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Synergistic effects of nanoarchitecture and oxygen vacancy in nickel molybdate hollow sphere towards a high-performance hybrid supercapacitor

Authors
Sivakumar, PeriyasamyRaj, C. JustinPark, JeongWonJung, Hyun
Issue Date
Dec-2021
Publisher
WILEY
Keywords
energy storage; hollow sphere; hybrid supercapacitor; NiMoO4; oxygen vacancy
Citation
INTERNATIONAL JOURNAL OF ENERGY RESEARCH, v.45, no.15, pp 21516 - 21526
Pages
11
Indexed
SCIE
SCOPUS
Journal Title
INTERNATIONAL JOURNAL OF ENERGY RESEARCH
Volume
45
Number
15
Start Page
21516
End Page
21526
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/4128
DOI
10.1002/er.7156
ISSN
0363-907X
1099-114X
Abstract
The facile design and fabrication of nanoarchitectured binary transition metal oxide electrode materials are essentially required for the advancement of high-performance supercapacitors (SCs). Herein, we prepared an oxygen-vacant NiMoO4 (Ov-NiMoO4) hollow sphere via a simple hydrothermal approach and subsequent heat treatment under an argon atmosphere. In particular, the oxygen vacancy is confirmed by using X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), Raman, and differential reflectance spectroscopy (DRS) UV-Vis spectra studies. Furthermore, the generation of the oxygen vacancy could enhance the electrical conductivity and improve Faradaic redox sites. Significantly, the Ov-NiMoO4 hollow sphere depicts a larger specific capacity (C-sp) of 496 mA h g(-1) at 1 A g(-1) than the bare-NiMoO4 (b-NiMoO4; 279 mA h g(-1)) thermally treated under air. Furthermore, the hybrid SC (HSC) is fabricated based on the Ov-NiMoO4//activated carbon, revealing a high specific capacitance (C-s) of 120 F g(-1) and providing a large energy density (ED) of 37.49 W h kg(-1) and power density (PD) of 36.61 kW kg(-1). Moreover, the HSC shows considerable cyclic stability of similar to 91.14% over 20 000 cycles. The results divulge that the poor crystallinity and the introduction of oxygen vacancies play a vital role in enhancing the charge-storage capability of the materials.
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