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Merging of Kirkendall growth and Ostwald ripening: CuO@MnO2 core-shell architectures for asymmetric supercapacitors.


ABSTRACT: Fabricating hierarchical core-shell nanostructures is currently the subject of intensive research in the electrochemical field owing to the hopes it raises for making efficient electrodes for high-performance supercapacitors. Here, we develop a simple and cost-effective approach to prepare CuO@MnO2 core-shell nanostructures without any surfactants and report their applications as electrodes for supercapacitors. An asymmetric supercapacitor with CuO@MnO2 core-shell nanostructure as the positive electrode and activated microwave exfoliated graphite oxide (MEGO) as the negative electrode yields an energy density of 22.1 Wh kg(-1) and a maximum power density of 85.6 kW kg(-1); the device shows a long-term cycling stability which retains 101.5% of its initial capacitance even after 10000 cycles. Such a facile strategy to fabricate the hierarchical CuO@MnO2 core-shell nanostructure with significantly improved functionalities opens up a novel avenue to design electrode materials on demand for high-performance supercapacitor applications.

SUBMITTER: Huang M 

PROVIDER: S-EPMC3970130 | biostudies-literature | 2014

REPOSITORIES: biostudies-literature

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Merging of Kirkendall growth and Ostwald ripening: CuO@MnO2 core-shell architectures for asymmetric supercapacitors.

Huang Ming M   Zhang Yuxin Y   Li Fei F   Wang Zhongchang Z   Alamusi   Hu Ning N   Wen Zhiyu Z   Liu Qing Q  

Scientific reports 20140331


Fabricating hierarchical core-shell nanostructures is currently the subject of intensive research in the electrochemical field owing to the hopes it raises for making efficient electrodes for high-performance supercapacitors. Here, we develop a simple and cost-effective approach to prepare CuO@MnO2 core-shell nanostructures without any surfactants and report their applications as electrodes for supercapacitors. An asymmetric supercapacitor with CuO@MnO2 core-shell nanostructure as the positive e  ...[more]

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