Effect of alkali metal doping on the properties and crystalline perfection of bis(thiourea)zinc(II) chloride crystals

The influence of sodium doping on the properties of bis(thiourea)zinc(II) chloride crystals has been described. The reduction in the intensity observed in powder X-ray diffraction of doped specimen and slight shifts in vibrational frequencies confirm the lattice stress as a result of doping. The incorporation of Na(I) into the crystal lattice was confirmed by energy dispersive X-ray spectroscopy. Surface morphological changes due to doping of the alkali metal are observed by scanning electron microscopy. The TG?CDTA studies reveal the purity of the material and no decomposition is observed up to the melting point. The high resolution X-ray diffraction studies reveal that the crystalline quality is improved considerably by doping with alkali metal. High transmittance is observed and cut off ?? is ~270?nm.     

Effect of magnesium doping on the properties and crystalline perfection of bis(thiourea)zinc(II) chloride crystals

In this article, the effect of magnesium doping on the properties of bis(thiourea)zinc(II) chloride (BTZC) crystals has been described. The incorporation of Mg(II) into the crystal lattice was confirmed by energy dispersive X-ray spectroscopy and quantified by inductively coupled plasma technique. The powder X-ray diffraction and FT-IR spectral analyses indicate that the crystal undergoes considerable stress as result of doping. SEM studies of pure and doped samples indicate the formation of structural defect centers in BTZC crystals. The TG?CDTA studies reveal the purity of the materials, and no decomposition is observed up to the melting point. Improved crystalline perfection by doping is observed by high-resolution X-ray diffraction. High transmittance is observed, and the cutoff ?? is ~295?nm.     

Effect of s-, p-, d-, and f-block elements on the structure and properties of ammonium dihydrogen phosphate crystals

The influence of the s-, p-, d-, and f-block elements (Cs, Sb, Pd, and Ce) doping on the properties of ammonium dihydrogen phosphate (ADP) crystals has been described. Incorporation of small quantity of dopants into the crystalline matrix is well confirmed by energy dispersive X-ray spectroscopy (EDS) and inductively coupled plasma (ICP) techniques. The reduction in the intensity observed in powder X-ray diffraction (XRD) of doped specimens and slight shifts in vibrational frequencies confirm the lattice stress. Surface morphological changes due to doping of metals are observed by scanning electron microscopy (SEM). The differential scanning calorimetry (DSC) curves show only a slight variation in endothermic peak temperatures. The sharpness of the DSC peaks shows the good degree of crystallinity of the material. The cell parameters have been determined using single crystal XRD analysis of pure ADP and ADP:Cs/ADP:Sb/ADP:Pd/ADP:Ce specimens. The influence of metals on the second harmonic generation (SHG) efficiency is also investigated.     

Alkali metal intercalated fullerene-like MS(2) (M = W, Mo) nanoparticles and their properties

Layered metal disulfides-MS(2) (M = Mo, W) in the form of fullerene-like nanoparticles and in the form of platelets (crystallites of the 2H polytype) have been intercalated by exposure to alkali metal (potassium and sodium) vapor using a two-zone transport method. The composition of the intercalated systems was established using X-ray energy dispersive spectrometer and X-ray photoelectron spectroscopy (XPS). The alkali metal concentration in the host lattice was found to depend on the kind of sample and the experimental conditions. Furthermore, an inhomogeneity of the intercalated samples was observed. The product consisted of both nonintercalated and intercalated phases. X-ray diffraction analysis and transmission electron microscopy of the samples, which were not exposed to the ambient atmosphere, showed that they suffered little change in their lattice parameters. On the other hand, after exposure to ambient atmosphere, substantial increase in the interplanar spacing (3-5 A) was observed for the intercalated phases. Insertion of one to two water molecules per intercalated metal atom was suggested as a possible explanation for this large expansion along the c-axis. Deintercalation of the hydrated alkali atoms and restacking of the MS(2) layers was observed in all the samples after prolonged exposure to the atmosphere. Electric field induced deintercalation of the alkali metal atoms from the host lattice was also observed by means of the XPS technique. Magnetic moment measurements for all the samples indicate a diamagnetic to paramagnetic transition after intercalation. Measurements of the transport properties reveal a semiconductor to metal transition for the heavily K intercalated 2H-MoS(2). Other samples show several orders of magnitude decrease in resistivity and two- to five-fold decrease in activation energies upon intercalation. These modifications are believed to occur via charge transfer from the alkali metal to the conduction band of the host lattice. Recovery of the pristine compound properties (diamagnetism and semiconductivity) was observed as a result of deintercalation.     

