纳米团簇
光催化
共价键
过电位
金属
催化作用
材料科学
纳米技术
化学工程
化学
光化学
物理化学
电极
有机化学
冶金
工程类
电化学
作者
Aimin Yao,Yuanxin Du,Meng Han,Yan Wang,Jiashen Hu,Qingtao Zhu,Hongting Sheng,Manzhou Zhu
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2022-08-10
卷期号:16 (1): 1527-1532
被引量:36
标识
DOI:10.1007/s12274-022-4725-4
摘要
Metal nanoclusters (NCs) with precise structure and ultrasmall size have attracted great interests in catalysis. However, the poor stability has limited its large-scale use. Herein, we proposed the “covalence bridge” strategy to effectively connect atomically precise metal NCs and metal-organic frameworks. Benefiting from the covalent linkage, the synthesized UiO-66-NH2-Au25(L-Cys)18 showed outstanding stability after 16 h photocatalysis. Moreover, the covalence bridge created a strong metal-support interaction between the two components and provided an effective charge transport channel and thereby enhanced photocatalytic activity. UiO-66-NH2-Au25(L-Cys)18 displayed an exceptional photocatalytic H2 production rate, which is 21 and 90 times higher than that of UiO-66-NH2/Au25(PET)18 (made by physically combination) and bare UiO-66-NH2, respectively. Thermodynamic and kinetic studies demonstrated that UiO-66-NH2-Au25(L-Cys)18 exhibited higher charge transfer efficiency, lower overpotential of water reduction and activation energy barrier compared with its counterparts.
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