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At least 91 records · Page 5

Non-resonant Microwave Absorption and Boundary Current Response of Ba{sub 0.34}K{sub 0.64}Fe{sub 2}As{sub 2} Superconducting Single Crystals

Boundary current response of Ba{sub 0.34}K{sub 0.64}Fe{sub 2}As{sub 2} (BaK122) single crystals was probed by non-resonant microwave absorption (NRMA) as a function of 100-KHz modulation field at an intermediate temperature, namely, 25 K, which is 10 K below the actual T{sub c}. The measurements were done for both field parallel and perpendicular to the iron arsenide plane configuration. A weak anisotropic effect is noted. However, it is observed that the boundary current response depends on the modulation field value and it increases as we increase the modulation field value from 1 to 9 G. Further, this boundary current response strongly depends on the microwave power. We have shown that these modulation field and microwave power dependence of the boundary current response of NRMA signals in BaK122 iron arsenide crystal can be qualitatively understood through the Dulcic model.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Experimental Investigation on the Low-Temperature Anomalies in Dysprosium Iron Garnet (DyIG)

The anomalous physical properties of dysprosium iron garnet Dy{sub 3}Fe{sub 5}O{sub 12} or DyIG single crystals have been revisited at low temperatures. This paper presents results of experimental investigation based on specific heat, magnetization, and Faraday rotation measurements. The distinguishing features are the occurrence of two types of anomalies in the temperature dependences of some judicious quantities. The first one coincides with the previous first-order spin reorientation transition at T{sub SR} = 15 K where the iron sublattice magnetization vector M{sub Fe} changes from the <111> axis at high temperature toward the low angular phases below T{sub SR}. The second one takes place around the “low-temperature Belov point” T{sub B} = 42 K, confirming what had already been predicted previously about the paraprocess effect in this ferrimagnet. The results are compared with previous findings and discussed taking into account the coexistence of some concomitant phenomena such the magnetodielectric and Schottky effects which cause anomalies, respectively near T{sub SR} and T{sub B}.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Hexanuclear and Heptanuclear Nickel(II) Complexes of with a Non-Schiff-Base Tetradentate Ligand: an Example of Slow Motion Ferromagnetic Phase Transition at Very Low Temperature

Hexanuclear and heptanuclear nickel(II) complexes with N,N′-bis(2-hydroxy-3,5-dimethylbenzyl-1,2-ethanediamine (H{sub 2}hdde), [Ni{sub 6}(hdde){sub 3}(OH){sub 4}(NO{sub 3}){sub 2}(H{sub 2}O){sub 2}]·2dmf (dmf = N,N-dimethylformamide) and [Ni{sub 7}(hdde){sub 3}(OH){sub 6}(dmac){sub 3}](ClO{sub 4}){sub 2} (dmac = N,N-dimethylacetamide), were investigated. The latter complex was newly synthesized and the single-crystal X-ray structure analysis revealed a wheel-shaped heptanuclear cluster. These complexes showed a ferromagnetic interaction in the temperature dependence of magnetic susceptibilities. The micro-SQUID data of the former complex did not show SMM property, whereas the AC susceptibility measurements suggested SMM-like behavior and the zero-field-cooled and field-cooled studies showed a ferromagnetic transition near 240 mK for the latter complex.

36 MATERIALS SCIENCE↗

Characterizing the Josephson Effect on Ba-122 Single-Crystal Junctions

This paper presents c-direction hybrid Josephson junctions with base electrodes of Co:BaFe{sub 2}As{sub 2} single crystals. To realize Josephson junctions, it applies standard photolithography technologies and a newly developed surface polishing method that was used. As conventional isotropic s-wave superconductor counter electrodes used double layers of Pb/In. The artificial barrier for the tunneling junctions consists of a thin sputtered Ti layer or a thermally evaporated Al layer; both layers were used as an insulator barrier. For characterizing the Josephson effects with TiO{sub x} barrier, we could realize I{sub c}R{sub N} products of about 13.7 μV and unconventional I{sub c}-T dependencies. The formation of Shapiro steps under the influence of microwave irradiation and magnetic field to the junctions will be discussed as well.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Signatures of Quantum Transport Steps in Bi{sub 2}Se{sub 3} Single Crystal