Effect of zinc(II) doping on thermal and optical properties of potassium hydrogen phthalate (KHP) crystals

The influence of doping the transition metal Zn(II) on potassium hydrogen phthalate (KHP) crystals has been studied. A close observation of FT-IR and XRD profiles of doped and undoped samples reveals some minor structural variations. It appears that the crystal undergoes considerable lattice stress as a result of doping the bivalent zinc. Furthermore, the possibility of cation vacancies aroused owing to the substitution of K¹⁺ by Zn²⁺ could result in a defective crystal system. Energy dispersive spectra reveal the incorporation of Zn(II) in the crystalline matrix of KHP crystals. Differential scanning calorimetry (DSC) and TG-DTA studies reveal the purity of the sample and no decomposition is observed below the melting point. Small quantity additions of Zn(II) enhance the fluorescence intensity of KHP crystals. The doping results in morphological changes and significantly improves the second harmonic generation (SHG) efficiency of the host crystal.     

N-(1-萘基)-琥珀酰亚胺化合物晶体结构的理论预测

用Materials Studio软件对N-(1-萘基)-琥珀酰亚胺多晶粉末的X射线衍射数据进行衍射峰指标化、晶胞参数优化和空间群搜索等理论计算, 可以确定晶体结构所属的晶系和空间群, 并初步给出和多晶粉末衍射数据相近的晶胞参数; 在已确定空间群范围内, 以密度泛函理论计算得到的最低能量构象作为初始分子结构, 对N-(1-萘基)-琥珀酰亚胺多晶进行晶体结构理论预测, 给出一系列假定的晶胞参数, 从中可以找到和经上述计算给出的晶胞参数一致的晶体结构；对其进行晶胞参数优化后, 得到晶体结构具有和多晶粉末X射线衍射数据相近的衍射曲线, 并与已有的单晶数据相吻合.     

Os(VIII) doping effects on the properties and crystalline perfection of potassium hydrogen phthalate (KHP) crystals

The effect of dopant, Os(VIII) on the growth process, crystalline perfection and properties of potassium hydrogen phthalate (KHP) single crystals grown by a slow evaporation solution growth technique has been investigated. The XRD analysis of black-colored doped specimen reveals slight structural changes as a result of doping. The SEM images exhibit defect centers and crystal voids. The complex formation of KHP with Os(VIII) is evidenced by the considerable shift in λ_max of the doped specimen and enhanced fluorescence intensity is observed by doping. Differential scanning calorimetry (DSC) and TG-DTA studies reveal the purity of the sample and no decomposition is observed up to the melting point. The high resolution X-ray diffraction (HRXRD) studies used to evaluate the crystalline perfection reveal some features on the capability of accommodating the dopant in the crystalline matrix. The diffraction curve (DC) patterns indicate that the high valence transition metal predominantly occupies the interstitial positions and the doping depresses the second harmonic generation (SHG) efficiency owing to the deterioration of crystalline perfection disturbing the charge transfer and nonlinearity.     

