Seedless polyol synthesis and CO oxidation activity of monodisperse (111)- and (100)-oriented rhodium nanocrystals in sub-10 nm sizes

Monodisperse sub-10 nm (6.5 nm) sized Rh nanocrystals with (111) and (100) surface structures were synthesized by a seedless polyol reduction in ethylene glycol, with poly(vinylpyrrolidone) as a capping ligand. When using [Rh(Ac)(2)](2) as the metal precursor, (111)-oriented Rh nanopolyhedra contain...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1999. - 26(2010), 21 vom: 02. Nov., Seite 16463-8
1. Verfasser: Zhang, Yawen (VerfasserIn)
Weitere Verfasser: Grass, Michael E, Huang, Wenyu, Somorjai, Gabor A
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2010
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Organometallic Compounds Polymers polyol Carbon Monoxide 7U1EE4V452 Rhodium DMK383DSAC
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245 1 0 |a Seedless polyol synthesis and CO oxidation activity of monodisperse (111)- and (100)-oriented rhodium nanocrystals in sub-10 nm sizes 
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520 |a Monodisperse sub-10 nm (6.5 nm) sized Rh nanocrystals with (111) and (100) surface structures were synthesized by a seedless polyol reduction in ethylene glycol, with poly(vinylpyrrolidone) as a capping ligand. When using [Rh(Ac)(2)](2) as the metal precursor, (111)-oriented Rh nanopolyhedra containing 76% (111)-twinned hexagons (in 2D projection) were obtained; whereas, when employing RhCl(3) as the metal precursor in the presence of alkylammonium bromide, such as tetramethylammonium bromide and trimethyl(tetradecyl)ammonium bromide, (100)-oriented Rh nanocubes were obtained with 85% selectivity. The {100} faces of the Rh nanocrystals are stabilized by chemically adsorbed Br(-) ions from alkylammonium bromides, which led to (100)-oriented nanocubes. Monolayer films of the (111)-oriented Rh nanopolyhedra and (100)-oriented Rh nanocubes were deposited on silicon wafers in a Langmuir-Blodgett trough to make model 2D nanoarray catalysts. These nanocatalysts were active for CO oxidation by O(2), and the turnover frequency was independent of nanoparticle shape, consistent with that previously observed for Rh(111) and Rh(100) single crystals 
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650 7 |a Carbon Monoxide  |2 NLM 
650 7 |a 7U1EE4V452  |2 NLM 
650 7 |a Rhodium  |2 NLM 
650 7 |a DMK383DSAC  |2 NLM 
700 1 |a Grass, Michael E  |e verfasserin  |4 aut 
700 1 |a Huang, Wenyu  |e verfasserin  |4 aut 
700 1 |a Somorjai, Gabor A  |e verfasserin  |4 aut 
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