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Anionic Chemistry Modulation Enabled Environmental Self-Charging Aqueous Zinc Batteries: The Case of Carbonate Ions.
Qu, Guangmeng; Wang, Lu; Zhao, Yongzheng; Wang, Dedong; Zhang, Xixi; Wang, Bin; Wang, Fengbo; Jing, Zhongxin; Xu, Xijin; Xu, Liqiang; Li, Hongfei.
Afiliação
  • Qu G; Shandong University, School of Chemistry and Chemical Engineering, CHINA.
  • Wang L; Shandong University, School of Chemistry and Chemical Engineering, CHINA.
  • Zhao Y; Shandong University, School of Chemistry and Chemical Engineering, CHINA.
  • Wang D; Shandong University, School of Chemistry and Chemical Engineering, CHINA.
  • Zhang X; University of Jinan, School of Physics and Technology, CHINA.
  • Wang B; Shandong University, School of Chemistry and Chemical Engineering, CHINA.
  • Wang F; Shandong University, School of Chemistry and Chemical Engineering, CHINA.
  • Jing Z; Shandong University, School of Chemistry and Chemical Engineering, CHINA.
  • Xu X; University of Jinan, School of Physics and Technology, CHINA.
  • Xu L; Southern University of Science and Technology, School of System Design and Intelligent Manufacturing, CHINA.
  • Li H; Southern University of Science and Technology, School of System Design and Intelligent Manufacturing, 1088 Xueyuan Avenue, Shenzhen, 518055, Shenzhen, CHINA.
Angew Chem Int Ed Engl ; : e202409774, 2024 Jul 02.
Article em En | MEDLINE | ID: mdl-38953785
ABSTRACT
Anionic chemistry modulation represents a promising avenue to enhance the electrochemical performance and unlock versatile applications in cutting-edge energy storage devices. Herein, we propose a methodology that involves anionic chemistry of carbonate anions to tailor the electrochemical oxidation-reduction reactions of bismuth (Bi) electrodes, where the conversion energy barrier for Bi (0) to Bi (III) has been significantly reduced, endowing anionic full batteries with enhanced electrochemical kinetics and chemical self-charging property. The elaborately designed batteries with an air-switch demonstrate rapid self-recharging capabilities, recovering over 80% of the electrochemical full charging capacity within a remarkably short timeframe of 1 hour and achieving a cumulative self-charging capacity of 5 Ah g-1. The aqueous self-charging battery strategy induced by carbonate anion, as proposed in this study, holds the potential for extending to various anionic systems, including seawater-based Cl- ion batteries. This work offers a universal framework for advancing next-generation multi-functional power sources.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article