铂纳米粒子
八面体
吸附
纳米颗粒
胶体
铂金
化学
齿合度
模板
无机化学
四面体
化学工程
纳米技术
材料科学
催化作用
结晶学
金属
有机化学
晶体结构
工程类
作者
José M. Gisbert-González,Juan M. Feliú,Adolfo Ferre-Vilaplana,Enrique Herrero
标识
DOI:10.1021/acs.jpcc.8b05195
摘要
The performance of many advanced catalytic systems depends not only on the size and composition but also on the specific shape of the metal nanoparticles (NPs) from which they are assembled. In turn, the shape of colloidal NPs depends on the specific capping agent involved in their synthesis, though the mechanism is still poorly understood. Here, supported by electrochemical experiments, Fourier transform infrared spectra, and density functional theory calculations, on well-defined surfaces, we show how a specific capping agent determines the shape of colloidal NPs. Solvated citrate can become simultaneously adsorbed on the Pt(111) surface through three dehydrogenated carboxylic groups, with each one of them in bidentate configuration. On the other two basal planes, citrate can be adsorbed through only two of them. For this reason, under the synthesis conditions, citrate is more favorably adsorbed on the Pt(111) than on the other two basal planes of platinum. This adsorption behavior explains why colloidal platinum NPs of tetrahedral and octahedral shape are produced when citrate is used as the capping agent in water. The mechanism for citrate would also determine the shape of other pure face-centered cubic metals and can inspire the engineering of future capping agents.
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