A New Family of Binary Layered Compounds of Platinum with Alkali Metals (A = K,Rb, Cs)

By reacting platinum with alkali metals (A = K, Rb, Cs) a new family of binary alkali metal platinides has been synthesized and characterized by chemical analysis, X‐ray powder diffraction, thermal analysis (DTA and DSC), and magnetic measurements. All three compounds exhibit similar XRD‐patterns with strong reflections that can be indexed on the basis of a rhombohedral crystal system (K_xPt: a = 2.6462(1), c = 17.123(1); Rb_xPt: a = 2.6415(1) Å, c = 17.871(1) Å; Cs_xPt: a = 2.6505(1) Å, c = 18.536(1) Å; x < ½. The a lattice constant is independent on the alkali metal used and of value close to the Pt–Pt distance in NaPt₂ (2.645Å). The c parameter increases monotonically with the growing atomic radius of the alkali metal. The average structure of the alloys consists of cubic close packed layers of platinum atoms with layers of disordered alkali metals in between. For all compounds besides the strong reflections small satellites are observed which cannot be indexed together with the rhombohedral peaks in any rational 3‐dimensional lattice. However, these satellites can be indexed as incommensurate modulations within the ab plane (found propagation vectors k = (0.1011, 0.2506, 0) for Cs_xPt, and k = (0.0168, 0.2785, 0) for Rb_xPt).     

Growth and characterization of a new nonlinear optical crystal: [(18C6)Li][Cd(SCN)3]

Single crystals of a new nonlinear optical compound [(18C6)Li][Cd(SCN)₃][(18-crown-6-ether) lithium(I) trithiocyanate cadmium(II), CLTC], with dimension of 22 mm × 8 mm × 2 mm, were grown from aqueous solutions for the first time via evaporation technique. Solubility of CLTC has been determined for various temperatures. The grown crystals were characterized by single crystal X-ray diffraction (XRD) study, powder X-ray diffraction, FT-IR techniques, UV–vis, elemental analysis, EDS analyses and SHG test. Single crystal XRD study has been carried out to identify the lattice parameters and CLTC crystallizes in orthorhombic system. FT-IR studies confirm the functional groups present in the grown crystal. The mechanical properties of the grown crystals have been studied using Vickers microhardness tester. The optical second harmonic generation effect has been measured by using the Kurtz powder technique to be 2 times as large as that of KDP (KH₂PO₄) crystal. From the optical spectrum, CLTC has good optical transmission in the entire visible region, which is an essential requirement for a nonlinear crystal.     

Growth, spectral, and thermal characterization of semicarbazone of p-hydroxy acetophenone (SPHA)

A new organic nonlinear optical material semicarbazone of p-hydroxy acetophenone (SPHA) was synthesized. Good quality single crystal of SPHA was successfully grown by slow evaporation method at room temperature. The crystal system was identified and lattice dimensions were measured from the single crystal X-ray diffraction (XRD) analysis. The various planes of reflection were identified from the powder XRD pattern. The presence of functional groups was qualitatively found by Fourier transform infrared (FTIR) spectral analysis. The proton and carbon nuclear magnetic resonance (¹HNMR and ¹³CNMR) spectral studies confirmed the presence of hydrogen and carbon bonded network in the grown crystal. The UV?CVisible absorption spectrum was recorded to study the optical transmittance in the range from 200 to 800?nm. The thermal stability of compound was determined by thermogravimetric and differential thermal analysis (TG-DTA) traces. The existence of second harmonic generation (SHG) signal was observed using Nd:YAG laser with fundamental wavelength of 1064?nm.     

Cation substitutional chemistry in the r(7)x(12)z-type structure for four lanthanum iodide examples

A series of quaternary lanthanide halide cluster compounds ALa(6)I(12)Z with transition metal interstitials (principally Os) and alkali or alkaline-earth metal cations (A = Na, Mg, Ca, Sr) have been synthesized by high temperature solid state techniques. The compounds were structurally characterized by single crystal and powder X-ray diffraction methods. The new compounds are isotypic (R3, Z = 3) with rhombohedral R(7)X(12)Z (R = Sc, Y, La-Lu; X = Cl, Br, I; Z = transition or main group element) and contain nominally octahedral R(6)X(12) units centered by interstitial Z. Here, the cation (A) rather than the seventh R occupies the isolated position between clusters along c as A(x)R(1-x) with 0 < x 相似文献   

Synthesis,growth, structural,spectroscopic, crystalline perfection,second harmonic generation (SHG) and thermal studies of 2-aminopyridinium picrate (2APP): A new nonlinear optical material

