过电位
铂金
催化作用
纳米笼
材料科学
化学
无机化学
铱
掺杂剂
氢
碳纤维
钯
微型多孔材料
化学工程
兴奋剂
有机化学
物理化学
电化学
复合数
复合材料
工程类
光电子学
电极
作者
Zhiqi Zhang,Yugang Chen,Liqi Zhou,Chi Chen,Zhen Han,Bingsen Zhang,Qiang Wu,Lijun Yang,Lingyu Du,Yongfeng Bu,Peng Wang,Xizhang Wang,Hui Yang,Zheng Hu
标识
DOI:10.1038/s41467-019-09596-x
摘要
Abstract Single-site catalysts feature high catalytic activity but their facile construction and durable utilization are highly challenging. Herein, we report a simple impregnation-adsorption method to construct platinum single-site catalysts by synergic micropore trapping and nitrogen anchoring on hierarchical nitrogen-doped carbon nanocages. The optimal catalyst exhibits a record-high electrocatalytic hydrogen evolution performance with low overpotential, high mass activity and long stability, much superior to the platinum-based catalysts to date. Theoretical simulations and experiments reveal that the micropores with edge-nitrogen-dopants favor the formation of isolated platinum atoms by the micropore trapping and nitrogen anchoring of [PtCl 6 ] 2- , followed by the spontaneous dechlorination. The platinum-nitrogen bonds are more stable than the platinum-carbon ones in the presence of adsorbed hydrogen atoms, leading to the superior hydrogen evolution stability of platinum single-atoms on nitrogen-doped carbon. This method has been successfully applied to construct the single-site catalysts of other precious metals such as palladium, gold and iridium.
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