We report signatures of quantum magneto transport steps in a Bi{sub 2}Se{sub 3} single crystal. The Bi{sub 2}Se{sub 3} crystal is grown by self-flux method through solid-state reaction. Details of its structural analysis along with physical properties in terms of low temperature and high field transport, thermal (heat capacity), Raman, X-ray photo electron and angle resolved photo electron spectroscopy were reported earlier (J. Sup. Novel. Mag. 30, 2031 2017). In a present short letter, we show the details of its 2 K and up to 14 Tesla magneto transport, exhibiting quantum transport (QT) like steps above say 11 Tesla field. The possible QT steps cannot be modelled with the SdH (Shubnikov-de Haas) or other possible quantum oscillations. The observed QT like steps are possibly the result of the mixed out-of-plane R{sub xy}(H) and in-plane R{sub xx}(H) contributions from the misaligned [00l] planes of the studied crystal and this may happen with other studied topological insulator (TI) crystals as well. Our careful assessment of crystal XRD data shows the same.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Signature of Ferromagnetic Phase at Low Temperature in Low-Doped La{sub 0.88}Ca{sub 0.12}MnO{sub 3} Single Crystal

The confirmation of ferromagnetism at low temperature in a low-doped manganites system is always debatable. It is for the first time, electrical, magnetic, and thermal properties have been measured for manganites single crystal of La{sub 0.88}Ca{sub 0.12}MnO{sub 3} by using a floating-zone method. The electrical resistivity shows a perceptible change of resistance at a low temperature which can be viewed as a signature of the ferromagnetic phase. The ferromagnetic phase of the investigated La{sub 0.88}Ca{sub 0.12}MnO{sub 3} single crystal with Curie temperature of T{sub C} = 120 K which is in closed agreement with ac-susceptibility measurement. An analysis of the specific heat suggests the transition peak (T{sub P}) coincides with the T{sub C} and attains 1.2 J mol{sup −1} K at 116 K. The magnetoresistance (MR) and temperature coefficient of resistance (TCR) were found to be 69% and 10% respectively, which expands its subtle potential for applications in spintronics and thermistor.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Synthesis of the Orthorhombic Dy{sub 1−x}Ho{sub x}MnO{sub 3} Single Crystals and Study of Their Magnetic Properties

In this report, we prepared for the first time the orthorhombic Dy{sub 1−x}Ho{sub x}MnO{sub 3} single crystals with x = 0, 0.1, 0.2, 0.3, and 0.4 using the flux technique. The post-growth processing and chemical and structural characterization of the synthesized samples were performed. Also, we examined the samples obtained by their magnetic properties and the magnetic anisotropy in wide ranges of temperatures and magnetic fields.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Oxygen Vacancy-Induced Room Temperature Ferromagnetism in Rutile TiO{sub 2}

As oxygen vacancies play an important role in ferromagnetism of rutile TiO{sub 2}, a method of γ-ray irradiates rutile TiO{sub 2} single crystals was subtly proposed to study the effect of oxygen vacancies on magnetic properties. Remarkably, room temperature ferromagnetism was observed in γ-ray irradiated rutile TiO{sub 2} single crystals, and the saturation magnetization is the strongest when dose is 4 × 10{sup 4} Gy which assigned to ESR results. Since the displacement threshold energy of Ti atom is much bigger than that of O atom, the defects produced by γ-irradiation are mainly oxygen vacancies. After irradiation, XPS, PL spectra indicate the presence of oxygen vacancies(V{sub O}), Ti{sup 3+}, and V{sub O}-Ti{sup 3+} composite defects.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Nonlinear Second Harmonics of Localized Shear Waves in an Anisotropic Layer Between Anisotropic Half Spaces Under the Conditions of Imperfect Contact

We construct a numerical-analytic solution of the problem of generation of the nonlinear second harmonics in the course of propagation of elastic symmetric localized shear waves in the crystalline layer of cubic system of the m3m class located between the crystalline half spaces of the same type and the same class of anisotropy under the conditions of imperfect sliding contact of components of the waveguide. We determine the analytic form of the functions of wave motions for nonlinear anharmonic perturbations in the form of longitudinal-shear-type waves. We also perform the numerical investigations of the amplitude-frequency characteristics of the second harmonics for monochromatic localized waves in a layer of a single crystal of germanium between the half spaces from the single crystal of silicon.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Hybrid CdS nanowires/Si heterostructure photodetector fabricated by intense pulsed light assisted - laser ablation in liquid

Synthesis of CdS nanowires NWs by combined intense pulsed light (IPL) and pulsed laser ablation in liquid is demonstrated for the first time. An IPL source providing 3 ms duration pulses was used to assist the synthesis of CdS nanowires by 7 ns pulsed laser ablation of cadmium target in thiourea and CTAB solution. The results showed a small increase in optical energy band gap of CdS NWs and a decrease of the nanowires diameter from 50 to 40 nm after combining the IPL. The intensity of the photoluminescence emission peak located at 458 nm was doubled when the IPL combined laser ablation process. In addition the synthesized CdS nanowires showed single crystalline pure hexagonal wurtzite phase with decreased particles agglomeration and smaller particle size. Raman spectra were improved too by revealing sharp and shifted peaks at 293 and 585 cm{sup −1}. The figures of merit of hybrid n-CdSNWs/p-Si heterojunction photodetector namely responsivity and minority carrier lifetime were found to be improved remarkably after using IPL assisted laser ablation.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Hydrogen sulfide as a source of hydrogen production

