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U. Roß

Publications and source records attributed to U. Roß.

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Atomic scale spectral control of thermal transport in phononic crystal superlattices

We present experimental and theoretical investigations of phonon thermal transport in (LaMnO$_3$)$_m$/(SrMnO$_3$)$_n$ superlattices (LMO/SMO SLs) with the thickness of individual layers $m,n = 3 - 10\;$ u.c. and the thickness ratio $m/n = 1, 2$. Optical transient thermal reflectivity measurements reveal a pronounced difference in the thermal conductivity between SLs with $m/n = 1$, and SLs with $m/n = 2$. State-of-the art electron microscopy techniques and ab-initio density functional calculations enables us to assign the origin of this difference to the absence ($m/n = 1$) or presence ($m/n = 2$) of spatially periodic, static oxygen octahedral rotation (OOR) inside the LMO layers. The experimental data analysis shows that the effective thermal conductance of the LMO/SMO interfaces strongly changes from $0.3$ GW/m$^2$K for $m/n = 2$ SLs with OOR to a surprisingly large value of $1.8$ GW/m$^2$K for $m/n = 1$ SLs without OOR. An instructive lattice dynamical model rationalizes our experimental findings as a result of coherent phonon transmission for $m/n = 1$ versus coherent phonon blocking in SLs with $m/n = 2$. We briefly discuss the possibilities to exploit these results for atomic-scale engineering of a crystalline phonon insulator. The thermal resistivity of this proposal for a thermal metamaterial surpasses the amorphous limit, although phonons still propagate coherently.

cond-mat.mtrl-sci

Strain-Driven Structure-Ferroelectricity Relationship in hexagonal TbMnO$_3$ Films

Thin films and heterostructures of hexagonal manganites as promising multiferroic materials have attracted a considerable interest recently. We report structural transformations of high quality epitaxial h-TMO/YSZ(111) films, analyzed by means of various characterization techniques. A phase transition from P63mc to P63mcm structure at TC~800 K was observed by temperature dependent Raman spectroscopy and optical ellipsometry. The latter probing directly electronic system, indicates its modification at the structural phase transition likely due to charge transfer from oxygen to Mn. In situ transmission electron microscopy (TEM) of the lamella samples displayed an irreversible P63mc-P63mcm transformation and vanishing of ferroelectric domains already at 410 K. After the temperature cycling (300K-1300K-300K) the room temperature TEM of h-TMO films revealed an inhomogeneous microstructure, containing ferroelectric and paraelectric nanodomains with P63mc and P63mcm structure, respectively. We point out a strong influence of stress relaxation, induced by temperature and by constrained sample geometry onto the structure and ferroelectricity in strain-stabilized h-TMO thin films.

cond-mat.str-el