Enhanced superconductivity close to a non-magnetic quantum critical point in electron-doped strontium titanate.

Studies on quantum critical points (QCP) have focused on magnetic QCPs to date. Remarkable phenomena such as superconductivity due to avoided criticality have been discovered, but we focus here on the non-magnetic counterpart, i.e., the superconductivity of SrTiO3 regarded as being close to a ferroelectric QCP. Here we prepare high-quality Sr1-xLaxTi(16O1-z18Oz)3 single crystals without localisation at low temperatures, which allow us to systematically investigate the La substitution of Sr as an alternative to introducing oxygen vacancies. Analysis of our data based on a theoretical model predicts an appearance of the ferroelectric QCP around 3 × 1018 cm-3. Because of the QCP, the superconducting dome of Sr1-xLaxTiO3 can be raised upwards. Furthermore, remarkable enhancement of Tc (~0.6 K) is achieved by 18O exchange on the Sr1-xLaxTiO3 crystals. These findings provide a new knob for observing intriguing physics around the ferroelectric QCP.

Reverse Offset Printing of Semidried Metal Acetylacetonate Layers and Its Application to a Solution-Processed IGZO TFT Fabrication.

The submicrometer resolution printing of various metal acetylacetonate complex inks including Fe, V, Mn, Co, Ni, Zn, Zr, Mo, and In was enabled by a robust ink formulation scheme which adopted a ternary solvent system where solubility, surface wettability, and drying as well as absorption behavior on a polydimethylsiloxane sheet were optimized. Hydrogen plasma in heated conditions resulted in bombarded, resistive, or conductive state depending on the temperature and the metal species. With a conductivity-bestowed layer of MoO x and a plasma-protecting layer of ZrO x situated on the top of an IGZO layer, a solution-processed TFT exhibiting an average mobility of 0.17 cm2/(V s) is demonstrated.

Effect of Minerals on Intestinal IgA Production Using Deep Sea Water Drinks.

Minerals are essential for life, as they are a vital part of protein constituents, enzyme cofactors, and other components in living organisms. Deep sea water is characterized by its cleanliness and stable low temperature, and its possible health- and medical benefits are being studied. However, no study has yet evaluated the physical properties of the numerous commercially available deep sea water products, which have varying water sources and production methods. We analyzed these products' mineral content and investigated their effect on living organism, focusing on immune functions, and investigated the relation between physiological immunoactivities and mineral intake. We qualitatively analyzed the mineral compositions of the deep sea water drinks and evaluated the drinks' physical properties using principal component analysis, a type of multivariate analysis, of their mineral content. We create an iron and copper-deficient rat model and administered deep sea water drinks for 8 weeks. We then measured their fecal immunoglobulin A (IgA) to evaluate immune function. Principal component analysis suggested that physical properties of deep sea water drinks could be determined by their sources. Administration of deep sea water drinks increased fecal IgA, thus tending to stimulate immune function, but the extent of this effect varied by drink. Of the minerals contained in deep sea water, iron showed positive correlations with the fecal IgA. The principal component analysis used in this study is suitable for evaluating deep sea water containing many minerals, and our results form a useful basis for comparative evaluations of deep sea water's bioactivity.

Large enhancement of superconducting transition temperature in single-element superconducting rhenium by shear strain.

Finding a physical approach for increasing the superconducting transition temperature (Tc) is a challenge in the field of material science. Shear strain effects on the superconductivity of rhenium were investigated using magnetic measurements, X-ray diffraction, transmission electron microscopy, and first-principles calculations. A large shear strain reduces the grain size and simultaneously expands the unit cells, resulting in an increase in Tc. Here we show that this shear strain approach is a new method for enhancing Tc and differs from that using hydrostatic strain. The enhancement of Tc is explained by an increase in net electron-electron coupling rather than a change in the density of states near the Fermi level. The shear strain effect in rhenium could be a successful example of manipulating Bardeen-Cooper-Schrieffer-type Cooper pairing, in which the unit cell volumes are indeed a key parameter.

Evaluation of the magnetic properties of cosmetic contact lenses with a superconducting quantum interference device.

We evaluated the magnetization of 21 cosmetic contact lens samples that included various coloring materials with a superconducting quantum interference device with regard to magnetic resonance (MR) safety. We found 7 samples were ferromagnetic; two had both ferromagnetic and diamagnetic properties; and the rest were diamagnetic. The saturated magnetization of the most ferromagnetic sample was 15.0 µJ/T, which yielded a magnetically induced displacement force of 90.0 µN when the spatial gradient of the static magnetic field was 6.0 T/m. The force was less than one-third of the gravitational force.

