Growth of ytterbium tartrate trihydrate crystals in silica and agar‐agar gels and their characterization

Single crystals of ytterbium tartrate trihydrate have been grown by gel method using silica and agar‐agar gels as media of growth. The medium of growth influences the morphology of grown crystals, silica gel yielding single and polycrystalline in the form of spherulites whereas agar‐agar gel leading to growth of single and twinned crystals. Materials grown as single crystals have been characterized by using optical and scanning electron microscopy (SEM), EDAX, XRD, FT‐IR, CHN and thermogravimetric techniques. The stoichiometry of the grown single crystals is suggested to be Yb(C₄H₄O₆) (C₄H₅O₆).3H₂O. The FT‐IR spectrum shows the presence of singly as well as doubly ionized tartrate ligands. Results of thermal analysis indicate that the material is thermally stable up to a temperature of 200 °C. (© 2006 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Real Structure of LiB3O5 (LBO) Crystals Grown in Li2O‐B2O3‐MoO3 System

The liquidus surface structure and field of LiB₃O₅ (LBO) primary crystallization have been revealed in Li₂O‐B₂O₃ ‐MoO₃ ternary system. The optimization of charge composition and growth conditions results in large volume optical quality LBO single crystals yielding. Crystallographic properties and real defect structure of grown LBO single crystals have been investigated by X‐ray powder diffraction method and X‐ray reflection topography. The volume of the crystals is partly free of any structural imperfections.     

Electrochemical growth and properties of LaMn1−xCoxO3 (0 < x ≤ 1) single crystals

Single crystals of LaMn_1−xCo_xO₃ (0 < x < 1) with distorted perovskite structure have been obtained by the electrodeposition technique at anode from flux melt using Cs₂MoO₄‐MoO₃ binary system as solvent. An investigation of magnetic and electrical properties of the obtained crystals as well as its comparison with those for ceramic samples of the same composition were carried out. A much weaker interplay between magnetic and electrical properties and a smaller ∼8% magnetoresistance were found in the ternary oxide crystals slightly doped by Co on the verge of transition to ferromagnetic state in comparison to the data have been reported for LaMnO_3+δ single crystals. (© 2003 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Micrometric single crystal germanates obtained using a double‐spherical mirror furnace

Micro‐crystals of two new compounds EuMnGe₂O₇ and SmMnGe₂O₇ were grown performing the flux method in a double‐spherical mirror furnace. One valuable advantage of this system was that the heating profile could be modified easily adjusting lamp positions and orientation as well. The micrometric crystals were observed and analyzed for chemical composition by scanning electron microscopy and energy dispersive spectroscopy. This furnace is perfectly suitable to grow at low price, low temperature and short time new materials as a single crystal for basic research or to obtain raw material. (© 2004 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Czochralski growth and constitutional studies on single crystals of potassium lithium niobate (KLN)

The ferroelectric phase of potassium lithium niobate K₃Li_2−xNb_5+xO₁₅ (KLN) is a very promising material for the conversion of infrared light to light in the visible region. However, growing of single crystals is known to be complicated due to the considerable anisotropy of the growth rate and the thermal expansion behaviour. The single crystals of KLN, Mg²⁺‐doped KLN, as well as the mixed crystals of potassium lithium tantalate niobate K₃Li₂(Nb_1−xTa_x)₅O₁₅ (KLTN) were grown by the Czochralski technique. The chemical analyses of the samples were performed by atomic absorption spectroscopy (AAS) and X‐ray fluorescence analysis (XRF). The element concentrations along the single crystals were measured by the electron microprobe analysis (EMPA) to clarify the segregation phenomena in the grown crystals. The elements distribution coefficients were also calculated. (© 2003 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Synthesis of single‐phase ZnAl2O4 nanoparticles via a wet chemical approach and evaluation of crystal structure characteristics

Single‐phase ZnAl₂O₄ nanoparticles were hydrothermally synthesized utilizing improvements to the preparation of the precursor materials. This synthesis differs from more general syntheses of ZnAl₂O₄ nanoparticles in that it minimizes the presence of ZnO impurities. The higher purity of our ZnAl₂O₄ nanoparticles allowed for more comprehensive X‐ray diffraction analysis as well as more sensitive spectroscopic evaluation. Moreover, pH control of the precursor solution dramatically improved the reproducibility of the synthesis. The lattice constant of the ZnAl₂O₄ samples synthesized by our technique is different from what is observed in particles fabricated using more common solid state reactions. This difference in lattice constants indicates the occurrence of a site exchange phenomenon between Zn²⁺ and Al³⁺ and/or oxygen deficiency. This suggests the possibility of tailoring novel functional spinel oxides for a wide array of future applications.     