Potentialities and perspectives of using the known processes of hydrogen sulfide decomposition (thermal, plasmochemical, electrochemical, and photochemical) to produce hydrogen are examined. The results of theoretical and experimental studies of hydrogen sulfide dissociation on the surface of single crystals are presented. The data on the low-temperature decomposition of H{sub 2}S on the sulfide and metal catalysts are discussed. The electronic structure of diatomic sulfur and thermodynamics of its formation in the processes of H{sub 2}S decomposition are considered. The decomposition of hydrogen sulfide on the heterogeneous catalysts placed under the solvent layer is shown to be promising. The mechanism of assimilation of hydrogen sulfide by colorless sulfur bacteria is proposed.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Aluminum hydrides with radical-anionic and dianionic acenaphthene-1,2-diimine ligands

The reaction of 1,2-bis[(2,6-diisopropylphenyl)imino]acenaphthene (dpp-bian) with LiAlH{sub 4} affords two products regardless of the solvent used (tetrahydrofuran or diethyl ether). These products were isolated as green and colorless crystals. Green crystals of the complex [(dpp-bian)Al(H){sub 2}Li(THF){sub 3}] (1) were obtained from tetrahydrofuran; colorless crystals of the complex [{dpp-bian(H_2)}Al(H){sub 2}Li(Et{sub 2}O){sub 2}] (2), from diethyl ether. The reactions of compound 1 with 2,6-di-tert-butyl-4-methylphenol and benzophenone gave monohydrides [(dpp-bian)Al(H)(OC{sub 6}H{sub 2}-2,6-Bu{sub 2}{sup t}-4-Me)][Li(THF){sub 4}] (3) and [(dpp-bian)Al(H)(OCHPh{sub 2})- Li(THF){sub 2}] (4), respectively. The diamagnetic aluminum hydride [(dpp-bian)AlH(THF)] (5) was synthesized by the reaction of dichloroalane HAlCl{sub 2} (in situ) with the disodium salt of dpp-bian in THF; the paramagnetic hydride [(dpp-bian)AlH(Cl)] (6) containing the dpp-bian radical anion was synthesized by the reaction of the monosodium salt (dpp-bian)Na with monochloroalane H{sub 2}AlCl (in situ) in diethyl ether. The reaction of compound 6 with tert-butyllithium gives the complex [(dpp-bian)AlBu{sup t}(Et{sub 2}O)] (7). Diamagnetic derivatives 1—5 and 7 were characterized by {sup 1}Н NMR spectroscopy; paramagnetic compound 6, by ESR spectroscopy. The molecular structures of compounds 1—7 were determined by single-crystal X-ray diffraction.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Cadmium(II) terephthalates based on trinuclear units {Cd_3(bdc)_3}: control of coordination structure dimensionality and luminescence properties

Two metal-organic coordination polymers based on cadmium(II) ions and terephthalic (1,4-benzenedicarboxylic) acid were synthesized in dimethylformamide or a mixture of dimethylformamide and methanol: [Cd{sub 3}(bdc){sub 3}(dmf){sub 4}] (1, bdc is 1,4-benzenedicarboxylate, dmf is N,N´-dimethylformamide) and [Cd{sub 3}(bdc){sub 3}(dmf){sub 2}] (2), respectively. According to the single-crystal X-ray diffraction data, both compounds are built up by the trinuclear carboxylate units {Cd_3(O_2CR)_6}. Compound 1 has a layered structure, whereas compound 2 has a three-dimensional structure due to the presence of additional coordination interactions between adjacent trinuclear units and the formation of polymer chains {Cd_3(dmf)_2(μ_2-O_2CR-κ"1,κ"1)_2(μ_2-O_2CR-κ"2,κ"1)_4(O_2CR-κ"1)2}. The synthesized compounds were characterized by IR spectroscopy, thermogravimetric analysis, elemental analysis, and powder X-ray diffrac- tion. The luminescence properties of these compounds provide evidence for the existence of both intraligand and charge-transfer transitions. The luminescence quantum yields for both compounds are 10%.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Ternary gallides of the Ce{sub 2+n}Rh{sub 3+3n}Ga{sub 1+2n} (n = 0—5) structure family

