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Dawid Pinkowicz

Publications and source records attributed to Dawid Pinkowicz.

4 recordsLinked to original sources

Polariton-polariton coherent coupling in a molecular spin-superconductor chip

The ability to establish coherent communication channels is key for scaling up quantum devices. Here, we engineer interactions between distant polaritons, hybrid spin-photon excitations formed at different lumped-element superconducting resonators within a chip. The chip consists of several resonator pairs, slightly detuned in frequency to make them addressable, capacitively coupled within each pair and inductively coupled to a common readout line. They interact locally with samples of PTMr and Tripak$^{-}$ organic free radicals, deposited onto their inductors, which provide model $S = 1/2$, $g \simeq 2$ spin ensembles. Frequency-dependent microwave transmission experiments, performed at very low temperatures, measure polariton frequencies as a function of magnetic field in different scenarios. When only one resonator within a pair hosts a molecular sample, the results evidence that spins couple remotely to the empty LER as well as to the local cavity mode. If both resonators interact with a spin ensemble, the magnetic field tunes the polariton frequencies relative to each other, on account of the different spin-photon interactions at each LER. When polaritons are brought into mutual resonance, an avoided level crossing emerges that gives direct spectroscopic evidence for a coherent polariton-polariton interaction mediated by the circuit. Pump-probe experiments reveal that the excitation of a polariton within a connected pair is felt, thus it can be read out, by the other one. These observations, backed by model calculations, illustrate the control and detection of distant photon-photon and spin-spin correlations and entanglement in a scalable modular chip.

quant-ph

Insight into magnetocaloric properties of Mn2Nb molecular magnet by relaxation calorimetry: A comprehensive case study

Magnetocaloric effect in [Nb$^\mathrm{IV}${($\mu$-CN)$_4$Mn$^\mathrm{II}$(H$_2$O)$_2$]}$_2\cdot$4H$_2$O]$_n$ molecular magnet is reported. The compound crystallizes in the tetragonal I4/m space group. It exhibits a phase transition to a long-range ferrimagnetically ordered state at $T_\mathrm{c}$ = 47.0(2) K. In order to calculate magnetocaloric properties relaxation calorimetry measurements are performed and a self-consistent scheme based on the magnetic entropy counting for the baseline determination is developed. The molecular field model is used to simulate the temperature and field dependence of the magnetic entropy change. The exchange coupling constant between the Mn$^\mathrm{II}$ and Nb$^\mathrm{IV}$ ions is estimated to be equal to -10.26 K. At the lowest temperatures and for the lowest applied field change values the inverse magnetocaloric effect is revealed, which seems to be characteristic for systems with antiferromagnetic coupling. The temperature dependence of exponent $n$ quantifying the field dependence of $\Delta S_\mathrm{M}$ is calculated on the basis of the experimental results and within the mean-field model. Its predicting power for the universality class of the critical behavior is discussed. Finally, the studied compound is employed as the working substance in the two most natural refrigeration cycles, i.e. the Brayton cycle and the Ericsson cycle, to assess its cooling effectiveness. A cascade system is suggested for the most efficient cooling performance.

cond-mat.mtrl-sci

Plasma-induced magnetic phase in 3D $\mathrm{Mn^{II}-Nb^{IV}}$ octacyanidometalate with magnetic sponge behavior

A new magnetic phase with $T_C = 72 \ \mathrm K$ was obtained by exposing the three-dimensional $\mathrm{\{ [Mn^{II}(H_2O)_2]_2[Nb^{IV}(CN)_8] \cdot 4H_2O \} _n}$ coordination ferrimagnet ($T_C = 49 \ \mathrm K$) to air, oxygen, nitrogen, and argon-based plasma. The X-ray powder diffraction pattern revealed that the unit cell shrank after plasma treatment, leading to a 20% enhancement of the superexchange couplings, as estimated from the mean-field approximation (MFA) model. Although no stable dehydrated form was found in the thermogravimetric analysis, the observed changes are attributed to the removal of crystallization water molecules. The plasma-induced magnetic phase could not be obtained by exposing the studied material to 0% relative humidity during dynamic vapor sorption. Instead, the material underwent a major structural reorganization after dehydration, necessitating an extended MFA model to reproduce the magnetic susceptibility. These findings demonstrate that plasma-induced changes can create unique magnetic phases in molecule-based systems that are otherwise unobtainable.

cond-mat.mtrl-sci

Plasma treatment as an unconventional molecular magnet engineering method

Molecular magnetism aims to design materials with unique properties at the molecular level, focusing on the systematic synthesis of new chemical compounds. In this paper, we propose an alternative route to engineer molecular magnetic materials through plasma irradiation. Our research indicates that the long-range magnetic order temperature in the three-dimensional $\mathrm{\{[Mn^{II}(H_2O)_2]_2[Nb^{IV}(CN)_8]\cdot 4H_2O\}_n}$ molecular ferrimagnet increases by 20 K after plasma treatment. The core structure of the compound does not reveal significant changes after plasma processing, as confirmed by the X-ray powder diffraction analysis. The observed results are attributed to the release of crystallized water molecules. The described procedure can serve as a viable approach to altering the magnetic properties of the molecular systems.

cond-mat.mtrl-sci