4.8 Article

Unlocking the self-supported thermal runaway of high-energy lithium-ion batteries

期刊

ENERGY STORAGE MATERIALS
卷 39, 期 -, 页码 395-402

出版社

ELSEVIER
DOI: 10.1016/j.ensm.2021.04.035

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资金

  1. Ministry of Science and Technology of China [2019YFE0100200]
  2. National Natural Science Foundation of China [52006115, 52076121]
  3. China National Postdoctoral Program for Innovative Talents [BX20190162]
  4. China Postdoctoral Science Foundation [2019M660631]
  5. Tsinghua University Initiative Scientific Research Program [2019Z02UTY06]
  6. US Department of Energy (DOE), Vehicle Technologies Office
  7. DOE [DE-AC02-06CH11357]
  8. U.S. China Clean Energy Research Center (CERC-CVC2)

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This study demonstrates that two endogenous oxygen pathways involved in strong exothermic reactions lead to uncontrollable states in the NMC811|graphite pouch cell, with significant safety concerns. Approximately 41% of thermal-induced oxygen reacts aggressively with ethylene carbonate at the cathode/electrolyte interface, accelerating the self-heating rate and triggering thermal runaway. The residual oxygen that survives the reaction with carbonate spreads to the lithiated anode, generating major heat and bringing the battery to the maximum destructive temperature during thermal runaway.
Layered Ni-rich LiNi(x)MnyCo(1-x-y)O(2) (NMC) materials are the most promising cathode materials for Li-ion batteries due to their favorable energy densities. However, the low thermal stability typically caused by detrimental oxygen release leads to significant safety concerns. Determining the pathways of oxygen evolution reaction is essential, as the ideal safety countermeasure is to break the reaction chain of thermal runaway. In this study, we demonstrate that two endogenous pathways of oxygen involved in strong exothermic reactions lead the NMC811|graphite pouch cell to an uncontrollable state, and we quantify the individual contribution of the pathways to thermal runaway. Approximately 41% of thermal-induced oxygen reacts aggressively with ethylene carbonate (EC) at the cathode/electrolyte interface with 16% heat generation, accelerating the self-heating rate and thereby further triggering thermal runaway. The residual oxygen that survives the reaction with carbonate spreads to the lithiated anode with major heat generation (65%), bringing the battery to the maximum destructive temperature during thermal runaway. By confirming the significant roles of EC and anode, a deeper understanding on battery fire was achieved. The revealed mechanism can help guide studies on stopping the two reaction pathways, allowing for the safer use of high-energy lithium-ion batteries in the future.

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