An effective growth method to improve the homogeneity of relaxor ferroelectric single crystal Pb(In1/2Nb1/2)O3‐ Pb(Mg1/3Nb2/3)O3‐PbTiO3

Compositional segregation usually has negative effects on the growth of solid solution ferroelectric single crystals of Pb(In_1/2Nb_1/2)O₃‐Pb(Mg_1/3Nb_2/3)O₃‐PbTiO₃ (abbr. PIN‐PMN‐PT or PIMNT). A modified Bridgman method was adopted in this work to control the segregation and improve the compositional homogeneity significantly. The characteristic of this work is to use multiround growths and gradient composition raw materials in order to keep the PbTiO₃ concentration constant during the crystal growth. As an example, the two‐round growth of ternary PIN‐PMN‐PT single crystal is conducted in the same Pt crucible with gradient raw materials, where the first‐round boule was used as the seed crystal for the second‐round growth. Our results show that the as‐grown (Ф80 mm × 270 mm) PIN‐PMN‐PT crystals exhibit higher phase transition temperatures (T_c∼180 °C, T_r/t∼110 °C) and larger coercive field (E_c∼5–5.5 kV/cm), which are much better than the performances of Pb(Mg_1/3Nb_2/3)O₃‐PbTiO₃ crystals, and similar dielectric and piezoelectric performances (ε∼5000, tanδ∼1.25%, d₃₃∼1500 pC/N, k_t∼60%). And about 85 percent of the crystal boule grown by the two‐round growth technique could maintain its compositions around the morphotropic phase boundary.     

Investigations on the crystallisation of potassium molybdenum bronzes from flux melts

Results are presented to identify the fields of primary crystallisation of red and blue potassium molybdenum oxide bronzes K_0.30MoO₃ and K_0.33MoO₃ in the ternary system K₂MoO₄–MoO₃–MoO₂. Starting from crystal growth experiments for the preparation of bronze crystals by electrolytic reduction the binary marginal systems K₂MoO₄–MoO₃ as well as MoO₃–MoO₂ and further pseudo‐binary sections have been investigated by differential thermo‐analysis, hot‐stage microscopy, and by quenching experiments under inert gas. We succeeded in determining phase transition temperatures in the binary section Mo₄O₁₁–K₂Mo₂O₇. Temperature and composition ranges have been found in this section to crystallise red and blue potassium molybdenum oxide bronzes. (© 2007 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

A new piezoelectric single crystal obtained by Ge doping in the SiO2 structure

The interest of Si_1–xGe_xO₂ single crystals with alpha‐quartz structure is connected to improvement of electromechanical coefficients and rise of α – β phase transition of quartz one. Growth of an α‐Si_xGe_1–xO₂ crystal was realized by a hydrothermal method of temperature gradient in autoclaves, made from Cr–Ni alloys. Nutrient material was prepared from synthetic quartz as crashed rods and placed in the bottom of autoclaves. There was loaded GeO₂ powder additive in proportions to quartz nutrient. Single crystals were investigated by electron microprobe analysis, X‐ray diffraction and atomic force microscopy. The most important result, which was obtained during the investigations, is an experimental proof of growth of α‐Si_xGe_1–xO₂ single crystals under the hydrothermal conditions. The present results thus open the possibility to tune the piezoelectric properties of these materials by varying the chemical composition. (© 2009 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Specific features of the flux growth of bulk crystals of high-temperature modification of BaB2O4

High-quality single crystals of the high-temperature phase of barium metaborate (α-BaB₂O₄) up to 100–120 g in weight are grown from a flux in the ternary system BaO-B₂O₃-Na₂O. The growth temperature is below the α → β phase transition temperature. The conditions necessary for growing α-BaB₂O₄ crystals under metastable conditions are determined and the morphology and optical quality of the crystals grown are investigated.     

Nano‐sized silver crystals and their dispersion over α‐alumina for ethylene epoxidation

Ethylene oxide catalyst is a high metal loading catalyst, in which silver crystals is impregnated on α‐Al₂O₃ support. In this type of catalyst, metal dispersion plays an important role on catalyst selectivity for desired products. In this work, silver nitrate and silver oxide together with oxalic and lactic acid as the raw materials were used with different impregnation techniques to make catalysts with high silver content and dispersion. It is also known that the use of promoters affect the metal dispersion on the catalyst support and for that cesium was used as the promoter to improve the silver crystal dispersion. Physical and chemical characteristics of the prepared catalysts, i.e., surface area, pore volume, silver content, nano‐sized silver crystals and their dispersion were measured using BET method, Atomic Absorption Spectroscopy, X‐ray diffraction and TEM. (© 2009 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Growth and characterization of large La1‐xPbxMnO3+δ (x=0.32–0.35) crystals

