Growth and Optical Spectra of Zn∶Er∶LiNbO_3 Crystals Using Bridgman Method

The growth of LiNbO3 single crystal with Er^3＋ and Zn^2＋ co-doped using Bridgman method and its characteristic absorption spectra and fluorescence spectra were reported. Large-size crystals initially containing Zn^2＋ （3%） and Er^3＋ （0.6%） with good optical quality were obtained using optimized conditions such as a growth rate of 0.8- 1.5 mm·h^-1 and a temperature gradient of about 30 - 35℃·cm^-1 across the solid-liquid interface and the sealed platinum crucible. X-ray diffraction and differential thermal analysis （DTA） were used to characterize the crystals. The results indicate that the concentration of Er^3＋ ions in crystals, their absorption intensity, and their fluorescence intensity decrease from the bottom to the top in the crystals. However, for the upper part of the crystal, the up-conversion fluorescence intensity is higher than that of the lower part excited by an 800 or 970 nm pump. The effects of the crystal lattice, their structural defect and their effective segregation of Er^3＋ ions were discussed with respect to the variations of the up-conversion fluorescence intensity.

Improvement of photorefractive properties in Hf:Fe:LiNbO_3 crystals with various [Li]/[Nb] ratios

Photorefractive properties of Hf：Fe：LiNbO3 crystals with various [Li]/[Nb] ratios have been investigated at 488 nm wavelength based on the two-wave coupling experiment. High diffraction efficiency and large recording sensitivity are observed and explained. The decrease in Li vacancies is suggested to be the main contributor to the increase in the photoconductivity and subsequently to the induction of the improvement of recording sensitivity. The saturation diffraction efficiency is measured up to 80.2%, and simultaneously the recording sensitivity of 0.91 cm/J is achieved to in the Hf：Fe：LiNbO3 crystal grown from the melt with the [Li]/[Nb] ratio of 1.20, which is significantly enhanced as compared with those of the Hf：Fe：LiNbO3 crystal with the [Li]/[Nb] ratio of 0.94 in melt under the same experimental conditions. Experimental results definitely show that increasing the [Li]/[Nb] ratio in crystal is an effective method＇for Hf：Fe：LiNbO3 crystal to improve its photorefractive properties.

OH^- absorption and nonvolatile holographic storage properties in Mg:Ru:Fe:LiNbO_3 crystal as a function of Mg concentration

Mg：Ru：Fe：LiN-bO3 crystals with various concentrations of MgO （in mole） and fixed content of RuO2 and Fe203 （in mass） are grown with the Czochralski method from the congruent melt. Their infrared transmission spectra are mea- sured and discussed to investigate the defect structure. With the increase of Mg2＋ concentration the blue nonvolatile holographic storage capability is enhanced. The nonvolatile holographic storage properties of dual-wavelength recording of Mg（7 mol%）：Ru：Fe：LiNbO3 nonvolatile diffraction efficiency, response time, and nonvolatile sensitivity reach 59.8%, 70 s, and 1.04 cm/J, respectively. Comparing Mg（7 mol%）：Ru：Fe：LiNbO3 with Ru：Fe：LiNbO3 crystal, the response time is shortened apparently. The nonvolatile diffraction efficiency and sensitivity are raised largely. The mechanism in blue photorefractive nonvolatile holographic storage is discussed.

Growth and Optical Spectra of Zn∶Er∶LiNbO_3 Crystals by Bridgman Method

The growth of LiNbO3 single crystal with Er^3＋/Zn^2＋ co-doped by the bridgman method and the characteristics of absorption spectra and fluorescence spectra were reported. By means of the optimized con- ditions such as growth rate of 0.8 - 1.5 mm · h^- 1, temperature gradient about 30 - 35℃ ·cm^-1 across the solid-liquid interface and sealed platinum, large size crystals containing Zn^2＋ （3%） and Er^3＋ （0.6%） with good optical quality were obtained. X-ray diffraction and DTA were used to characterize the crystals. The results indicate that the concentration of Er^3＋ ions in crystals decrease along the growth direction, the absorption intensity and the fluorescence intensity ions also decrease along the growth direction. of Er^3＋ However, for the upper part crystal, the upconversion fluorescence intensity is higher than that of the lower part crystal excited with 800 or 970 nm pump. The effects of crystal lattice, structure defect and effective segregation of Er^3＋ ions were discussed in respect to the variations were discussed of upconversion fluorescence intensity.

