Xueqing Min , Li Wang , Min Shen , Guoqiang Ma , Xiangming He
{"title":"A multifunctional additive extending the calendar life of Ni-rich cathode-based lithium-ion batteries for electric vehicles","authors":"Xueqing Min , Li Wang , Min Shen , Guoqiang Ma , Xiangming He","doi":"10.1016/j.mattod.2024.12.021","DOIUrl":null,"url":null,"abstract":"<div><div>Lithium-ion batteries (LIBs) with Ni-rich cathode are expected to conquer range anxiety for electric vehicles (EVs). However, they suffer from rapid performance fading under inadequate thermal management, particularly during EV applications in summer, due to vigorous parasitic reactions between the Ni-rich materials and the electrolyte and consequent chemical crosstalk at elevated temperature. To address the challenge, a triple-functional additive named triallyl cyanurate (TAC) is proposed in this study, and the mechanism of its function is validated theoretically and experimentally. In detail, TAC builds strong solid electrolyte interphase (SEI) through reduction to protect the anode, forms robust cathode electrolyte interphase (CEI) via oxidation decomposition due to preferable adsorption to restrain the parasitic reactions between the cathode and the electrolyte, and inhibits LiPF<sub>6</sub> hydrolysis to remove HF to lower the corrosivity of the electrolyte. Encouragingly, the TAC-containing electrolyte significantly extends the cycle life of Ah-level pouch cells with various Ni-rich cathodes by 2.5 times at room temperature and 45 °C, as well as extending the high-temperature storage capability by up to 2.8 times. The successful exploration of functional TAC as electrolyte additive presents a promising multi-in-one strategy for additive design, paving a new avenue to boost the application of Ni-rich cathode in LIBs.</div></div>","PeriodicalId":387,"journal":{"name":"Materials Today","volume":"83 ","pages":"Pages 157-165"},"PeriodicalIF":21.1000,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Materials Today","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1369702124002980","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Lithium-ion batteries (LIBs) with Ni-rich cathode are expected to conquer range anxiety for electric vehicles (EVs). However, they suffer from rapid performance fading under inadequate thermal management, particularly during EV applications in summer, due to vigorous parasitic reactions between the Ni-rich materials and the electrolyte and consequent chemical crosstalk at elevated temperature. To address the challenge, a triple-functional additive named triallyl cyanurate (TAC) is proposed in this study, and the mechanism of its function is validated theoretically and experimentally. In detail, TAC builds strong solid electrolyte interphase (SEI) through reduction to protect the anode, forms robust cathode electrolyte interphase (CEI) via oxidation decomposition due to preferable adsorption to restrain the parasitic reactions between the cathode and the electrolyte, and inhibits LiPF6 hydrolysis to remove HF to lower the corrosivity of the electrolyte. Encouragingly, the TAC-containing electrolyte significantly extends the cycle life of Ah-level pouch cells with various Ni-rich cathodes by 2.5 times at room temperature and 45 °C, as well as extending the high-temperature storage capability by up to 2.8 times. The successful exploration of functional TAC as electrolyte additive presents a promising multi-in-one strategy for additive design, paving a new avenue to boost the application of Ni-rich cathode in LIBs.
期刊介绍:
Materials Today is the leading journal in the Materials Today family, focusing on the latest and most impactful work in the materials science community. With a reputation for excellence in news and reviews, the journal has now expanded its coverage to include original research and aims to be at the forefront of the field.
We welcome comprehensive articles, short communications, and review articles from established leaders in the rapidly evolving fields of materials science and related disciplines. We strive to provide authors with rigorous peer review, fast publication, and maximum exposure for their work. While we only accept the most significant manuscripts, our speedy evaluation process ensures that there are no unnecessary publication delays.