阴极
电池(电)
量子点
电化学
材料科学
同种类的
锂(药物)
碳纤维
纳米颗粒
纳米技术
介孔材料
化学工程
氧化还原
电极
硫黄
化学
催化作用
复合材料
物理
物理化学
有机化学
冶金
复合数
工程类
内分泌学
医学
功率(物理)
量子力学
热力学
作者
Lu Qiao,Longtao Ren,Rongrong Zhang,Jing Chen,Minggui Xu,Jun Liu,Haijun Xu,Wen Liu,Zheng Chang,Xiaoming Sun
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2021-06-07
卷期号:35 (12): 10219-10226
被引量:23
标识
DOI:10.1021/acs.energyfuels.1c00716
摘要
Lithium–sulfur (Li–S) batteries are a prospective battery technology with high energy density, whereas the successful implementation of Li–S batteries is still impeded by many challenges, especially the shuttling effect of lithium polysulfides (LiPSs) and sluggish redox kinetics. Therefore, it is urgent to find a novel host material that could tackle these problems with a cost-effective manner. Herein, the mesoporous and hollow carbon sphere embedded with homogeneous VN quantum dots (noted as VN-H-C) is constructed and applied as an efficient host for a sulfur cathode, which features both physical and chemical trapping ability for soluble LiPSs. More importantly, VN quantum dots can significantly accelerate the electrochemical conversion of LiPSs. As a consequence, the S@VN-H-C cathode exhibits a high specific capacity of 856.5 mAh g–1 at 1 C and maintains 602.5 mAh g–1 after 500 cycles with a low capacity decay rate of only 0.059% per cycle. This study provides a feasible strategy for designing nanostructured materials as effective sulfur hosts in Li–S batteries.
科研通智能强力驱动
Strongly Powered by AbleSci AI