Lithiation‐Induced Vacancy Engineering of Co3O4 with Improved Faradic Reactivity for High‐Performance Supercapacitor

By Yu Zhang, Yuxiang Hu, Zhiliang Wang, Tong'en Lin, Xiao-bo Zhu, Bin Luo, Han Hu, W. Xing, Zifeng Yan, Lianzhou Wang. Advanced Functional Materials, 2020

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Transition metal oxides are promising electrode candidates for supercapacitor because of their low cost, high theoretical capacity, and good reversibility. However, intrinsically poor electrical conductivity and sluggish reaction kinetics of these oxides normally lead to low specific capacity and slow rate capability of the devices. Herein, a commonly used cobalt oxide is used as an example to demonstrate that lithiation process as a new strategy to enhance its electrochemical performance for supercapacitor application. Detailed characterization reveals that electrochemical lithiation of Co3O4 crystal reduces the coordination of the CoO band, leading to substantially increased oxygen vacancies (octahedral Co2+ sites). These vacancies further trigger the formation of a new electronic state in the bandgap, resulting in remarkably improved electrical conductivity and accelerated faradic reactions. The lithiated Co3O4 exhibits a noticeably enhanced specific capacity of 260 mAh g−1 at 1 A g−1, approximately fourfold enhancement compared to that of pristine Co3O4 (66 mAh g−1). The hybrid supercapacitor assembled with lithiated Co3O4//N‐doped activated carbon achieves high energy densities in a broad range of power densities, e.g., 76.7 Wh kg−1 at 0.29 kW kg−1, 46.9 Wh kg−1 at a high power density of 18.7 kW kg−1, outperforming most of the reported hybrid supercapacitors.

Subfields: Electrical and Electronic Engineering, Electronic, Optical and Magnetic Materials, Renewable Energy, Sustainability and the Environment

View Paper: https://www.semanticscholar.org/paper/7b3776907a60526483584f70863f5cc66ef1f8b3