Source abstract
Abstract
The layer-structured cathode materials with high specific capacities are highly required to meet the demands of high-energy-density Li-ion batteries. However, the oxygen loss and the transition metal migration at the deep delithiation state lead to the generation of the surface spinels, which was believed to be responsible for the fade of the reversible capacity and the discharge potential. Different from the conventional “additive” surface modification such as surface coating and surface doping, we hereby apply a “subtraction” strategy to reconstruct the surface of LiCoO 2 by quenching it in an aqueous solution of KAl(SO 4 ) 2 . Such salt-solution quenching merges the Li + /H + ion-exchange in the acidic solution and the Al 3+ doping in molten salt to form a Co 3 O 4 -like ((Co,Al) 3 O 4 ) spinel on the LiCoO 2 surface. A combined investigation of the crystalline and electronic structural characterizations and density functional theory calculations correlates the presence of the “artificial” (Co,Al) 3 O 4 surface spinel and the suppressed structural degradation of LiCoO 2 at high potentials (4.6 V vs Li + /Li). The LiCo 2 O 4 -like spinel observed on naked Li 1– x CoO 2 is energetically apt to transform to Co 3 O 4 spinel. In contrast, the specifically fabricated spinel hinders the Co migration and the subsequent formation of the LiCo 2 O 4 -like spinel, while the high binding energy of oxygen in the LiCoO 2 /(Co,Al) 3 O 4 heterojunction prevents the oxygen escape. Therefore, the presence of the LiCo 2 O 4 -like spinel as an electrochemical intermediate facilitates the structural degradation from LiCoO 2 to Co 3 O 4 while the artificial spinel (Co,Al) 3 O 4 passivates the LiCoO 2 surface by preventing the formation of the LiCo 2 O 4 -like spinel intermediate. These findings clarify the role of the surface spinels generated by different ways and their impacts on the evolution of the structure and electrochemical behaviors of the layer-structured cathode materials and inspire new strategies on improving the performances of the cathode materials.
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Affiliations
Key Laboratory for Renewable Energy, Chinese Academy of Sciences, Beijing Key Laboratory for New Energy Materials and Devices, Institute of Physics, Chinese Academy of Sciences, Beijing 100190, China
College of Material Science and Optoelectronic Technology, University of Chinese Academy of Sciences, Beijing 100049, China
Laboratory for Advanced Materials and Electron Microscopy, Institute of Physics, Chinese Academy of Sciences, Beijing 100190, China
School of Physical Sciences, University of Chinese Academy of Sciences, Beijing 100049, China
National Center for Nanoscience and Technology, Chinese Academy of Sciences, Beijing 100190, China
Max Planck Institute for Chemical Physics of Solids, Dresden 01187, Germany
National Synchrotron Radiation Research Center, Hsinchu 30076, Taiwan
Qingdao Industrial Energy Storage Research Institute, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, Qingdao 266101, China
Funding
Agence Nationale de la Recherche · National Natural Science Foundation of China · Chinese Academy of Sciences