材料科学
电解质
催化作用
氧化物
稀土
金属
锂(药物)
无机化学
硫黄
金属锂
星团(航天器)
化学工程
纳米技术
电极
冶金
有机化学
程序设计语言
化学
物理化学
内分泌学
工程类
医学
计算机科学
作者
Meiling Shu,Yangyang Dong,Mengdi Ni,Dong Cai,Honglong Ning,Shuo Yang,Xuemei Zhou,Duo Chen,Zhi Yang
标识
DOI:10.1021/acsami.4c18159
摘要
Developing high-energy-density lithium–sulfur batteries faces serious polysulfide shuttle effects and sluggish conversion kinetics, often necessitating the excessive use of electrolytes, which in turn adversely affects battery performance. Our study introduces a meticulously designed electrocatalyst, Cu–CeO2–x@N/C, to enhance lean-electrolyte lithium–sulfur battery performance. This catalyst, featuring in situ synthesized Cu clusters, regulates oxygen vacancies in CeO2 and forms Cu–CeO2–x heterojunctions, thereby diminishing sulfur conversion barriers and hastening reaction kinetics through the generation of S32–/S3*– intermediates. Besides, the three-dimensional conductive networks, composed of Cu and nitrogen-doped carbon matrices with high electrolyte affinity, effectively confine sparse electrolytes proximal to the catalyst locations, thereby facilitating rapid transport of Li+/electron to the active sites. As a result, the 1% Cu–CeO2–x@N/C cell demonstrated robust performance, achieving an initial discharge capacity of 793.2 mAh/g at 5 C over 500 cycles and maintaining a capacity of 719.9 mAh/g at 0.3 C with an electrolyte-to-sulfur ratio of 5 μL mg–1 and a high sulfur loading of 5.4 mg cm–2 after 60 cycles. These findings highlight the catalyst design for high-performance lean-electrolyte lithium–sulfur batteries, further paving the way for their commercialization.
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