Absorption and fluorescence lineshape theory for polynomial potentials

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Standard

Absorption and fluorescence lineshape theory for polynomial potentials. / Anda, Andre; De Vico, Luca; Hansen, Thorsten; Abramavičius, Darius.

I: Journal of Chemical Theory and Computation, Bind 12, Nr. 12, 2016, s. 5979-5989.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Harvard

Anda, A, De Vico, L, Hansen, T & Abramavičius, D 2016, 'Absorption and fluorescence lineshape theory for polynomial potentials', Journal of Chemical Theory and Computation, bind 12, nr. 12, s. 5979-5989. https://doi.org/10.1021/acs.jctc.6b00997

APA

Anda, A., De Vico, L., Hansen, T., & Abramavičius, D. (2016). Absorption and fluorescence lineshape theory for polynomial potentials. Journal of Chemical Theory and Computation, 12(12), 5979-5989. https://doi.org/10.1021/acs.jctc.6b00997

Vancouver

Anda A, De Vico L, Hansen T, Abramavičius D. Absorption and fluorescence lineshape theory for polynomial potentials. Journal of Chemical Theory and Computation. 2016;12(12):5979-5989. https://doi.org/10.1021/acs.jctc.6b00997

Author

Anda, Andre ; De Vico, Luca ; Hansen, Thorsten ; Abramavičius, Darius. / Absorption and fluorescence lineshape theory for polynomial potentials. I: Journal of Chemical Theory and Computation. 2016 ; Bind 12, Nr. 12. s. 5979-5989.

Bibtex

@article{fa8fd5880f7d443bafc4f97766841946,
title = "Absorption and fluorescence lineshape theory for polynomial potentials",
abstract = "The modeling of vibrations in optical spectra relies heavily on the simplifications brought about by using harmonic oscillators. However, realistic molecular systems can deviate substantially from this description. We develop two methods which show that the extension to arbitrarily shaped potential energy surfaces is not only straightforward, but also efficient. These methods are applied to an electronic two-level system with potential energy surfaces of polynomial form and used to study anharmonic features such as the zero-phonon line shape and mirror-symmetry breaking between absorption and fluorescence spectra. The first method, which constructs vibrational wave functions as linear combinations of the harmonic oscillator wave functions, is shown to be extremely robust and can handle large anharmonicities. The second method uses the cumulant expansion, which is readily solved, even at high orders, thanks to an ideally suited matrix theorem.",
author = "Andre Anda and {De Vico}, Luca and Thorsten Hansen and Darius Abramavi{\v c}ius",
year = "2016",
doi = "10.1021/acs.jctc.6b00997",
language = "English",
volume = "12",
pages = "5979--5989",
journal = "Journal of Chemical Theory and Computation",
issn = "1549-9618",
publisher = "American Chemical Society",
number = "12",

}

RIS

TY - JOUR

T1 - Absorption and fluorescence lineshape theory for polynomial potentials

AU - Anda, Andre

AU - De Vico, Luca

AU - Hansen, Thorsten

AU - Abramavičius, Darius

PY - 2016

Y1 - 2016

N2 - The modeling of vibrations in optical spectra relies heavily on the simplifications brought about by using harmonic oscillators. However, realistic molecular systems can deviate substantially from this description. We develop two methods which show that the extension to arbitrarily shaped potential energy surfaces is not only straightforward, but also efficient. These methods are applied to an electronic two-level system with potential energy surfaces of polynomial form and used to study anharmonic features such as the zero-phonon line shape and mirror-symmetry breaking between absorption and fluorescence spectra. The first method, which constructs vibrational wave functions as linear combinations of the harmonic oscillator wave functions, is shown to be extremely robust and can handle large anharmonicities. The second method uses the cumulant expansion, which is readily solved, even at high orders, thanks to an ideally suited matrix theorem.

AB - The modeling of vibrations in optical spectra relies heavily on the simplifications brought about by using harmonic oscillators. However, realistic molecular systems can deviate substantially from this description. We develop two methods which show that the extension to arbitrarily shaped potential energy surfaces is not only straightforward, but also efficient. These methods are applied to an electronic two-level system with potential energy surfaces of polynomial form and used to study anharmonic features such as the zero-phonon line shape and mirror-symmetry breaking between absorption and fluorescence spectra. The first method, which constructs vibrational wave functions as linear combinations of the harmonic oscillator wave functions, is shown to be extremely robust and can handle large anharmonicities. The second method uses the cumulant expansion, which is readily solved, even at high orders, thanks to an ideally suited matrix theorem.

U2 - 10.1021/acs.jctc.6b00997

DO - 10.1021/acs.jctc.6b00997

M3 - Journal article

C2 - 27759961

AN - SCOPUS:85005987384

VL - 12

SP - 5979

EP - 5989

JO - Journal of Chemical Theory and Computation

JF - Journal of Chemical Theory and Computation

SN - 1549-9618

IS - 12

ER -

ID: 170741573