4.7 Article

Assembly of flexible CoMoO4@NiMoO4•xH2O and Fe2O3 electrodes for solid-state asymmetric supercapacitors

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SCIENTIFIC REPORTS
卷 7, 期 -, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/srep41088

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资金

  1. National Natural Science Foundation of China [51572058, 91216123, 51174063, 51502057]
  2. Natural Science Foundation of Heilongjiang Province [E201436]
  3. International Science & Technology Cooperation Program of China [2013DFR10630, 2015DFE52770]
  4. Specialized Research Fund for the Doctoral Program of Higher Education [SRFDP 20132302110031]
  5. Natural Science Foundation of Heilongjiang Province of China [E2016062]
  6. China Postdoctoral Science Foundation [2014M561345]
  7. Heilongjiang Postdoctoral Science Foundation [LBH-Z14105]

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In this work, CoMoO4@NiMoO4 center dot xH(2)O core-shell heterostructure electrode is directly grown on carbon fabric (CF) via a feasible hydrothermal procedure with CoMoO4 nanowires (NWs) as the core and NiMoO4 nanosheets (NSs) as the shell. This core-shell heterostructure could provide fast ion and electron transfer, a large number of active sites, and good strain accommodation. As a result, the CoMoO4@NiMoO4 center dot xH(2)O electrode yields high-capacitance performance with a high specific capacitance of 1582 F g(-1), good cycling stability with the capacitance retention of 97.1% after 3000 cycles and good rate capability. The electrode also shows excellent mechanical flexibility. Also, a flexible Fe2O3 nanorods/CF electrode with enhanced electrochemical performance was prepared. A solid-state asymmetric supercapacitor device is successfully fabricated by using flexible CoMoO4@NiMoO4 center dot xH(2)O as the positive electrode and Fe2O3 as the negative electrode. The asymmetric supercapacitor with a maximum voltage of 1.6 V demonstrates high specific energy (41.8 Wh kg(-1) at 700 W kg(-1)), high power density (12000 W kg(-1) at 26.7 Wh kg(-1)), and excellent cycle ability with the capacitance retention of 89.3% after 5000 cycles (at the current density of 3A g(-1)).

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