Singlet Fermionic Dark Matter with Dark ZZ

We present a fermionic dark matter model mediated by the hidden gauge boson. We assume the QED-like hidden sector which consists of a Dirac fermion and U(1)$_X$ gauge symmetry, and introduce an additional scalar electroweak doublet field with the U(1)$_X$ charge as a mediator. The hidden U(1)$_X$ symmetry is spontaneously broken by the electroweak symmetry breaking and there exists a massive extra neutral gauge boson in this model which is the mediator between the hidden and visible sectors. Due to the U(1)$_X$ charge, the additional scalar doublet does not couple to the Standard Model fermions, which leads to the Higgs sector of type I two Higgs doublet model. The new gauge boson couples to the Standard Model fermions with couplings proportional to those of the ordinary $Z$ boson but very suppressed, thus we call it the dark $Z$ boson. We study the phenomenology of the dark $Z$ boson and the Higgs sector, and show the hidden fermion can be the dark matter candidate.Comment: 10 pages, 3 figure

Potassium-doped BaFe2As2 superconducting thin films with a transition temperature of 40 K

We report the growth of potassium-doped BaFe2As2 thin films, where the major charge carriers are holes, on Al2O3 (0001) and LaAlO3 (001) substrates by using an ex-situ pulsed laser deposition technique. The measured Tc's are 40 and 39 K for the films grown on Al2O3 and LaAlO3, respectively and diamagnetism indicates that the films have good bulk superconducting properties below 36 and 30 K, respectively. The X-ray diffraction patterns for both films indicated a preferred c-axis orientation, regardless of the substrate structures of LaAlO3 and Al2O3. The upper critical field at zero temperature was estimated to be about 155 T.Comment: 6 pages including 3 figure

Ultraviolet photodepletion spectroscopy of dibenzo-18-crown-6-ether complexes with alkali metal cations

Ultraviolet photodepletion spectra of dibenzo-18-crown-6-ether complexes with alkali metal cations (M+-DB18C6, M = Cs, Rb, K, Na, and Li) were obtained in the gas phase using electrospray ionization quadrupole ion-trap reflectron time-of-flight mass spectrometry. The spectra exhibited a few distinct absorption bands in the wavenumber region of 35450−37800 cm^(−1). The lowest-energy band was tentatively assigned to be the origin of the S_0-S_1 transition, and the second band to a vibronic transition arising from the “benzene breathing” mode in conjunction with symmetric or asymmetric stretching vibration of the bonds between the metal cation and the oxygen atoms in DB18C6. The red shifts of the origin bands were observed in the spectra as the size of the metal cation in M^+-DB18C6 increased from Li^+ to Cs^+. We suggested that these red shifts arose mainly from the decrease in the binding energies of larger-sized metal cations to DB18C6 at the electronic ground state. These size effects of the metal cations on the geometric and electronic structures, and the binding properties of the complexes at the S_0 and S_1 states were further elucidated by theoretical calculations using density functional and time-dependent density functional theories