锂(药物)
硫黄
材料科学
化学工程
纳米技术
化学
生物
冶金
工程类
内分泌学
作者
Jung Tae Kim,Adwitiya Rao,Heng‐Yong Nie,Yang Hu,Weihan Li,Feipeng Zhao,Sixu Deng,Xiaoge Hao,Jiamin Fu,Jing Luo,Hui Duan,Changhong Wang,Chandra Veer Singh,Xueliang Sun
标识
DOI:10.1038/s41467-023-42109-5
摘要
All-solid-state lithium-sulfur batteries offer a compelling opportunity for next-generation energy storage, due to their high theoretical energy density, low cost, and improved safety. However, their widespread adoption is hindered by an inadequate understanding of their discharge products. Using X-ray absorption spectroscopy and time-of-flight secondary ion mass spectrometry, we reveal that the discharge product of all-solid-state lithium-sulfur batteries is not solely composed of Li2S, but rather consists of a mixture of Li2S and Li2S2. Employing this insight, we propose an integrated strategy that: (1) manipulates the lower cutoff potential to promote a Li2S2-dominant discharge product and (2) incorporates a trace amount of solid-state catalyst (LiI) into the S composite electrode. This approach leads to all-solid-state cells with a Li-In alloy negative electrode that deliver a reversible capacity of 979.6 mAh g-1 for 1500 cycles at 2.0 A g-1 at 25 °C. Our findings provide crucial insights into the discharge products of all-solid-state lithium-sulfur batteries and may offer a feasible approach to enhance their overall performance.
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