多硫化物
材料科学
硫黄
成核
化学工程
阳极
溶解
锂(药物)
石墨氮化碳
阴极
碳纤维
氮化物
图层(电子)
纳米技术
催化作用
化学
复合材料
复合数
冶金
电极
物理化学
有机化学
电解质
内分泌学
工程类
医学
光催化
作者
Wenhao Sun,Lingyong Xu,Zihao Song,Hai Lin,Zhaoqing Jin,Weikun Wang,Anbang Wang,Yaqin Huang
标识
DOI:10.1002/adfm.202313112
摘要
Abstract Lithium‐sulfur (Li‐S) batteries have received tremendous academic and industrial attentions owing to their ultrahigh energy density. However, technical challenges including lithium dendrite formation, polysulfide shuttling and sluggish sulfur reaction kinetics limit their cycle life, rate capability and areal capacity, especially at practically high sulfur loadings. Here, coordination‐engineered graphite carbon nitrides is proposed to effectively address these challenges. On the anode a layer of novel N‐rich graphitic carbon nitride (g‐C 3 N 5 ) is applied, in which tricoordinated N atoms display strong affinity to Li + , to guide lithium deposition and efficiently inhibit dendrite formation. Besides, a layer of defective g‐C 3 N 5 carrying highly active bicoordinated N vacancies and cyano N atoms is applied on the cathode, which significantly adsorb polysulfides and catalyze the reversible conversion, as well as the nucleation and dissolution of Li 2 S thereby outcompeting polysulfide shuttling and raising kinetics at high sulfur loading. This coordination‐engineering strategy based on g‐C 3 N 5 enables Li‐S batteries exhibiting high stability and low capacity‐fading‐rate (0.03% per cycle) in 400 cycles at the high current rate of 4 C, as well as Li‐S pouch cells showing a high areal capacity of 11.69 mAh cm −2 at a high sulfur loading of 9.02 mg cm −2 , demonstrating the feasibility of Li‐S batteries in practical applications.
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