Revealing the Charge Storage Mechanism of Nickel Oxide Electrochromic Supercapacitors

Nickel oxide (NiO) is considered one of the most promising positive anode materials for electrochromic supercapacitors. Nevertheless, a detailed mechanism of the electrochromic and energy storage process has yet to be unraveled. In this research, the charge storage mechanism of a NiO electrochromic...

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Veröffentlicht in:ACS applied materials & interfaces 2020-09, Vol.12 (35), p.39098-39107
Hauptverfasser: Luo, Zhihui, Liu, Lei, Yang, Xiaoyong, Luo, Xuan, Bi, Peng, Fu, Zhenjin, Pang, Aimin, Li, Wei, Yi, Yong
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Sprache:eng
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Zusammenfassung:Nickel oxide (NiO) is considered one of the most promising positive anode materials for electrochromic supercapacitors. Nevertheless, a detailed mechanism of the electrochromic and energy storage process has yet to be unraveled. In this research, the charge storage mechanism of a NiO electrochromic electrode was investigated by combining the in-depth experimental and theoretical analyses. Experimentally, a kinetic analysis of the Li-ion behavior based on the cyclic voltammetry curves reveals the major contribution of surface capacitance versus total capacity, providing fast reaction kinetics and a highly reversible electrochromic performance. Theoretically, our model uncovers that Li ions prefer to adsorb at fcc sites on the NiO(1 1 1) surface, then diffuse horizontally over the plane, and finally migrate in the bulk. More significantly, the calculated theoretical surface capacity (106 mA h g–1) accounts for about 77.4% of the total experimental capacity (137 mA h g–1), indicating that the surface storage process dominates the whole charge storage, which is in accordance with the experimental results. This work provides a fundamental understanding of transition-metal oxides for application in electrochromic supercapacitors and can also promote the exploration of novel electrode materials for high-performance electrochromic supercapacitors.
ISSN:1944-8244
1944-8252
1944-8252
DOI:10.1021/acsami.0c09606