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A preparative-scale reaction using platinum clusters with a single-digit atomicity realized
by Staff Writers
Tokyo, Japan (SPX) Sep 27, 2017


Figure (A) shows the chemical structure of the complexes, (B) shows the chromatogram of the HPLC separation with size exclusion columns, (C) shows the MALDI-TOF-mass spectra of the isolated platinum complexes measured with DCTB matrix, and (D) shows the optimized geometric structures with platinum as blue, sulfur as yellow, and a-carbon atoms in grey.

Subnanometer noble-metal clusters have been studied previously for these possibilities in catalytic applications. For example, it is known that platinum is used as a catalyst for a fuel cell, which is conductive and exhibits magnetism. Platinum is indispensable as a material for the next-generation energy grid, but it is "rare metal" whose reserves are limited. In order to make effective use of resources, it is essential to improve the atomic level accuracy of subnanometer metal clusters and increase the amount of synthesis.

While several different synthesis methods have been developed from multi-nuclear metal complexes or stable ligand-protected "magic number" clusters, the precursors were not scalable and the exact preservation of atomicity was never provided. This may have been due, in part, to the high metal-to-ligand binding energy that requires extremely high calcination temperature, which results in the aggregation of the clusters.

Scientists at Tokyo Tech investigated platinum-thiolates because they may lead to the formation of bare metal clusters through reductive metal-sulfur bond cleavage. These platinum-thiolates have been shown to form tiara-like complexes that are stable enough for isolation.

Takane Imaoka, Kimihisa Yamamoto and colleagues studied the monodispersed subnanometer platinum clusters, and their catalytic activity for preparative-scale reactions through non-destructive conversion from platinum thiolate complexes to platinum tiara-like clusters. Prior to this study, only one example of a platinum thiolate tiara-like complex with full chemical identification has been published.

As a basis for this study, they began the investigation with basic reactions between PtCl4 and n-octanethiol. Results of these basic reactions suggested that platinum thiolates initially undergo a linear chain growth, followed by entropically favorable formation of smaller cyclic compounds. Based on these results, they optimized the synthesis protocol in two steps that resulted in a crude product with platinum tiara-like complexes of various ring sizes.

The platinum tiara-like complexes where further isolated into their pure clusters based on ring sizes through size exclusion chromatography based on preparative recycling HPLC. To affirm the potential of these complexes to be used as precursors for atom-precise platinum clusters, the thermostability and catalytic activity of the complexes were investigated.

These scientists discovered that the tiara-like platinum thiolate complexes were suitable as precursors for the synthesis of monodispersed zero-valent platinum clusters with a specific atomicity: a reaction that previous chemical methods could not realize. This is the first method to demonstrate a preparative-scale reaction using atom precise clusters with a single digit atomicity, which is expected to be useful in producing high-performance catalysts.

Further investigation on the stability and support effect is necessary for the complete understanding of the catalyst system by clusters of such a small size.

Research paper

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Quantum twisted Loong confirms the physical reality of wavefunctions
Beijing, China (SPX) Sep 25, 2017
Quantum mechanics, as a pillar of modern civilization, has benefited human society for a century, in which wavefunctions played a crucial role. In the past 100 years, what most people did was 'Shut up and calculate', and wavefunctions always gave us a correct probability list of measurement outcomes. However, the debate on the following deeper philosophical issue behind it still persists: ... read more

Related Links
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