纳米团簇
硫黄
溶解
过渡金属
金属
无机化学
化学
材料科学
有机化学
物理化学
催化作用
电极
电解质
作者
Binwei Zhang,Tian Sheng,Yunxiao Wang,Shulei Chou,Kenneth Davey,Shixue Dou,Shi Zhang Qiao
标识
DOI:10.1002/anie.201811080
摘要
Abstract Room‐temperature sodium–sulfur (RT‐Na/S) batteries hold significant promise for large‐scale application because of low cost of both sodium and sulfur. However, the dissolution of polysulfides into the electrolyte limits practical application. Now, the design and testing of a new class of sulfur hosts as transition‐metal (Fe, Cu, and Ni) nanoclusters (ca. 1.2 nm) wreathed on hollow carbon nanospheres (S@M‐HC) for RT‐Na/S batteries is reported. A chemical couple between the metal nanoclusters and sulfur is hypothesized to assist in immobilization of sulfur and to enhance conductivity and activity. S@Fe‐HC exhibited an unprecedented reversible capacity of 394 mAh g −1 despite 1000 cycles at 100 mA g −1 , together with a rate capability of 220 mAh g −1 at a high current density of 5 A g −1 . DFT calculations underscore that these metal nanoclusters serve as electrocatalysts to rapidly reduce Na 2 S 4 into short‐chain sulfides and thereby obviate the shuttle effect.
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