Optical Property of LiNbO_3 Crystal Codoped with In, Mg and Fe

In 2O 3, MgO and Fe 2O 3 were doped in LiNbO3 and Czochralski method was used to grow In:Mg:Fe:LiNbO 3 crystals. The OH - extension transmission spectra, light scattering resistance ability, two wave coupled diffraction efficiency and response time of the crystal were measured. Codoping In and Mg in crystal will improve its light scattering resistance ability and response time. Doping In can increase the ability to replace antisite Nb and decrease the doping quantity of Mg. All these are propitious to improve the optical homogeneity of crystal. Doping Fe can improve the photorefractive sensitivity for LiNbO 3 crystal. We discussed the site of In, Mg and Fe in LiNbO 3 crystals and the influence of the absorption peak of OH - transmission spectra on photorefractive property for LiNbO 3 crystal.

Effect of Hf^(4+) doping on structure and enhancement of upconversion luminescence in Yb:Tm:LiNbO_3 crystals

A series of Yb：Tm：LiNbO_3 crystals doped with x mol% Hf^（4＋）ions（x = 2, 4, and 6） were grown by the Czochralski method. The dopant occupancy and defect structure of Hf：Yb：Tm：LiNbO_3 crystals were investigated by x-ray diffraction and infrared transmission spectra. The influence of Hf^（4＋）ions concentration on UV–VIS–NIR absorption spectra of Hf：Yb：Tm：LiNbO_3 crystals was discussed. The upconversion luminescence of Hf：Yb：Tm：LiNbO_3 crystals was obtained under 980 nm excitation. Strong emissions were observed at 475 nm in the blue wavelength range and 651 nm in the red wavelength range. Remarkably, enhancement of the red and blue upconversion luminescence was achieved by tridoping Hf^（4＋）ions.

Study on the Growth and Photorefractive Properties of In:Fe:Cu:LiNbO_3 Crystals

Fe（0.2 mol%）：Cu（0.04 mol%）：LiNbO3 crystals with different doping concentration of In^3＋ （0, 1.0, 2.0, 3.0mol%） were grown by Czochralski method, and then oxidized and reduced. The infrared transmittance spectra of crystals were measured to investigate the location of doping ion and its threshold concentration. The photorefractive properties of the crystals were tested by two beam coupling experiment. The results showed that the threshold concentration of In ions is 2.0～ 3.0 mol% and In ions take the place of NbLi^4＋ to form （ InLi^2＋） before reaching its threshold concentration, and then the location of normal Nb ions. In the （2.0 mol%）：Fe：Cu：LiNbO3 crystal with the oxidation treatment having the highest diffraction efficiency （η = 45.8%）, the photo-damage resistance threshold value R of In（3.0 mol%）：Fe：Cu：LiNbO3 was 3.67×10^4 W/cm^2 which was two orders of magnitude higher than that of Fe：Cu：LiNbO3 crystal （4.30×10^2 W/cm^2）. And the photo-damage resistance ability was enhanced by oxidized treatment. The In（2.0～3.0 mol%）：Fe：Cu：LiNbO3 crystals with oxidized treatment have the best photorefractive properties.

