3D flower-like oxygen-deficient non-stoichiometry zinc cobaltite for high performance hybrid supercapacitors
- Authors
- Sivakumar, Periyasamy; Nakhanivej, Puritut; Raj, Chellam Justin; Park, Ho Seok
- Issue Date
- 10-Jun-2021
- Publisher
- WILEY
- Keywords
- 3D architecture; flower like morphology; hybrid supercapacitor; non‐ stoichiometry; oxygen deficiency
- Citation
- INTERNATIONAL JOURNAL OF ENERGY RESEARCH, v.45, no.7, pp 10832 - 10842
- Pages
- 11
- Indexed
- SCIE
SCOPUS
- Journal Title
- INTERNATIONAL JOURNAL OF ENERGY RESEARCH
- Volume
- 45
- Number
- 7
- Start Page
- 10832
- End Page
- 10842
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/4803
- DOI
- 10.1002/er.6566
- ISSN
- 0363-907X
1099-114X
- Abstract
- Non-stoichiometry and defect engineering of nanostructured materials plays a vital role in controlling the electronic structure, which results in enhancing the electrochemical performances. Herein, we report three-dimensional (3D) oxygen-deficient flower-like non-stoichiometry zinc cobaltite (Zn1.5Co1.5O4-delta) for hybrid supercapacitor applications. In particular, XRD, XPS and Raman analyses confirm the oxygen-deficiency of the non-stoichiometry Zn1.5Co1.5O4-delta. The oxygen-deficient non-stoichiometry and 3D hierarchical porous structure of Zn1.5Co1.5O4-delta offer the efficient utilization of abundant electrochemical active sites and the rapid transportation of ion/electron. Accordingly, the Zn1.5Co1.5O4-delta electrode achieves the high specific capacitance of 763.32 F g(-1) at 1 A g(-1), which is superior to those of ZnCo2O4 (613.14 F g(-)1), Co3O4 (353.88 F g(-1)) and ZnO (248.59 F g(-1)). The hybrid supercapacitor cells, configuring Zn1.5Co1.5O4-delta as the positive electrode and activated carbon as negative electrodes, respectively, deliver the maximum energy/power densities (40.49 W h kg(-1) at 397.37 W kg(-1) and 20.87 W h kg(-1) at 50.08 kW kg(-1)) and outstanding cycle stability with capacitance retention of 89.42% over 20 000 cycles.
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Collections - College of Natural Science > Department of Chemistry > 1. Journal Articles

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