF was dramatically improved as compared to those of its CuOx NRs/CF counterpart and also most reported Cu-based water splitting electrocatalysts.
AbstractList The preparation of low-cost and efficient bifunctional catalysts towards water splitting is essential for the production of clean H₂ energy. Herein, a hierarchical Co₃O₄-decorated CuO–Cu₂O nanorod core–shell structure was in situ grown on a Cu foam (denoted as CuOₓ@Co₃O₄ NRs/CF) and investigated as a bifunctional catalyst for both the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) in alkaline solution. Benefiting from its large electrochemical surface area and the synergetic effects between the CuOₓ core and Co₃O₄ shell, CuOₓ@Co₃O₄ NRs/CF exhibited considerable catalytic activity, which resulted in a small overpotential of 240 mV for the OER and 242 mV for the HER at a current density of 50 mA cm⁻², along with low Tafel slopes of 46 and 61 mV dec⁻¹, respectively. Remarkably, CuOₓ@Co₃O₄ NRs/CF could continuously produce O₂ or H₂ for at least 24 h with negligible decline in catalytic activity, and it gave rise to high faradaic efficiencies of 99.7% and 96.4% for the OER and HER, respectively. The electrochemical performance of CuOₓ@Co₃O₄ NRs/CF was dramatically improved as compared to those of its CuOₓ NRs/CF counterpart and also most reported Cu-based water splitting electrocatalysts.
The preparation of low-cost and efficient bifunctional catalysts towards water splitting is essential for the production of clean H2 energy. Herein, a hierarchical Co3O4-decorated CuO–Cu2O nanorod core–shell structure was in situ grown on a Cu foam (denoted as CuOx@Co3O4 NRs/CF) and investigated as a bifunctional catalyst for both the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) in alkaline solution. Benefiting from its large electrochemical surface area and the synergetic effects between the CuOx core and Co3O4 shell, CuOx@Co3O4 NRs/CF exhibited considerable catalytic activity, which resulted in a small overpotential of 240 mV for the OER and 242 mV for the HER at a current density of 50 mA cm−2, along with low Tafel slopes of 46 and 61 mV dec−1, respectively. Remarkably, CuOx@Co3O4 NRs/CF could continuously produce O2 or H2 for at least 24 h with negligible decline in catalytic activity, and it gave rise to high faradaic efficiencies of 99.7% and 96.4% for the OER and HER, respectively. The electrochemical performance of CuOx@Co3O4 NRs/CF was dramatically improved as compared to those of its CuOx NRs/CF counterpart and also most reported Cu-based water splitting electrocatalysts.
Author Yue-Qing, Zheng
Zhou, Qianqian
Qian, Jinjie
Hu, Yue
Guo, Fenya
Ting-Ting, Li
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Snippet The preparation of low-cost and efficient bifunctional catalysts towards water splitting is essential for the production of clean H2 energy. Herein, a...
The preparation of low-cost and efficient bifunctional catalysts towards water splitting is essential for the production of clean H₂ energy. Herein, a...
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StartPage 14431
SubjectTerms Catalysis
Catalysts
Catalytic activity
Clean energy
cobalt oxide
Cobalt oxides
copper
copper nanoparticles
Core-shell structure
Electrocatalysts
Electrochemical analysis
Electrochemistry
energy
foams
Heterostructures
hydrogen
Hydrogen evolution reactions
hydrogen production
Metal foams
Nanorods
oxygen
Oxygen evolution reactions
oxygen production
Splitting
surface area
Tafel slopes
Water splitting
Title Self-supported hierarchical CuOx@Co3O4 heterostructures as efficient bifunctional electrocatalysts for water splitting
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