电解质
材料科学
电化学
硫黄
离子电导率
电池(电)
电极
快离子导体
化学工程
阴极
锂(药物)
无机化学
化学
冶金
物理化学
热力学
医学
功率(物理)
物理
工程类
内分泌学
作者
Daiwei Wang,Li‐Ji Jhang,Rong Kou,Meng Liao,Shiyao Zheng,Heng Jiang,Pei Shi,Guo‐Xing Li,Kui Meng,Donghai Wang
标识
DOI:10.1038/s41467-023-37564-z
摘要
Abstract Lithium-sulfur all-solid-state batteries using inorganic solid-state electrolytes are considered promising electrochemical energy storage technologies. However, developing positive electrodes with high sulfur content, adequate sulfur utilization, and high mass loading is challenging. Here, to address these concerns, we propose using a liquid-phase-synthesized Li 3 PS 4 -2LiBH 4 glass-ceramic solid electrolyte with a low density (1.491 g cm −3 ), small primary particle size (~500 nm) and bulk ionic conductivity of 6.0 mS cm −1 at 25 °C for fabricating lithium-sulfur all-solid-state batteries. When tested in a Swagelok cell configuration with a Li-In negative electrode and a 60 wt% S positive electrode applying an average stack pressure of ~55 MPa, the all-solid-state battery delivered a high discharge capacity of about 1144.6 mAh g −1 at 167.5 mA g −1 and 60 °C. We further demonstrate that the use of the low-density solid electrolyte increases the electrolyte volume ratio in the cathode, reduces inactive bulky sulfur, and improves the content uniformity of the sulfur-based positive electrode, thus providing sufficient ion conduction pathways for battery performance improvement.
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