Huang–Rhys factor
E27438
The Huang–Rhys factor is a dimensionless parameter in solid-state and molecular spectroscopy that quantifies the strength of electron–phonon (vibronic) coupling during electronic transitions.
All labels observed (1)
| Label | Occurrences |
|---|---|
| Huang–Rhys factor canonical | 2 |
How this entity was disambiguated
This entity first appeared as the object of triple T210290 — resolving that mention is where its identity was fixed. The disambiguator weighed these candidate entities and picked the highlighted one (or “None”, minting a new entity). This is how homonymy is resolved: the same surface form can point to different entities.
Target entity: Huang–Rhys factor Context triple: [Franck–Condon principle, relatedTo, Huang–Rhys factor]
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A.
Franck–Condon principle
The Franck–Condon principle is a rule in molecular spectroscopy that explains the intensity distribution of vibronic transitions by assuming electronic transitions occur much faster than nuclear motion, making vertical transitions between vibrational states most probable.
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B.
Rayleigh–Schrödinger perturbation theory
Rayleigh–Schrödinger perturbation theory is a fundamental method in quantum mechanics for approximating the energies and states of a system by treating interactions as small corrections to an exactly solvable problem.
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C.
Feynman–Hellmann theorem
The Feynman–Hellmann theorem is a result in quantum mechanics that relates the derivative of an energy eigenvalue with respect to a parameter in the Hamiltonian to the expectation value of the corresponding derivative of the Hamiltonian.
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D.
Born–Huang expansion
The Born–Huang expansion is a quantum mechanical method that systematically improves upon the Born–Oppenheimer approximation by including couplings between electronic and nuclear motions in molecular systems.
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E.
Born–Oppenheimer approximation
The Born–Oppenheimer approximation is a fundamental method in molecular quantum mechanics that simplifies calculations by treating nuclear motion as much slower than electronic motion, allowing their behaviors to be separated.
- F. None of above. chosen
- G. Unsure - the case is ambiguous/there is not enough information to decide.
Target entity: Huang–Rhys factor Target entity description: The Huang–Rhys factor is a dimensionless parameter in solid-state and molecular spectroscopy that quantifies the strength of electron–phonon (vibronic) coupling during electronic transitions.
-
A.
Franck–Condon principle
The Franck–Condon principle is a rule in molecular spectroscopy that explains the intensity distribution of vibronic transitions by assuming electronic transitions occur much faster than nuclear motion, making vertical transitions between vibrational states most probable.
-
B.
Rayleigh–Schrödinger perturbation theory
Rayleigh–Schrödinger perturbation theory is a fundamental method in quantum mechanics for approximating the energies and states of a system by treating interactions as small corrections to an exactly solvable problem.
-
C.
Feynman–Hellmann theorem
The Feynman–Hellmann theorem is a result in quantum mechanics that relates the derivative of an energy eigenvalue with respect to a parameter in the Hamiltonian to the expectation value of the corresponding derivative of the Hamiltonian.
-
D.
Born–Huang expansion
The Born–Huang expansion is a quantum mechanical method that systematically improves upon the Born–Oppenheimer approximation by including couplings between electronic and nuclear motions in molecular systems.
-
E.
Born–Oppenheimer approximation
The Born–Oppenheimer approximation is a fundamental method in molecular quantum mechanics that simplifies calculations by treating nuclear motion as much slower than electronic motion, allowing their behaviors to be separated.
- F. None of above. chosen
Statements (48)
| Predicate | Object |
|---|---|
| instanceOf |
dimensionless physical quantity
ⓘ
spectroscopic parameter ⓘ |
| appearsIn | Poisson distribution of phonon sideband intensities ⓘ |
| appliesTo |
color centers in crystals
ⓘ
defect centers in solids ⓘ electronic transitions ⓘ molecular electronic spectra ⓘ optical absorption ⓘ photoluminescence ⓘ |
| dependsOn |
displacement between ground and excited state potential energy surfaces
ⓘ
effective phonon mode energy ⓘ |
| determines |
relative intensity of phonon sidebands
ⓘ
relative intensity of vibronic peaks ⓘ weight of zero-phonon line ⓘ |
| estimatedFrom |
fit to vibronic sideband intensities
ⓘ
temperature dependence of luminescence ⓘ |
| field |
molecular spectroscopy
ⓘ
optical spectroscopy ⓘ solid-state physics ⓘ |
| governs | relative probability of n-phonon transitions ⓘ |
| hasProperty | dimensionless ⓘ |
| influences |
Debye–Waller factor
ⓘ
Stokes shift ⓘ shape of optical absorption spectra ⓘ shape of optical emission spectra ⓘ |
| introducedBy |
A. M. Rhys
ⓘ
Kun Huang ⓘ |
| mathematicalRole | average number of phonons involved in an electronic transition ⓘ |
| quantifies |
electron–phonon coupling strength
ⓘ
vibronic coupling strength ⓘ |
| relatedTo |
Franck–Condon principle
ⓘ
surface form:
Franck–Condon factors
Franck–Condon principle ⓘ phonon sidebands ⓘ vibronic progression ⓘ zero-phonon line ⓘ |
| symbol | S ⓘ |
| typicalRange |
much less than 1 for weak coupling
ⓘ
of order 1 or larger for strong coupling ⓘ |
| usedIn |
color center spectroscopy
ⓘ
nitrogen-vacancy center spectroscopy ⓘ organic molecular crystals ⓘ quantum emitter characterization ⓘ rare-earth ion spectroscopy ⓘ semiconductor defect spectroscopy ⓘ single-molecule spectroscopy ⓘ |
| usedInModel |
configuration coordinate model
ⓘ
harmonic oscillator approximation ⓘ |
| yearProposed | 1950 ⓘ |
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Subject: Huang–Rhys factor Description of subject: The Huang–Rhys factor is a dimensionless parameter in solid-state and molecular spectroscopy that quantifies the strength of electron–phonon (vibronic) coupling during electronic transitions.
Referenced by (2)
Full triples — surface form annotated when it differs from this entity's canonical label.