Influence of Oxidation and Reduction Treatments on the Photorefractive Properties of Mg:In:Fe:LiNbO_3 Crystals

A series of Mg：In：Fe：LiNbO3 crystals were grown by Czochralski technique; their absorption spectra and photo scattering resistance ability after oxidation or reduction treatment were measured by light spot distortion method, and their response time and exponential gain coefficient were tested by two-beam coupling experiment. Besides, the effective carrier concentration has been calculated. The results showed that the absorption edges of reduced and oxidized crystals are respectively shifted to violet and Einstein compared with those of the growth state crystal. From oxidation state to growth state to reduction state of the samples, the photo scattering resistance ability and response time decrease while the exponential gain coefficient and concentration of effective carriers increase. The reduction treatment was necessary for the Mg：In：Fe：LiNbO3 crystals to enhance their photorefractive properties.

Holographic Storage Properties of In:Fe:Mn:LiNbO_3 Crystals

In：Fe：Mn：LiNbO3（LN） crystals were grown in air atmosphere by Czochralski method with different concentration of In （0, 1, 2, 3 mol%） in the melts, while the contents of Fe2O3 and MnO were 0.1 and 0.5 mol%, respectively. The location of doping ions was analyzed by Ultravioletvisible absorption spectra and differential thermal analysis. The diffraction efficiency （η）, writing time （τw） and erasure time （τe） of the crystals were measured by two-beam coupling experiment. The dynamic range and photorefractive sensitivity have also been calculated. The results showed that with the increase of In ions in the melt, the absorption edge of In：Fe：Mn：LN crystal shifts to the violet firstly and then makes the Einstein shift, the Curie temperature of crystal increases firstly and then decreases, the storage ratio speeds up, diffraction efficiency decreases, and dynamic range and photorefractive sensitivity increase. The mechanism of holographic storage properties of In：Fe： Mn：LN crystal with different doping concentration of In^3＋ was investigated, suggesting the In： Fe：Mn：LN crystals are excellent holographic storage materiel with better synthetical properties than Fe：Mn：LN crystals.

The Effect of Oxidation/Reduction Disposing on Optical Properties of Mg:Fe:Mn:LiNbO_3 Crystals

The congruent tri-doped Mg:Mn:Fe:LiNbO 3 crystal has been grown by Czochralski method. Some crystal samples are reduced in Li 2CO 3 powder at 500 ℃ for 24 hours or oxidized for 10 hours at 1100 ℃ in Nb 2O 5 powder. Compared with As-grown Mg:Mn:Fe:LiNbO 3, the absorption edge in UV-Vis. absorption spectrum of the oxidized sample and the reduced shifts to the violet and the red, respectively. Reduction increases the absorption of crystals in visible light region. In two-wave coupling experiments, the writing time, maximum diffraction efficiency and the erasure time of crystal samples in the same conditions are determined. The results indicate that oxidation and reduction disposing has great effect on the holographic recording properties of these crystals. The reduced crystal exhibits the fastest response time of 160 s among the crystal series. The mechanism of post-disposing effect on the holographic recording properties of Mg:Mn:Fe:LiNbO 3 crystals are investigated.

Accelerated Sequential Deposition Reaction via Crystal Orientation Engineering for Low-Temperature,High-Efficiency Carbon-Electrode CsPbBr_(3) Solar Cells

Low-temperature,ambient processing of high-quality CsPbBr_(3)films is demanded for scalable production of efficient,low-cost carbon-electrode perovskite solar cells(PSCs).Herein,we demonstrate a crystal orientation engineering strategy of PbBr_(2)precursor film to accelerate its reaction with CsBr precursor during two-step sequential deposition of CsPbBr_(3)films.Such a novel strategy is proceeded by adding CsBr species into PbBr_(2)precursor,which can tailor the preferred crystal orientation of PbBr_(2)film from[020]into[031],with CsBr additive staying in the film as CsPb_(2)Br_(5)phase.Theoretical calculations show that the reaction energy barrier of(031)planes of PbBr_(2)with CsBr is lower about 2.28 eV than that of(O2O)planes.Therefore,CsPbBr_(3)films with full coverage,high purity,high crystallinity,micro-sized grains can be obtained at a low temperature of 150℃.Carbon-electrode PSCs with these desired CsPbBr_(3)films yield the record-high efficiency of 10.27%coupled with excellent operation stability.Meanwhile,the 1 cm^(2)area one with the superior efficiency of 8.00%as well as the flexible one with the champion efficiency of 8.27%and excellent mechanical bending characteristics are also achieved.

