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Ultrafast Vibrational Dynamics at the Solid/Water Interface

No doubt, water is the most important liquid on the planet. In addition to the obligatory need for water in life, water is widely used in diverse applications. In most applications if not all, water is interfaced with different materials, at different phases depending on the application. This unique value of water originates from its chemical structure, which is based on hydrogen bonding. Although these chemical bonding in bulk liquid and vapor water have extensively been investigated, in interfacial water are not yet fully understood. This thesis presents an investigation of ultrafast vibrational dynamics of hydrogen bonding in interfacial water. In a first chapter, the experimental technique and tools needed for the study of interfacial vibrational dynamics are exposed. In the first part of a second chapter, vibrational coherence dynamics of free OH stretch modes at the alumina/water interface are investigated. And in the second part, vibrational coherence dynamics of hydrogen bonded OH stretch modes at the calcium fluoride/water interface are investigated. To understand the dynamics of vibrational energy flow within an interfacial network of hydrogen bonding, the investigation of vibrational coupling dynamics at the calcium fluoride/water interface takes place in a third chapter. Unlike what has already been reported in this topic, in our work, the vibrational energy will be initially deposited at the second vibrational excited state, through an overtone transition. / Chemistry

Identiferoai:union.ndltd.org:TEMPLE/oai:scholarshare.temple.edu:20.500.12613/2615
Date January 2014
CreatorsBoulesbaa, Abdelaziz
ContributorsBorguet, Eric, Dai, Hai-Lung, Spano, Francis C., Yodh, Arjun G.
PublisherTemple University. Libraries
Source SetsTemple University
LanguageEnglish
Detected LanguageEnglish
TypeThesis/Dissertation, Text
Format87 pages
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Relationhttp://dx.doi.org/10.34944/dspace/2597, Theses and Dissertations

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