昌黎源影寺塔

昌黎源影寺塔石守仁、王恩林、徐永江源影寺塔位于河北省昌黎县城西北侧的源影寺内，河北省人民政府于１９５６年和１９８２年两次公布此塔为省重点文物保护单位。源影寺塔的原名早已失传。据明万历年间昌黎知县杨于陛“重修古塔寺记”所载：“明万历四十八年庚申重九日（...

Lattice Dynamics at Zone-Center of Sulphide and Selenide Spinels

A rigid-ion model is used to calculate the force constants and effective dynamical charges of sulphide and selenide spinels. The Raman and infrared phonon modes of normal cubic sulphide spinels MCr2S4 （M = Mn, Co, Fe, Hg, Zn, and Cd） and selenide spinels MCr2Se4 （M = Hg, Zn, and Cd） are calculated at the first Brillouin zone-centre using above model, The significant outcome of the present work is （i） the interatomic interaction between Cr-S （Se） dominates over the Cr-S（Se） and S-S（Se-Se） type of interatomic interactions, （ii） the effective dynamical charges of the bivalent metal ions are nearly zero, and （iii） the selenide spinels are less ionic than the sulphide spinels and the ionicity decreases as MnCr2S4 〉 FeCr2S4 〉 CoCr2S4 〉 and CdOr2C4 〉 ZnCr2C4 〉 HgCr2C4 （C = S and Se）. The zone-center phonon frequencies, calculated using these parameters, are found to be in very good agreement with the observed results.

Spin—Polarized States of Nuclear Matter

The equations of state of spin-polarized nuclear matter and pure neutron matter are studied in the framework of the Brueckner–Hartree–Fock theory including a three-body force. The energy per nucleon EA(δ) calculated in the full range of spin polarization for symmetric nuclear matter and pure neutron matter fulfills a parabolic law. In both the cases the spin-symmetry energy is calculated as a function of the baryonic density along with the related quantities such as the magnetic susceptibility and the Landau parameter G0. The main effect of the three-body force is to strongly reduce the degenerate Fermi gas magnetic susceptibility even more than the value with only two-body force. The equation of state is monotonically increasing with the density for all spin-aligned configurations studied here so that no any signature is found for a spontaneous transition to a ferromagnetic state.

Iron porphyrin with appended guanidyl group for significantly improved electrocatalytic carbon dioxide reduction activity and selectivity in aqueous solutions

Iron porphyrins have high activity and selectivity for electrocatalytic CO_(2)reduction reaction(CO_(2)RR)in nonaqueous solutions,but they usually display poor or moderate selectivity for CO_(2)RR in aqueous solutions because of the competitive hydrogen evolution reaction.Using water as the electrocatalytic reaction solvent is more favored because not only it is cheap,green and abundant but also it can sufficiently provide protons required for CO_(2)RR.Therefore,developing Fe porphyrins as electrocatalysts for efficient and selective CO_(2)RR in aqueous solutions is of both fundamental and practical significance.Herein,we report the design and synthesis of Fe porphyrin 1 with an appended guanidyl group and its electrocatalytic features for CO_(2)RR in both nonaqueous and aqueous solutions.In acetonitrile,Fe porphyrin 1 and its guanidyl-free analogue,tetrakis(3,4,5-trimethoxyphenyl)porphyrin 2,are both efficient for electrocatalytic CO_(2)-to-CO conversion,but the turnover frequency with 1(3.9´10^(5)s^(-1))is one order of magnitude larger than that with 2(1.7´10^(4)s^(-1)),showing the critical role of the appended guanidyl group in improving electrocatalytic CO_(2)RR activity.More importantly,in 0.1 mol L^(-1)KHCO_(3)aqueous solutions,1 showed very high selectivity for electrocatalytic CO_(2)-to-CO conversion with a Faradaic efficiency of 96%,while 2 displayed a Faradaic efficiency of 65%for the CO_(2)-to-CO conversion.This work is of significance to show the effect of appended guanidyl group on improving both activity and selectivity of Fe porphyrins for CO_(2)RR electrocatalysis.

Transport Properties of Ferrite Perovskite Material

Transport properties of LaFeO3 in the temperature range of 2 K 〈 T 〈 300 K have been explored for the first time using interaction potential developed by the author and found that our computed results on transport properties follow the same trend as that of available experimental values. These are scientifically and technologically important materials with orthorhombic perovskite-like structure and space group Pbnm. Lanthanum ferrite, LaFeO3 is semiconducting and antiferrom agnetically ordered at zero. The thermodynamics of perovskite-type or related materials of potential use in, e.g., solid oxide fuel cells have been studied to a rather limited extent only.

