Thermally excited Trivelpiece–Gould modes as a pure electron plasma temperature diagnostic

Thermally excited plasma modes are observed in trapped, near-thermal-equilibrium pure electron plasmas over a temperature range of 0.05<kT<5 eV. The modes are excited and damped by thermal fluctuations in both the plasma and the receiver electronics. The thermal emission spectra together with a plasma-antenna coupling coefficient calibration uniquely determine the plasma (and load) temperature. This calibration is obtained from the mode spectra themselves when the receiver-generated noise absorption is measurable; or from separate wave reflection/absorption measurements; or from kinetic theory. This nondestructive temperature diagnostic agrees well with standard diagnostics, and may be useful for expensive species such as antimatter

Thermally excited fluctuations as a pure electron plasma temperature diagnostic

Thermally excited charge fluctuations in pure electron plasma columns provide a diagnostic for the plasma temperature over a range of 0.05 0.2, so that Landau damping is dominant and well modeled by theory. The third method compares the total (frequency-integrated) number delta N of fluctuating image charges on the wall antenna to a simple thermodynamic calculation. This method works when lambda(D)/R-p > 0.2

Bessel bridges decomposition with varying dimension. Applications to finance

We consider a class of stochastic processes containing the classical and well-studied class of Squared Bessel processes. Our model, however, allows the dimension be a function of the time. We first give some classical results in a larger context where a time-varying drift term can be added. Then in the non-drifted case we extend many results already proven in the case of classical Bessel processes to our context. Our deepest result is a decomposition of the Bridge process associated to this generalized squared Bessel process, much similar to the much celebrated result of J. Pitman and M. Yor. On a more practical point of view, we give a methodology to compute the Laplace transform of additive functionals of our process and the associated bridge. This permits in particular to get directly access to the joint distribution of the value at t of the process and its integral. We finally give some financial applications to illustrate the panel of applications of our results

Hubbard chains network on corner-sharing tetrahedra: origin of the heavy fermion state in LiV_2O_4

We investigate the Hubbard chains network model defined on corner-sharing tetrahedra (the pyrochlore lattice) which is a possible microscopic model for the heavy fermion state of LiV_2O_4. Based upon this model, we can explain transport, magnetic, and thermodynamic properties of LiV_2O_4. We calculate the spin susceptibility, and the specific heat coefficient, exploiting the Bethe ansatz exact solution of the 1D Hubbard model and bosonization method. The results are quite consistent with experimental observations. We obtain the large specific heat coefficient $\gamma\sim 222 {\rm mJ/mol K^2}$.Comment: 5 pages, 2 figures, a postscript file of Figure 1 is not included, to appear in Physical Review

A microfabricated surface-electrode ion trap for scalable quantum information processing

We demonstrate confinement of individual atomic ions in a radio-frequency Paul trap with a novel geometry where the electrodes are located in a single plane and the ions confined above this plane. This device is realized with a relatively simple fabrication procedure and has important implications for quantum state manipulation and quantum information processing using large numbers of ions. We confine laser-cooled Mg-24 ions approximately 40 micrometer above planar gold electrodes. We measure the ions' motional frequencies and compare them to simulations. From measurements of the escape time of ions from the trap, we also determine a heating rate of approximately five motional quanta per millisecond for a trap frequency of 5.3 MHz.Comment: 4 pages, 4 figure

Pressure Induced Quantum Critical Point and Non-Fermi-Liquid Behavior in BaVS3

The phase diagram of BaVS3 is studied under pressure using resistivity measurements. The temperature of the metal to nonmagnetic Mott insulator transition decreases under pressure, and vanishes at the quantum critical point p_cr=20kbar. We find two kinds of anomalous conducting states. The high-pressure metallic phase is a non-Fermi liquid described by Delta rho = T^n where n=1.2-1.3 at 1K < T < 60K. At p<p_cr, the transition is preceded by a wide precursor region with critically increasing resistivity which we ascribe to the opening of a soft Coulomb gap.Comment: 4 pages, 5 eps figures, problem with figure correcte

Electronic phase diagram of Cr-doped VO2 epitaxial films studied by in situ photoemission spectroscopy

Through in situ photoemission spectroscopy (PES), we investigated the changes in the electronic structure of Cr-doped VO2 films coherently grown on TiO2 (001) substrates. The electronic phase diagram of CrxV1-xO2 is drawn by a combination of electric and spectroscopic measurements. The phase diagram is similar to that of bulk CrxV1-xO2, while the temperature of metal-insulator transition (TMIT) is significantly suppressed by the epitaxial strain effect. In the range of x = 0-0.04, where TMIT remains unchanged as a function of x, the PES spectra show dramatic change across TMIT, demonstrating the characteristic spectral changes associated with the Peierls phenomenon. In contrast, for x > 0.04, the TMIT linearly increases, and the metal-insulator transition (MIT) may disappear at x = 0.08-0.12. The PES spectra at x = 0.08 exhibit pseudogap behavior near the Fermi level, whereas the characteristic temperature-induced change remains almost intact, suggesting the existence of local V-V dimerization. The suppression of V-V dimerization with increasing x was confirmed by polarization-dependent x-ray absorption spectroscopy. These spectroscopic investigations reveal that the energy gap and V 3d states are essentially unchanged with 0 $\le$ x $\le$ 0.08 despite the suppression of V-V dimerization. The invariance of the energy gap with respect to x suggests that the MIT in CrxV1-xO2 arises primarily from the strong electron correlations, namely the Peierls-assisted Mott transition. Meanwhile, the pseudogap at x = 0.08 eventually evolves to a full gap (Mott gap) at x = 0.12, which is consistent with the disappearance of the temperature-dependent MIT in the electronic phase diagram. These results demonstrate that a Mott insulating phase without V-V dimerization is stabilized at x > 0.08 as a result of the superiority of Mott instability over the Peierls one.Comment: 27 pages, 3 main figures, 5 supplementary figures. arXiv admin note: text overlap with arXiv:2005.0030