Electrochemical noise analysis of the effects of a magnetic field on cathodic hydrogen evolution

The effect of a static magnetic field on the evolution of hydrogen gas from a small platinum electrode in an aqueous electrolyte has been studied by recording the noise spectrum of overpotential voltage fluctuations at a constant current density of ?50 mA mm^?2. A 1/f² variation of the power spectrum characteristic of droplet coalescence is found for frequencies >10 Hz. The overpotential for hydrogen evolution decreases with applied field. When the production of gas bubbles is quasiperiodic, there is a threshold field of 0.5 T beyond which the size of the bubbles released is approximately doubled. This is explained by enhanced coalescence of small bubbles swept across the electrode surface by forced convection due to the Lorentz force.     

A novel threefold‐interpenetrating primitive cubic network based on a dinuclear Zn2 node

In the mixed‐ligand metal–organic polymeric compound poly[[μ₂‐1,4‐bis(imidazol‐1‐yl)benzene](μ₂‐terephthalato)dizinc(II)], [Zn₂(C₈H₄O₄)₂(C₁₂H₁₀N₄)]_n or [Zn₂(bdc)₂(bib)]_n [H₂bdc is terephthalic acid and bib is 1,4‐bis(imidazol‐1‐yl)benzene], the asymmetric unit contains one Zn^II ion, with two half bdc anions and one half bib molecule lying around inversion centers. The Zn^II ion is in a slightly distorted tetrahedral environment, coordinated by three carboxylate O atoms from three different bdc anions and by one bib N atom. The crystal structure is constructed from the secondary building unit (SBU) [Zn₂(CO₂)₂N₂O₂], in which the two metal centers are held together by two bdc linkers with bis(syn,syn‐bridging bidentate) bonding modes. The SBU is connected by bdc bridges to form a two‐dimensional grid‐like (4,4)‐layer, which is further pillared by the bib ligand. Topologically, the dinuclear SBU can be considered to be a six‐connected node, and the extended structure exhibits an elongated primitive approximately cubic framework. The three‐dimensional framework possesses a large cavity with dimensions of approximately 10 × 13 × 17 Å in cross‐section. The potential porosity is filled with mutual interpenetration of two identical equivalent frameworks, generating a novel threefold interpenetrating network with an α‐polonium topology [Abrahams, Hoskins, Robson & Slizys (2002). CrystEngComm, 4 , 478–482].     

Synthesis and Structure of Three Novel Complexes Based on 4-Chlorophenyloxyacetic Acid

Three new metal–organic complexes, [CoL₂(H₂O)₄] 1, [CdL₂(H₂O)₂] 2, and [CuL₂(H₂O)₂] 3 [HL = 4-chlorophenyloxyacetic acid], have been synthesized and characterized by IR spectra, elemental analysis, fluorescence spectra, and single-crystal X-ray diffraction. Compounds 1, 2, and 3 are all zero-dimensional dimers. The carboxylate ligand exhibits different coordination modes in all compounds. These compounds exhibit interesting supramolecular architecture according to O–H···O and C–H···Cl interactions. Compounds 1, 2, and 3 develop to different framework though they all are from same ligands, which will be helpful to design of different materials.

[Supplemental materials are available for this article. Go to the publisher's online edition of Molecular Crystals and Liquid Crystals to view the free supplemental file: CCDC 902676, 902674, 902675 contains the supplementary crystallographic data for this article. These data can be obtained free of charge via www.ccdc.cam.ac.uk/conts/retrieving.html (or from the Cambridge Crystallographic Data Centre, 12, Union Road, Cambridge CB2 1EZ, UK; Fax: C44 1223 336033; e-mail: deposit@ccdc.cam.ac.uk).]     

Lanthanide-ion-tuned magnetic properties in a series of three-dimensional cyano-bridged Ln(III)W(V) assemblies

The reaction of [W(CN)(8)](3-) with Ln(3+) and pyrazine in acetonitrile yielded a series of isostructural compounds formulated as Ln(H(2)O)(4)(pyrazine)(0.5)W(CN)(8) (Ln = La(1), Ce(2), Pr(3), Nd(4), Sm(5), Eu(6), Gd(7)). The Ln(iii) and W(v) centers in the structure are linked through cyanide groups to form two-dimensional (2D) layers, which are further pillared by pyrazine, generating 3D frameworks. The magnetic behavior for compounds 1-7 were driven by the lanthanide ions involved. The Ln(iii) and W(v) ions in compounds 2 and 5 are ferromagnetically coupled with magnetic ordering occurring at 2.8 K, comparable with magnetic ordering with the critical temperature of 1.9 K for compound 4. In addition, the antiferromagnetic interactions were observed in compounds 3 and 7, while no significant magnetic couplings were found in compounds 1 and 6.     

