Ligand-Controlled Co-reduction versus Electroless Co-deposition: Synthesis of Nanodendrites with Spatially Defined Bimetallic Distributions

被引:40
作者
Ortiz, Nancy [1 ]
Weiner, Rebecca G. [1 ]
Skrabalak, Sara E. [1 ]
机构
[1] Indiana Univ, Dept Chem, Bloomington, IN 47405 USA
基金
美国国家科学基金会;
关键词
alloy; core-shell; palladium; platinum; nanoparticles; shape control; PALLADIUM NANOPARTICLES; DEPOSITION; NANOCRYSTALS; REACTIVITY; OLEYLAMINE; CATALYSTS; COLLOIDS; METALS; GREEN;
D O I
10.1021/nn5052822
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The predictable synthesis of bimetallic nanostructures via co-reduction of two metal precursors is challenging due to our limited understanding of precursor ligand effects. Here, the influence of different metalligand environments is systematically examined in the synthesis of PdPt nanostructures as a model bimetallic system. Nanodendrites with different spatially defined PdPt compositions are achieved, where the local ligand environments of metal precursors dictate if temporally separated co-reduction dominates to achieve coreshell nanostructures or whether electroless co-deposition proceeds to facilitate alloyed nanostructure formation. As the properties of bimetallic nanomaterials depend on crystal ordering and composition, chemical routes to structurally defined bimetallic nanomaterials are critically needed. The approaches reported here should be applicable to other bimetallic compositions given the established reactivity of coordination complexes available for use as precursors.
引用
收藏
页码:12461 / 12467
页数:7
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