ReaxFF Simulations of Self-Assembled Monolayers On Silver Surfaces and Nanocrystals

Fuente: arXiv
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Autores principales: Lahouari, Adam, Piquemal, Jean-Philip, Richardi, Johannes
Formato: Preprint
Publicado: 2023
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author Lahouari, Adam
Piquemal, Jean-Philip
Richardi, Johannes
author_facet Lahouari, Adam
Piquemal, Jean-Philip
Richardi, Johannes
contents The self-assembled monolayers of alkane thiolates on Ag (111) surfaces and nanoparticles are studied using molecular dynamics. Reactive force fields allow simulations of very large systems such as nanoparticles of 10 nm. Stable (sqrt(7) X sqrt(7))R19.1° assemblies are obtained as experimentally observed for these systems. Only nanoparticles smaller than 4 nm show a spontaneous restructuration of the metallic core. The preferred adsorption site is found to be in an on-top position, in good agreement with recent X-ray absorption near edge structure experiments. Moreover, similar distances between the sulfur headgroups are found on the facets and edges.
format Preprint
id arxiv_https___arxiv_org_abs_2307_10858
institution arXiv
publishDate 2023
record_format arxiv
spellingShingle ReaxFF Simulations of Self-Assembled Monolayers On Silver Surfaces and Nanocrystals
Lahouari, Adam
Piquemal, Jean-Philip
Richardi, Johannes
Chemical Physics
The self-assembled monolayers of alkane thiolates on Ag (111) surfaces and nanoparticles are studied using molecular dynamics. Reactive force fields allow simulations of very large systems such as nanoparticles of 10 nm. Stable (sqrt(7) X sqrt(7))R19.1° assemblies are obtained as experimentally observed for these systems. Only nanoparticles smaller than 4 nm show a spontaneous restructuration of the metallic core. The preferred adsorption site is found to be in an on-top position, in good agreement with recent X-ray absorption near edge structure experiments. Moreover, similar distances between the sulfur headgroups are found on the facets and edges.
title ReaxFF Simulations of Self-Assembled Monolayers On Silver Surfaces and Nanocrystals
topic Chemical Physics
url https://arxiv.org/abs/2307.10858