The structures of nine ternary intermetallic compounds (IMCs) of the cerium—rhodium—gallium system containing 50 at.% rhodium were determined by single-crystal X-ray diffraction. The compounds are built up of alternating Ce{sub 2}Rh{sub 3}Ga fragments with the Mg{sub 2}Cu{sub 3}Si (MgZn{sub 2} type) or Mg{sub 2}Ni{sub 3}Si (MgCu{sub 2} type) structure and CeRh{sub 3}Ga{sub 2} fragments with the CeCo{sub 3}B{sub 2} (CaCu{sub 5} type) structure and form a homologous series of the composition R{sub 2+n}T{sub 3+3n}M{sub 1+2n} (n = 0—5). These compounds can be classified into trigonal (R-3m) or hexagonal (P6{sub 3}/mmc) branches depending on the Laves phase-type fragment.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Three-dimensional copper(II) carboxylates based on 4,4′,4″-benzene-1,3,5-triyltris(benzoic acid)

The homochiral coordination polymers [Cu{sub 4}(CH{sub 3}OH)(H{sub 2}O){sub 4}(Hbtb)(S-mal){sub 2}]•4H{sub 2}O and [Cu{sub 4}(CH{sub 3}OH)(H{sub 2}O){sub 4}(Hbtb)(R-mal){sub 2}]•4H{sub 2}O were synthesized by heating S- or R-malic acid (H{sub 3}mal), 4,4′,4″-benzene-1,3,5-triyltris(benzoic acid) (H{sub 3}btb), and copper(II) acetate in an aqueous methanolic solution. The reaction with copper(II) nitrate in aqueous dioxane afforded the coordination framework [Cu{sub 6}(C{sub 4}H{sub 8}O{sub 2}){sub 3}(H{sub 2}O){sub 3}(btb){sub 4}]•4C{sub 4}H{sub 8}O{sub 2}•10H{sub 2}O, which does not contain chiral ligands. The compositions and crystal structures of the new compounds were determined by single-crystal X-ray diffraction and confirmed by X-ray powder diffraction, IR spectroscopy, thermogravimetric and elemental analysis.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Synthesis and crystal structure of the coordination polymer [{Li(H_2O)_3}{sub 2}(C{sub 36}H{sub 36}N{sub 24}O{sub 12})]Cl{sub 2}•6H{sub 2}O

The coordination polymer of the composition [{Li(H_2O)_3}{sub 2}(C{sub 36}H{sub 36}N{sub 24}O{sub 12})]Cl{sub 2}•6H{sub 2}O (1) was synthesized by heating an aqueous solution of lithium chloride and cucurbit[6]uril (CB[6]). According to single-crystal X-ray diffraction data, solvated lithium cations in compound 1 form coordination bonds with oxygen atoms of CB[6] molecules. Compound 1 was characterized by X-ray diffraction, IR spectroscopy, thermogravimetric and elemental analysis. Luminescence spectra of the new compound were measured.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Coordination polymers based on zinc(II) and manganese(II) with 1,4-cyclohexanedicarboxylic acid

Three new metal-organic coordination polymers were obtained namely, [Mn{sub 3}(chdc){sub 3}-(NMP){sub 2}(DMF){sub 2}] (1, chdc{sup 2–} is trans-1,4-cyclohexanedicarboxylate, NMP is N-methylpyrrolidone, DMF is N,N-dimethylformamide), [Zn{sub 3}(chdc){sub 3}(NMP){sub 2}]•2NMP (2), and [Zn{sub 3}(chdc){sub 3}(ur)-(DMF){sub 0.5}]•DMF (3, ur is the urotropine). The crystal structures of polymers 1, 2, and 3 were determined by single-crystal X-ray crystallography. All three compounds were found to contain a trinuclear secondary building unit {M_3(OOC)_6}. Coordination polymers 1 and 2 have a layered structure, while polymer 3 has a three-dimensional coordination framework with isolated pores formed due to the presence of urotropine bridging molecules. Compounds 1 and 3 were characterized by IR spectroscopy, thermogravimetric and elemental analysis data, powder X-ray diffraction. Compound 3 was also characterized by UV-Vis diffuse reflectance spectrum.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Synthesis and structural features of new pentacoordinated monofluorosilanes containing C,O-chelate ligands based on 2-amino acid N-methylamides

Pentacoordinated monofluorosilanes R{sup 1}SO{sub 2}NHCHR{sub 2}C(O)N(Me)CH{sub 2}SiMe{sub 2}F containing moieties of N′-methyl-N-(organosulfonyl)-2-amino acid amides of glycine, alanine, and leucine as C,O-chelating ligands were synthesized via the reaction of corresponding disiloxanes with BF{sub 3}•Et{sub 2}O. The structures of obtained compounds were investigated by single-crystal X-ray diffraction analysis.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