纳米笼
石墨烯
材料科学
多硫化物
硫黄
锂硫电池
阴极
碳纤维
溶解
纳米技术
储能
电池(电)
化学工程
电极
电化学
复合材料
化学
复合数
有机化学
催化作用
物理化学
功率(物理)
物理
量子力学
工程类
电解质
冶金
作者
Yifei Yuan,Guoqiang Tan,Jianguo Wen,Jun Lü,Lu Ma,Cong Liu,Xiaobing Zuo,Reza Shahbazian‐Yassar,Tianpin Wu,Khalil Amine
标识
DOI:10.1002/adfm.201706443
摘要
Abstract The encapsulation of sulfur within carbon matrices is widely utilized in the cathode of a rechargeable lithium–sulfur battery, whose energy density largely depends on the design of the carbon structure. Here, an advanced graphene nanocage structure with the capability of hosting both cyclo‐S 8 and smaller sulfur molecules (S 2–4 ) is reported. The cage inner cavity is partially filled with S 8 to form a yolk–shell structure that enables free volumetric variation of S 8 during (de)lithiation. In the graphene shell of the cage, S 8 are downsized to S 2–4 to activate extra sulfur loading sites within graphene layers. Importantly, the graphene shell exhibits inward volumetric variation upon (de)lithiation of the loaded S 2–4 , and the overall electrode strain is thus minimized. This prototyped design promises an ultimate solution to maximize sulfur loading in carbon matrices as well as to circumvent the polysulfide dissolution problem and boost the commercialization of lithium‐sulfur batteries in the future.
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