多硫化物
杂原子
吸附
材料科学
硫黄
介孔材料
锂硫电池
化学工程
锂(药物)
阴极
X射线光电子能谱
无机化学
化学
有机化学
电解质
物理化学
电极
烷基
冶金
催化作用
内分泌学
工程类
医学
作者
Felix Hippauf,Winfried Nickel,Guang‐Ping Hao,Kai Schwedtmann,Lars Giebeler,Steffen Oswald,Lars Borchardt,Susanne Doerfler,Jan J. Weigand,Stefan Kaskel
标识
DOI:10.1002/admi.201600508
摘要
Polysulfide shuttling is a crucial factor in lithium sulfur batteries responsible for capacity fading and degradation. Liquid phase adsorption in combination with nuclear magnetic resonance and X‐ray photoelectron spectroscopy are used to elucidate and quantify polysulfide retention in typical porous cathode materials used in lithium sulfur batteries without cell assembly to achieve a more fundamental understanding of liquid phase adsorption phenomena as a responsible mechanism for polysulfide retention. The individual impact of each pore size increment is quantified on the polysulfide adsorption (PSA). Ultramicropores show eight times higher PSA (1.48 mmol cm −3 ) than mesopores. Strong heteroatom‐doped ultramicropores show even stronger interactions with polysulfides leading to 25 times higher adsorption compared to hydrophobic mesopores. These findings allow to precisely tailor pore structure and heteroatom distribution of cathode materials for next generation lithium sulfur batteries with prolonged cycle life and reduced capacity fading.
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