arXiv subjects

Narcis Avarvari

Publications and source records attributed to Narcis Avarvari.

4 recordsLinked to original sources

arXiv2025

Stretching helical molecular springs: the peculiar evolution of electron transport in helicene junctions

Single-molecule junctions represent electromechanical systems at the edge of device miniaturization. Despite extensive studies on the interplay between mechanical manipulation and electron transport in molecular junctions, a thorough understanding of conducting molecular springs remains elusive. Here, we investigate the impact of mechanical elongation and compression on the electron transport and electronic structure of helicene-based spring-like single-molecule junctions, utilizing 2,2'-dithiol-[6]helicene and thioacetyl-[13]helicene molecules bridging two gold electrodes. We observe robust, reversible U-shaped conductance variations with interelectrode distance. Ab-initio electronic structure and quantum transport calculations reveal that this behavior stems from destructive quantum interference, induced mainly by modifications of the coupling at the metal-molecule interface as a peculiar outcome of the helical backbone deformation. These findings highlight the central role of the helical geometry in combination with contact properties in the electromechanical response of conducting molecular springs, offering insights for designing functional electromechanical devices that leverage similar mechanisms.

cond-mat.mes-hall↗

arXiv2024

Gapped magnetic ground state in the spin-liquid candidate $\kappa$-(BEDT-TTF)$_2$Ag$_2$(CN)$_3$ suggested by magnetic spectroscopy

The nature of the magnetic ground state of highly frustrated systems remained puzzling to this day. Here, we have performed multifrequency electron spin resonance (ESR) measurements on a putative quantum spin liquid compound $\kappa$-(BEDT-TTF)$_2$Ag$_2$(CN)$_3$, which is a rare example of $S = 1/2$ spins on a triangular lattice. At high temperatures, the spin susceptibility exhibits a weak temperature dependence which can be described by the Heisenberg model with an antiferromagnetic exchange interaction of strength $J/k_B \approx 175$ K. At low temperatures, however, the rapid drop of the static spin susceptibility, together with monotonic decrease of the ESR linewidth indicates that strong singlet correlations develop below a pairing energy scale $T^*$ accompanied by a spin gap. On the other hand, a weak Curie-like spin susceptibility and the angular dependence of the linewidth suggest additional contribution from impurity spins. We propose the gradual formation of spin singlets with an inhomogeneous spin gap at low temperatures.

cond-mat.str-el↗

arXiv2024

Single-molecule junctions map the interplay between electrons and chirality

The interplay of electrons with a chiral medium has a diverse impact across science and technology, influencing drug separation, chemical reactions, and electronic transport. In particular, such electronchirality interactions can significantly affect charge and spin transport in chiral conductors, ranging from bulk semiconductors down to individual molecules. Consequentially, these interactions are appealing for spintronic manipulations. However, an atomistic mapping of the different electron chirality interactions and their potential for spintronics has yet to be reached. Here, we find that single molecule junctions based on helicene molecules behave as a combined magnetic diode and spin valve device. This dual functionality is used to identify the coexistence of different electron chirality interactions at the atomic scale. Specifically, we find that the magnetic diode behavior arises from an interaction between the angular momentum of electrons in a chiral medium and magnetic fields, whereas the spin valve functionality stems from an interaction between the electron spin and a chiral medium. The coexistence of these two interactions in the same atomic scale system is then used to identify the distinct properties of each interaction. This work uncovers the different electron chirality interactions available at the atomic level. The found concurrent existence of such interactions can broaden the available methods for spintronics by combining their peculiar functionalities.

cond-mat.mes-hall↗

arXiv2013

Charge-sensitive vibrational modes in the (EDT-TTF-OX)_2AsF_6 chiral molecular conductors

Infrared and Raman spectra of the three chiral molecular conductors (EDT-TTF-OX)_2AsF_6, comprising two salts based on enantiopure EDT-TTF-OX donor molecules and one based on their racemic mixture, have been measured as a function of temperature. In the frequency range of the C=C stretching vibrations of EDT-TTF-OX, charge-sensitive modes are identified based on theoretical calculations for neutral and oxidized EDT-TTF-OX using density functional theory (DFT) methods. The positions of the C=C stretching modes in both Raman and infrared spectra of the (EDT-TTF-OX)_2AsF_6 materials are analyzed assuming linear relationship between the frequency and charge on the molecule. The charge density on the EDT-TTF-OX donor molecule is estimated to be +0.5 in all the investigated materials and does not change with temperature. Therefore it is suggested, that M-I transition observed in (EDT-TTF-X)_2AsF_6 chiral molecular conductors at low temperature is not related to the charge ordering mechanism.

cond-mat.mtrl-sci↗