电解质
材料科学
过电位
阴极
介电谱
锂(药物)
电化学
硫黄
化学工程
无机化学
传质
电极
冶金
化学
色谱法
物理化学
内分泌学
工程类
医学
作者
Yifan Zhao,Jian Zhang,Juchen Guo
标识
DOI:10.1021/acsami.1c08615
摘要
The implementation of a low electrolyte/sulfur (E/S) ratio is essential to achieving high specific energy for lithium∥sulfur (Li∥S) batteries. In reality, however, the lean electrolyte condition results in low achievable capacity and inferior cyclability. In this study, we probe the interfacial processes on the sulfur cathode under the lean electrolyte condition using operando electrochemical impedance spectroscopy (EIS) and a galvanostatic intermittent titration technique (GITT). The operando EIS reveals a significant and rapid increase in the charge-transfer resistance during the transition from high-order polysulfides to low-order ones at a low E/S ratio, which is induced by a kinetic bottleneck at the interphase due to Li-ion mass transfer limitation. The GITT results confirm the kinetic bottleneck by revealing a large discharge overpotential during the transition phase. We further demonstrate that improving the adsorption of dissolved high-order polysulfides, a key step in the interfacial processes, can alleviate the kinetic limitation, thus enhancing the achievable capacity under the lean electrolyte condition.
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