Revealing spatially heterogeneous relaxation in a model nanocomposite
Abstract
The detailed nature of spatially heterogeneous dynamics of glycerol-silica nanocomposites is unraveled by combining dielectric spectroscopy with atomistic simulation and statistical mechanical theory. Analysis of the spatial mobility gradient shows no glassy layer, but the -relaxation time near the nanoparticle grows with cooling faster than the -relaxation time in the bulk and is ~20 times longer at low temperatures. The interfacial layer thickness increases from ~1.8 nm at higher temperatures to ~3.5 nm upon cooling to near bulk Tg. A real space microscopic description of the mobility gradient is constructed by synergistically combining high temperature atomistic simulation with theory. Our analysis suggests that the interfacial slowing down arises mainly due to an increase of the local cage scale barrier for activated hopping induced by enhanced packing and densification near the nanoparticle surface. As a result, the theory is employed to predict how local surface densification can be manipulated to control layer dynamics and shear rigidity over a wide temperature range.
- Authors:
-
- Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)
- Univ. of Illinois, Urbana, IL (United States)
- Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Univ. of Tennessee, Knoxville, TN (United States)
- Publication Date:
- Research Org.:
- Oak Ridge National Laboratory (ORNL), Oak Ridge, TN (United States). Oak Ridge Leadership Computing Facility (OLCF)
- Sponsoring Org.:
- USDOE Office of Science (SC)
- OSTI Identifier:
- 1265978
- Alternate Identifier(s):
- OSTI ID: 1421239
- Grant/Contract Number:
- AC05-00OR22725
- Resource Type:
- Accepted Manuscript
- Journal Name:
- Journal of Chemical Physics
- Additional Journal Information:
- Journal Volume: 143; Journal Issue: 19; Journal ID: ISSN 0021-9606
- Publisher:
- American Institute of Physics (AIP)
- Country of Publication:
- United States
- Language:
- English
- Subject:
- 36 MATERIALS SCIENCE; 37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY; relaxation times; surface dynamics; nanocomposites; interface dynamics; dielectrics
Citation Formats
Cheng, Shiwang, Mirigian, Stephen, Carrillo, Jan-Michael Y., Bocharova, Vera, Sumpter, Bobby G., Schweizer, Kenneth S., and Sokolov, Alexei P. Revealing spatially heterogeneous relaxation in a model nanocomposite. United States: N. p., 2015.
Web. doi:10.1063/1.4935595.
Cheng, Shiwang, Mirigian, Stephen, Carrillo, Jan-Michael Y., Bocharova, Vera, Sumpter, Bobby G., Schweizer, Kenneth S., & Sokolov, Alexei P. Revealing spatially heterogeneous relaxation in a model nanocomposite. United States. https://doi.org/10.1063/1.4935595
Cheng, Shiwang, Mirigian, Stephen, Carrillo, Jan-Michael Y., Bocharova, Vera, Sumpter, Bobby G., Schweizer, Kenneth S., and Sokolov, Alexei P. Wed .
"Revealing spatially heterogeneous relaxation in a model nanocomposite". United States. https://doi.org/10.1063/1.4935595. https://www.osti.gov/servlets/purl/1265978.
@article{osti_1265978,
title = {Revealing spatially heterogeneous relaxation in a model nanocomposite},
author = {Cheng, Shiwang and Mirigian, Stephen and Carrillo, Jan-Michael Y. and Bocharova, Vera and Sumpter, Bobby G. and Schweizer, Kenneth S. and Sokolov, Alexei P.},
abstractNote = {The detailed nature of spatially heterogeneous dynamics of glycerol-silica nanocomposites is unraveled by combining dielectric spectroscopy with atomistic simulation and statistical mechanical theory. Analysis of the spatial mobility gradient shows no glassy layer, but the -relaxation time near the nanoparticle grows with cooling faster than the -relaxation time in the bulk and is ~20 times longer at low temperatures. The interfacial layer thickness increases from ~1.8 nm at higher temperatures to ~3.5 nm upon cooling to near bulk Tg. A real space microscopic description of the mobility gradient is constructed by synergistically combining high temperature atomistic simulation with theory. Our analysis suggests that the interfacial slowing down arises mainly due to an increase of the local cage scale barrier for activated hopping induced by enhanced packing and densification near the nanoparticle surface. As a result, the theory is employed to predict how local surface densification can be manipulated to control layer dynamics and shear rigidity over a wide temperature range.},
doi = {10.1063/1.4935595},
journal = {Journal of Chemical Physics},
number = 19,
volume = 143,
place = {United States},
year = {Wed Nov 18 00:00:00 EST 2015},
month = {Wed Nov 18 00:00:00 EST 2015}
}
Web of Science
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Works referencing / citing this record:
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