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Carla Slebodnick

Publications and source records attributed to Carla Slebodnick.

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Anomalous Thermal Transport Reveals Weak First-Order Melting of Charge Density Waves in 2H-TaSe2

How ordered phases melt in low-dimensional quantum materials remain difficult to resolve because the relevant fluctuations are dynamic and charge neutral. In this work, we show that thermal transport provides a sensitive probe of these hidden fluctuations in the layered transition metal dichalcogenide 2H-TaSe2. We observe a striking V-shaped temperature dependence of the thermal conductivity that cannot be explained by conventional phonon-phonon scattering. Instead, it originates from scattering by persistent local charge-density-wave (CDW) correlations, consistent with our phenomenological model linking thermal transport to spatial CDW fluctuation. Electron diffraction reveals short-range periodic lattice distortions persisting to at least 300 K, while X-ray diffraction shows thermal hysteresis of the CDW wavevector. Together, these results reveal a dislocation- and fluctuation-driven weak first-order melting of the CDW state.

cond-mat.str-el

Double Helical Conformation and Extreme Rigidity in a Rodlike Polyelectrolyte

The ubiquitous biomacromolecule DNA has an axial rigidity persistence length of ~50 nm, driven by its elegant double helical structure. While double and multiple helix structures appear widely in nature, only rarely are these found in synthetic non-chiral macromolecules. Here we describe a double helical conformation in the densely charged aromatic polyamide poly(2,2'-disulfonyl-4,4'-benzidine terephthalamide) or PBDT. This double helix macromolecule represents one of the most rigid simple molecular structures known, exhibiting an extremely high axial persistence length (~1 micrometer). We present X-ray diffraction, NMR spectroscopy, and molecular dynamics (MD) simulations that reveal and confirm the double helical conformation. The discovery of this extreme rigidity in combination with high charge density gives insight into the self-assembly of molecular ionic composites with high mechanical modulus (~1 GPa) yet with liquid-like ion motions inside, and provides fodder for formation of new 1D-reinforced composites.

cond-mat.soft