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Degradation of High‐Nickel‐Layered Oxide Cathodes from Surface to Bulk: A Comprehensive Structural, Chemical, and Electrical Analysis
Author(s) -
Ko DongSu,
Park JunHo,
Yu Byong Yong,
Ahn Docheon,
Kim Kihong,
Han Heung Nam,
Jeon Woo Sung,
Jung Changhoon,
Manthiram Arumugram
Publication year - 2020
Publication title -
advanced energy materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 10.08
H-Index - 220
eISSN - 1614-6840
pISSN - 1614-6832
DOI - 10.1002/aenm.202001035
Subject(s) - cathode , materials science , degradation (telecommunications) , battery (electricity) , chemical engineering , nickel , energy dispersive x ray spectroscopy , oxide , transition metal , ion , electrode , scanning electron microscope , composite material , metallurgy , chemistry , electronic engineering , power (physics) , physics , biochemistry , organic chemistry , quantum mechanics , engineering , catalysis
Multiple applications of lithium‐ion batteries in energy storage systems and electric vehicles require highly stable electrode materials for long‐term battery operation. Among the various cathode materials, high‐Ni cathode materials enable a high energy density. However, cathode degradation accompanied by complex chemical and structural changes results in capacity and voltage fading in batteries. Cathode degradation remains poorly understood; the majority of studies have only explored the oxidation states of transition‐metal ions in localized areas and have rarely evaluated chemical degradation in complete particles after prolonged cycling. This study systematically investigates the degradation of a high‐Ni cathode by comparing the chemical, structural, and electrical changes in pristine and 500 times‐cycled cathodes. Electron probe micro‐analysis and X‐ray energy dispersive spectroscopy reveal changes in the Ni:O ratio from 1:2 to 1:1 over a large area inside the secondary particle. Electron energy loss spectroscopy analysis related to structural changes is performed for the entire primary particle area to visualize the oxidation state of transition‐metal ions in two dimensions. The results imply that the observed monotonic capacity fade without unusual changes is due to the continuous formation of the Ni 2+ phase from the surface to the bulk through chemical and structural degradation.