Hydrogen bond dynamics of interfacial water molecules revealed from two-dimensional vibrational sum-frequency generation spectroscopy

Abstract Vibrational sum-frequency generation (vSFG) spectroscopy allows the study of the structure and dynamics of interfacial systems. In the present work, we provide a simple recipe, based on a narrowband IR pump and broadband vSFG probe technique, to computationally obtain the two-dimensional vS...

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Autores principales: Deepak Ojha, Thomas D. Kühne
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Lenguaje:EN
Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/7f11097867f74482837116da9323123e
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spelling oai:doaj.org-article:7f11097867f74482837116da9323123e2021-12-02T13:57:38ZHydrogen bond dynamics of interfacial water molecules revealed from two-dimensional vibrational sum-frequency generation spectroscopy10.1038/s41598-021-81635-42045-2322https://doaj.org/article/7f11097867f74482837116da9323123e2021-01-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-81635-4https://doaj.org/toc/2045-2322Abstract Vibrational sum-frequency generation (vSFG) spectroscopy allows the study of the structure and dynamics of interfacial systems. In the present work, we provide a simple recipe, based on a narrowband IR pump and broadband vSFG probe technique, to computationally obtain the two-dimensional vSFG spectrum of water molecules at the air–water interface. Using this technique, to study the time-dependent spectral evolution of hydrogen-bonded and free water molecules, we demonstrate that at the interface, the vibrational spectral dynamics of the free OH bond is faster than that of the bonded OH mode.Deepak OjhaThomas D. KühneNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-6 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Deepak Ojha
Thomas D. Kühne
Hydrogen bond dynamics of interfacial water molecules revealed from two-dimensional vibrational sum-frequency generation spectroscopy
description Abstract Vibrational sum-frequency generation (vSFG) spectroscopy allows the study of the structure and dynamics of interfacial systems. In the present work, we provide a simple recipe, based on a narrowband IR pump and broadband vSFG probe technique, to computationally obtain the two-dimensional vSFG spectrum of water molecules at the air–water interface. Using this technique, to study the time-dependent spectral evolution of hydrogen-bonded and free water molecules, we demonstrate that at the interface, the vibrational spectral dynamics of the free OH bond is faster than that of the bonded OH mode.
format article
author Deepak Ojha
Thomas D. Kühne
author_facet Deepak Ojha
Thomas D. Kühne
author_sort Deepak Ojha
title Hydrogen bond dynamics of interfacial water molecules revealed from two-dimensional vibrational sum-frequency generation spectroscopy
title_short Hydrogen bond dynamics of interfacial water molecules revealed from two-dimensional vibrational sum-frequency generation spectroscopy
title_full Hydrogen bond dynamics of interfacial water molecules revealed from two-dimensional vibrational sum-frequency generation spectroscopy
title_fullStr Hydrogen bond dynamics of interfacial water molecules revealed from two-dimensional vibrational sum-frequency generation spectroscopy
title_full_unstemmed Hydrogen bond dynamics of interfacial water molecules revealed from two-dimensional vibrational sum-frequency generation spectroscopy
title_sort hydrogen bond dynamics of interfacial water molecules revealed from two-dimensional vibrational sum-frequency generation spectroscopy
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/7f11097867f74482837116da9323123e
work_keys_str_mv AT deepakojha hydrogenbonddynamicsofinterfacialwatermoleculesrevealedfromtwodimensionalvibrationalsumfrequencygenerationspectroscopy
AT thomasdkuhne hydrogenbonddynamicsofinterfacialwatermoleculesrevealedfromtwodimensionalvibrationalsumfrequencygenerationspectroscopy
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