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In this Letter, we describe quantitative magnetic imaging of superconducting vortices in RbEuFe_4As_4 in order to investigate the unique interplay between the magnetic and superconducting sublattices. Our scanning Hall microscopy data reveal a pronounced suppression of the superfluid density near the magnetic ordering temperature in good qualitative agreement with a recently developed model describing the suppression of superconductivity by correlated magnetic fluctuations. These results indicate a pronounced exchange interaction between the superconducting and magnetic subsystems in RbEuFe_4As_4, with important implications for future investigations of physical phenomena arising from the interplay between them.The class of possible thermodynamic conversions can be extended by introducing an auxiliary system called catalyst, which assists in state conversion while its own state remains unchanged. We reveal a complete characterization of catalytic state conversion in quantum and single-shot thermodynamics by allowing an infinitesimal correlation between the system and the catalyst. Specifically, we prove that a single thermodynamic potential, which provides the necessary and sufficient condition for the correlated-catalytic state conversion, is given by the standard nonequilibrium free energy defined with the Kullback-Leibler divergence. This resolves the conjecture raised by Wilming, Gallego, and Eisert [Entropy 19, 241 (2017)ENTRFG1099-430010.3390/e19060241] and by Lostaglio and Müller [Phys. Rev. Lett. MLN2238 123, 020403 (2019)PRLTAO0031-900710.1103/PhysRevLett.123.020403] in the positive. Moreover, we show that, with the aid of the work storage, any quantum state can be converted into another by paying the work cost equal to the nonequilibrium free energy difference. Our result would serve as a step towards establishing resource theories of catalytic state conversion in the fully quantum regime.Fast-ion driven Alfvén waves with frequency close to the ion cyclotron frequency (f=0.58f_ci) excited by energetic ions from a neutral beam are stabilized via a controlled energetic ion density ramp for the first time in a fusion research plasma. The scaling of wave amplitude with injection rate is consistent with theory for single mode collisional saturation near marginal stability. The wave is identified as a shear-polarized global Alfvén eigenmode excited by Doppler-shifted cyclotron resonance with fast ions with sub-Alfvénic energetic ions, a first in fusion research plasmas.Electronic excitations near the surface of water ice lead to the desorption of adsorbed molecules, through a so far debated mechanism. A systematic study of photon-induced indirect desorption, revealed by the spectral dependence of the desorption (7-13 eV), is conducted for Ar, Kr, N_2, and CO adsorbed on H_2O or D_2O amorphous ices. The mass and isotopic dependence and the increase of intrinsic desorption efficiency with photon energy all point to a mechanism of desorption induced by collisions between adsorbates and energetic H/D atoms, produced by photodissociation of water. This constitutes a direct and unambiguous experimental demonstration of the mechanism of indirect desorption of weakly adsorbed species on water ice, and sheds new light on the possibility of this mechanism in other systems. It also has implications for the description of photon-induced desorption in astrochemical models.Neutrinoless double-β (0νββ) decay of certain atomic isotopes, if observed, will have significant implications for physics of neutrinos and models of physics beyond the standard model. In the simplest scenario, if the mass of the light neutrino of the standard model has a Majorana component, it can mediate the decay. Systematic theoretical studies of the decay rate in this scenario, through effective field theories matched to ab initio nuclear many-body calculations, are needed to draw conclusions about the hierarchy of neutrino masses, and to plan the design of future experiments. However, a recently identified short-distance contribution at leading order in the effective field theory amplitude of the subprocess nn→pp(ee) remains unknown, and only lattice quantum chromodynamics (QCD) can directly and reliably determine the associated low-energy constant. While the numerical computations of the correlation function for this process are underway with lattice QCD, the connection to the physical amplitude, and hence this short-distance contribution, is missing. A complete framework that enables this complex matching is developed in this Letter. The complications arising from the Euclidean and finite-volume nature of the corresponding correlation function are fully resolved, and the value of the formalism is demonstrated through a simple example. The result of this work, therefore, fills the gap between first-principles studies of the nn→pp(ee) amplitude from lattice QCD and those from effective field theory, and can be readily employed in the ongoing lattice-QCD studies of this process.Quantum systems are typically characterized by the inherent fluctuation of their physical observables. Despite this fundamental importance, the investigation of the fluctuations in interacting quantum systems at finite temperature continues to pose considerable theoretical and experimental challenges. Here we report the characterization of atom number fluctuations in weakly interacting Bose-Einstein condensates. Technical fluctuations are mitigated through a combination of nondestructive detection and active stabilization of the cooling sequence. We observe fluctuations reduced by 27% below the canonical expectation for a noninteracting gas, revealing the microcanonical nature of our system. The peak fluctuations have near linear scaling with atom number ΔN_0,p^2∝N^1.134 in an experimentally accessible transition region outside the thermodynamic limit. Our experimental results thus set a benchmark for theoretical calculations under typical experimental conditions.Nanoscopic clustering in a 2D disordered phase is observed for oxygen on Ru(0001) at low coverages and high temperatures. We study the coexistence of quasistatic clusters (with a characteristic length of ∼9  Å) and highly mobile atomic oxygen which diffuses between the energy-inequivalent, threefold hollow sites of the substrate. We determine a surprisingly low activation energy for diffusion of 385±20  meV. The minimum of the O-O interadsorbate potential appears to be at lower separations than previously reported.

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