Metal–organic framework templated fabrication of Cu7S4@Ni(OH)2 core–shell nanoarrays for high-performance supercapacitors

Well-controlled core–shell nanostructured arrays are highly attractive and rational combination of hybrid electrochemical active materials as promising candidate electrodes for supercapacitors still remains a great challenge. In this work, ultrathin Ni(OH)2 nanosheets as the “shell” were anchored on...

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Bibliographic Details
Published inInorganic chemistry frontiers Vol. 7; no. 2; pp. 427 - 436
Main Authors Zhou, Yan, Zhao, Shihang, Yu, Xianbo, Li, Yanli, Chen, Hongmei, Han, Lei
Format Journal Article
LanguageEnglish
Published London Royal Society of Chemistry 21.01.2020
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Summary:Well-controlled core–shell nanostructured arrays are highly attractive and rational combination of hybrid electrochemical active materials as promising candidate electrodes for supercapacitors still remains a great challenge. In this work, ultrathin Ni(OH)2 nanosheets as the “shell” were anchored on Cu7S4 nanorods as the “core” to form core–shell hybrid nanoarrays on copper foam (CF), which were firstly fabricated by a facile metal–organic framework templated synthetic strategy with a three-step procedure of in situ interface growth, sulfurization and hydrothermal synthesis. The core–shell Cu7S4@Ni(OH)2/CF hybrid nanoarrays as binder-free electrodes show a high specific capacitance of 1072.5 F g−1 (482.6 C g−1) at a current density of 1 A g−1, superior rate capacity of 86.4% at 10 A g−1 and an outstanding cycling stability of 94.5% capacitance retention after 10 000 cycles. What's more, the assembled asymmetric supercapacitor device based on Cu7S4@Ni(OH)2/CF as a positive electrode and activated carbon (AC) as a negative electrode shows a high energy density of 52.5 W h kg−1 at a power density of 750 W kg−1 with decent cycling stability. This strategy can be extended to form other unique copper sulfide-based core–shell nanoarray architectures with enhanced electrochemical activity for high-performance energy storage devices.
ISSN:2052-1545
2052-1553
DOI:10.1039/c9qi01180c