材料科学
阴极
无定形固体
原子层沉积
图层(电子)
化学工程
沉积(地质)
硫黄
多硫化物
纳米技术
电解质
电化学
电极
储能
冶金
有机化学
物理化学
工程类
古生物学
功率(物理)
物理
化学
生物
量子力学
沉积物
作者
Dingtao Ma,Yongliang Li,Jingbo Yang,Hongwei Mi,Shan Luo,Libo Deng,Chaoyi Yan,Muhammad Rauf,Peixin Zhang,Xueliang Sun,Xiangzhong Ren,Jianqing Li,Han Zhang
标识
DOI:10.1002/adfm.201705537
摘要
Abstract The room temperature (RT) sodium–sulfur batteries (Na–S) hold great promise for practical applications including energy storage and conversion due to high energy density, long lifespan, and low cost, as well based on the abundant reserves of both sodium metal and sulfur. Herein, freestanding (C/S/BaTiO 3 )@TiO 2 (CSB@TiO 2 ) electrode with only ≈3 wt% of BaTiO 3 additive and ≈4 nm thickness of amorphous TiO 2 atomic layer deposition protective layer is rational designed, and first used for RT Na–S batteries. Results show that such cathode material exhibits high rate capability and excellent durability compared with pure C/S and C/S/BaTiO 3 electrodes. Notably, this CSB@TiO 2 electrode performs a discharge capacity of 524.8 and 382 mA h g −1 after 1400 cycles at 1 A g −1 and 3000 cycles at 2 A g −1 , respectively. Such superior electrochemical performance is mainly attributed from the “BaTiO 3 ‐C‐TiO 2 ” synergetic structure within the matrix, which enables effectively inhibiting the shuttle effect, restraining the volumetric variation and stabilizing the ionic transport interface.
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