电解质
电化学
阳极
化学
硫黄
阴极
钠
电极
环丁砜
普鲁士蓝
无机化学
储能
溶剂
化学工程
有机化学
物理化学
工程类
功率(物理)
物理
量子力学
作者
Wenxi Kuang,Xunzhu Zhou,Ziqiang Fan,Xiaomin Chen,Zhuo Yang,Jian Chen,Xiaoyan Shi,Lin Li,Ronghua Zeng,Jiazhao Wang,Shulei Chou
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2024-07-29
卷期号:9 (8): 4111-4118
被引量:5
标识
DOI:10.1021/acsenergylett.4c01445
摘要
Sodium-ion batteries (SIBs) with abundant sodium resources have been considered to be competitive candidates for large-scale energy storage systems. However, undesirable instability of the electrode/electrolyte interface (EEI) at the electrode surface in a commercial ester-based electrolyte results in the unsatisfactory electrochemical performance of SIBs. Herein, robust sulfur-containing inorganic-rich EEI is simultaneously constructed on both Prussian blue (PB) cathode and hard carbon (HC) anode via the film-forming additive, named sulfolane (SL). SL largely participates in the inner Na+ sheath, weakening the coordination of Na+-solvent with accelerated Na+ desolvation and inducing the additive-derived sulfur-containing inorganic-rich interfacial chemistry. These merit the improved reversible capacity, rate performance, and cycling stability of the HC||PB full cell with SL-containing electrolyte. More importantly, the HC||PB pouch cell delivers a high capacity retention of 78.3% after 500 cycles, demonstrating the feasibility of SL in SIBs. This work provides valuable guidance to develop sulfur-containing inorganic-rich interfacial chemistry for advanced SIBs.
科研通智能强力驱动
Strongly Powered by AbleSci AI