离解(化学)
钌
碱土金属
氢
分解水
材料科学
无机化学
化学
化学物理
催化作用
物理化学
碱金属
光催化
有机化学
作者
Dong Liu,Xu Li,Sicheng Li,Airong Xu,Yuanhua Sun,Tong Liu,Meng‐Yuan Liu,Huijuan Wang,Xiaokang Liu,Tao Yao,Tao Ding
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2024-06-03
卷期号:17 (8): 6993-7000
被引量:9
标识
DOI:10.1007/s12274-024-6726-y
摘要
Atomic clusters typically exhibit distinctive electronic structures and physicochemical properties. However, as the size decreases, their ability to adsorb and dissociate water also diminishes, thereby affecting chemical reactions involving water molecules. Enhancing the adsorption and dissociation capabilities of atomic clusters towards water molecules and elucidating the mechanisms underlying their performance enhancement have become important research directions. Herein, employing the carrier-anchored strategy, Ru-O-Ru atomic clusters were prepared and displayed excellent activity and durability in the hydrogen evolution reaction. Specifically, the Ru-O-Ru atomic clusters exhibited only 86 mV overpotential at 100 mA·cm−2 and superior membrane-electrode-assembly activity than commercial Ru/C catalyst. Synchrotron radiation-based Fourier transform infrared spectroscopic measurements revealed that the modification of oxygen in Ru-O-Ru units promoted the reorientation of water molecules from a H-up orientation to H-down, therefore, enhanced the formation of strong hydrogen-bond network of interfacial water on the surface of Ru-O-Ru clusters, leading to enhanced adsorption and dissociation of water and accelerated Volmer step. Those findings provide a potential strategy and deep insights for the development of atomic clusters in electrocatalysts.
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