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EnglishThe excited electronic states of nearby molecules are in general coupled via Coulomb interaction even in the absence of wavefunction overlap. When two different organic molecules having a nearly resonant excited state are close enough, the dipole-dipole interaction can significantly affect their optical response. Even though they do not chemically interact, concerning their coupling to light, such molecules do not act independently, but rather as a 'virtual heterodimer' the response of which stems from, but is different from that of each molecule alone. We discuss here a simple and general model to estimate their resonant nonlinear susceptibilities.
| Titolo: | Optical nonlinearities of hybrid pairs of organic molecules |
| Autori: | |
| Data di pubblicazione: | 2013 |
| Rivista: | |
| Parole Chiave: | INORGANIC QUANTUM-WELLS; ENERGY-TRANSFER; EXCITONS; NANOSTRUCTURES |
| Digital Object Identifier (DOI): | http://dx.doi.org/10.1088/0953-8984/25/41/415303 |
| Appare nelle tipologie: | 1.1 Articolo in rivista |
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http://hdl.handle.net/11384/28990
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