Structural and excited-state properties of oligoacene crystals from first principles
Artikel i vetenskaplig tidskrift, 2016

Molecular crystals are a prototypical class of van der Waals (vdW) bound organic materials with excited-state properties relevant for optoelectronics applications. Predicting the structure and excited-state properties of molecular crystals presents a challenge for electronic structure theory, as standard approximations to density functional theory (DFT) do not capture long-range vdW dispersion interactions and do not yield excited-state properties. In this work, we use a combination of DFT including vdW forces, using both nonlocal correlation functionals and pairwise correction methods, together with many-body perturbation theory (MBPT) to study the geometry and excited states, respectively, of the entire series of oligoacene crystals, from benzene to hexacene. We find that vdW methods can predict lattice constants within 1% of the experimental measurements, on par with the previously reported accuracy of pairwise approximations for the same systems. We further find that excitation energies are sensitive to geometry, but if optimized geometries are used MBPT can yield excited-state properties within a few tenths of an eV from experiment. We elucidate trends in MBPT-computed charged and neutral excitation energies across the acene series and discuss the role of common approximations used in MBPT.


T. Rangel

UC Berkeley

Lawrence Berkeley National Laboratory

Kristian Berland

Universitetet i Oslo

S. Sharifzadeh

Boston University

F. Brown-Altvater

UC Berkeley

Lawrence Berkeley National Laboratory

K. Lee

Lawrence Berkeley National Laboratory

Per Hyldgaard

Elektronikmaterial och system

L. Kronik

Weizmann Institute of Science Israel

J. B. Neaton

Lawrence Berkeley National Laboratory

UC Berkeley

Kavli Energy NanoSciences Institute at Berkeley

Physical Review B

24699950 (ISSN) 24699969 (eISSN)

Vol. 93 115206


Nanovetenskap och nanoteknik