Kinetic Control and Thermodynamic Selection in the Synthesis of Atomically Precise Gold Nanoclusters

被引:206
作者
Wu, Zhikun [1 ,2 ]
MacDonald, Mark A. [3 ,4 ]
Chen, Jenny [1 ]
Zhang, Peng [3 ,4 ]
Jin, Rongchao [1 ]
机构
[1] Carnegie Mellon Univ, Dept Chem, Pittsburgh, PA 15213 USA
[2] Chinese Acad Sci, Inst Solid State Phys, Key Lab Mat Phys, Anhui Key Lab Nanomat & Nanotechnol, Hefei 230031, Peoples R China
[3] Dalhousie Univ, Dept Chem, Halifax, NS B3H 4J3, Canada
[4] Dalhousie Univ, Inst Mat Res, Halifax, NS B3H 4J3, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
LIGAND-EXCHANGE REACTIONS; AU CLUSTERS; CIRCULAR-DICHROISM; KDA GOLD; SIZE; NANOPARTICLES; LUMINESCENCE; MONODISPERSE; OXIDATION; AU-38;
D O I
10.1021/ja2028102
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This work presents a combined approach of kinetic control and thermodynamic selection for the synthesis of monodisperse 19 gold atom nanoclusters protected by thiolate groups. The step of kinetic control allows the formation of a proper size distribution of initial size-mixed Au-n(SR)(m) nanoclusters following the reduction of a gold precursor. Unlike the synthesis of Au-25(SR)(18) nanodusters, which involves rapid reduction of the gold precursor by NaBH4 followed by size focusing, the synthesis of 19-atom nanoclusters requires slow reduction effected by a weaker reducing agent, borane tert-butylamine complex. The initially formed mixture of nanodusters then undergoes size convergence into a monodisperse product by means of a prolonged aging process. The nanocluster formula was determined to be Au-19(SC2H4Ph)(13). This work demonstrates the importance of both kinetic control of the initial size distribution of nanoclusters prior to size focusing and subsequent thermodynamic selection of stable nanoclusters as the final product.
引用
收藏
页码:9670 / 9673
页数:4
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