Effect of nanocatalysis in colloidal solution on the tetrahedral and cubic nanoparticle SHAPE: Electron-transfer reaction catalyzed by platinum nanoparticles

被引:161
作者
Narayanan, R [1 ]
El-Sayed, MA [1 ]
机构
[1] Georgia Inst Technol, Sch Chem & Biochem, Laser Dynam Lab, Atlanta, GA 30332 USA
关键词
D O I
10.1021/jp0493780
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The stability of tetrahedral and cubic platinum nanoparticles during the catalysis of the electron-transfer reaction between hexacyanoferrate (III) and thiosulfate ions in colloidal solution at room temperature was studied by using TEM and HRTEM. Before the reaction, the dominantly tetrahedral nanoparticles have a shape distribution of 55 +/- 4% regular tetrahedral, 22 +/- 2% distorted tetrahedral, and 23 +/- 2% spherical nanoparticles, and the dominantly cubic nanoparticles have an initial shape distribution of 56 4% regular cubes, 13 +/- 1% distorted cubes, and 31 +/- 3% truncated octahedral nanoparticles. The amount of tetrahedral nanoparticles decreases by 60 +/- 5% after the first cycle and by 62 +/- 4% after the second cycle of the reaction. In the case of cubic nanoparticles, the amount of cubic nanoparticles decreases by 39 +/- 5% after the first cycle and by 66 +/- 5% after the second cycle compared to before the reaction. After the first and second cycles of the reaction, there are a greater percentage of distorted tetrahedral and distorted cubic nanoparticles present. The rate of the dissolution of the surface Pt atoms is faster for the tetrahedral nanoparticles than for the cubic nanoparticles. This suggests that tetrahedral nanoparticles, with their sharp corners and edges, are more sensitive and more liable to shape changes during nanocatalysis. The presence of just hexacyanoferrate ions in the solution with the nanoparticles is found to increase the amount of distorted tetrahedral and distorted cubes present much more than during the reaction. The presence of only the thiosulfate ions does not seem to affect the size or shape distribution which might result from the capping ability of this anion and thus protects the nanoparticles.
引用
收藏
页码:5726 / 5733
页数:8
相关论文
共 49 条
[1]   Shape-controlled synthesis of colloidal platinum nanoparticles [J].
Ahmadi, TS ;
Wang, ZL ;
Green, TC ;
Henglein, A ;
ElSayed, MA .
SCIENCE, 1996, 272 (5270) :1924-1926
[2]  
[Anonymous], 1994, CLUSTERS COLLOIDS TH, P459, DOI DOI 10.1002/9783527616077.CH6
[3]  
[Anonymous], 1964, STABILITY CONSTANTS
[5]   (2,2'-bipyridine-N,N')(mu-thiosulfato)-cadmium(II) [J].
Baggio, S ;
Pardo, MI ;
Baggio, R ;
Garland, MT .
ACTA CRYSTALLOGRAPHICA SECTION C-CRYSTAL STRUCTURE COMMUNICATIONS, 1997, 53 :727-729
[6]   Nanoscale colloidal metals and alloys stabilized by solvents and surfactants - Preparation and use as catalyst precursors [J].
Bonnemann, H ;
Braun, G ;
Brijoux, W ;
Brinkmann, R ;
Tilling, AS ;
Seevogel, K ;
Siepen, K .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1996, 520 (1-2) :143-162
[7]  
Bonnemann H, 2002, SYNTH METHODS ORGANO, V10, P209
[8]  
Bowker M., 2001, STUD SURF SCI CATAL, V133, P3, DOI DOI 10.1016/S0167-2991(01)81946-7
[9]   Dendrimer-encapsulated Pd nanoparticles as fluorous phase-soluble catalysts [J].
Chechik, V ;
Crooks, RM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (06) :1243-1244
[10]  
Chusuei CC, 2001, TOP CATAL, V14, P71