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Exploring the bottlenecks of anionic redox in Li-rich layered sulfides

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  • Sujoy Saha

    (Collège de France, Chaire de Chimie du Solide et de l’Energie
    Sorbonne Université
    Réseau sur le Stockage Electrochimique de l’Energie (RS2E))

  • Gaurav Assat

    (Collège de France, Chaire de Chimie du Solide et de l’Energie
    Sorbonne Université
    Réseau sur le Stockage Electrochimique de l’Energie (RS2E))

  • Moulay Tahar Sougrati

    (Réseau sur le Stockage Electrochimique de l’Energie (RS2E)
    Institut Charles Gerhardt
    ALISTORE-European Research Institute)

  • Dominique Foix

    (Réseau sur le Stockage Electrochimique de l’Energie (RS2E)
    Université de Pau)

  • Haifeng Li

    (University of Illinois at Chicago)

  • Jean Vergnet

    (Collège de France, Chaire de Chimie du Solide et de l’Energie
    Sorbonne Université
    Réseau sur le Stockage Electrochimique de l’Energie (RS2E))

  • Soma Turi

    (Collège de France, Chaire de Chimie du Solide et de l’Energie)

  • Yang Ha

    (Advanced Light Source, Lawrence Berkeley National Laboratory)

  • Wanli Yang

    (Advanced Light Source, Lawrence Berkeley National Laboratory)

  • Jordi Cabana

    (University of Illinois at Chicago)

  • Gwenaëlle Rousse

    (Collège de France, Chaire de Chimie du Solide et de l’Energie
    Sorbonne Université
    Réseau sur le Stockage Electrochimique de l’Energie (RS2E))

  • Artem M. Abakumov

    (Center for Energy Science and Technology, Skolkovo Institute of Science and Technology)

  • Jean-Marie Tarascon

    (Collège de France, Chaire de Chimie du Solide et de l’Energie
    Sorbonne Université
    Réseau sur le Stockage Electrochimique de l’Energie (RS2E))

Abstract

Anionic redox chemistry has emerged as a new paradigm to design higher-energy lithium ion-battery cathode materials such as Li-rich layered oxides. However, they suffer from voltage fade, large hysteresis and sluggish kinetics, which originate intriguingly from the anionic redox activity itself. To fundamentally understand these issues, we decided to act on the ligand by designing new Li-rich layered sulfides Li1.33 – 2y/3Ti0.67 – y/3FeyS2, among which the y = 0.3 member shows sustained reversible capacities of ~245 mAh g−1 due to cumulated cationic (Fe2+/3+) and anionic (S2−/Sn−, n

Suggested Citation

  • Sujoy Saha & Gaurav Assat & Moulay Tahar Sougrati & Dominique Foix & Haifeng Li & Jean Vergnet & Soma Turi & Yang Ha & Wanli Yang & Jordi Cabana & Gwenaëlle Rousse & Artem M. Abakumov & Jean-Marie Tar, 2019. "Exploring the bottlenecks of anionic redox in Li-rich layered sulfides," Nature Energy, Nature, vol. 4(11), pages 977-987, November.
  • Handle: RePEc:nat:natene:v:4:y:2019:i:11:d:10.1038_s41560-019-0493-0
    DOI: 10.1038/s41560-019-0493-0
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    Cited by:

    1. Shunsuke Sasaki & Souvik Giri & Simon J. Cassidy & Sunita Dey & Maria Batuk & Daphne Vandemeulebroucke & Giannantonio Cibin & Ronald I. Smith & Philip Holdship & Clare P. Grey & Joke Hadermann & Simon, 2023. "Anion redox as a means to derive layered manganese oxychalcogenides with exotic intergrowth structures," Nature Communications, Nature, vol. 14(1), pages 1-11, December.

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