| Autor: |
Rodrigues TS; Departamento de Química Fundamental, Instituto de Química, Universidade de São Paulo , Av. Prof. Lineu Prestes, 748, 05508-000 São Paulo, SP, Brazil., da Silva AG; Departamento de Química Fundamental, Instituto de Química, Universidade de São Paulo , Av. Prof. Lineu Prestes, 748, 05508-000 São Paulo, SP, Brazil., Gonçalves MC; Departamento de Química Fundamental, Instituto de Química, Universidade de São Paulo , Av. Prof. Lineu Prestes, 748, 05508-000 São Paulo, SP, Brazil., Fajardo HV; Departamento de Química, Universidade Federal de Ouro Preto , 35400-000 Ouro Preto, MG, Brasil., Balzer R; Departamento de Química, Universidade Federal de Santa Catarina , 88040-900 Florianópolis, SC, Brasil., Probst LF; Departamento de Química, Universidade Federal de Santa Catarina , 88040-900 Florianópolis, SC, Brasil., da Silva AH; Departamento de Engenharia Química, Universidade Federal de São Carlos , 13565-905 São Carlos, SP, Brasil., Assaf JM; Departamento de Engenharia Química, Universidade Federal de São Carlos , 13565-905 São Carlos, SP, Brasil., Camargo PH; Departamento de Química Fundamental, Instituto de Química, Universidade de São Paulo , Av. Prof. Lineu Prestes, 748, 05508-000 São Paulo, SP, Brazil. |
| Abstrakt: |
We report herein a systematic investigation on the effect of the size of silver (Ag) nanoparticles employed as starting materials over the morphological features and catalytic performances of AgPt nanoshells produced by a combination of galvanic replacement between Ag and PtCl6(2-) and PtCl6(2-) reduction by hydroquinone. More specifically, we focused on Ag nanoparticles of four different sizes as starting materials, and found that the outer diameter, shell thickness, and the number of Pt surface atoms of the produced nanoshells increased with the size of the starting Ag nanoparticles. The produced AgPt nanoshells were supported into SiO2, and the catalytic performances of the AgPt/SiO2 nanocatalysts toward the gas-phase oxidation of benzene, toluene, and o-xylene (BTX oxidation) followed the order: AgPt 163 nm/SiO2 > AgPt 133 nm/SiO2 > AgPt 105 nm/SiO2 > AgPt 95 nm/SiO2. Interestingly, bigger AgPt nanoshell sizes lead to better catalytic performances in contrast to the intuitive prediction that particles having larger outer diameters tend to present poorer catalytic activities due to their lower surface to volume ratios as compared to smaller particles. This is in agreement with the H2 chemisorption results, and can be assigned to the increase in the Pt surface area with size due to the presence of smaller NPs islands at the surface of the nanoshells having larger outer diameters. This result indicates that, in addition to the overall diameters, the optimization of the surface morphology may play an important role over the optimization of catalytic activities in metal-based nanocatalysts, which can be even more pronounced that the size effect. Our data demonstrate that the control over surface morphology play a very important role relative to the effect of size to the optimization of catalytic performances in catalysts based on noble-metal nanostructures. |
