溢出效应
催化作用
纳米颗粒
氢
贵金属
氢溢流
材料科学
离解(化学)
分解水
电解水
异源的
制氢
纳米技术
化学工程
电解
化学
物理化学
工程类
光催化
经济
有机化学
微观经济学
生物化学
电极
电解质
基因
作者
Yike Xu,Junyi Du,Jingyun Jiang,Yumin Miao,Zechao Zhuang,Zhenyu Liu,Yuanyuan Yan,Rongrong Pan,Jin Wook Yang,Meiling Wang,Shaonan Gu,Lixing Kang,Dingsheng Wang
标识
DOI:10.1002/anie.202502227
摘要
Introducing OH-interaction sites to accelerate water dissociation can increase hydrogen coverage on active site surfaces and thus accelerate H-spillover, leading to an enhanced hydrogen evolution reaction (HER). Recent studies on single-atom catalysts (SACs) combined with nano-metal-particles (NMPs) have developed various homologous NMP-SACs, however, synthesizing the heterologous NMP-SACs remains a significant challenge. Particularly for HER catalysts under alkaline conditions, the ideal heterologous structure requires a synergy between non-noble NMPs with strong oxophilicity and noble-metal SAs with suitable hydrogen binding energy. Herein, we report a facile pyrolysis-confinement strategy to create the heterologous NMP-SACs, comprising Co NMP (Con) and Pt SACs (Pt1) confined within N-doped hollow polyhedral carbons (Con-Pt1@NPC). This catalyst demonstrates outstanding HER activity and superior stability in alkaline electrolyzer. Calculations reveal that Co nanoparticles serve as an H-pump, dissociating water to supply hydrogen to Pt1 sites, thereby enhancing the HER through a short C site→C-Pt bridge site→ Pt site hydrogen spillover pathway.
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