Many‐body response of benzene at monolayer MoS2: Van der Waals interactions and spectral broadening. Issue 21 (11th April 2020)

• Record Type: Journal Article
• Authors: Umerbekova, Alina; Pavanello, Michele
• Other Names: Wasserman Adam guestEditor.; Pavanello Michele guestEditor.
• Is Part Of: International journal of quantum chemistry. Volume 120:Issue 21(2020)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2020-04-11
• Subjects: linear response -- many body dispersion -- TDDFT -- van der Waals; Quantum chemistry -- Periodicals; 541.28
• DOI: 10.1002/qua.26243
• Languages: English
• ISSNs: 0020-7608

Abstract

Abstract: Models of surface enhancement of molecular electronic response properties are challenging for two reasons: (a) molecule‐surface interactions require a simultaneous solution of the molecular and the surface dynamic response (a daunting task), and (b) when solving for the electronic structure of the combined molecule + surface system, it is not trivial to single out the particular physical effects responsible for enhancement. To tackle this problem, in this work, we apply a formally exact decomposition of the system's response function into subsystem contributions by using subsystem density functional theory (DFT), which grants access to dynamic polarizabilities and optical spectra. In order to access information about the interactions between the subsystems, we extend a previously developed subsystem‐based adiabatic connection fluctuation‐dissipation theorem of DFT to separate the additive from the nonadditive correlation energy and identify the nonadditive correlation as the van der Waals interactions. As an example, we choose benzene adsorbed on monolayer MoS2 . We isolate the contributions to benzene's dynamic response arising from the interaction with the surface, and for the first time, we evaluate the enhancements to the effectiveness of C 6 coefficients as a function of benzene‐MoS2 distance and adsorption site. We also quantify the spectral broadening of the benzene's electronic excited states due to their interaction with the surface. We find that the broadening has a similar decay law with the molecule‐surface distance as the leading van der Waals interactions (ie, R −6 ) and that the surface enhancement of dispersion interactions between benzene molecules is less than 5% but is still large enough (0.5 kcal/mol) to likely play a role in the prediction of interface morphologies. Abstract : To tackle the problem of accurate modeling surface enhancement of molecular electronic response properties, a formally exact decomposition of the system's response function into subsystem contributions is developed by using subsystem DFT, which grants access to dynamic polarizabilities and optical spectra. A previously developed subsystem‐based adiabatic connection fluctuation‐dissipation theorem of DFT is extended to distinguish between additive and nonadditive correlation energies, such as van der Waals interactions.