1992
DOI: 10.1016/0301-0104(92)80198-5
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An analysis of models for resonant transer of excitation using quantum electrodynamics

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Cited by 95 publications
(156 citation statements)
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“…Such a description of molecular interactions in terms of virtual photons has found extensive applications in other areas of chemical physics. It has, for example, a pivotal role in the description of chiroptical behaviour associated with intermolecular interactions, as in induced circular dichroism [30][31][32], and it has recently enjoyed extensive application in the theory of intermolecular energy transfer per se [20][21][22][23][24][25] -areas in which Craig and Thirunamachandran have made a number of important contributions. Such considerations here form the basis for a common representation of bimolecular probability amplitudes in terms of the photophysical interactions of the individual molecules A and B, as will be detailed in Sections 4 and 5.…”
Section: Theoretical Framework For Bimolecular Excitationmentioning
confidence: 99%
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“…Such a description of molecular interactions in terms of virtual photons has found extensive applications in other areas of chemical physics. It has, for example, a pivotal role in the description of chiroptical behaviour associated with intermolecular interactions, as in induced circular dichroism [30][31][32], and it has recently enjoyed extensive application in the theory of intermolecular energy transfer per se [20][21][22][23][24][25] -areas in which Craig and Thirunamachandran have made a number of important contributions. Such considerations here form the basis for a common representation of bimolecular probability amplitudes in terms of the photophysical interactions of the individual molecules A and B, as will be detailed in Sections 4 and 5.…”
Section: Theoretical Framework For Bimolecular Excitationmentioning
confidence: 99%
“…When the intermolecular distance R is less than the reduced wavelength ~ = A/2'rr (where A is the wavelength corresponding to the energy being transferred) then the transfer is commonly termed a non-radiative or radiationless process and treated as a longitudinal (Coulombic) interaction [14]; alternatively it may be understood to be mediated by virtual photon coupling [15][16][17][18][19][20][21][22][23][24]. From either viewpoint, although it may occur at some interval after initial molecular photoexcitation, each individual transfer of energy is essentially instantaneous, subject to the obvious constraint of causality.…”
Section: Introductionmentioning
confidence: 99%
“…In its QED formulation, this emerges as a second-order perturbational process mediated by intermolecular propagation of a virtual photon [8][9][10][11][12][13][14]. The advantage of such a quantum electrodynamical treatment is that it extends the traditional F~Srster theory of short-range (near-zone) dipole-dipole radiationless transfer to arbitrary A-B separations R, thus establishing a continuous connection with long-range (far-zone) radiative transfer.…”
Section: A* +B--a+b* (13)mentioning
confidence: 99%
“…Following the extensive analysis of the energy transfer between a pair of molecules in vacuum [8][9][10][11][12][13][14], the medium-induced modifications of the process have also been considered recently [17]. The formalism developed [17] will now be extended to higher-order bimolecular processes that involve real incoming and outgoing photons in addition to the virtual ones.…”
Section: Definition Of Bimolecular Ratesmentioning
confidence: 99%
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