The synthesis under controlled oxygen partial pressure and the characterization of a layered perovskite system Sr(2)V(1-x)Mo(x)O(4).

We have successfully synthesized Sr(2)V(1-x)Mo(x)O(4) from x = 0.3 to 1.0 by an improved process. The layered compound Sr(2)VO(4) is an antiferromagnetic insulator with S = 1/2, while the isostructural Sr(2)MoO(4) is a Pauli paramagnetic metal. The solid solution Sr(2)V(1-x)Mo(x)O(4) of these materials is expected to show a metal-insulator transition. In this paper we report the synthetic process and the results of the magnetic susceptibility and the electrical resistivity. The selection of the starting materials and the adjustment of O(2) partial pressure of less than 10(-12) atm were indispensable for the synthesis. The reducing conditions during the sintering had been determined rationally, according to thermodynamical analysis. Kondo-like behavior in both resistivity and magnetic susceptibility were observed in a limited range of V-containing samples.

Superconductivity in carrier-doped silicon carbide.

We report growth and characterization of heavily boron-doped 3C-SiC and 6H-SiC and Al-doped 3C-SiC. Both 3C-SiC:B and 6H-SiC:B reveal type-I superconductivity with a critical temperature Tc=1.5 K. On the other hand, Al-doped 3C-SiC (3C-SiC:Al) shows type-II superconductivity with Tc=1.4 K. Both SiC:Al and SiC:B exhibit zero resistivity and diamagnetic susceptibility below Tc with effective hole-carrier concentration n higher than 1020 cm-3. We interpret the different superconducting behavior in carrier-doped p-type semiconductors SiC:Al, SiC:B, Si:B and C:B in terms of the different ionization energies of their acceptors.

Single-molecule magnet behavior in heterometallic M(II)-Mn(III)(2)-M(II) tetramers (M(II) = Cu, Ni) containing Mn(III) salen-type dinuclear core.

The linear-type heterometallic tetramers, [Mn(III)(2)(5-MeOsaltmen)(2)M(II)(2)(L)(2)](CF(3)SO(3))(2) x 2H(2)O (MII = Cu, 1a; Ni, 2a), where 5-MeOsaltmen(2-) = N,N'-(1,1,2,2-tetramethylethylene) bis(5-methoxysalicylideneiminate), and H(2)L = 3-{2-[(2-hydroxy-benzylidene)-amino]-2-methyl-propylimino}-butan-2-one oxime, have been synthesized and characterized from structural and magnetic points of view. These two compounds are isostructural and crystallize in the same monoclinic P2(1)/n space group. The structure has a [M(II)-NO-Mn(III)-(O)(2)-Mn(III)-ON-M(II)] skeleton, where -NO- is a linking oximato group derived from the non-symmetrical Schiff-base complex [M(II)(L)] and -(O)(2)- is a biphenolato bridge in the out-of-plane [Mn(2)(5-MeOsaltmen)(2)](2+) dimer. The solvent-free compounds, 1b and 2b, have also been prepared by drying of the parent compounds, 1a and 2a, respectively, at 100 degrees C under dried nitrogen. After this treatment, the crystallinity is preserved, and 1b and 2b crystallize in a monoclinic P2(1)/c space group without significant changes in their structures in comparison to 1a and 2a. Magnetic measurements on 1a and 1b revealed antiferromagnetic Mn(III)---Cu(II) interactions via the oximato group and weak ferromagnetic Mn(III)---Mn(III) interactions via the biphenolato bridge leading to an S(T) = 3 ground state. On the other hand, the diamagnetic nature of the square planar Ni(II) center generates an S(T) = 4 ground state for 2a and 2b. At low temperature, these solvated (a) and desolvated (b) compounds display single-molecule magnet behavior modulated by their spin ground state.

A heterometal single-molecule magnet of [MnIII2NiII2Cl2(salpa)2].

The tetranuclear complex [MnIII2NiII2Cl2(salpa)2] (salpa = N-(2-hydroxybenzyl)-3-amino-1-propanol) has a spin ground state of S = 6 and was confirmed to be an SMM based on a steplike feature of the magnetization hysteresis loop at 0.55 K.