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P2-Type Moisture-Stable and High-Voltage-Tolerable Cathodes for High-Energy and Long-Life Sodium-Ion Batteries.
Yuan, Siqi; Yu, Lei; Qian, Guannan; Xie, Yingying; Guo, Penghui; Cui, Guijia; Ma, Jun; Ren, Xiangyu; Xu, Zhixin; Lee, Sang-Jun; Lee, Jun-Sik; Liu, Yijin; Ren, Yang; Li, Linsen; Tan, Guoqiang; Liao, Xiaozhen.
Afiliação
  • Yuan S; Shanghai Electrochemical Energy Devices Research Center, Department of Chemical Engineering, Shanghai Jiao Tong University, Shanghai 200240, People's Republic of China.
  • Yu L; Key Laboratory for Soft Chemistry and Functional Materials, Nanjing University of Science and Technology, Nanjing 210094, People's Republic of China.
  • Qian G; Stanford Synchrotron Radiation Lightsource, SLAC National Accelerator Laboratory, Menlo Park, California 94025, United States.
  • Xie Y; Chemical Sciences and Engineering Division, Argonne National Laboratory, Lemont, Illinois 60439, United States.
  • Guo P; School of Materials Science & Engineering, Beijing Institute of Technology, Beijing 100081, People's Republic of China.
  • Cui G; Shanghai SodaEn New Energy Technology Co., Ltd, Shanghai 200240, People's Republic of China.
  • Ma J; In-Situ Center for Physical Sciences, School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai 200240, People's Republic of China.
  • Ren X; School of Materials Science and Engineering, Shanghai Jiao Tong University, Shanghai 200240, China.
  • Xu Z; Shanghai Electrochemical Energy Devices Research Center, Department of Chemical Engineering, Shanghai Jiao Tong University, Shanghai 200240, People's Republic of China.
  • Lee SJ; Stanford Synchrotron Radiation Lightsource, SLAC National Accelerator Laboratory, Menlo Park, California 94025, United States.
  • Lee JS; Stanford Synchrotron Radiation Lightsource, SLAC National Accelerator Laboratory, Menlo Park, California 94025, United States.
  • Liu Y; Stanford Synchrotron Radiation Lightsource, SLAC National Accelerator Laboratory, Menlo Park, California 94025, United States.
  • Ren Y; Department of Physics, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong 999077, People's Republic of China.
  • Li L; Shanghai Electrochemical Energy Devices Research Center, Department of Chemical Engineering, Shanghai Jiao Tong University, Shanghai 200240, People's Republic of China.
  • Tan G; School of Materials Science & Engineering, Beijing Institute of Technology, Beijing 100081, People's Republic of China.
  • Liao X; Shanghai Electrochemical Energy Devices Research Center, Department of Chemical Engineering, Shanghai Jiao Tong University, Shanghai 200240, People's Republic of China.
Nano Lett ; 23(5): 1743-1751, 2023 Mar 08.
Article em En | MEDLINE | ID: mdl-36811529
ABSTRACT
P2-Na0.67Ni0.33Mn0.67O2 represents a promising cathode for Na-ion batteries, but it suffers from severe structural degradation upon storing in a humid atmosphere and cycling at a high cutoff voltage. Here we propose an in situ construction to achieve simultaneous material synthesis and Mg/Sn cosubstitution of Na0.67Ni0.33Mn0.67O2 via one-pot solid-state sintering. The materials exhibit superior structural reversibility and moisture insensitivity. In-operando XRD reveals an essential correlation between cycling stability and phase reversibility, whereas Mg substitution suppressed the P2-O2 phase transition by forming a new Z phase, and Mg/Sn cosubstitution enhanced the P2-Z transition reversibility benefiting from strong Sn-O bonds. DFT calculations disclosed high chemical tolerance to moisture, as the adsorption energy to H2O was lower than that of the pure Na0.67Ni0.33Mn0.67O2. A representative Na0.67Ni0.23Mg0.1Mn0.65Sn0.02O2 cathode exhibits high reversible capacities of 123 mAh g-1 (10 mA g-1), 110 mAh g-1 (200 mA g-1), and 100 mAh g-1 (500 mA g-1) and a high capacity retention of 80% (500 mA g-1, 500 cycles).
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article