Single crystal growth, spectroscopic, relative second harmonic generation (SHG) efficiency and thermal analysis of 2-aminopyridinium picrate (2APP) is reported for the first time. Crystals were grown by the slow evaporation solution technique using methanol as a solvent. The crystal system and lattice parameters were confirmed by single crystal and powder XRD analyses. FT-IR and FT-Raman spectroscopic studies were carried out to identify the functional groups and vibrational modes present in the grown crystal. Crystalline perfection of the grown crystal was assessed by high-resolution XRD and the results reveal that the crystal is reasonably good. SHG efficiency was measured using Kurtz powder technique. Thermogravimetric (TG) and differential thermal analysis (DTA) studies were carried out and show that the grown single crystal is stable up to 223 °C.     

Growth, spectral studies, thermal and dielectric aspects of l-lysine doped triglycine sulpho phosphate (TGSP) crystals

Single crystals of ferroelectric material triglycine sulpho phosphate (TGSP) have been grown by slow evaporation method. The effect of l-lysine addition on the growth of TGSP crystal has been studied for various concentrations (5, 10 and 20 mol%). Unit cell parameters were determined from powder XRD analysis. Functional groups present in the grown crystal were confirmed from the vibrational frequencies of recorded FTIR and FT-Raman spectrum. The l-lysine doping into the crystal lattice has been qualitatively confirmed by spectral analysis. Thermogravimetric studies confirm that the lysine is incorporated into TGSP crystals. Dielectric studies reveal that the incorporation of lysine into TGSP enhances its dielectric strength.     

Synthesis growth and characterization of l-valine nickel (II) chloride

A new semi organic nonlinear optical crystal, l-valine nickel chloride has been synthesized and good optical quality single crystals were grown by slow evaporation technique. The growth conditions of the crystals are studied and the grown crystals are confirmed by powder X-ray diffraction studies. The grown crystal was characterized by using powdered XRD, FT-IR, UV?CVis?CNIR, EDAX, and TG?CDTA. The crystalline nature and its various planes of reflections were observed by the powder XRD. The presence of various functional groups was confirmed by FT-IR spectroscopic technique. The UV?CVis?CNIR spectrum indicates that the crystal has very good absorption in the entire visible and near IR region spectrum suggesting the suitability of the material for NLO applications. The decomposition temperatures and mass loss have been estimated from the thermogravimetric analysis.     

ChemInform Abstract: Crystal Structures of New Alkali Metal-Rich Oxometallates: Rubidium Aluminate Tetrahydroxide,Rb9(AlO4)(OH)4, Rubidium Orthogallate,Rb5GaO4, Cesium bis-Chromate(IV) Oxide,Cs10(CrO4)2O,and Cesium Diindate,Cs8In2O7.

The crystal structures of several new alkali metal oxometallates are determined by single crystal XRD.     

Synthesis and Crystal Structure of [K（2,2,2-crypt）]_3Sb_（11）

The title complex [K(2,2,2-crypt)]3Sb11 has been prepared by the reaction of K3Cd2Sb with Cu-C≡CH in ethylenediamine in the presence of 2,2,2-crypt, and characterized by low temperature X-ray structure analysis. The crystal is of orthorhombic system, space group C2221 with a = 15.475(3), b = 22.807(5), c = 24.834(6), V = 8765(3)3, Dc = 1.960 g/cm3, C54H108K3N6O18Sb11, Mr = 2586.01, F(000) = 4944, μ = 3.531 mm-1, Z = 4, R = 0.0442 and wR = 0.1053 for 10265 observed reflections (I > 2σ(I)). The "naked" Sb113- anion is stable due to the completely sequestered alkali metal cations through ion-ion interactions.     

