Hydration-dependent dynamics of deeply cooled water under strong confinement

We have measured the hydration-level dependence of the single-particle dynamics of water confined in the ordered mesoporous silica MCM-41. The dynamic crossover observed at full hydration is absent at monolayer hydration. The monolayer dynamics are significantly slower than those of water in a fully...

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Main Authors: Bertrand, Christopher E., Liu, K.-H., Mamontov, Eugene, Chen, Sow-Hsin
Other Authors: Massachusetts Institute of Technology. Department of Nuclear Science and Engineering
Format: Article
Language:en_US
Published: American Physical Society 2014
Online Access:http://hdl.handle.net/1721.1/89038
https://orcid.org/0000-0001-6588-2428
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author Bertrand, Christopher E.
Liu, K.-H.
Mamontov, Eugene
Chen, Sow-Hsin
author2 Massachusetts Institute of Technology. Department of Nuclear Science and Engineering
author_facet Massachusetts Institute of Technology. Department of Nuclear Science and Engineering
Bertrand, Christopher E.
Liu, K.-H.
Mamontov, Eugene
Chen, Sow-Hsin
author_sort Bertrand, Christopher E.
collection MIT
description We have measured the hydration-level dependence of the single-particle dynamics of water confined in the ordered mesoporous silica MCM-41. The dynamic crossover observed at full hydration is absent at monolayer hydration. The monolayer dynamics are significantly slower than those of water in a fully hydrated pore at ambient temperatures. At low temperatures, the opposite is found to be true. These results underscore the importance of water's tetrahedral hydrogen-bond network in accounting for its low temperature dynamic properties.
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spelling mit-1721.1/890382022-10-01T04:59:45Z Hydration-dependent dynamics of deeply cooled water under strong confinement Bertrand, Christopher E. Liu, K.-H. Mamontov, Eugene Chen, Sow-Hsin Massachusetts Institute of Technology. Department of Nuclear Science and Engineering Chen, Sow-Hsin Bertrand, Christopher E. Liu, K.-H. We have measured the hydration-level dependence of the single-particle dynamics of water confined in the ordered mesoporous silica MCM-41. The dynamic crossover observed at full hydration is absent at monolayer hydration. The monolayer dynamics are significantly slower than those of water in a fully hydrated pore at ambient temperatures. At low temperatures, the opposite is found to be true. These results underscore the importance of water's tetrahedral hydrogen-bond network in accounting for its low temperature dynamic properties. United States. Dept. of Energy. Office of Basic Energy Sciences (Contract DE-FG02-90ER45429) 2014-08-25T18:37:32Z 2014-08-25T18:37:32Z 2013-04 2013-03 Article http://purl.org/eprint/type/JournalArticle 1539-3755 1550-2376 http://hdl.handle.net/1721.1/89038 Bertrand, C. E., K.-H. Liu, E. Mamontov, and S.-H. Chen. “Hydration-Dependent Dynamics of Deeply Cooled Water Under Strong Confinement.” Phys. Rev. E 87, no. 4 (April 2013). © 2013 American Physical Society https://orcid.org/0000-0001-6588-2428 en_US http://dx.doi.org/10.1103/PhysRevE.87.042312 Physical Review E Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use. application/pdf American Physical Society American Physical Society
spellingShingle Bertrand, Christopher E.
Liu, K.-H.
Mamontov, Eugene
Chen, Sow-Hsin
Hydration-dependent dynamics of deeply cooled water under strong confinement
title Hydration-dependent dynamics of deeply cooled water under strong confinement
title_full Hydration-dependent dynamics of deeply cooled water under strong confinement
title_fullStr Hydration-dependent dynamics of deeply cooled water under strong confinement
title_full_unstemmed Hydration-dependent dynamics of deeply cooled water under strong confinement
title_short Hydration-dependent dynamics of deeply cooled water under strong confinement
title_sort hydration dependent dynamics of deeply cooled water under strong confinement
url http://hdl.handle.net/1721.1/89038
https://orcid.org/0000-0001-6588-2428
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