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Self-Assembly of a Linear Alkylamine Bilayer around a Cu Nanocrystal: Molecular Dynamics
被引:3
作者:
Yan, Tianyu
[1
]
Fichthorn, Kristen A.
[1
,2
]
机构:
[1] Penn State Univ, Dept Chem Engn, University Pk, PA 16802 USA
[2] Penn State Univ, Dept Phys, 104 Davey Lab, University Pk, PA 16802 USA
基金:
美国国家科学基金会;
关键词:
SUM-FREQUENCY GENERATION;
COPPER NANOWIRES;
ATOMISTIC SIMULATIONS;
GOLD NANOPARTICLES;
HIGH-PERFORMANCE;
MONOLAYERS;
SURFACES;
LIGANDS;
HEXADECYLAMINE;
CONFORMATION;
D O I:
10.1021/acs.jpcb.1c02043
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:
Copper nanocrystals are often grown with the help of alkylamine capping agents, which direct the nanocrystal shape. However, the role of these molecules is still unclear. We characterized the assembly of aqueous tetradecylamine (TDA) around a Cu nanocrystal and found that TDA exhibits a temperature-dependent bilayer structure. The bilayer involves an inner layer, in which TDA binds to Cu via the amine group and tends to orient the alkyl tail perpendicular to the surface, and an outer layer whose structure depends on temperature. At low temperatures, alkylamines in the inner layer form bundles with no apparent relation to the crystal facets. Alkylamines in the outer layer tend to orient their long axes perpendicular to the Cu surfaces, with interdigitation into the inner layer. At high temperatures, alkylamines in the inner layer lose their bundle structure, and outer-layer alkylamines tend to orient themselves tangential to the Cu surfaces, forming a "web" above inner-layer TDA. TDA exhibits a rapid interlayer exchange at typical synthesis temperatures, consistent with experiment. The variety in the assemblies seen here and in other studies of alkanethiols around gold nanocrystals indicates a richness in the assemblies that can be achieved by modulating the interaction between the strongly binding end group and the surface.
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页码:4178 / 4186
页数:9
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