多硫化物
硫黄
材料科学
电解质
锂(药物)
化学工程
碳纤维
氧化还原
碳纳米管
锂硫电池
纳米技术
电极
化学
物理化学
复合材料
冶金
复合数
工程类
内分泌学
医学
作者
Xiaomin Zhang,Tingzhou Yang,Yongguang Zhang,Xingbo Wang,Jiayi Wang,Yebao Li,Aiping Yu,Xin Wang,Zhongwei Chen
标识
DOI:10.1002/adma.202208470
摘要
Single-atom catalysts (SACs) pave new possibilities to improve the utilization efficiency of sulfur electrodes arising from polysulfide shuttle effects and sluggish kinetics due to their excellent applicability in atomic-scale reaction mechanisms and structure-activity relationships. Herein, nitrogen (N)-anchored SACs on the highly ordered N-doped carbon nanotube arrays are reported as the sulfur host for fast redox conversion in lithium-sulfur (Li-S) batteries. The cube structure of the aligned carbon nanotubes can promote the rapid mass transfer under high sulfur loadings, and abundant single-atom active sites further accelerate the conversion of lithium polysulfides (LiPSs). The synergistic enhancement effect induced by adjacent single atoms with interatomic distances <1 nm further accelerates the rapid multi-step reaction of sulfur at high sulfur loadings. As a result, the obtained Li-S batteries exhibit outstanding cycle stability with a high areal capacity of 5.6 mAh cm-2 after 100 cycles under a high sulfur loading of 7.2 mg cm-2 (electrolyte to sulfur ratio is ≈3.7 mL g-1 ). Even assembled into a pouch cell, it still delivers a high capacity of 953.4 mAh g-1 after 100 cycles at 0.1 C, contributing to the development of the practically viable Li-S batteries.
科研通智能强力驱动
Strongly Powered by AbleSci AI