TY - JOUR
T1 - State of charge-capacity-pressure coupled effects on combustion characteristics and suppression of thermal runaway gases in lithium iron phosphate batteries
AU - Yu, Lin
AU - Wang, Yuhui
AU - Wu, Xingtong
AU - Li, Fangzhou
AU - Wang, Qing
AU - Wang, Kuo
AU - Hao, Wenhao
AU - Zhang, Jianqi
AU - Qian, Xinming
N1 - Publisher Copyright:
© 2026 Elsevier Ltd. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
PY - 2026/11/15
Y1 - 2026/11/15
N2 - Against the backdrop of global energy transition and rapid development of energy storage systems, thermal safety and combustion-explosion risks of Lithium iron phosphate (LFP) batteries in confined high-pressure environments have become key bottlenecks; however, gas-generation combustion kinetics and suppression mechanisms under coupled state of charge (SOC), capacity, and pressure remain unclear. In this study, prismatic LFP batteries with varying SOCs (50%, 75%, 100%) and capacities (25, 52, 100 Ah) were tested under 1 and 2 atm conditions. Thermal runaway (TR) gases were analyzed by GC–MS. Four electrolyte systems with 25% and 50% fractions (EC:DMC:EMC = 1:1:1, EC:DMC:3:7, EC:DMC:1:1, EC:EMC:DEC = 3:5:2) and suppressants (TMP, DMMP, water vapor) were investigated. Combustion kinetics were simulated using CHEMKIN-Pro. Results show that lower SOC reduces peak temperature and delays TR, while higher capacity and pressure increase gas generation, pressure accumulation, and H₂ formation, intensifying thermal runaway risk. Combustion behavior is primarily governed by H₂ content and jointly influenced by pressure and capacity. High-SOC small cells (25 Ah, 100% SOC) exhibit the highest H₂ fraction, flame speed, and temperature (64.7%, 129.75 cm/s, 2386.68 K). LFS increases with H₂ content but decreases significantly with pressure. Elevated pressure suppresses flame propagation and heat release while shifting the risk from instantaneous deflagration to delayed accumulation. Electrolyte vapor dilution reduces combustion intensity, while composition sensitivity becomes more significant under high-capacity and high-pressure conditions. At 50% fraction, EC:EMC:DEC = 3:5:2 shows the highest hazard, with NHG difference reaching 32.62 (100 Ah, 2 atm). At 25% fraction, EC:DMC = 1:1 is most hazardous under 25 Ah and 100% SOC conditions. Under this condition, TMP and DMMP strongly suppress combustion through O/OH radical scavenging, significantly outperforming water vapor, with TMP showing slightly higher inhibition efficiency. These findings provide useful guidance for combustion suppression and battery safety design in confined high-pressure environments.
AB - Against the backdrop of global energy transition and rapid development of energy storage systems, thermal safety and combustion-explosion risks of Lithium iron phosphate (LFP) batteries in confined high-pressure environments have become key bottlenecks; however, gas-generation combustion kinetics and suppression mechanisms under coupled state of charge (SOC), capacity, and pressure remain unclear. In this study, prismatic LFP batteries with varying SOCs (50%, 75%, 100%) and capacities (25, 52, 100 Ah) were tested under 1 and 2 atm conditions. Thermal runaway (TR) gases were analyzed by GC–MS. Four electrolyte systems with 25% and 50% fractions (EC:DMC:EMC = 1:1:1, EC:DMC:3:7, EC:DMC:1:1, EC:EMC:DEC = 3:5:2) and suppressants (TMP, DMMP, water vapor) were investigated. Combustion kinetics were simulated using CHEMKIN-Pro. Results show that lower SOC reduces peak temperature and delays TR, while higher capacity and pressure increase gas generation, pressure accumulation, and H₂ formation, intensifying thermal runaway risk. Combustion behavior is primarily governed by H₂ content and jointly influenced by pressure and capacity. High-SOC small cells (25 Ah, 100% SOC) exhibit the highest H₂ fraction, flame speed, and temperature (64.7%, 129.75 cm/s, 2386.68 K). LFS increases with H₂ content but decreases significantly with pressure. Elevated pressure suppresses flame propagation and heat release while shifting the risk from instantaneous deflagration to delayed accumulation. Electrolyte vapor dilution reduces combustion intensity, while composition sensitivity becomes more significant under high-capacity and high-pressure conditions. At 50% fraction, EC:EMC:DEC = 3:5:2 shows the highest hazard, with NHG difference reaching 32.62 (100 Ah, 2 atm). At 25% fraction, EC:DMC = 1:1 is most hazardous under 25 Ah and 100% SOC conditions. Under this condition, TMP and DMMP strongly suppress combustion through O/OH radical scavenging, significantly outperforming water vapor, with TMP showing slightly higher inhibition efficiency. These findings provide useful guidance for combustion suppression and battery safety design in confined high-pressure environments.
KW - Combustion kinetics
KW - Gas combustion
KW - High-pressure environment
KW - Radical scavenging
KW - State of charge (SOC)
KW - Thermal runaway
UR - https://www.scopus.com/pages/publications/105044601313
U2 - 10.1016/j.est.2026.123586
DO - 10.1016/j.est.2026.123586
M3 - Article
AN - SCOPUS:105044601313
SN - 2352-152X
VL - 178
JO - Journal of Energy Storage
JF - Journal of Energy Storage
M1 - 123586
ER -