We propose and analyze a scheme for parametrically cooling bilayer cuprates based on the selective driving of a $c$-axis vibrational mode. The scheme exploits the vibration as a transducer making the Josephson plasma frequencies time-dependent. We sh
ow how modulation at the difference frequency between the intra- and interbilayer plasmon substantially suppresses interbilayer phase fluctuations, responsible for switching $c$-axis transport from a superconducting to resistive state. Our calculations indicate that this may provide a viable mechanism for stabilizing non-equilibrium superconductivity even above $T_c$, provided a finite pair density survives between the bilayers out of equilibrium.
We show that superconducting interlayer coupling, which coexists with and is depressed by stripe order in La1.885Ba0.115CuO4, can be enhanced by excitation with near-infrared laser pulses. For temperatures lower than Tc = 13 K, we observe a blue-shif
t of the equilibrium Josephson plasma resonance, detected by terahertz-frequency reflectivity measurements. Key to this measurement is the ability to probe the optical properties at frequencies as low as 150 GHz, detecting the weak interlayer coupling strengths. For T > Tc a similar plasma resonance, absent at equilibrium, is induced up to the spin-ordering temperature TSO = 40 K. These effects are reminiscent but qualitatively different from the light-induced superconductivity observed by resonant phonon excitation in La1.675Eu0.2Sr0.125CuO6.5. Importantly, enhancement of the below-Tc interlayer coupling and its appearance above Tc are preferentially achieved when the near-infrared pump light is polarized perpendicular to the superconducting planes, likely due to more effective melting of stripe order and the less effective excitation of quasiparticles from the Cooper pair condensate when compared to in-plane excitation.
75As nuclear magnetic resonance (NMR) experiments were performed on Ba(Fe1-xMnx)2As2 (xMn = 2.5%, 5% and 12%) single crystals. The Fe layer magnetic susceptibility far from Mn atoms is probed by the75As NMR line shift and is found similar to that of
BaFe2As2, implying that Mn does not induce charge doping. A satellite line associated with the Mn nearest neighbours (n.n.) of 75As displays a Curie-Weiss shift which demonstrates that Mn carries a local magnetic moment. This is confirmed by the main line broadening typical of a RKKY-like Mn-induced staggered spin polarization. The Mn moment is due to the localization of the additional Mn hole. These findings explain why Mn does not induce superconductivity in the pnictides contrary to other dopants such as Co, Ni, Ru or K.
75As NMR and susceptiblity were measured in a Ba(Fe1-xCox)2As2 single crystal for x=6% for various field H values and orientations. The sharpness of the superconducting and magnetic transitions demonstrates a homogeneity of the Co doping x better tha
n +-0.25%. On the nanometer scale, the paramagnetic part of the NMR spectra is found very anisotropic and very narrow for H//ab which allows to rule out the interpretation of Ref.[6] in terms of strong Co induced electronic inhomogeneities. We propose that a distribution of hyperfine couplings and chemical shifts due to the Co effect on its nearest As explains the observed linewidths and relaxations. All these measurements show that Co substitution induces a very homogeneous electronic doping in BaFe2As2, from nano to micrometer lengthscales, on the contrary to the K doping.
75As NMR and susceptiblity were measured in a Ba(Fe1-xCox)2As2 single crystal for x=6%. Nuclear Magnetic Resonance (NMR) spectra and relaxation rates allow to show that all Fe sites experience an incommensurate magnetic ordering below T=31K. Comparis
on with undoped compound allows to estimate a typical moment of 0.05 muB. Anisotropy of the NMR widths can be interpreted using a model of incommensurability with a wavevector (1/2-eps,0,l) with eps of the order of 0.04. Below TC=21.8K, a full volume superconductivity develops as shown by susceptibility and relaxation rate, and magnetic order remains unaffected, demonstrating coexistence of both states on each Fe site.
