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Unraveling H+/Zn2+ Sequential Conversion Reactions in Tellurium Cathodes for Rechargeable Aqueous Zinc Batteries.
Wang, Jinzhi; Du, Junzhe; Zhao, Jingwen; Wang, Yantao; Tang, Yue; Cui, Guanglei.
Afiliação
  • Wang J; Qingdao Industrial Energy Storage Research Institute, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, Qingdao 266101, China.
  • Du J; Center of Materials Science and Optoelectronics Engineering, University of Chinese Academy of Sciences, Beijing 100049, China.
  • Zhao J; Qingdao Industrial Energy Storage Research Institute, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, Qingdao 266101, China.
  • Wang Y; Qingdao Industrial Energy Storage Research Institute, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, Qingdao 266101, China.
  • Tang Y; Qingdao Industrial Energy Storage Research Institute, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, Qingdao 266101, China.
  • Cui G; School of Future Technology, University of Chinese Academy of Sciences, Beijing 100190, China.
J Phys Chem Lett ; 12(41): 10163-10168, 2021 Oct 21.
Article em En | MEDLINE | ID: mdl-34643403
Progress toward practical rechargeable aqueous zinc (Zn) batteries is impeded by the low energy density. The use of tellurium (Te) cathodes featuring multielectron redox reactions offers one possible approach to mitigating this dilemma. However, the corresponding energy-storage mechanisms in aqueous electrolytes are not established yet. Here, we uncover a H+/Zn2+-involved sequential conversion reaction with 6e- transfer for Te-based cathodes, which accounts for the outstanding capacity (over 460 mAh g-1 at 50 mA g-1). Two distinct redox processes, corresponding to TeO2 ↔ Te and Te ↔ ZnTe, are explicitly revealed within the electrochemical window of routine aqueous Zn electrolytes. The mechanism elucidated here complements the understanding of energy-dense Te centers and propels the exploration of high-capacity electrodes for multivalent battery chemistries.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: J Phys Chem Lett Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: J Phys Chem Lett Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China