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Dresden 2020 – wissenschaftliches Programm

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O: Fachverband Oberflächenphysik

O 70: Frontiers in Electronic-Structure Theory - Focus on Electron-Phonon Interactions IV (joint session O/CPP/DS/HL)

O 70.2: Vortrag

Mittwoch, 18. März 2020, 15:30–15:45, GER 38

Fully Anharmonic, Non-Perturbative First-Principles Theory of Electronic-Vibrational Coupling in SolidsMarios Zacharias, Matthias Scheffler, and •Christian Carbogno — Fritz-Haber-Institut der Max-Planck-Gesellschaft, Berlin

The coupling between nuclear vibrations and the electronic structure plays a pivotal role for many material properties, including optical absorption and electronic transport. In this regard, however, today’s state-of-the-art methodologies rely on two approximations [1]: the harmonic (phonon) approximation for the nuclear motion and the linear response description of the electronic structure with respect to harmonic displacements. In this work, we overcome both these approximations by performing fully anharmonic ab initio molecular dynamics (aiMD) calculations and by accounting for the non-perturbative, self-consistent response of the wave functions along the aiMD trajectory. By this means, we obtain fully anharmonic, vibronically renormalized spectral functions, from which macroscopic material properties like temperature-dependent band gaps and electronic transport coefficients are obtained. We validate our approach using silicon as an example, for which the traditional electron-phonon coupling formalism is recovered. Using cubic SrTiO3 as example, we further demonstrate that anharmonic electronic-vibrational coupling effects are not captured in traditional formalisms, but they play a decisive role here and in other complex materials like perovskites.

[1] F. Giustino, Rev. Mod. Phys. 89, 015003 (2017).

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