Charge transfer dynamics across the interface of 3,4,9,10-perylenetetracarboxylic dianhydride (PTCDA) organic molecules and the reduced rutile TiO2 (110) 1 × 1 surface has been investigated using core-hole clock implementation of resonant photoemission spectroscopy (RPES). It is found that ultrafast charge transfer from PTCDA molecules to TiO2 substrate takes place on the time scale of 8–20 fs due to their strong electronic coupling. Moreover, the charge transfer time scale at the PTCDA/TiO2 (110) interface shows evident orientational dependence which varies with the molecular site owing to different electronic coupling strength
Charge transfer phenomena at metal/organic interfaces are a crucial step affecting the efficiencies ...
Orbital-specific femtosecond charge transfer dynamics between Fe(II)-tetraphenylporphyrin molecules ...
We present for the first time two-dimensional resonant inelastic x-ray scattering (RIXS) maps of mul...
Charge transfer dynamics across the interface of 3,4,9,10-perylenetetracarboxylic dianhydride (PTCDA...
The electronic structure, molecular orientations, and interfacial energy level alignment of 3,4,9,10...
Resonant core spectroscopies are applied to a study of the excited electron transfer dynamics on a l...
Charge transfer rates at metal/organic interfaces affect the efficiencies of devices for organic bas...
Resumen del póster presentado a la 13th European Conference on Surface Crystallography and Dynamics,...
The interfacial interaction and charge transfer dynamics between a F<sub>16</sub>CuPc molecular thin...
The application of the resonant photoemission spectroscopy (RPES) to various organic molecule based ...
The adsorption of Zn-tetraphenylporphyrin (ZnTPP) on nanoporous hierarchically organized anatase TiO...
We investigate by first-principles simulations the resonant electron-transfer lifetime from the exci...
Core-hole clock spectroscopy and near-edge x-ray-absorption fine structure measurements have been us...
The surface reduction of rutile TiO2(110) generates a state in the band gap whose excess electrons a...
The surface reduction of rutile TiO2(110) generates a state in the band gap whose excess electrons a...
Charge transfer phenomena at metal/organic interfaces are a crucial step affecting the efficiencies ...
Orbital-specific femtosecond charge transfer dynamics between Fe(II)-tetraphenylporphyrin molecules ...
We present for the first time two-dimensional resonant inelastic x-ray scattering (RIXS) maps of mul...
Charge transfer dynamics across the interface of 3,4,9,10-perylenetetracarboxylic dianhydride (PTCDA...
The electronic structure, molecular orientations, and interfacial energy level alignment of 3,4,9,10...
Resonant core spectroscopies are applied to a study of the excited electron transfer dynamics on a l...
Charge transfer rates at metal/organic interfaces affect the efficiencies of devices for organic bas...
Resumen del póster presentado a la 13th European Conference on Surface Crystallography and Dynamics,...
The interfacial interaction and charge transfer dynamics between a F<sub>16</sub>CuPc molecular thin...
The application of the resonant photoemission spectroscopy (RPES) to various organic molecule based ...
The adsorption of Zn-tetraphenylporphyrin (ZnTPP) on nanoporous hierarchically organized anatase TiO...
We investigate by first-principles simulations the resonant electron-transfer lifetime from the exci...
Core-hole clock spectroscopy and near-edge x-ray-absorption fine structure measurements have been us...
The surface reduction of rutile TiO2(110) generates a state in the band gap whose excess electrons a...
The surface reduction of rutile TiO2(110) generates a state in the band gap whose excess electrons a...
Charge transfer phenomena at metal/organic interfaces are a crucial step affecting the efficiencies ...
Orbital-specific femtosecond charge transfer dynamics between Fe(II)-tetraphenylporphyrin molecules ...
We present for the first time two-dimensional resonant inelastic x-ray scattering (RIXS) maps of mul...