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We present a comparative study of magnetic excitations in the first two Ruddlesden-Popper members of the Hg-family of high-temperature superconducting cuprates, which are chemically nearly identical and have the highest critical temperature ($T_mathrm{c}$) among all cuprate families. Our inelastic photon scattering experiments reveal that the two compounds paramagnon spectra are nearly identical apart from an energy scale factor of $sim130%$ that matches the ratio of $T_mathrm{c}$s, as expected in magnetic Cooper pairing theories. By relating our observations to other cuprates, we infer that the strength of magnetic interactions determines how high $T_mathrm{c}$ can reach. Our finding can be viewed as a magnetic analogue of the isotope effect, thus firmly supporting models of magnetically mediated high-temperature superconductivity.
Besides superconductivity, copper-oxide high temperature superconductors are susceptible to other types of ordering. We use scanning tunneling microscopy and resonant elastic x-ray scattering measurements to establish the formation of charge ordering
Recent experiments in the cuprates have seen evidence of a transient superconducting state upon optical excitation polarized along the c-axis [R. Mankowsky et al., Nature 516, 71 (2014)]. Motivated by these experiments we propose an extension of the
The discovery of high temperature superconductivity in the cuprates in 1986 triggered a spectacular outpouring of creative and innovative scientific inquiry. Much has been learned over the ensuing 28 years about the novel forms of quantum matter that
Soon after the discovery of the first high temperature superconductor by Georg Bednorz and Alex Mueller in 1986 the late Sir Nevill Mott answering his own question Is there an explanation? [Nature v 327 (1987) 185] expressed a view that the Bose-Eins
Superconductivity in organic conductors is often tuned by the application of chemical or external pressure. With this type of tuning, orbital overlaps and electronic bandwidths are manipulated, whilst the properties of the molecular building blocks r