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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2021
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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) |
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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 |
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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 |
_version_ |
1718392268830801920 |