Thermal runaway aspect of ultrahigh-nickel cathode-based lithium-ion batteries at increasing charge states

被引:8
作者
Oh, Juyoung [1 ]
Mehrotra, Ayushi [2 ]
Lee, Yejun [2 ]
Kim, Bohoon [3 ]
Yoh, Jack J. [2 ]
机构
[1] Seoul Natl Univ, Inst Adv Machines & Design, 1 Gwanakro, Seoul 08826, South Korea
[2] Seoul Natl Univ, Dept Aerosp Engn, 1 Gwanakro, Seoul 08826, South Korea
[3] Samsung SDI, Syst Verificat Grp, 150-20 Gongse Ro, Youngin Si 17084, Gyeonggi Do, South Korea
基金
新加坡国家研究基金会;
关键词
Ultrahigh-nickel cathode; Lithium-ion batteries; State of charge; Calorimetry; Thermal runaway; Silicon-suboxide-graphite anodes; CALORIMETRY; KINETICS; MODEL; ELECTROLYTE; STABILITY; MECHANISM; GRAPHITE; FAILURE;
D O I
10.1016/j.est.2023.109887
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
High-nickel cathode-based lithium-ion batteries (LIBs) are the core of sustainable innovation in electric vehicles (EV). However, there exists a fire hazard associated with thermal runaway (TR) during charging due to chemical instability of the abundant nickel oxides produced. While the subject of TR in LIBs has been considered in the past, research on the ultrahigh-nickel (Ni content >90 wt%) cathode materials subjected to a wide range of state of charge (SOC) is limited. The LIB is transforming towards going ultrahigh in Ni content to improve the performance of EVs, and ultimately resolving safety issues associated with TR related fire accidents is an immediate goal. The current study presents a correlation amongst the LIB components, SOCs, and Ni contents on two classes of cathodes, namely high-Ni at 88 % and ultrahigh-Ni at 91 % Ni. The exothermic reaction involving anode and electrolyte in a full cell was intensified at SOCs >75 %, leading to the dissociation of cathode materials and a significant self-heating via repeated reactions. When self-heating rate exceeded 1000 C/min, the reaction developed into a TR, elucidating that a 3 % increase from 88 % to 91 % Ni content brought forward the likelihood of TR with a much shorter delay time.
引用
收藏
页数:13
相关论文
共 41 条
[1]   Contribution of the structural changes of LiNi0.8Co0.15Al0.05O2 cathodes on the exothermic reactions in Li-ion cells [J].
Bang, HJ ;
Joachin, H ;
Yang, H ;
Amine, K ;
Prakash, J .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2006, 153 (04) :A731-A737
[2]   Multi-scale thermal stability study of commercial lithium-ion batteries as a function of cathode chemistry and state-of-charge [J].
Barkholtz, Heather M. ;
Preger, Yuliya ;
Ivanov, Sergei ;
Langendorf, Jill ;
Torres-Castro, Loraine ;
Lamb, Joshua ;
Chalamala, Babu ;
Ferreira, Summer R. .
JOURNAL OF POWER SOURCES, 2019, 435
[3]   Thermal stability of the Li(Ni0.8Co0.15Al0.05)O2 cathode in the presence of cell components [J].
Belharouak, I. ;
Vissers, D. ;
Amine, K. .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2006, 153 (11) :A2030-A2035
[4]   Thermal stability of LiPF6-EC:EMC electrolyte for lithium ion batteries [J].
Botte, GG ;
White, RE ;
Zhang, ZM .
JOURNAL OF POWER SOURCES, 2001, 97-8 :570-575
[5]   Quantification of heat energy leading to failure of 18650 lithium-ion battery abused by external heating [J].
Chombo, Pius Victor ;
Laoonual, Yossapong .
JOURNAL OF LOSS PREVENTION IN THE PROCESS INDUSTRIES, 2022, 79
[6]   Modulated temperature differential scanning calorimetry: A novel approach to pharmaceutical thermal analysis [J].
Coleman, NJ ;
Craig, DQM .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1996, 135 (1-2) :13-29
[7]   Experimental study on the runaway behaviors of Panasonic 21,700 LiNi0.8Co0.15Al0.05O2 battery used in electric vehicle under thermal failure [J].
Duh, Yih-Shing ;
Lin, Ying-Cih ;
Ho, Ta-Cheng ;
Kao, Chen-Shan .
JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY, 2022, 147 (21) :12005-12018
[8]   Mitigating Thermal Runaway of Lithium-Ion Batteries [J].
Feng, Xuning ;
Ren, Dongsheng ;
He, Xiangming ;
Ouyang, Minggao .
JOULE, 2020, 4 (04) :743-770
[9]   Thermal runaway mechanism of lithium ion battery for electric vehicles: A review [J].
Feng, Xuning ;
Ouyang, Minggao ;
Liu, Xiang ;
Lu, Languang ;
Xia, Yong ;
He, Xiangming .
ENERGY STORAGE MATERIALS, 2018, 10 :246-267
[10]  
FRIEDMAN HL, 1964, J POLYM SCI POL SYM, P183