Boosting the zinc-ion storage ability of MnO2 cathode by depositing oxygen-deficient CuOx layer
MnO2 is subject to intensified examination as the foremost promising cathode material for aqueous zinc-ion batteries (AZIBs). However, achieving high stability and fast kinetics simultaneously is extremely challenging. Herein, an α-MnO2 cathode has been successfully engineered with an oxygen-deficie...
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Published in | Journal of energy storage Vol. 86; p. 111257 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier Ltd
10.05.2024
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Abstract | MnO2 is subject to intensified examination as the foremost promising cathode material for aqueous zinc-ion batteries (AZIBs). However, achieving high stability and fast kinetics simultaneously is extremely challenging. Herein, an α-MnO2 cathode has been successfully engineered with an oxygen-deficient CuOx coating utilizing active screen plasma technology. The CuOx coating, abundant in oxygen vacancies (OVs), promotes the dissociation of adsorbed water molecules and the ensuing formation of hydroxyl groups, thereby bestowing several benefits on the electrochemical performance. At the atomic level, the OVs serve to markedly fortify electron transport and expedite charge transfer. At the molecular level, the introduction of negatively-charged hydroxyl groups augments surface wettability, which in turn improves the Zn2+ diffusion kinetics and promotes the aggregation of a higher concentration of Zn2+ in the vicinity of the cathode. Furthermore, the CuOx layer is instrumental in preserving the integrity of the electrode structure by inhibiting the Mn dissolution. The integration of these multifaceted advantages culminates in a cathode that manifests a remarkable specific capacity (345 mA h g-1 at 0.2 A g-1) and exemplary cyclic stability (240 mA h g−1 after 1200 cycles at 0.5 A g−1). Conclusively, pouch cells with a large area (5 × 7 cm2) have been fabricated, demonstrating extraordinary flexibility and practical utility.
•An oxygen-deficient CuOx coating is first applied to the MnO2 cathode.•Oxygen vacancies promote the dissociation of adsorbed water and the subsequent generation of hydroxyl groups.•The integration of oxygen vacancies and hydroxyl groups lead to simultaneous improvements in electrical conductivity and surface wettability.•The CuOx-coated MnO2 cathode manifests a remarkable specific capacity and exemplary cyclic stability. |
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AbstractList | MnO2 is subject to intensified examination as the foremost promising cathode material for aqueous zinc-ion batteries (AZIBs). However, achieving high stability and fast kinetics simultaneously is extremely challenging. Herein, an α-MnO2 cathode has been successfully engineered with an oxygen-deficient CuOx coating utilizing active screen plasma technology. The CuOx coating, abundant in oxygen vacancies (OVs), promotes the dissociation of adsorbed water molecules and the ensuing formation of hydroxyl groups, thereby bestowing several benefits on the electrochemical performance. At the atomic level, the OVs serve to markedly fortify electron transport and expedite charge transfer. At the molecular level, the introduction of negatively-charged hydroxyl groups augments surface wettability, which in turn improves the Zn2+ diffusion kinetics and promotes the aggregation of a higher concentration of Zn2+ in the vicinity of the cathode. Furthermore, the CuOx layer is instrumental in preserving the integrity of the electrode structure by inhibiting the Mn dissolution. The integration of these multifaceted advantages culminates in a cathode that manifests a remarkable specific capacity (345 mA h g-1 at 0.2 A g-1) and exemplary cyclic stability (240 mA h g−1 after 1200 cycles at 0.5 A g−1). Conclusively, pouch cells with a large area (5 × 7 cm2) have been fabricated, demonstrating extraordinary flexibility and practical utility.
•An oxygen-deficient CuOx coating is first applied to the MnO2 cathode.•Oxygen vacancies promote the dissociation of adsorbed water and the subsequent generation of hydroxyl groups.•The integration of oxygen vacancies and hydroxyl groups lead to simultaneous improvements in electrical conductivity and surface wettability.•The CuOx-coated MnO2 cathode manifests a remarkable specific capacity and exemplary cyclic stability. |
ArticleNumber | 111257 |
Author | Wang, Zhen Feng, Pan Huang, Zhiquan Tian, Wubian Chen, Jian Xu, Hui Tao, Xiao |
Author_xml | – sequence: 1 givenname: Zhen surname: Wang fullname: Wang, Zhen organization: Jiangsu Key Laboratory of Advanced Metallic Materials, School of Materials Science and Engineering, Southeast University, Nanjing 211189, China – sequence: 2 givenname: Hui surname: Xu fullname: Xu, Hui organization: School of Material Science and Engineering, Jiangsu University, Zhenjiang, Jiangsu 212013, China – sequence: 3 givenname: Xiao surname: Tao fullname: Tao, Xiao organization: Jiangsu Key Laboratory of Advanced Metallic Materials, School of Materials Science and Engineering, Southeast University, Nanjing 211189, China – sequence: 4 givenname: Pan surname: Feng fullname: Feng, Pan email: pan.feng@seu.edu.cn organization: Jiangsu Key Laboratory of Advanced Metallic Materials, School of Materials Science and Engineering, Southeast University, Nanjing 211189, China – sequence: 5 givenname: Zhiquan surname: Huang fullname: Huang, Zhiquan organization: Jiangsu Key Laboratory of Advanced Metallic Materials, School of Materials Science and Engineering, Southeast University, Nanjing 211189, China – sequence: 6 givenname: Wubian surname: Tian fullname: Tian, Wubian organization: Jiangsu Key Laboratory of Advanced Metallic Materials, School of Materials Science and Engineering, Southeast University, Nanjing 211189, China – sequence: 7 givenname: Jian surname: Chen fullname: Chen, Jian email: j.chen@seu.edu.cn organization: Jiangsu Key Laboratory of Advanced Metallic Materials, School of Materials Science and Engineering, Southeast University, Nanjing 211189, China |
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Keywords | MnO2 cathode Zinc-ion storage Oxygen-deficient CuOx |
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Title | Boosting the zinc-ion storage ability of MnO2 cathode by depositing oxygen-deficient CuOx layer |
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