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      Direct Observation of Reductive Coupling Mechanism between Oxygen and Iron/Nickel in Cobalt‐Free Li‐Rich Cathode Material: An in Operando X‐Ray Absorption Spectroscopy Study

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      https://www.riss.kr/link?id=O112125115

      • 저자
      • 발행기관
      • 학술지명
      • 권호사항
      • 발행연도

        2021년

      • 작성언어

        -

      • Print ISSN

        1614-6832

      • Online ISSN

        1614-6840

      • 등재정보

        SCOPUS;SCIE

      • 자료형태

        학술저널

      • 수록면

        n/a-n/a   [※수록면이 p5 이하이면, Review, Columns, Editor's Note, Abstract 등일 경우가 있습니다.]

      • 구독기관
        • 전북대학교 중앙도서관  
        • 성균관대학교 중앙학술정보관  
        • 부산대학교 중앙도서관  
        • 전남대학교 중앙도서관  
        • 제주대학교 중앙도서관  
        • 중앙대학교 서울캠퍼스 중앙도서관  
        • 인천대학교 학산도서관  
        • 숙명여자대학교 중앙도서관  
        • 서강대학교 로욜라중앙도서관  
        • 충남대학교 중앙도서관  
        • 한양대학교 백남학술정보관  
        • 이화여자대학교 중앙도서관  
        • 고려대학교 도서관  
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      부가정보

      다국어 초록 (Multilingual Abstract)

      Li‐rich cathodes possess high capacity and are promising candidates in next‐generation high‐energy density Li‐ion batteries. This high capacity is partly attributed to its poorly understood oxygen‐redox activity. The present Li‐rich cathod...

      Li‐rich cathodes possess high capacity and are promising candidates in next‐generation high‐energy density Li‐ion batteries. This high capacity is partly attributed to its poorly understood oxygen‐redox activity. The present Li‐rich cathodes contain expensive and environmentally‐incompatible cobalt as a main transition metal. In this work, cobalt‐free, iron‐containing Li‐rich cathode material (nominal composition Li1.2Mn0.56Ni0.16Fe0.08O2) is synthesized, which exhibits excellent discharge capacity (≈250 mAh g−1) and cycling stability. In operando, X‐ray absorption spectroscopy at Mn, Fe, and Ni K edges reveals its electrochemical mechanism. X‐ray absorption near edge structure (XANES) features of Fe and Ni K edges show unusual behavior: when an electrode is charged to 4.5 V, Fe and Ni K edges’ XANES features shift to higher energies, evidence for Fe3+→Fe4+ and Ni2+→Ni4+ oxidation. However, when charged above 4.5 V, XANES features of Fe and Ni K edges shift back to lower energies, indicating Fe4+→Fe3+ and Ni4+→Ni3+ reduction. This behavior can be linked to a reductive coupling mechanism between oxygen and Fe/Ni. Though this mechanism is observed in Fe‐containing Li‐rich materials, the only electrochemically active metal in such cases is Fe. Li1.2Mn0.56Ni0.16Fe0.08O2 has multiple electrochemically active metal ions; Fe and Ni, which are investigated simultaneously and the obtained results will assist tailoring of cost‐effective Li‐rich materials.
      A cobalt‐free Li‐rich cathode material in which Ni and Fe are electrochemically active is synthesized and its electrochemical reaction mechanism is investigated using in operando X‐Ray Absorption Spectroscopy. Both Ni and Fe in the material are found to undergo reductive coupling with oxygen, during charging above 4.5 V versus Li+/Li, contributing to the anomalous capacity observed in the first charge.

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