纳米反应器
过电位
催化作用
空位缺陷
插层(化学)
硫系化合物
材料科学
化学
Atom(片上系统)
碳纤维
化学工程
纳米技术
结晶学
物理化学
无机化学
复合数
电极
光电子学
计算机科学
电化学
工程类
嵌入式系统
复合材料
生物化学
作者
Feilong Gong,Yuheng Liu,Yang Zhao,Wei Liu,Guang‐Zhi Zeng,Guoqing Wang,Yonghui Zhang,Lihua Gong,Jian Liu
标识
DOI:10.1002/anie.202308091
摘要
Abstract The coordination structure determines the electrocatalytic performances of single atom catalysts (SACs), while it remains a challenge to precisely regulate their spatial location and coordination environment. Herein, we report a universal sub‐nanoreactor strategy for synthesis of yolk‐shell MoS 2 supported single atom electrocatalysts with dual‐anchored microenvironment of vacancy‐enriched MoS 2 and intercalation carbon toward robust hydrogen‐evolution reaction. Theoretical calculations reveal that the “E‐Lock” and “E‐Channel” are conducive to stabilize and activate metal single atoms. A group of SACs is subsequently produced with the assistance of sulfur vacancy and intercalation carbon in the yolk‐shell sub‐nanoreactor. The optimized C−Co−MoS 2 yields the lowest overpotential (η 10 =17 mV) compared with previously reported MoS 2 ‐based electrocatalysts to date, and also affords a 5–9 fold improvement in activity even comparing with those as‐prepared single‐anchored analogues. Theoretical results and in situ characterizations unveil its active center and durability. This work provides a universal pathway to design efficient catalysts for electro‐refinery.
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