Large crystals of La_0.63Pb_0.37Mn O_3+δ with small La(Pb)‐ deficiency of about 0.005‐0.01 at.% were grown by high temperature solution growth method. The structure of the grown crystals was determined as rhombohedral with R‐3 space group by single‐crystal X‐ray diffractometry. The surface morphology of the crystals and the exact chemical composition was examined by scanning electron microscopy and energy dispersive X‐ray analysis methods, respectively. The IR‐transmission spectrum reveals the presence of Mn³⁺O₆‐ and Mn⁴⁺O₆‐ octahedra in the lattice of La_0.63Pb_0.37Mn O_3+δ crystals. (© 2009 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Growth of single-crystalline sodium titanate and sodium tungstate one-dimensional nanostructures: Bio-inspired approach using oyster shell

Using oyster shell, single-crystalline Na₂Ti₆O₁₃ and Na₂W₄O₁₃ one-dimensional nanostructures (ODNS) were simply synthesized from granular TiO₂ and WO₃ particles by thermal heating at 700 °C. The oyster shell was used as a source of both sodium and carbon dioxide, which have an effect on unidirectional growth of single-crystalline Na₂Ti₆O₁₃ and Na₂W₄O₁₃ from TiO₂ and WO₃. The growth of sodium metal oxide ODNS from metal oxide particles was reproduced by replacing oyster shell with chemical reagents (NaCl, CaCO₃) or gas (CO₂), allowing identification of the main factors for the growth of ODNS. The characteristics of biological material (i.e., oyster shell) lend certain advantages in the fabrication of sodium metal oxide ODNS: (a) low processing temperature with high yield; (b) an eco-friendly method; and (c) no requirement of additional processes such as separation or washing. This work suggests a new approach for using biological material for the crystal growth of nanostructured materials.     

Growth and characterization of L‐prolinium tartrate – A new organic NLO material

Single crystals of L‐Prolinium tartrate (C₅H₁₀NO₂)⁺ (C₄H₅O₆)^‐, a new organic non‐linear optical material of size: 15 × 10 × 10 mm³ were grown using submerged seed solution growth method. Characterization of the crystals was made using single crystal X‐ray diffraction and density determination. Spectroscopic, thermal, optical and mechanical studies were carried out. These studies show that the crystals are thermally stable upto 161°C, transparent for the fundamental and second harmonic generation of Nd: YAG (λ = 1064 nm) laser and possess good mechanical strength. Second harmonic generation (SHG) conversion efficiency was investigated to explore the NLO characteristics of this material using Kurtz and Perry method and it was found that the SHG conversion efficiency is about 90% of that of the standard KDP crystals. Laser damage threshold study was also carried out. (© 2007 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Characterization of large‐sized Nd:YAG single crystals grown by horizontal directional solidification

Nd³⁺‐doped Y₃Al₅O₁₂ single crystals have been grown by the horizontal directional solidification (HDS) method in different thermal zone. The Grashof (G_r), Prandtl (P_r), Marangoni (M_a) and Rayleigh (R_a) numbers of melt in HDS system have been discussed for our experimental system to understand the mechanism of melt flow patterns and concentration gradient of dopant. The concentration gradient of Nd³⁺ ions was explained with melt flow processes during crystal growth in different thermal zone, and results indicated that high growth temperature will be helpful for uniformity of dopant in HDS‐grown single crystal. The main microscopic growth defects such as bubbles and irregular inclusions in HDS‐grown Nd:YAG crystals were observed, and the causes were discussed as well. (© 2012 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Induced growth of Pb0.97La0.02(Zr0.66Sn0.27Ti0.07)O3 antiferroelectric single crystals with a platinum wire

Relaxor antiferroelectric (Pb,La)(Zr,Sn,Ti)O₃ (PLZST) with the composition near the morphotropic phase boundary shows excellent electrical properties. However, the crystal growth of PLZST is limited by the incongruent melting of the materials. Crystal growth of PLZST was induced by a platinum wire in the flux solution with 50 wt% PbO‐PbF₂‐B₂O₃ as a solvent. The obtained PLZST single crystals are optical transparent with light yellow color. The size of the crystals in regular rectangular shape varies from 0.5 mm to 1 mm. The PLZST single crystals exhibit tetragonal phase structure. The element contents of the crystals were measured by inductively coupled plasma atomic emission spectrometry. The results show that the composition of as‐grown crystals is a little bit deviated from the starting composition. The single crystals show two dielectric peaks at 115 °C and 182 °C, corresponding to antiferroelectric‐ferroelectric and ferroelectric‐paraelectric phase transitions. The dielectric data of as‐grown crystals indicate there is typical relaxor behavior near 182 °C. The value of relaxor factor n is 1.49642.     