Magnetic ordering in doped Cd(1-x)Co(x)Se diluted magnetic quantum dots

In this study, we report structural, vibrational, and magnetic data providing evidence of random ion displacement in the core of CdSe quantum dots on the Cd(2+) sites by Co(2+) ions (between x = 0 and 0.30). Structural evidence for core doping is obtained by analyzing the powder X-ray diffraction (pXRD), data which exhibits a linear lattice compression with increasing Co(2+) concentration, in accord with Vegard's law. Correlated with the pXRD shift, a hardening of the CdSe longitudinal optical phonon mode and a new local vibrational mode are observed which track Co(2+) doping concentration. Consistent with the observed core doping, superconducting quantum interference device (SQUID) measurements indicate a surprising increase for the onset of spin glass behavior by an order of magnitude over bulk Co:CdSe. Correlation of SQUID results, pXRD, and Raman measurements suggests that the observed enhancement of magnetic superexchange between Co(2+) dopant ions in this confined system arises from changes in the nature of coupling in size-restricted materials.     

Spectral, optical, and thermal studies of pure and Zn(II)-doped l-histidine hydrochloride monohydrate (LHHC) crystals

The influence of doping the transition metal Zn(II) on the growth, spectral, optical, and thermal properties of l-histidine hydrochloride monohydrate (LHHC) crystals grown by slow solvent evaporation method has been investigated. Structural characterizations of the grown crystals were carried out by single crystal X-ray diffraction analysis and it shows slight structural changes as a result of doping. The FT-IR spectral study reveals the presence of various functional groups and confirms the slight distortion of the structure of the crystals due to doping. The energy dispersive X-ray analysis reveals the incorporation of Zn(II) in the crystalline matrix of LHHC crystal. The UV?CVis spectral study was carried out to analyze the optical transmittance of the grown crystals and found that the transmittance is very high in the visible and UV regions for both pure and doped crystals. The second harmonic generation (SHG) for the grown crystals was confirmed by Nd:YAG laser. The scanning electron microscopy reveals the presence of defect centers and crystal voids. The thermal stability and purity of the grown crystals were analyzed by thermogravimetry, differential thermal analysis, and differential scanning calorimetry techniques.     

Crystal structure of YbCu6In6 and mixed valence behavior of Yb in YbCu(6-x)In(6+x) (x = 0, 1, and 2) solid solution

High quality single crystals of YbCu(6)In(6) have been grown using the flux method and characterized by means of single crystal X-ray diffraction data. YbCu(6)In(6) crystallizes in the CeMn(4)Al(8) structure type, tetragonal space group I4/mmm, and the lattice constants are a = b = 9.2200(13) ? and c = 5.3976(11) ?. The crystal structure of YbCu(6)In(6) is composed of pseudo-Frank-Kasper cages filled with one ytterbium atom in each ring. The neighboring cages share corners along [100] and [010] to build the three-dimensional network. YbCu(6-x)In(6+x) (x = 0, 1, and 2) solid solution compounds were obtained from high frequency induction heating and characterized using powder X-ray diffraction. The magnetic susceptibilities of YbCu(6-x)In(6+x) (x = 0, 1, and 2) were investigated in the temperature range 2-300 K and showed Curie-Weiss law behavior above 50 K, and the experimentally measured magnetic moment indicates mixed valent ytterbium. A deviation in inverse susceptibility data at 200 K suggests a valence transition from Yb(2+) to Yb(3+) as the temperature decreases. An increase in doping of Cu at the Al2 position enhances the disorder in the system and enhancement in the trivalent nature of Yb. Electrical conductivity measurements show that all compounds are of a metallic nature.     

双金属同构金属-有机框架材料CAU-21-Al/M的合成、 氮气吸附及复合膜性能

通过掺杂金属的方式实现了双金属同构金属-有机框架材料的制备, 采用X射线粉末衍射(PXRD)确定了多种金属在双金属CAU-21材料中的最大掺杂量, 使用扫描电子显微镜(SEM)观察了掺杂金属对材料形貌的影响. 热重分析(TGA)结果表明, CAU-21系列材料均具有较好的热稳定性. 氮气气体吸附测试及以CAU-21-Al/M为填料的混合基质膜对N₂气的渗透实验结果与掺杂金属离子尺寸大小呈相反的关系, 证实了双金属可实现对孔道结构及气体吸附性能的调控.