This paper summarizes the mitigation strategies for the thermal runaway of lithium-ion batteries. The mitigation strategies function at the material level, cell level, and system level. A time-sequence map with states and flows that describe the evolution of the physical and/or chemical processes has been proposed to interpret the mechanisms, both at the cell level and at the system level. At the cell level, the time-sequence map helps clarify the relationship between thermal runaway and fire. At the system level, the time-sequence map depicts the relationship between the expected thermal runaway propagation and the undesired fire pathway. Mitigation strategies are fulfilled by cutting off a specific transformation flow between the states in the time sequence map. The abuse conditions that may trigger thermal runaway are also summarized for the complete protection of lithium-ion batteries. This perspective provides directions for guaranteeing the safety of lithium-ion batteries for electrical energy storage applications in the future.
This article reports the thermal runaway mechanism of a 25-Ah large-format lithium-ion battery without internal short circuit induced by Joule heat. In this condition, chemical crosstalk is believed to be the mechanism. Specifically, cathode-produced oxygen is consumed by the anode with great heat generation. This finding is important for better design of LIBs to avoid thermal runaway via the optimization of all battery components.
We report the crystal orientation tuning of LiFePO(4) nanoplates for high rate lithium battery cathode materials. Olivine LiFePO(4) nanoplates can be easily prepared by glycol-based solvothermal process, and the largest crystallographic facet of the LiFePO(4) nanoplates, as well as so-caused electrochemical performances, can be tuned by the mixing procedure of starting materials. LiFePO(4) nanoplates with crystal orientation along the ac facet and bc facet present similar reversible capacities of around 160 mAh g(-1) at 0.1, 0.5, and 1 C-rates but quite different ones at high C-rates. The former delivers 156 mAh g(-1) and 148 mAh g(-1) at 5 C-rate and 10 C-rate, respectively, while the latter delivers 132 mAh g(-1) and only 28 mAh g(-1) at 5 C-rate and 10 C-rate, respectively, demonstrating that the crystal orientation plays important role for the performance of LiFePO(4) nanoplates. This paves a facile way to prepare high performance LiFePO(4) nanoplate cathode material for lithium ion batteries.
More than LiP service: The adsorption of red phosphorus into porous carbon provides a composite anode material for lithium-ion batteries. The amorphous nano phosphorus, in the carbon matrix, shows highly reversible lithium storage with high coulombic efficiencies and stable cycling capacity of 750 mAh per gram composite.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.