Yang J, Lee Jim Yang, Too Heng-Phon, Valiyaveettil S
Department of Chemical and Biomolecular Engineering, National University of Singapore, 10 Kent Ridge Crescent, Singapore 119260.
J Phys Chem B. 2006 Jan 12;110(1):125-9. doi: 10.1021/jp055306c.
We report herewith the synthesis of hollow Pt nanospheres by using bis(p-sulfonatophenyl)phenylphosphine to selectively remove the Ag cores of Ag-Pt core-shell nanoparticles. Core-shell Ag-Pt nanoparticles were first obtained by the successive reduction method with a discontinuous Pt shell to allow the BSPP passage. Transmission electron microscopy imaging of the core-shell Ag-Pt nanoparticles before and after BSPP dissolution showed little changes in the particle size, indicating that the removal of the Ag cores had occurred isomorphously. The hollow Pt nanospheres, together with the predecessor Ag-Pt core-shell particles of the same size, were transferred from water to toluene and surface modified by dodecylamine in toluene. This allows the catalytic activities of solid and hollow Pt particles in room temperature methanol oxidation reaction to be compared under conditions of identical particle size and the same surface environment. The measured higher specific activity of the Pt hollow nanospheres could then be attributed unambiguously to the larger specific surface area prevalent in the porous hollow structure.
我们在此报告通过使用双(对磺基苯基)苯基膦选择性去除Ag-Pt核壳纳米颗粒的Ag核来合成中空Pt纳米球。首先通过连续还原法获得核壳Ag-Pt纳米颗粒,其具有不连续的Pt壳以允许BSPP通过。BSPP溶解前后核壳Ag-Pt纳米颗粒的透射电子显微镜成像显示粒径变化很小,表明Ag核的去除是同构发生的。将中空Pt纳米球与相同尺寸的前身Ag-Pt核壳颗粒一起从水转移到甲苯中,并在甲苯中用十二胺进行表面改性。这使得在相同粒径和相同表面环境的条件下能够比较实心和中空Pt颗粒在室温甲醇氧化反应中的催化活性。然后可以明确地将测得的Pt中空纳米球的较高比活性归因于多孔中空结构中普遍存在的较大比表面积。