Computational Condensed Matter Physics Group

Abstract:

We study the effect of size on the vibrational modes and frequencies of nanoparticles, by applying a newly developed, robust, and efficient first-principles-based method that we present in outline. We focus on rutile TiO₂, a technologically important material whose bulk exhibits a softening of a transverse acoustic mode close to q=(12,12,14), which becomes unstable with the application of negative pressure. We demonstrate that, under these conditions, nanoparticles above a critical size exhibit unstable localized modes and we calculate their characteristic localization length and decomposition with respect to bulk phonons. We propose that such localized soft modes could initiate coherent structural phase transformations in small nanoparticles above a critical size.

Abstract:

Interlayer organic cations in quasi-two-dimensional halide perovskites are a versatile tuning vehicle for the optoelectronic properties of these complex systems, but chemical intuition for this design route is yet to be established. Here, we use density functional theory, the GW approximation, and the Bethe-Salpeter equation approach to understand the contribution of the organic cation to the quasiparticle band gap and exciton binding energy of layered perovskites. We show that organic cations in quasi-two-dimensional perovskites contribute significantly to the dielectric screening in these systems, countering quantum confinement effects on the quasiparticle band gap and the exciton binding energy. Using a simple electrostatics model inspired by parallel-plate capacitors, we decouple the organic cation and inorganic layer contributions to the effective dielectric constants and show that dielectric properties of layered perovskites are broadly tunable via the interlayer cation, providing a direct means of tuning photophysical properties for a variety of applications.

Abstract:

The dependence of ab initio many-body perturbation theory within the GW approximation on the eigensystem used in calculating quasiparticle corrections limits this method's predictive power. Here, we investigate the accuracy of the recently developed Wannier-localized optimally tuned screened range-separated hybrid (WOT-SRSH) functional as a generalized Kohn-Sham starting point for single-shot GW (G0W0) calculations for a range of semiconductors and insulators. Comparison to calculations based on well-established functionals, namely, PBE, PBE0, and HSE, as well as to self-consistent GW schemes and to experiment, shows that band gaps computed via G0W0@WOT-SRSH have a level of precision and accuracy that is comparable to that of more advanced methods such as quasiparticle self-consistent GW and eigenvalue self-consistent GW. We also find that G0W0@WOT-SRSH improves the description of states deeper in the valence band manifold. Finally, we show that G0W0@WOT-SRSH significantly reduces the sensitivity of computed band gaps to ambiguities in the underlying WOT-SRSH tuning procedure.

Abstract:

Halogen mixing in lead-halide perovskites is an effective route for tuning the band gap in light emission and multijunction solar cell applications. Here we report the effect of halogen mixing on the optoelectronic properties of lead-halide perovskites from theory and experiment. We applied the virtual crystal approximation within density functional theory, the <i>GW</i> approximation, and the Bethe-Salpeter equation to calculate structural, vibrational, and optoelectronic properties for a series of mixed halide perovskites. We separately perform spectroscopic measurements of these properties and analyze the impact of halogen mixing on quasiparticle band gaps, effective masses, absorption coefficients, charge-carrier mobilities, and exciton binding energies. Our joint theoretical-experimental study demonstrates that iodide-bromide mixed-halide perovskites can be modeled as homovalent alloys, and local structural distortions do not play a significant role for the properties of these mixed species. Our study outlines a general theoretical-experimental framework for future investigations of novel chemically mixed systems.