多硫化物
材料科学
法拉第效率
阳极
电解质
锂(药物)
电极
阴极
化学工程
锂硫电池
原子层沉积
电镀(地质)
无机化学
图层(电子)
纳米技术
化学
物理化学
内分泌学
工程类
地质学
医学
地球物理学
作者
Hyunki Sul,Amruth Bhargav,Arumugam Manthiram
标识
DOI:10.1002/aenm.202200680
摘要
Abstract The development of practical lithium–sulfur (Li–S) batteries with prolonged cycle life and high Coulombic efficiency is limited by both parasitic reactions from dissolved polysulfides and mossy lithium deposition. To address these challenges, here lithium trithiocarbonate (Li 2 CS 3 )‐coated lithium sulfide (Li 2 S) is employed as a dual‐function cathode material to improve the cycling performance of Li–S batteries. Interestingly, at the cathode, Li 2 CS 3 forms an oligomer‐structured layer on the surface to suppress polysulfide shuttle. The presence of Li 2 CS 3 alters the conventional sulfur reaction pathway, which is supported by material characterization and density functional theory calculation. At the anode, a stable in situ solid electrolyte interphase layer with a lower Li‐ion diffusion barrier is formed on the Li‐metal surface to engender enhanced lithium plating/stripping performance upon cycling. Consequently, the obtained anode‐free full cells with Li 2 CS 3 exhibit a superior capacity retention of 51% over 125 cycles, whereas conventional Li 2 S cells retain only 26%. This study demonstrates that Li 2 CS 3 inclusion is an efficient strategy for designing high‐energy‐density Li–S batteries with extended cycle life.
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