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Novel piperidinium-based ionic liquid as electrolyte additive for high voltage lithium-ion batteries
Conventional carbonate-based electrolyte is prone to oxidative decomposition at high voltage (over 4.5 V vs. Li/Li(+)), which leads to the bad oxidation stability and inferior cycling performance of lithium ion batteries (LIBs). To solve these problems, a novel ionic liquid (IL) N-butyronitrile-N-me...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8698397/ https://www.ncbi.nlm.nih.gov/pubmed/35424023 http://dx.doi.org/10.1039/d1ra01454d |
Sumario: | Conventional carbonate-based electrolyte is prone to oxidative decomposition at high voltage (over 4.5 V vs. Li/Li(+)), which leads to the bad oxidation stability and inferior cycling performance of lithium ion batteries (LIBs). To solve these problems, a novel ionic liquid (IL) N-butyronitrile-N-methylpiperidinium bis(fluorosulfonyl)imide (PP(1,CN)FSI) was synthesized and explored as the additive to the LiPF(6)–ethylene carbonate (EC)/dimethyl carbonate (DMC) electrolyte. For the cell performance, the addition of PP(1,CN)FSI not only inhibits overcharge phenomenon, but also improves discharge capacity, thus enhancing capacity retention capability. Compared to the cell with blank electrolyte, the capacity retentions of adding 15 wt% PP(1,CN)FSI into the electrolyte were improved to 96.8% and 97% from 82.8% and 78.7% at 0.2 C and 5 C, respectively. The effects of PP(1,CN)FSI on the LNMO cathode surface were further investigated by electrochemical impedance spectroscopy (EIS), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). It reveals that PP(1,CN)FSI addition drives the formation of solid electrolyte interphase (SEI) film which suppresses oxidative decomposition of the electrolyte and protects the structure cathode material. |
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