多硫化物
材料科学
锂硫电池
重量分析
牙髓(牙)
化学工程
储能
电池(电)
硫黄
电解质
有机化学
电极
化学
热力学
冶金
物理
工程类
病理
物理化学
功率(物理)
医学
作者
Shengzhi Li,Zhuzuan Chen,Jie Chen,Xintao Luo,Xueqing Qiu,Yong Qian
标识
DOI:10.1002/aenm.202405461
摘要
Abstract Natural binders play attractive roles in stabilizing lithium–sulfur (Li–S) battery systems due to their polymeric skeleton and abundant functional structures, but the complex extraction and modification hinder the practical use. Here, lignocellulose, the unbleached product of the pulp industry, is directly developed as a robust binder in Li–S batteries. Benefiting from various oxygen‐containing functional groups woven strong hydrogen‐bonded network framework, robust mechanical stability, lithium polysulfide anchoring capacity, and high‐speed Li + transport channel. The Li–S cell battery delivers an initial discharge capacity of 996 mAh·g⁻¹ at a current density of 0.5 C and can stably run 500 cycles. Moreover, an Ah‐scale pouch cell is constructed and delivers notable gravimetric and volumetric energy densities of 322 Wh·kg⁻¹ and 432 Wh·L⁻ 1 , respectively. This work expands the application boundaries of bulk lignocellulose pulp in advanced energy storage systems.
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