过电位
锇
海水
吉布斯自由能
氢原子
图层(电子)
Atom(片上系统)
活动层
化学物理
化学
材料科学
纳米技术
海洋学
物理化学
地质学
热力学
催化作用
钌
有机化学
嵌入式系统
烷基
电极
物理
薄膜晶体管
生物化学
电化学
计算机科学
作者
Yang Gao,Yurui Xue,Wei Han,Siao Chen,Xuchen Zheng,Changrui Xing,Yuliang Li
摘要
Atomic thick two-dimensional (2D) materials with exciting physical, chemical, and electronic properties are gaining increasing attention in next-generation science and technology, showing great promise in catalysis and energy science. However, the precise design and synthesis of efficient catalytic systems based on such materials still face many difficulties, especially in how to control the preparation of structurally determined, highly active, atomic-scale distribution of material systems. Here, we report that a highly active zerovalent osmium single-atom-layer with a thickness of single atom size has been successfully and controllably self-organized on the surface of 2D graphdiyne (GDY) material. Detailed characterizations showed that the incomplete charge transfer effect between the Os atoms and GDY not only stabilized the catalytic system but also improved the intrinsic activity, making the Gibbs free energy reach the best and resulting in remarkable performance with a small overpotential of 49 mV at 500 mA cm-2, large specific j0 of 18.6 mA cm-2, and turnover frequency of 3.89 H2 s-1 at 50 mV. In addition, the formation of sp-C-Os bonds guarantees the high long-term stability of 800 h at a large current density of 500 mA cm-2 in alkaline simulated seawater.
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