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Bottom-up precise synthesis of stable platinum dimers on graphene.


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.

SUBMITTER: Yan H 

PROVIDER: S-EPMC5715161 | biostudies-literature | 2017 Oct

REPOSITORIES: biostudies-literature

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Bottom-up precise synthesis of stable platinum dimers on graphene.

Yan Huan H   Lin Yue Y   Wu Hong H   Zhang Wenhua W   Sun Zhihu Z   Cheng Hao H   Liu Wei W   Wang Chunlei C   Li Junjie J   Huang Xiaohui X   Yao Tao T   Yang Jinlong J   Wei Shiqiang S   Lu Junling J  

Nature communications 20171020 1


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 Pt<sub>2</sub> dimers can be fabricated with a bottom-up approach on graphene using atomic layer deposition, through proper nucleation sites creation, Pt<sub>1</sub> single-atom deposition and attaching a secondary Pt atom selectively on  ...[more]

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