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Abstract We examine key aspects of the theory of the Bardeen–Cooper–Schrieffer (BCS) to Bose–Einstein condensation (BEC) crossover, focusing on the temperature dependence of the chemical potential, μ. We identify an accurate method of determining the change of μ in the cuprate high temperature superconductors from angle-resolved-photoemission data (along the ‘nodal’ direction), and show that μ varies by less than a few percent of the Fermi energy over a range of temperatures from far below to several times above the superconducting transition temperature, T c . This shows, unambiguously, that not only are these materials always on the BCS side of the crossover (which is a phase transition in the d-wave case), but are nowhere near the point of the crossover (where the chemical potential approaches the band bottom).

Superconductivity reported in metals driven away from equilibrium via optical pumping has been proposed to arise from nonlinear coupling between electrons and optically excited phonons. The authors use an exact approach to show that here, disorder, which disfavors superconductivity, emerges even though the system is translationally invariant.

We consider the quench of an atomic impurity via a single Rydberg excitation in a degenerate Fermi gas. The Rydberg interaction with the background gas particles induces an ultralong-range potential that binds particles to form dimers, trimers, tetramers, etc. Such oligomeric molecules were recently observed in atomic Bose-Einstein condensates. Understanding the effects of a correlated background on molecule formation, absent in bosonic baths, is crucial to explain ongoing experiments with Fermi gases. In this work we demonstrate with a functional determinant approach that quantum statistics and fluctuations have clear observable consequences. We show that the occupation of molecular states is predicated on the Fermi statistics, which suppresses molecular formation in an emergent molecular shell structure. At high gas densities this leads to spectral narrowing, which can serve as a probe of the quantum gas thermodynamic properties. Rydberg excitations in Fermi gases go beyond traditional impurity problems, creating an opportunity for studies of mesoscopic interactions in synthetic quantum matter.

The exploration of large-scale many-body phenomena in quantum materials has produced many important experimental discoveries, including novel states of entanglement, topology and quantum order as found for example in quantum spin ices, topological insulators and semimetals, complex magnets, and high- T _c superconductors. Yet, the sheer scale of solid-state systems and the difficulty of exercising exacting control of their quantum mechanical degrees of freedom limit the pace of rational progress in advancing the properties of these and other materials. With extraordinary effort to counteract natural processes of dissipation, precisely engineered ultracold quantum simulators could point the way to exotic new materials. Here, we look instead to the quantum mechanical character of the arrested state formed by a quenched ultracold molecular plasma. This novel class of system arises spontaneously, without a deliberate engineering of interactions, and evolves naturally from state-specified initial conditions, to a long-lived final state of canonical density, in a process that conflicts with classical notions of plasma dissipation and neutral dissociation. We take information from experimental observations to develop a conceptual argument that attempts to explain this state of arrested relaxation in terms of a minimal phenomenological model of randomly interacting dipoles of random energies. This model of the plasma forms a starting point to describe its observed absence of relaxation in terms of many-body localization (MBL). The large number of accessible Rydberg and excitonic states gives rise to an unconventional web of many-body interactions that vastly exceeds the complexity of MBL in a conventional few-level scheme. This experimental platform thus opens an avenue for the coupling of dipoles in disordered environments that will demand the development of new theoretical tools.

In spite of the fact that systemic administration of MDMA elicits serotonin syndrome, direct intracranial administration fails to reproduce the effect. To reconcile these findings, it has been suggested that the cause of serotonin syndrome is attributed mainly to MDMA hepatic metabolites, and less likely to MDMA itself. Recently, however, this explanation has been challenged, and alternative hypotheses need to be explored. Here, we tested the hypothesis that serotonin syndrome is the result of excessive 5HT simultaneously in many brain areas, while MDMA administered intracranially fails to cause serotonin syndrome because it produces only a localized effect at the delivery site and not to other parts of the brain. This hypothesis was examined using adult male Sprague Dawley rats by comparing 5HT responses in the right and left hemispheric frontal cortices, right and left hemispheric diencephalons, and medullar raphe nucleus. Occurrence of serotonin syndrome was confirmed by measuring change in body temperature. Administration routes included intraperitoneal (IP), intracerebroventricular (ICV) and reverse microdialysis. First, we found that IP administration caused excessive 5HT in all five sites investigated and induced hypothermia, suggesting the development of the serotonin syndrome. In contrast, ICV and reverse microdialysis caused excessive 5HT only in regions of delivery sites without changes in body-core temperature, suggesting the absence of the syndrome. Next, chemical dyes were used to trace differences in distribution and diffusion patterns between administration routes. After systemic administration, the dyes were found to be evenly distributed in the brain. However, the dyes administered through ICV or reverse microdialysis injection still remained in the delivery sites, poorly diffusing to the brain. In conclusion, intracranial MDMA administration in one area has no or little effect on other areas, which must be considered a plausible reason for the difference in MDMA-elicited serotonin syndrome between systemic and intracranial administrations.