电解质
二甲氧基乙烷
阳极
电化学
化学
溶剂化
电池(电)
溶剂
阴极
锂(药物)
化学工程
电极
储能
无机化学
有机化学
物理化学
热力学
内分泌学
工程类
功率(物理)
物理
医学
作者
Jing Zhou,Yang Ding,Yingyu Wang,Haoyu Li,Jiayi Shang,Yu Cao,Hua Wang
标识
DOI:10.1016/j.jcis.2023.12.012
摘要
Sodium ion batteries (SIBs) are considered reliable supplies for next-generation energy devices. However, there is a limited understanding of strategies to prevent the performance deterioration of SIBs under extreme temperature conditions. This study aimed to address this challenge by developing modified electrolyte chemistry to achieve stable wide-temperature SIBs. Weakly Na+-solvating solvent 2-methyltetrahydrofuran (MeTHF) was used to promote the kinetics of Na+ de-solvation. Moreover, 1,2-dimethoxyethane (DME) was introduced as a co-solvent because of the high solubility for Na salts and the coupling reaction mechanism with the Bi electrode. The formulated electrolyte not only endows an anion-dominated NaF-rich solid electrolyte interface (SEI) layer, but also reduces the energy required for the Na+ across the SEI layer (from 291.2 to 89.6 meV). Consequently, Na||Bi half batteries achieve stable cycles at 400 mA g−1 at −20, 20 and 60 °C, respectively. Meanwhile, the extreme operating temperature of the batteries can be extended to −40 and 80 °C, which exceeds those of most current lithium/sodium-based batteries. Furthermore, full batteries employing Na3V2(PO4)3 as the cathode material exhibit stable operation over a wide temperature range of −20 to 60 °C. This electrolyte design strategy presented in this study shows significant promise for enabling wide-temperature SIBs with improved performance.
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