晶体硅太阳电池双层电极优化分析与实验研究

相对于单层电极结构,优化的前表面双层电极能够明显减小功率损失,改善晶体硅太阳电池的电学特性．本文对晶体硅太阳电池的双层电极进行了优化分析和实验研究.通过扫描电子显微镜观测将双层电极的截面抽象为更接近于实际的半椭圆型,建立了太阳电池前表面的双层电极模型,理论分析了双层电极的电学损失和光学损失.结合丝网印刷后光诱导电镀太阳电池的实验,得到了理论和实验上的最优化光诱导电镀增厚电极厚度与丝网印刷电极宽度的关系.所得到的理论和实验结果符合良好.由于并不涉及电极制备的具体技术,双层电极理论模型普遍适用于多种类型的双层电极结构.     

The Effect of Angle Restriction on the Topological Characteristics of Minicircle Networks

Networks of topologically linked minicircle polymers are found in diverse natural systems and are a subject of intense research in nanotechonology. In a recent report the authors introduced a new theoretical model to study the effects of polymer density on the formation and on the topological properties of minicircle networks. Three key topological characteristics were identified in the formation and characterization of a network: the critical percolation density, the average saturation density and the mean valence of the network. In this work we report how these characteristics change when an orientation bias is imposed on the minicircles forming the network. We observe that such restrictions have significant effects on the key topological characteristics of the network. In particular while the effects of restriction of the tilting angle can be predicted we find that those of the azimuthal angle can have somewhat unexpected results.     

Equivalence of the Wei potential model and Tietz potential model for diatomic molecules

By employing the dissociation energy and the equilibrium bond length for a diatomic molecule as explicit parameters, we generate improved expressions for the well-known Rosen-Morse, Manning-Rosen, Tietz, and Frost-Musulin potential energy functions. It is found that the well-known Tietz potential function that is conventionally defined in terms of five parameters [T. Tietz, J. Chem. Phys. 38, 3036 (1963)] actually only has four independent parameters. It is shown exactly that the Wei [Phys. Rev. A 42, 2524 (1990)] and the well-known Tietz potential functions are the same solvable empirical function. When the parameter h in the Tietz potential function has the values 0, +1, and -1, the Tietz potential becomes the standard Morse, Rosen-Morse, and Manning-Rosen potentials, respectively.     

Thermodynamical behavior of E′ centers in quartz from sediments: Potential for paleothermometry and geochronometry

The thermodynamical behaviors of E′ centers in 8 quartz samples from core XJ33-2-1 recovered in the Zhujiang Mouth Basin were measured by electron spin resonance (ESR) technique. The E′ ESR spectral intensity of samples before any laboratory treatment was measured and expressed asI ₁. The samples were then annealed at 300°C or 350°C for 60 min. The E′ ESR spectral intensity measured after this procedure is expressed asI ₂. The ratios ofI ₁, toI ₂ for the samples increase with the sample depth (from 320 to 3972 m), showing that there is a correlation between this ratio and the storage temperature of samples. Therefore the ratio ofI ₁/I ₂ can be used as an ESR paleothermometer. Besides the temperature, we must take into account the period of time for which the samples have been buried since their deposition, because we find that the ratiosI ₁/I ₂ (from 0.293 to 0.941) are closely related to the sediment ages (from 1.5 to 27.5 Ma), with a correlation coefficient of 0.98 or 0.99 obtained by linear or exponential regression, respectively. This relation can be explained by the increase of E′ center concentration in quartz samples with the sedimentation age.     

Synthesis,structural characterization and catalytic activity of benzimidazole‐functionalized Pd(II) N‐heterocyclic carbene complexes

Two Pd(II)–NHC complexes bearing benzimidazole and pyridine groups have been successfully prepared and fully characterized by NMR and X‐ray diffraction analysis. The structure of palladium complexes are a typical square‐planar with palladium surrounded by two pairs of trans‐arranged benzimidazole and carbene ligands. The Pd–NHC complexes have been proved to be a highly efficient catalyst for the Mizoroki–Heck coupling reaction of aryl halides with various substituted acrylates under mild conditions in excellent yields. Copyright © 2013 John Wiley & Sons, Ltd.