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Evolution of the electrochemical interface in sodium ion batteries with ether electrolytes

Author

Listed:
  • Kaikai Li

    (Tsinghua University
    The Hong Kong Polytechnic University
    The Hong Kong Polytechnic University)

  • Jun Zhang

    (Tsinghua University)

  • Dongmei Lin

    (The Hong Kong Polytechnic University)

  • Da-Wei Wang

    (The University of New South Wales)

  • Baohua Li

    (Tsinghua University)

  • Wei Lv

    (Tsinghua University)

  • Sheng Sun

    (Shanghai University)

  • Yan-Bing He

    (Tsinghua University)

  • Feiyu Kang

    (Tsinghua University
    Tsinghua University)

  • Quan-Hong Yang

    (Tsinghua University
    Tianjin University)

  • Limin Zhou

    (The Hong Kong Polytechnic University
    The Hong Kong Polytechnic University)

  • Tong-Yi Zhang

    (Shanghai University)

Abstract

Ether based electrolytes have surfaced as alternatives to conventional carbonates allowing for enhanced electrochemical performance of sodium-ion batteries; however, the primary source of the improvement remains poorly understood. Here we show that coupling titanium dioxide and other anode materials with diglyme does enable higher efficiency and reversible capacity than those for the combination involving ester electrolytes. Importantly, the electrolyte dependent performance is revealed to be the result of the different structural evolution induced by a varied sodiation depth. A suit of characterizations show that the energy barrier to charge transfer at the interface between electrolyte and electrode is the factor that dominates the interfacial electrochemical characteristics and therefore the energy storage properties. Our study proposes a reliable parameter to assess the intricate sodiation dynamics in sodium-ion batteries and could guide the design of aprotic electrolytes for next generation rechargeable batteries.

Suggested Citation

  • Kaikai Li & Jun Zhang & Dongmei Lin & Da-Wei Wang & Baohua Li & Wei Lv & Sheng Sun & Yan-Bing He & Feiyu Kang & Quan-Hong Yang & Limin Zhou & Tong-Yi Zhang, 2019. "Evolution of the electrochemical interface in sodium ion batteries with ether electrolytes," Nature Communications, Nature, vol. 10(1), pages 1-10, December.
    • Handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-08506-5
    DOI: 10.1038/s41467-019-08506-5
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    Cited by:

    1. Perveen, Tahira & Siddiq, Muhammad & Shahzad, Nadia & Ihsan, Rida & Ahmad, Abrar & Shahzad, Muhammad Imran, 2020. "Prospects in anode materials for sodium ion batteries - A review," Renewable and Sustainable Energy Reviews, Elsevier, vol. 119(C).
    2. Yue, Xiyan & Qiao, Bozheng & Wang, Jiajia & Xie, Zhengkun & Liu, Zhao & Yang, Zhengpeng & Abudula, Abuliti & Guan, Guoqing, 2023. "Layered metal chalcogenide based anode materials for high performance sodium ion batteries: A review," Renewable and Sustainable Energy Reviews, Elsevier, vol. 185(C).
    3. Bartoli, Mattia & Piovano, Alessandro & Elia, Giuseppe Antonio & Meligrana, Giuseppina & Pedraza, Riccardo & Pianta, Nicolò & Tealdi, Cristina & Pagot, Gioele & Negro, Enrico & Triolo, Claudia & Gomez, 2024. "Pristine and engineered biochar as Na-ion batteries anode material: A comprehensive overview," Renewable and Sustainable Energy Reviews, Elsevier, vol. 194(C).
    4. Minxia Jiang & Yingjie Hu & Baoguang Mao & Yixin Wang & Zhen Yang & Tao Meng & Xin Wang & Minhua Cao, 2022. "Strain-regulated Gibbs free energy enables reversible redox chemistry of chalcogenides for sodium ion batteries," Nature Communications, Nature, vol. 13(1), pages 1-13, December.
    5. Qiulong Wei & Xiaoqing Chang & Danielle Butts & Ryan DeBlock & Kun Lan & Junbin Li & Dongliang Chao & Dong-Liang Peng & Bruce Dunn, 2023. "Surface-redox sodium-ion storage in anatase titanium oxide," Nature Communications, Nature, vol. 14(1), pages 1-9, December.
    6. Ziyang Lu & Huijun Yang & Yong Guo & Hongxin Lin & Peizhao Shan & Shichao Wu & Ping He & Yong Yang & Quan-Hong Yang & Haoshen Zhou, 2024. "Consummating ion desolvation in hard carbon anodes for reversible sodium storage," Nature Communications, Nature, vol. 15(1), pages 1-13, December.

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