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Yongfei Ji

Publications and source records attributed to Yongfei Ji.

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Raman Images of a Single Molecule in a Highly Confined Plasmonic Field

Under the local plasmonic excitation, the Raman images of a single molecule can now reach sub-nanometer resolution. We report here a theoretical description of the interaction between a molecule and a highly confined plasmonic field. It is shown that when the spatial distribution of the plasmonic field is comparable with the size of the molecule, the optical transition matrix of the molecule becomes to be dependent on the position and the spatial distribution of the plasmonic field, resulting in spatially resolved Raman image of a molecule. It is found that the resonant Raman image reflects the electronic transition density of the molecule. In combination with the first principles calculations, the simulated Raman image of a porphyrin derivative adsorbed on the silver surface nicely reproduces its experimental counterpart. The present theory provides the basic framework for describing linear and nonlinear responses of molecules under the highly confined plasmonic field.

cond-mat.mes-hall

Evidence of Photocatalytic Dissociation of Water on TiO2 with Atomic Resolution

Photocatalytic water splitting reaction on TiO2 surface is one of the fundamental issues that bears significant implication in hydrogen energy technology and has been extensively studied. However, the existence of the very first reaction step, the direct photo-dissociation of water, has been disregarded. Here, we provide unambiguously experimental evidence to demonstrate that adsorbed water molecules on reduced rutile TiO2(110)-1\times1 surface can be dissociated under UV irradiation using low temperature scanning tunneling microscopy. It is identified that a water molecule at fivefold coordinated Ti (Ti5c) site can be photocatalytically dissociated, resulting in a hydroxyl at Ti5c and another hydroxyl at bridge oxygen row. Our findings reveal a missing link in the photocatalytic water splitting reaction chain, which greatly contribute to the detailed understanding of underlying mechanism.

physics.chem-ph