Role of Crystal Seed in Aluminum Hydroxide Crystallization from Ammonia System with Added NH_(4)Al(SO_(4))_(2)·12H_(2)O

A method to promote aluminum hydroxide crystal growth through pickling Al(OH)_(3)as seed in the ammonia system was proposed to overcome these defects.The experimental results show that,under the conditions of pickling time of 15 min,the acid concentration of 10%,the addition of 70 g/L pickling-Al(OH)_(3)seed,and the coarse granular Al(OH)_(3)products(d0.5=85.667)can be obtained.The characterization results show that the phase of the product is gibbsite,consistent with the seed.Moreover,the steps and ledges can be formed on pickling Al(OH)_(3)seed surface under the ammonia system,effectively promoting crystal growth.During crystal growth,the roughness of the crystal surface was first increased and then decreased,and the lamellar structure was deposited on the crystal seed surface.The final particles are approximately round,the surface is compact and dense.The growth of the product is surface reaction controlled.In addition,the content of the AlO_(6)unit is increased and contributed to Al(OH)_(3)crystal growth.

Modulating perovskite crystallization and band alignment using coplanar molecules for high-performance indoor photovoltaics

The proper bandgap and exceptional photostability enable CsPbI_(3) as a potential candidate for indoor photovoltaics(IPVs),but indoor power conversion efficiency(PCE) is impeded by serious nonradiative recombination stemming from challenges in incomplete DMAPbI_(3) conversion and lattice structure distortion.Here,the coplanar symmetric structu re of hexyl sulfide(HS) is employed to functionalize the CsPbI_(3) layer for fabricating highly efficient IPVs.The hydrogen bond between HS and DMAI promotes the conversion of DMAPbI_(3) to CsPbI_(3),while the copianar symmetric structure enhances crystalline order.Simultaneously,surface sulfidation during HS-induced growth results in the in situ formation of PbS,spontaneously creating a CsPbI_(3) N-P homojunction to enhance band alignment and carrier mobility.As a result,the CsPbI_(3)&HS devices achieve an impressive indoor PCE of 39.90%(P_(in):334.6 μW cm^(-2),P_(out):133.5 μW cm^(-2)) under LED@2968 K,1062 lux,and maintain over 90% initial PCE for 800 h at ^(3)0% air ambient humidity.

Synthesis,crystal structure and photo-physical properties of tris(4-methyl-2,5-diphenylpyridine)iridium for OLED

Organic light-emitting diodes(OLEDs)have important applications in the field of next-generation displays and lighting,and phosphorescent iridium complexes are an important class of electroluminescent phosphorescent materials.In this paper,Ir(bmppy)_(3),tris(4-methyl-2,5-diphenylpyridine)iridium,was synthesized and elvaluted for photo-physical characteristics.Single crystals suitale for X-ray diffraction(XRD)were grown from a mixture solvent of dichloromethane and absolute ethanol.The composition and structur of Ir(bmppy)_(3)were determined by element analysis,NMR spectra and XRD.The complex crystallizes in the monoclinic symmetry with the space group P21/c with a slightly distorted octahedral configuration.As measured by UV-Visible and photoluminescence spectra,Ir(bmppy)_(3) displays a maximum emission at at 527 nm at ambient temperature,a typical green-emitting profile.The complex has potential for application in the OLED industry.

