期刊
INTERNATIONAL JOURNAL OF ENERGY RESEARCH
卷 46, 期 14, 页码 19402-19413出版社
WILEY
DOI: 10.1002/er.8511
关键词
additive; electrolyte; layered Ni-rich oxide cathode; lithium-ion batteries; sulfite functional group
资金
- National Research Foundation of Korea (NRF) [NRF-2017R1A6A1A06015181, 2022R1A2C2008968]
- Technology Innovation Program [20011905]
- Ministry of Trade, Industry & Energy (MOTIE, Korea)
- National Research Foundation of Korea [2022R1A2C2008968] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
This study introduces a functional additive, 1,2-propyleneglycol sulfite (PGS), to improve the interfacial stability of Ni-rich NCM cathode materials by creating artificial cathode-electrolyte interphase (CEI) layers that inhibit electrolyte decomposition. The addition of 2.0 wt% PGS significantly enhances the cycling performance of the cells.
Ni-rich LiNixCoyMnzO2 (NCM) cathode material has received a lot of attention as an advanced cathode material for lithium-ion batteries (LIBs). However, increasing internal resistance triggered by continuous electrolyte decomposition has become an important issue, as it seriously decreases the cycling retention of cells. Herein, this study will describe the means of a functional additive to improve the interfacial stability of Ni-rich NCM cathode materials, 1,2-propyleneglycol sulfite (PGS), which has a -SO3- functional group. The PGS can create layers of artificial cathode-electrolyte interphase (CEI) through electrochemical oxidation reactions, which inhibit electrolyte decomposition in the cell. The cells without the PGS additive suffered seriously from low-cycling retention (57.1%) after 100 cycles, but their cycling performance increased to 76.9% for the cell with 2.0 wt% PGS. Electrolyte decomposition is subsequently suppressed considerably in cells, indicating that artificial CEI layers incorporated by the electrochemical reaction of PGS improve the interfacial stability. First-principle calculations reveal that PGS exhibited a higher oxidation preference and stronger Ni2+ affinity compared with solvents, and inhibited the formation of detrimental F--like species.
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