Under low temperature (LT) conditions (−80 °C∼0 °C), lithium‐ion batteries (LIBs) may experience the formation of an extensive solid electrolyte interface (SEI), which can cause a series of detrimental effects such as Li+ deposition and irregular dendritic filament growth on the electrolyte surface. These issues ultimately lead to the degradation of the LT performance of LIBs. As a result, new electrode/electrolyte materials are necessary to address these challenges and enable the proper functioning of LIBs at LT. Given that most electrochemical reactions in lithium‐ion batteries occur at the electrode/electrolyte interface, finding solutions to mitigate the negative impact caused by SEI is crucial to improve the LT performance of LIBs. In this article, we analyze and summarize the recent studies on electrode and electrolyte materials for low temperature lithium‐ion batteries (LIBs). These materials include both metallic materials like tin, manganese, and cobalt, as well as non‐metallic materials such as graphite and graphene. Modified materials, such as those with nano or alloying characteristics, generally exhibit better properties than raw materials. For instance, Sn nanowire‐Si nanoparticles (SiNPs−In‐SnNWs) and tin dioxide carbon nanotubes (SnO2@CNT) have faster Li+ transport rates and higher reversible capacity at LT. However, it′s important to note that when operating under LT, the electrolyte may solidify, leading to difficulty in Li+ transmission. The compatibility between the electrolyte and electrode can affect the formation of the solid electrolyte interphase (SEI) and the stability of the electrode/electrolyte system. Therefore, a good electrode/electrolyte system is crucial for successful operation of LIBs at LT.
Due to excellent electrochemical performances, mixed transition metal oxides (TMOs) as electrode materials have attracted scholarly attention. However, the issues of volume expansion, unstable structure, and low electrical conductivity have limited their development for lithium battery (LIB). Drawing on the strategy of MOFs derivation synthesis combined with low temperature hydrothermal method, this study successfully synthesized the three‐dimensional (3D) NiCo2O4@Fe2O3 with a flower‐like crossing channel and a surface crumpled structure. As anode for LIBs, NiCo2O4@Fe2O3 exhibits more reliable performance than Ni−Co oxides. Our experiments verified that the Ni−Co composite electrical conductivity and cycling stability were both improved by the Fe2O3 coating. Under the high current density of 1000 mA g−1, the capacity decay rate of NiCo2O4@Fe2O3 tends to be stable after 60 cycles, and the capacity remains at 945 mAh g−1 after 400 cycles. Besides, the specific crossing porous‐channel structure mode improved the composite's carrier transport efficiency, and coulombic efficiency reached 100 % after 400 cycles. Noteworthy is the fact that the crumpled surface structure formed by the 2D Ni−Co nanosheets promotes the construction of heterostructures, further enhances the interface capacitance effect, and strengthens the rating capacity.
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