Water is characterized by large molecular electric dipole moments and strong interactions between molecules; however, hydrogen bonds screen the dipole–dipole coupling and suppress the ferroelectric order. The situation changes drastically when water is confined: in this case ordering of the molecular dipoles has been predicted, but never unambiguously detected experimentally. In the present study we place separate H2O molecules in the structural channels of a beryl single crystal so that they are located far enough to prevent hydrogen bonding, but close enough to keep the dipole–dipole interaction, resulting in incipient ferroelectricity in the water molecular subsystem. We observe a ferroelectric soft mode that causes Curie–Weiss behaviour of the static permittivity, which saturates below 10 K due to quantum fluctuations. The ferroelectricity of water molecules may play a key role in the functioning of biological systems and find applications in fuel and memory cells, light emitters and other nanoscale electronic devices.

We demonstrate on synthetic eumelanin that biomolecular conductivity models should account for temperature and hydration effects coherently.

Transport, magnetic and optical investigations on EuRbFe 4 As 4 single crystals evidence that the ferromagnetic ordering of the Eu 2+ magnetic moments at T N = 15 K, below the superconducting transition (Tc = 36 K), affects superconductivity in a weak but intriguing way. Upon cooling below T N , the zero resistance state is preserved and the superconductivity is affected by the in-plane ferromagnetism mainly at domain boundaries; a perfect diamagnetism is recovered at low temperatures. The infrared conductivity is strongly suppressed in the far-infrared region below Tc, associated with the opening of a complete superconducting gap at 2∆ = 10 meV. A gap smaller than the weak coupling limit suggests the strong orbital effects or, within a multiband superconductivity scenario, the existence of a larger yet unrevealed gap.New members of the iron-pnictide family, the so-called 1144-compounds, attract interest recently because the alternating layers of alkaline A and alkaline-earth B cations produce two different kinds of As sites [1][2][3][4]. These materials can be viewed as the intergrowth of A-122 and B-122 iron-pnictides and they are naturally hole doped. The parent compounds are superconducting with transition temperatures T c around 35 K, higher than most of the 122materials; no spin-density-wave order has been observed. Among all possible candidates, Eu-based 1144-systems are even more intriguing, since the Eu-sublattice orders ferromagnetically below a critical temperature T N ≈ 15 K [5,6], similar to the 122-counterpart EuFe 2 As 2 [7-11]. Ferromagnetic order deep inside the superconducting state is very rare, in general [12,13]; hence the "ferromagnetic superconductor" EuRbFe 4 As 4 might pave the way towards realization of a "superconducting ferromagnet" [14-16]. However, the exact nature of the Eu magnetic order and its effect on superconductivity is unresolved [5, 6] because single crystals have been synthesized only recently.In this Letter we focus on the interplay between superconductivity and ferromagnetism in EuRbFe 4 As 4 single crystals. We report comprehensive investigations comprising transport, magnetic and optical measurements combined with microscopic studies of the vortex dynamics. The infrared spectra show a clear gap opening around 80 cm −1 below T c = 36 K that is slightly reduced compared to the value expected from the BCS theory. We relate this small value to the multiband character of superconductivity as well as to the depairing (orbital) effects of super-currents screening the ferromagnetic domains. A surprisingly weak effect on the superconducting condensate has been observed upon magnetic ordering indicating a rather weak interaction between Eu-and Fe-sublattices.Single crystals of EuRbFe 4 As 4 are obtained according to Ref. [4,5,17,18]; they exhibit shiny ab-faces of approximately 1 mm in size. The structure of the compound is presented in Fig. 1(a). The crystals are characterized by x-ray, electrical transport, and magnetic susceptibility measurements. In Fig. 1(a) we plot the dc ...

Intermolecular hydrogen bonds impede long-range (anti-)ferroelectric order of water. We confine H 2 O molecules in nanosized cages formed by ions of a dielectric crystal. Arranging them in channels at a distance of~5 Å with an interchannel separation of~10 Å prevents the formation of hydrogen networks while electric dipole-dipole interactions remain effective. Here, we present measurements of the temperature-dependent dielectric permittivity, pyrocurrent, electric polarization and specific heat that indicate an order-disorder ferroelectric phase transition at T 0 ≈ 3 K in the water dipolar lattice. Ab initio molecular dynamics and classical Monte Carlo simulations reveal that at low temperatures the water molecules form ferroelectric domains in the ab-plane that order antiferroelectrically along the channel direction. This way we achieve the long-standing goal of arranging water molecules in polar order. This is not only of high relevance in various natural systems but might open an avenue towards future applications in biocompatible nanoelectronics.