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Influence of restricted environment and ionic interactions on water solvation dynamics

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dc.contributor.author Pant, Debi D.
dc.date.accessioned 2024-02-02T15:24:55Z
dc.date.available 2024-02-02T15:24:55Z
dc.date.issued 1998
dc.identifier.uri https://pubs.aip.org/aip/jcp/article-abstract/109/22/9995/476569/Influence-of-restricted-environment-and-ionic
dc.identifier.uri http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/14060
dc.description.abstract Polar solvation dynamics of water sequestered inside Aerosol OT (AOT) reverse micelles have been investigated as a function of the surfactant countercation, specifically replacing for and For Ca-AOT reverse micelles, the solvation dynamics for the smallest micelles probed occurs on a subnanosecond time scale. The K-AOT reverse micelles display an additional ultrafast component that is attributable to bulklike water motion. As previously reported for Na-AOT reverse micelles [Riter, Willard, and Levinger, J. Phys. Chem. B 102, 2705 (1998)], solvent mobility increases with increasing micellar size for both Ca-AOT and K-AOT reverse micelles. The solvation dynamics in strongly ionic aqueous solutions of and have also been investigated. The 10 M electrolyte solutions display water motion on significantly shorter time scales with substantial ultrafast components. These results show that the micellar interfacial structure plays a significant role in immobilizing intramicellar water and that solvent immobilization in the reverse micelles is not merely a result of solvent–ion interactions. en_US
dc.language.iso en en_US
dc.publisher AIP en_US
dc.subject Physics en_US
dc.subject Polar solvation dynamics en_US
dc.subject Water solvation en_US
dc.subject K-AOT en_US
dc.title Influence of restricted environment and ionic interactions on water solvation dynamics en_US
dc.type Article en_US


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