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 in | Journal of materials chemistry. A, Materials for energy and sustainability Vol. 6; no. 29; pp. 14431 - 14439 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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. |
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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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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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