Intermolecular vibrational energy transfer in monolayers of isotopically mixed rhenium carbonyl complexes at solid–liquid interfaces is investigated with the help of ultrafast 2D Attenuated Total Reflectance Infrared (2D ATR IR) spectroscopy in dependence of plasmonic surface enhancement effects. Dielectric and plasmonic materials are used to demonstrate that plasmonic effects have no impact on the vibrational energy transfer rate in a regime of moderate IR surface enhancement (enhancement factors up to ca. 30). This result can be explained with the common image-dipole picture. The vibrational energy transfer rate thus can be used as a direct observable to determine intermolecular distances on surfaces, regardless of their plasmonic propert...
We present two-dimensional infrared (2D IR) spectra of organic monolayers immobilized on thin metall...
In this thesis, two multidimensional spectroscopic methods — two-dimensional infrared (2D IR) spectr...
Surface-enhanced Raman scattering (SERS) is typically assumed to occur at individual molecules negle...
Intermolecular vibrational energy transfer in monolayers of isotopically mixed rhenium carbonyl comp...
We investigate the ultrafast vibrational dynamics of monolayers from adsorbed rhenium-carbonyl CO-re...
Vibrational energy transfer (VET) between two isotopologues of [Re(dcb)(CO)3Br] immobilized on a TiO...
Ultrafast vibrational dynamics of small molecules on platinum (Pt) layers in water are investigated ...
Knowledge of vibrational energy transfer on a metal nanoparticle/liquid interface is essential for u...
In a recent work (J. Phys. Chem. C 2016, 120, 3350-3359), we have introduced the concept of surface-...
Knowledge of vibrational energy transfer on a metal nanoparticle/liquid interface is essential for u...
A novel type of surface vibrational sum-frequency generation spectroscopy is presented that enables ...
Two-dimensional infrared spectroscopy of vibrational probes at an electrode surface shows promise fo...
Ultrafast two-dimensional infrared spectroscopy (2D IR) has been advanced in recent years toward mea...
We present an experimental and theoretical study of vibrational excitation of the C–O stretch vibrat...
We present an experimental and theoretical investigation into the coupling of C-O stretch vibrations...
We present two-dimensional infrared (2D IR) spectra of organic monolayers immobilized on thin metall...
In this thesis, two multidimensional spectroscopic methods — two-dimensional infrared (2D IR) spectr...
Surface-enhanced Raman scattering (SERS) is typically assumed to occur at individual molecules negle...
Intermolecular vibrational energy transfer in monolayers of isotopically mixed rhenium carbonyl comp...
We investigate the ultrafast vibrational dynamics of monolayers from adsorbed rhenium-carbonyl CO-re...
Vibrational energy transfer (VET) between two isotopologues of [Re(dcb)(CO)3Br] immobilized on a TiO...
Ultrafast vibrational dynamics of small molecules on platinum (Pt) layers in water are investigated ...
Knowledge of vibrational energy transfer on a metal nanoparticle/liquid interface is essential for u...
In a recent work (J. Phys. Chem. C 2016, 120, 3350-3359), we have introduced the concept of surface-...
Knowledge of vibrational energy transfer on a metal nanoparticle/liquid interface is essential for u...
A novel type of surface vibrational sum-frequency generation spectroscopy is presented that enables ...
Two-dimensional infrared spectroscopy of vibrational probes at an electrode surface shows promise fo...
Ultrafast two-dimensional infrared spectroscopy (2D IR) has been advanced in recent years toward mea...
We present an experimental and theoretical study of vibrational excitation of the C–O stretch vibrat...
We present an experimental and theoretical investigation into the coupling of C-O stretch vibrations...
We present two-dimensional infrared (2D IR) spectra of organic monolayers immobilized on thin metall...
In this thesis, two multidimensional spectroscopic methods — two-dimensional infrared (2D IR) spectr...
Surface-enhanced Raman scattering (SERS) is typically assumed to occur at individual molecules negle...