Microscopic properties of nanopore water from its time-dependent dielectric response

Author(s)
Jürgen Köfinger, Christoph Dellago
Abstract

We present a simple kinetic model for the orientational dynamics of a chain of hydrogen-bonded molecules due to the diffusion of orientational defects. We derive an event-driven algorithm which allows us to do kinetic simulations for chains from nanoscopic to macroscopic lengths, spanning huge orders of magnitude in time. Our simulations and analytical calculations show that nanopore water exhibits Debye behavior arising from the diffusive dynamics of orientational defects. For the limits of short and long chains we derive analytical expressions for the relaxation times which allow to extract the diffusion constant, the effective interaction, and the excitation energy of these defects from dielectric spectroscopy experiments. We also discuss the possibility to use such experiments to detect if the two possible kinds of orientational defects differ in excitation energy and diffusion constant.

Organisation(s)
Computational and Soft Matter Physics
External organisation(s)
National Institute of Diabetes and Digestive and Kidney Diseases
Journal
Physical Review B
Volume
82
No. of pages
14
ISSN
1098-0121
DOI
https://doi.org/10.1103/PhysRevB.82.205416
Publication date
2010
Peer reviewed
Yes
Austrian Fields of Science 2012
103036 Theoretical physics, 103009 Solid state physics, 104022 Theoretical chemistry, 103029 Statistical physics
Portal url
https://ucrisportal.univie.ac.at/en/publications/fc4a30f1-381a-444c-b8c9-26493861b694