多硫化物
双功能
材料科学
阳极
阴极
锂(药物)
枝晶(数学)
化学工程
纳米技术
有机化学
化学
物理化学
内分泌学
催化作用
几何学
工程类
医学
电解质
数学
电极
作者
Qiang Cai,Jia Jin,Zhaodi Fan,Chao Li,Zixiong Shi,Jingyu Sun,Zhongfan Liu
标识
DOI:10.1002/adma.202005967
摘要
Abstract Lithium–sulfur (Li–S) batteries have heretofore attracted tremendous interest due to low cost and high energy density. In this realm, both the severe shuttling of polysulfide and the uncontrollable growth of dendritic lithium have greatly hindered their commercial viability. Recent years have witnessed the rapid development of rational approaches to simultaneously regulate polysulfide behaviors and restrain lithium dendritic growth. Nevertheless, the major obstacles for high‐performance Li–S batteries still lie in little knowledge of bifunctional material candidates and inadequate explorations of advanced technologies for customizable devices. Herein, a “two‐in‐one” strategy is put forward to elaborate V 8 C 7 –VO 2 heterostructure scaffolds via the 3D printing (3DP) technique as dual‐effective polysulfide immobilizer and lithium dendrite inhibitor for Li–S batteries. A thus‐derived 3DP‐V 8 C 7 –VO 2 /S electrode demostrates excellent rate capability (643.5 mAh g −1 at 6.0 C) and favorable cycling stability (a capacity decay of 0.061% per cycle at 4.0 C after 900 cycles). Importantly, the integrated Li–S battery harnessing both 3DP hosts realizes high areal capacity under high sulfur loadings (7.36 mAh cm −2 at a sulfur loading of 9.2 mg cm −2 ). This work offers insight into solving the concurrent challenges for both S cathode and Li anode throughout 3DP.
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