On the Iso‐Diameter Growth of β ‐BaB2O4 (BBO) Crystals by Flux Pulling Method

The iso‐diameter growth of β ‐BaB₂O₄ (BBO) crystals by the flux pulling method have been studied based on the phase equilibrium diagram in the BaB₂O₄‐Na₂O pseudo‐binary system and from the interface stability. The mathematical expressions for the cooling rate in the growth of the crystals with constant diameter under stable growth conditions are derived, the experimental phenomena such as diameter contraction and difficulty to grow a lengthy crystal by the flux pulling method are explained, the prerequisite for iso‐diameter BBO crystal growth from the flux is suggested; a new continuous charging flux pulling method is introduced to grow large‐sized high quality crystals with a relative high growth rate.     

Single‐crystal growth and characterization of mullite‐type orthorhombic Bi2M4O9 (M = Al3+, Ga3+, Fe3+)

Pure and homogeneous single crystals of orthorhombic mullite‐type Bi₂M₄O₉ (M = Al³⁺, Ga³⁺, Fe³⁺), and a mixed Bi₂Fe_1.7Ga_2.3O₉ crystal from an equimolar Ga/Fe composition were grown by the top seeded solution growth (TSSG) method. All these compounds melt incongruently in the range of about 800 and 1100 °C. In case of bismuth gallate and ferrate inclusion‐free crystals with dimensions up to several cubic centimeters can be grown. Limited solubility in Bi₂O₃ and the high steepness of the liquidus curve are the reasons for getting only small imperfect bismuth aluminate crystals. In contrast to ceramic materials preparation reported in literature, divalent calcium and strontium could not be incorporated into the mullite‐type structure during the melt growth process. Several fundamental physical properties like heat capacity, thermal expansion, heat conductivity, elastic constants, high‐pressure behavior and oxygen diffusivity were determined by different research groups using single‐crystalline samples from the as‐grown materials. Furthermore, the refractive indices of Bi₂Ga₄O₉ were measured in the range of 0.430 and 0.700 μm. Such as many other bismuth containing compounds the refractive indices of Bi₂Ga₄O₉ are larger than 2, and Bi₂Ga₄O₉ is an optic biaxial positive crystal. (© 2009 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Czochralski Growth of Potassium Lithium Niobate Single Crystals with Low Li Content and Their Characterization

Single crystalline and crack free potassium lithium niobate (KLN) single crystals with low Li content were grown by the Czochralski method. The crystal composition can be written as K_2.60Li_1.17Nb_5.44O₁₅ (=K_2.95Li_1.33Nb_6.17O₁₇) which contain relatively fewer Li ions than ferroelectric K₃Li₂Nb₅O₁₅ crystals. All experimental results show that the deficiency of the Li ions in the KLN crystals strongly influences their physical properties. Especially, the as‐grown crystals do not indicate any signature for a ferroelectric phase transition in contrast to the ferroelectric K₃Li₂Nb₅O₁₅ crystals. However, due to ionic conduction, the temperature dependence of the dielectric constant of such KLN‐2 crystals show a broad anomaly near 300°C. In addition, the existence of proton defects can be revealed by infrared absorption spectroscopy near 3500 cm^‐1 in as‐grown crystals.     

Growth aspects of barium oxalate monohydrate single crystals in gel medium

Single crystals of barium oxalate monohydrate (BaC₂O₄.H₂O, BOM) were grown in pure form by controlled diffusion of Ba²⁺ using the gel technique at different temperatures. Starting from aqueous Ba²⁺ chloride (BaCl₂) and acetic acid (C₂H₂O₄) in gel, this method offers a low‐cost and an easiest alternative to other preparation methods for the production of barium oxalate bulky single crystals. The optimal conditions for the growth of BOM crystals in silica gel were found by investigating different growth parameters such as gel pH, gel aging and crystallization temperature. Irrespective of all such crystallization environments, growth rate of the crystals were initially less and then exhibited supersaturation effect leading to non‐linearity. Gel aging and temperature has profound effect on nucleation density that resulted less number of crystals of maximum size in the gel matrix. Perfect single crystals were grown on gels of higher pH. The macropore morphology and porosity was controlled by changing age of the gel. It has been found that temperature has a fabulous effect in controlling the nucleation density by altering the supersaturation conditions for the formation of critical nuclei. The entire growth kinetics informed that the grown crystals were derived by the one dimensional diffusion controlled process. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)