Adsorption kinetic process of thiol ligands on gold nanocrystals

被引:20
作者
Cheng, Hao [1 ]
Yang, Lina [1 ]
Jiang, Yong [1 ]
Huang, Yuanyuan [1 ]
Sun, Zhihu [1 ]
Zhang, Jing [2 ]
Hu, Tiandou [2 ]
Pan, Zhiyun [1 ]
Pan, Guoqiang [1 ]
Yao, Tao [1 ]
Bian, Qing [3 ]
Wei, Shiqiang [1 ]
机构
[1] Univ Sci & Technol China, Natl Synchrotron Radiat Lab, Hefei 230029, Peoples R China
[2] Chinese Acad Sci, Inst High Energy Phys, Beijing Synchrotron Radiat Facil, Beijing 100049, Peoples R China
[3] PLAUST, Inst Sci, Nanjing 210007, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
SELF-ASSEMBLED MONOLAYERS; PLACE-EXCHANGE REACTIONS; POLYCRYSTALLINE GOLD; AU NANOPARTICLES; X-RAY; SURFACE; DYNAMICS; SIZE; NANOTECHNOLOGY; DISULFIDES;
D O I
10.1039/c3nr04020h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Understanding the kinetic mechanism during ligand adsorption on gold nanocrystals is important for designing and fine-tuning their properties and implications. Here, we report a kinetic study on the adsorption process of dodecanethiol ligands on Au nanocrystals of 3.3 nm by an in situ time-resolved X-ray absorption fine structure technique. A two-step process of dodecanethiol adsorption on Au NC surfaces is proposed based on the obtained ligand coverage, which shows a quick increase from 0 to 0.40 within the first 20 min, followed by a much slower increase to the limiting value of 0.94. In-depth analysis suggests that the first stage involves the quick adsorption of dodecanethiol to the corner and edge sites of Au NCs surfaces, leading to remarkable surface Au-Au bond length relaxation (from 2.79 to 2.81 angstrom) and pronounced gold-to-ligand charge transfer. The second step that corresponds to the much slower adsorption process to the surface facets could be described by the Langmuir kinetics equation with an adsorption rate constant of 0.0132 min(-1) and an initial coverage of 0.41, in good agreement with the initially preferable adsorption of thiols to the most favorable sites.
引用
收藏
页码:11795 / 11800
页数:6
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