Analyses of Reaction Mechanisms among Different Sulfonation Reagents and m-Diphenylamine and Crystal Structures of the Formed Compounds

In the traditional process, m-phenylenediamine reacts with fuming sulfuric acid at high temperature to get intermediates, and then after dehydration occurs intramolecular rearrangement to get 2,4-diaminobenzenesulfonic acid. Traditional methods need to consume a lot of fuming sulfuric acid or concentrated sulfuric acid, resulting in high industrial large-scale production cost, more waste, and posing a serious environmental pollution risk. In this thesis, three different sulfonation reagents were used for the sulfonation reaction of m-phenylenediamine, and the reaction mechanisms and crystal structures of the three pathways were investigated. The three routes are: 1) one-step synthesis of monosulfonated compound 1 from raw material and sulfur trioxide (SO3);2) rapid reaction of raw material and chlorosulfonic acid to synthesize bisulfonated compound 2;3) direct eutectic crystallization of raw material and ordinary sulfuric acid to obtain compound 3. The crystal structure of the compounds synthesized by three paths was analyzed by X-ray single crystal diffraction, and compound 1 was characterized by NMR, Fourier infrared spectra, UV-visible spectrum and Mass spectrometry. The one-step synthesis of SO3 as a sulfonation reagent has the advantages of mild reaction conditions, simple operation and low cost.

Study of Temperature Enhancement of the Photorefractive Effect in Ce：Fe：LiNbO_3 Crystal

in the range of 20 to 120 ℃, the two-beam coupling exponential gain coefficient and the four-wave mixing phase conjugation reflectivity have been investigated. It is shown that the values such as the gain, the phase conjugation reflectivity and the response speed increase as the temperature increases. At about 55, 71 and 110℃, extraordinary enhancement of the gain and the phase conjugation reflectivity were observed.The mechanism is analyzed by the phase change in the crystal at these temperatures.

TEMPERATURE DEPENDENCE OF TWO-BEAM COUPLING IN Ce: LiNbO_3 CRYSTAL

The effect of temperature on photorefractive process is a significant problem inphotorefractive nonlinear optics. The temperature dependence of photoretiactive effect in semiinsulating semiconductive material Cr: GaAs was investigated by CHENG Li-jen et al., and they thought that the band gap of conventional oxide photorefractive crystal was too wide, so it is difficult to observe the temperature dependence of photorefractive effect in a general experimental condition. But the point of view has been proved not true by our experiment

Nonlinear Talbot self-healing in periodically poled LiNbO_3 crystal [Invited]

The nonlinear Talbot effect is a near-field nonlinear diffraction phenomenon in which the self-imaging of periodic objects is formed by the second harmonics of the incident laser beam. We demonstrate the first, to the best of our knowledge, example of nonlinear Talbot self-healing, i.e., the capability of creating defect-free images from faulty nonlinear optical structures. In particular, we employ the tightly focused femtosecond infrared optical pulses to fabricate LiNbO_(3) nonlinear photonic crystals and show that the defects in the form of the missing points of two-dimensional square and hexagonal periodic structures are restored in the second harmonic images at the first nonlinear Talbot plane. The observed nonlinear Talbot self-healing opens up new possibilities for defect-tolerant optical lithography and printing.

Oxidation and reduction treatment of photorefractive Fe:LiNbO_3 crystal

Lithitum niobate （LiNbO3, LN） crystal is an important type of photorefractive materi-als, its photorefractive property can be improved effectively by doping. For example, theoptical damage resistanee and the photorefractive sensitivity of LN crystal can be inerasedby doping Mg and Fe, respectively. Modest treatment of oxidation and reduction

Transmission Spectral Characteristics of Photonic Crystals Milled in Annealed Proton-Exchange LiNbO_3 Waveguide

Transmission spectra of triangular lattice photonic crystals milled in the top surface of an annealed proton- exchange waveguide are numerically simulated. The effects of the finite depth, conical shape, trapezoidal shape and hybrid shape of holes are theoretically analyzed. Due to the difficulty of milling high aspect-ratio cylindrical holes in lithium niobate （LiNbO3 ）, a compromised solution is proposed to improve the overlap between shallow holes and the waveguide mode, and useful transmission spectra with strong contrast and sharp band edges are achieved.