硫黄
可扩展性
电子
材料科学
碳纤维
计算机科学
纳米技术
化学工程
复合材料
物理
工程类
冶金
复合数
量子力学
数据库
作者
Nana Wang,Xiao Zhang,Zhengyu Ju,Xingwen Yu,Yunxiao Wang,Yi Du,Zhongchao Bai,Shi Xue Dou,Guihua Yu
标识
DOI:10.1038/s41467-021-24873-4
摘要
Increasing the energy density of lithium-sulfur batteries necessitates the maximization of their areal capacity, calling for thick electrodes with high sulfur loading and content. However, traditional thick electrodes often lead to sluggish ion transfer kinetics as well as decreased electronic conductivity and mechanical stability, leading to their thickness-dependent electrochemical performance. Here, free-standing and low-tortuosity N, O co-doped wood-like carbon frameworks decorated with carbon nanotubes forest (WLC-CNTs) are synthesized and used as host for enabling scalable high-performance Li-sulfur batteries. EIS-symmetric cell examinations demonstrate that the ionic resistance and charge-transfer resistance per unit electro-active surface area of S@WLC-CNTs do not change with the variation of thickness, allowing the thickness-independent electrochemical performance of Li-S batteries. With a thickness of up to 1200 µm and sulfur loading of 52.4 mg cm
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