TY - JOUR
T1 - Cation-Disordered Li3VO4
T2 - Reversible Li Insertion/Deinsertion Mechanism for Quasi Li-Rich Layered Li1+ x[V1/2Li1/2]O2 (x = 0-1)
AU - Rozier, Patrick
AU - Iwama, Etsuro
AU - Nishio, Nagare
AU - Baba, Kazuhisa
AU - Matsumura, Keisuke
AU - Kisu, Kazuaki
AU - Miyamoto, Junichi
AU - Naoi, Wako
AU - Orikasa, Yuki
AU - Simon, Patrice
AU - Naoi, Katsuhiko
N1 - Funding Information:
This study was supported by the Global Innovation Research Organization in TUAT, JSPS Grant-in-Aid for Scientific Research (KAKENHI) A under Grant No. JP25249140, KAKENHI C under Grant No. JP17K05962, KAKENHI Grand-in-Aid for Young Scientists B under Grant No. JP16K17970, and the Center of Innovation Program from Japan Science and Technology Agency (A-STEP; AS282S002d).
Funding Information:
This study was supported by the Global Innovation Research Organization in TUAT, JSPS Grant-in-Aid for Scientific Research (KAKENHI) A under Grant No. JP25249140, KAKENHI C under Grant No. JP17K05962, KAKENHI Grand-in-Aid for Young Scientists B under Grant No. JP16K17970, and the Center of Innovation Program from Japan Science and Technology Agency (A-STEP; AS282S002d). The synchrotron radiation experiments were performed at the BL14B2 of SPring-8 with the approval of the Japan Synchrotron Radiation Research Institute (JASRI) (Proposal No. 2016B1544) and at the BL8S1 of the Aichi Synchrotron Radiation Center (Aichi, Japan) (Proposal No. 201606105).
Publisher Copyright:
© 2018 American Chemical Society.
PY - 2018/8/14
Y1 - 2018/8/14
N2 - The reversible lithiation/delithiation mechanism of the cation-disordered Li3VO4 material was elucidated, including the understanding of structural and electrochemical signature changes during cycling. The initial exchange of two Li induces a progressive and irreversible 7migration of Li and V ions from tetrahedral to octahedral sites, confirmed by the combination of in situ/operando X-ray diffraction and X-ray absorption fine structure analyses. The resulting cation-disordered Li3VO4 can smoothly and reversibly accommodate two Li and shows a Li+ diffusion coefficient larger by 2 orders of magnitude than the one of pristine Li3VO4, leading to improved electrochemical performance. This cation-disordered Li3VO4 negative electrode offers new opportunities for designing high-energy and high-power supercapacitors. Furthermore, it opens new paths for preparing disordered compounds with the general hexagonal close-packing structure, including most polyanionic compounds, whose electrochemical performance can be easily improved by simple cation mixing.
AB - The reversible lithiation/delithiation mechanism of the cation-disordered Li3VO4 material was elucidated, including the understanding of structural and electrochemical signature changes during cycling. The initial exchange of two Li induces a progressive and irreversible 7migration of Li and V ions from tetrahedral to octahedral sites, confirmed by the combination of in situ/operando X-ray diffraction and X-ray absorption fine structure analyses. The resulting cation-disordered Li3VO4 can smoothly and reversibly accommodate two Li and shows a Li+ diffusion coefficient larger by 2 orders of magnitude than the one of pristine Li3VO4, leading to improved electrochemical performance. This cation-disordered Li3VO4 negative electrode offers new opportunities for designing high-energy and high-power supercapacitors. Furthermore, it opens new paths for preparing disordered compounds with the general hexagonal close-packing structure, including most polyanionic compounds, whose electrochemical performance can be easily improved by simple cation mixing.
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U2 - 10.1021/acs.chemmater.8b00721
DO - 10.1021/acs.chemmater.8b00721
M3 - Article
AN - SCOPUS:85051413979
VL - 30
SP - 4926
EP - 4934
JO - Chemistry of Materials
JF - Chemistry of Materials
SN - 0897-4756
IS - 15
ER -