Probing Glass Formation in Perylene Derivatives via Atomic-Scale Simulations and Bayesian Regression
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| Title: | Probing Glass Formation in Perylene Derivatives via Atomic-Scale Simulations and Bayesian Regression |
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| Authors: | Lindgren, Eric, 1997, Swenson, Jan, 1966, Müller, Christian, 1980, Erhart, Paul, 1978 |
| Source: | Karbider som vätefällor i stål Fasbeteende och elektroniska egenskaper hos halogenid-perovskiter från simulering på atomskala Acceptor Blandningar med Hög Entropi för Stabila Organiska Solceller Sveriges Neutronforskarskola - SwedNESS Sockers roll för stabilisering och kryokonservering av proteiner Journal of Physical Chemistry B. 129(26):6613-6619 |
| Subject Terms: | Hydrocarbons, Glass transition, Diffusion, Aromatic compounds, Transport properties |
| Description: | While the structural dynamics of chromophores are of interest for a range of applications, it is experimentally very challenging to resolve the underlying microscopic mechanisms. At the same time, glassy dynamics are also challenging for atomistic simulations due to the underlying dramatic slowdown over many orders of magnitude. Here, we address this issue by combining atomic scale simulations with autocorrelation function analysis and Bayesian regression, and apply this approach to a set of perylene derivatives as prototypical chromophores. The predicted glass transition temperatures and kinetic fragilities are in semiquantitative agreement with experimental data. We suggest that the remaining error could be caused by an overestimation of the intermolecular cohesion by the force field used in this work. By analyzing the underlying dynamics via the normal vector autocorrelation function, we are able to connect the β and α-relaxation processes in these materials to caged (or librational) dynamics and cooperative rotations of the molecules, respectively. The workflow presented in this work serves as a stepping stone toward understanding glassy dynamics in many-component mixtures of perylene derivatives and is readily extendable to other systems of chromophores. |
| File Description: | electronic |
| Access URL: | https://research.chalmers.se/publication/547324 https://research.chalmers.se/publication/547324/file/547324_Fulltext.pdf |
| Database: | SwePub |
Nájsť tento článok vo Web of Science | Abstract: | While the structural dynamics of chromophores are of interest for a range of applications, it is experimentally very challenging to resolve the underlying microscopic mechanisms. At the same time, glassy dynamics are also challenging for atomistic simulations due to the underlying dramatic slowdown over many orders of magnitude. Here, we address this issue by combining atomic scale simulations with autocorrelation function analysis and Bayesian regression, and apply this approach to a set of perylene derivatives as prototypical chromophores. The predicted glass transition temperatures and kinetic fragilities are in semiquantitative agreement with experimental data. We suggest that the remaining error could be caused by an overestimation of the intermolecular cohesion by the force field used in this work. By analyzing the underlying dynamics via the normal vector autocorrelation function, we are able to connect the β and α-relaxation processes in these materials to caged (or librational) dynamics and cooperative rotations of the molecules, respectively. The workflow presented in this work serves as a stepping stone toward understanding glassy dynamics in many-component mixtures of perylene derivatives and is readily extendable to other systems of chromophores. |
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| ISSN: | 15205207 15206106 |
| DOI: | 10.1021/acs.jpcb.5c00837 |