材料科学
电解质
电化学
阳极
电极
法拉第效率
储能
阴极
化学工程
多孔性
锂(药物)
纳米技术
复合材料
化学
医学
功率(物理)
物理
物理化学
量子力学
工程类
内分泌学
作者
Songjie Li,Jiazhe Gao,Yinjun Ou,Xuehua Liu,Liting Yang,Yifeng Cheng,Jincang Zhang,Li‐Ming Wu,Chunfu Lin,Renchao Che
出处
期刊:Small
[Wiley]
日期:2023-07-28
卷期号:19 (48): e2303763-e2303763
被引量:7
标识
DOI:10.1002/smll.202303763
摘要
Lithium-ion batteries (LIBs) are very popular electrochemical energy-storage devices. However, their applications in extreme environments are hindered because their low- and high-temperature electrochemical performance is currently unsatisfactory. In order to build all-climate LIBs, it is highly desirable to fully understand the underlying temperature effects on electrode materials. Here, based on a novel porous-microspherical yttrium niobate (Y0.5 Nb24.5 O62 ) model material, this work demonstrates that the operation temperature plays vital roles in electrolyte decomposition on electrode-material surfaces, electrochemical kinetics, and crystal-structure evolution. When the operation temperature increases, the reaction between the electrolyte and the electrode material become more intensive, causing the formation of thicker solid electrolyte interface (SEI) films, which decreases the initial Coulombic efficiency. Meanwhile, the electrochemical kinetics becomes faster, leading to the larger reversible capacity, higher rate capability, and more suitable working potential (i.e., lower working potential for anodes and higher working potential for cathodes). Additionally, the maximum unit-cell-volume change becomes larger, resulting in poorer cyclic stability. The insight gains here can provide a universal guide for the exploration of all-climate electrode materials and their modification methods.
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