3,555 research outputs found

    Study of corrections for anomalous coupling limits due to the possible background BSM contributions

    Full text link
    The search of the anomalous couplings is one of the possible ways to find any deviation from the Standard Model. The effective field theory is used to parameterize the anomalous couplings in the Lagrangian with the operators of higher dimensions, constructed from the SM fields. In the classical way, the limits on the Wilson coefficients of these operators are set based on beyond the Standard Model contributions induced for signal process, whereas the ones induced for background processes are assumed to be negligible. This article provides a study of the corrections to the limits on Wilson coefficients by accounting beyond the Standard Model contributions induced for background processes. The studies of Z(ννˉ)γjjZ(\nu\bar{\nu})\gamma jj and W(ν)γjjW(\ell\nu)\gamma jj productions in pppp collisions with s=13\sqrt{s}=13 TeV and conditions of the ATLAS experiment at the LHC are used as example. Cases of collected during Run II and expected from Run III integrated luminosities of 139 fb1^{-1} and 300 fb1^{-1} are considered. The expected 95% CL limits on coefficients fT0/Λ4f_\text{T0}/\Lambda^4, fT5/Λ4f_\text{T5}/\Lambda^4, fM0/Λ4f_\text{M0}/\Lambda^4 and fM2/Λ4f_\text{M2}/\Lambda^4 are obtained both in classical way and in the way, where the corrections from background anomalous contributions are applied. Corrected one-dimensional limits from Z(ννˉ)γjjZ(\nu\bar{\nu})\gamma jj and W(ν)γjjW(\ell\nu)\gamma jj productions are up to 9.1% and 4.4% (depending on operator) tighter than the classical ones respectively. Corrected combined limits are up to 3.0% (depending on operator) tighter than the classical ones. Corrections to two-dimensional limits are also obtained, corrected contours are more stringent, than the classical ones, and the maximal improvement is of 17.2%

    The increase of ultrasound measurements accuracy with the use of two-frequency sounding

    Get PDF
    In the article the new method for detection of the temporary position of the received echo signal is considered. The method consists in successive emission of sounded impulses on two frequencies and also the current study is concerned with the analysis of ultrasound fluctuation propagation time to and from the deflector on every frequency. The detailed description of the mathematical tool is presented in the article. The math tool used allows the authors to decrease the measurement error with help of calculations needed

    Spin-polarized electronic structure of the core-shell ZnO/ZnO:Mn nanowires probed by x-ray absorption and emission spectroscopy

    Full text link
    The combination of x-ray spectroscopy methods complemented with theoretical analysis unravels the coexistence of paramagnetic and antiferromagnetic phases in the Zn_0.9Mn_0.1O shell deposited onto array of wurtzite ZnO nanowires. The shell is crystalline with orientation toward the ZnO growth axis, as demonstrated by X-ray linear dichroism. EXAFS analysis confirmed that more than 90% of Mn atoms substituted Zn in the shell while fraction of secondary phases was below 10%. The value of manganese spin magnetic moment was estimated from the Mn K{\beta} X-ray emission spectroscopy to be 4.3{\mu}B which is close to the theoretical value for substitutional Mn_Zn. However the analysis of L_2,3 x-ray magnetic circular dichroism data showed paramagnetic behaviour with saturated spin magnetic moment value of 1.95{\mu}B as determined directly from the spin sum rule. After quantitative analysis employing atomic multiplet simulations such difference was explained by a coexistence of paramagnetic phase and local antiferromagnetic coupling of Mn magnetic moments. Finally, spin-polarized electron density of states was probed by the spin-resolved Mn K-edge XANES spectroscopy and consequently analyzed by band structure calculations.Comment: Supplementary information available at http://www.rsc.org/suppdata/ja/c3/c3ja50153a/c3ja50153a.pdf J. Anal. At. Spectrom., 201
    corecore