氨硼烷
石墨烯
材料科学
成核
脱氢
铂金
金属
纳米技术
Atom(片上系统)
结晶学
催化作用
纳米颗粒
化学工程
化学
生物化学
有机化学
计算机科学
工程类
冶金
嵌入式系统
作者
Huan Yan,Yue Lin,Hong Peng Wu,Wenhua Zhang,Zhihu Sun,Hao Cheng,Wei Liu,Chunlei Wang,Junjie Li,Xiaohui Huang,Tao Yao,Jinlong Yang,Shiqiang Wei,Junling Lu
标识
DOI:10.1038/s41467-017-01259-z
摘要
Abstract Supported metal clusters containing only a few atoms are of great interest. Progress has been made in synthesis of metal single-atom catalysts. However, precise synthesis of metal dimers on high-surface area support remains a grand challenge. Here, we show that Pt2 dimers can be fabricated with a bottom–up approach on graphene using atomic layer deposition, through proper nucleation sites creation, Pt1 single-atom deposition and attaching a secondary Pt atom selectively on the preliminary one. Scanning transmission electron microscopy, x-ray absorption spectroscopy, and theoretical calculations suggest that the Pt2 dimers are likely in the oxidized form of Pt2Ox. In hydrolytic dehydrogenation of ammonia borane, Pt2 dimers exhibit a high specific rate of 2800 molH2 molPt−1 min−1 at room temperature, ~17- and 45-fold higher than graphene supported Pt single atoms and nanoparticles, respectively. These findings open an avenue to bottom–up fabrication of supported atomically precise ultrafine metal clusters for practical applications.
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