Determination of impurity elements in MnZn ferrites by inductively coupled plasma mass spectrometry

An inductively coupled plasma mass spectrometry(ICP-MS) method was developed for the determination of Na, Mg, Al,K, Ca, Ti, Cr, Co, Ni, Cu, Ga, As, Mo, Ag, Cd and Pb in MnZn ferrites. The sample was digested by HNO3+HCl with microwave digestion followed by dilution with ultrapure water, then the above 16 impurity elements in the solution were analyzed directly by ICP-MS. The impurity elements were introduced by the helium gas or hydrogen gas into the octopole reaction system(ORS) to eliminate the polyatomic interferences caused by the high salty matrixes. The matrix effect was minimized through matrix matching,and Be, Y and Rh were used as internal standard elements. The working parameters of the instrument were optimized. The results show that the method has good precision and high accuracy. The detection limits for the investigated elements are in the range of0.9-37.5 ng/L, the relative standard deviation of each element is within 1.1%-4.8%, and the recovery of each element is 90%-108%.

Interaction mechanism between carboxylmethyl cellulose and iron ore concentrates in iron ore agglomeration

Carboxylmethyl cellulose(CMC) has become a commercial organic binder in agglomeration of iron ore concentrates. The relative molecular mass and degree of substitution(DS) of CMC have a large impact on its binding performance. The interaction mechanism between CMC and iron ore particles was analyzed through Zeta potential measurements, adsorption measurements and infrared spectra. The results show that the interaction is chemical adsorption-oriented and the CMC's adsorption performance is related to the properties of CMC as well as the type of iron oxides. CMC has a greater affinity to Fe2O3 than Fe3O4, and CMC with higher relative molecular mass shows a higher adsorption isotherm. Pelletization of practical iron ore concentrates added with CMC further illustrates that CMC with higher relative molecular mass or DS exhibits a better binding performance, which is consistent with the results of adsorption tests.

Atomistic simulation of dynamical and defect properties of multiferroic hexagonal YMnO_3

Atomistic simulation has been performed to investigate the dynamical and defect properties of multiferroic hexagonal YMnO3 with newly developed interaction potentials. Dynamical calculation reveals that phonon vibrations of hexagonal YMnO3 are quite different from those of orthorhombic YMnO3. Defect calculation finds that O Frenkel is the most probable intrinsic disorder, and Mn antisite defect is favorable to exist, especially for Mn ions entering the Y2 sites. It is also found that holes prefer to localize at O2sites rather than at Mn3+ sites, while the electron can be localized at the Mn3+ site. The disproportionation of Mn3+ ions is unlikely to occur in hexagonal YMnO3.

Chiral cyanide-bridged 1D Fe~Ⅲ-Mn~Ⅲ heterobimetallic chains: Synthesis, structures and magnetic properties

Two couples of enantiomerically pure chiral cyano-bridged heterobimetallic one-dimensional (1D) chain complexes: [Mn((R,R)-Salphen)Fe(Tp)(CN)3],, (1) and [Mn((S,S)-Salphen)Te(Tp)(CN)3]n (2) (Salphen = N,N'-l,2-diphenylethylenebis (salicylideneiminato) dianion, Tp = tris(pyrazolyl) hydroborate), [Mn((R,R)-Salphen)Fe(Tp*)(CN)3·2H2O],, (3) and [Mn((S,S)-Salphen)Fe(Tp*)(CN)3.2H20],, (4) (Tp* = hydridotris (3,5-dimethylpyrazol-l-yl) borate), have been successfully synthesized by the reactions of MnⅢ schiff-base complexes with the tricyanometalate building block, [(Lxp)Fe(CN)3]- (Lyp = Tp or Tp*). All complexes are made up of neutral cyano-bridged zigzag double chains with (-Fe-CN-Mn-NC-),, as the repeating unit. Circular dichroism (CD) spectra confirm the enantiomeric nature of the optically active complexes. Magnetic studies demonstrate that ferromagnetic interactions are operative in these complexes. The ferromagnetic couplings become weak in the chains with the bending of the Mn-N=C angles.

Controlling Thermodynamic Properties of Ferromagnetic Group-Ⅳ Graphene-Like Nanosheets by Dilute Charged Impurity

Using the Kane-Mele Hamiltonian, Dirac theory and self-consistent Born approximation, we investigate the effect of dilute charged impurity on the electronic heat capacity and magnetic susceptibility of two-dimensional ferromagnetic honeycomb structure of group-Ⅳ elements including silicene, germanene and stanene within the Green's function approach. We also find these quantities in the presence of applied external electric field. Our results show that the silicene(stanene) has the maximum(minimum) heat capacity and magnetic susceptibility at uniform electric fields. From the behavior of theses quantities, the band gap has been changed with impurity concentration, impurity scattering strength and electric field. The analysis on the impurity-dependent magnetic susceptibility curves shows a phase transition from ferromagnetic to paramagnetic and antiferromagnetic phases. Interestingly, electronic heat capacity increases(decreases) with impurity concentration in silicene(germanene and stanene) structure.