Nd3+A位置换对(Pb0.5Ca0.5)(Fe0.5Nb0.5)O3陶瓷微波介电性能的影响

研究了Nd3+离子A位置换改性(Pb0.5Ca0.5)(Fe0.5Nb0.5)O3陶瓷的微波介电性能.[(Pb0.5Ca0.5)1-xNdx](Fe0.5Nb0.5)O3(PCNFN)陶瓷的微波介电性能得到改善是由于少量过剩的Nd3+与(Pb,Ca)2+的固溶能够消除氧空位.当x=0.02时,能够形成单相的钙钛矿相,随着Nd3+置换量的增加,过剩的Nd3+将导致第二相焦绿石的形成,焦绿石会恶化PCNFN的微波介电性能.PCNFN介电性能随x的增加而下降是由于焦绿石相随x增加的结果.当x=0.02-0.05,PCNFN陶瓷有很好的微波介电性能,介电常数K>100,Qf值为5385-5797GHz,频率温度系数TCF随Nd3+含量的增加从正的变为负的.     

掺SrLi1／4Nb3／4O3的SrTiO3缺陷化学研究

利用Ｈ２／Ｈ２Ｏ体系获得不同的氧分压,上电极法 掺杂ＳｒＬｉ１／４Ｎｂ３／４Ｏ３的ＳｒＴｉＯ３瓷体在８００－１２００℃,Ｐｏ２＝１０＾１７－１０＾５Ｐａ的电导率。通过ｌｏｇＰｏ２－ｌｏｇσ图,计算出半导化活化焓约为２８７．７ｋＪ／ｍｏｌ,讨论了ＳｒＬｉ１／４Ｎｂ３／４Ｏ３掺杂的ＳｒＴｉＯ３在不同氧分压区域的主ｎ型半导体化向ｐ型半导化转变的特点。     

Mn改性Na0.5Bi2.5Nb2O9高温压电陶瓷的研究

采用固相法获得了Mn改性的Na0.5Bi2.5Nb2O9(NBN+xmol%MnCO3,0≤x≤10.0)铋层状压电陶瓷,并系统地研究了Mn(掺杂)对NBN基陶瓷显微结构与电性能的影响.结果表明,所有获得的样品都是居里点在700℃以上的单一相铁电体.加入Mn显著地提高了NBN系列陶瓷的机械品质因素Qm,明显改善了陶瓷的压电与机电性能.当MnCO3掺杂量为8.0mol%时,陶瓷获得最佳电性能:tanδ=0.749%,d33=20 pC/N,Qm=3120,kp=12.37%,kt=21.09%,Pr=7.01μC/cm2.NBN+xmol%MnCO3(x=8.0)陶瓷经700℃退极化处理后,其d33保持为原来的75%(~15 pC/N),表明该材料在高温领域下具有良好的应用前景.     

Enhanced energy storage and photoluminescence properties in ErBiO3-doped (Na0.5Bi0.5)TiO3-SrTiO3 ceramics

Journal of Materials Science - (1-x)(0.75Na0.5Bi0.5TiO3-0.25SrTiO3)-xErBiO3 (NBST-xEB, x?=?0–0.04) ceramics were fabricated through a solid state reaction method. Scanning...     

Synthesis and characterization of PVP/TbL(phen)0.5 x 7H2O nanorods

The luminescent complex terbium (III)-trimesic acid (TMA)-1,10-phenanthroline (phen) nanorod was synthesized in the polyvinylpyrrolidone (PVP) matrix by a co-precipitation method. The chemical formula of the synthesized complex was speculated to be PVP/TbL(phen)0.5 x 7H2O by inductively coupled plasma-atomic emission spectroscopy (ICP-AES), elemental analysis and Fourier-transform infrared spectroscopy (FTIR). The X-ray diffraction pattern (XRD) of PVP/TbL(phen)0.5 x 7H2O indicated that it was a crystalline complex. The transmission electron microscopy (TEM) result showed that the complex was nanorods with diameters of about 80-100 nm. The thermogravimetric curve (TGA) analysis exhibited that the complex has good stability below 400 degrees C. UV-Vis diffuse reflectance spectra showed that there is a maximum absorption at 300 nm. The photoluminescence analyses (PLA) showed that the synthesized complex emitted the characteristic green fluorescence of Tb (III) ions under ultraviolet light excitation. The emission peaks of PVP/TbL(phen)0.5 x 7H2O at 488, 542, 581, and 618 nm using 278 nm as exciting wavelength can be assigned to the 5D4 --> 7F6, 5D4 --> 7F5, 5D4 --> 7F4, and 5D4 --> 7F3 electron transitions of the Tb3+ ions, respectively.     

Thermomechanical Analysis of (Cu0.5Tl0.5)-1223 Substituted by Pr and La

The thermomechanical analysis (TMA) of Cu 0.5 Tl 0.5 Ba 2 Ca 2 x R x Cu 3 O 10 δ,where R=Pr and La,with 0.0≤x≤0.15,was carried out in temperature range from 450 to 1145 K.The samples were prepared by singlestep solid state reaction technique.The prepared samples were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM).The superconductivity of the prepared samples was investigated by electrical resistivity measurement.The results showed that low substitution content enhanced the (Cu 0.5 Tl 0.5)1223 phase formation,while the higher substitution content degraded this phase.The higher superconducting transition temperatures T c were found to be 114 K and 109 K at x= 0.025 for Pr-and La-substitutions,respectively.The average linear thermal expansion coefficient increased as x increased,while the shrinkage temperature decreased as x increased.Those results were emphasized by porosity and Vickers microhardness calculations.Debye temperature θ D was calculated from the linear thermal expansion coefficient data and correlated to T c to estimate the electron-phonon coupling λ ep.     

Dielectric and piezoelectric properties of PbFe1/2Nb1/2O3-PbTiO3 ceramics from the morphotropic phase boundary compositional range

Dielectric, X-ray, and piezoelectric studies of highly-resistive Li-doped (1-x)PbFe(1/2)Nb(1/2)O(3)-(x)PbTiO(3) (PFN-xPT) ceramics from the 0 ≤ x ≤ 0.2 range fabricated by solid-state synthesis and usual sintering have been carried out. Distinct anomalies of dielectric and piezoelectric parameters, corresponding to the transition between rhombohedral (monoclinic) and tetragonal ferroelectric phases, have been observed in pure PFN and PFN-xPT compositions with PbTiO(3) content up to 8 mol.%. The x,T-phase diagram of the PFN-xPT solid solution system has been constructed using these data.     

La0.5Ca0.5MnO3中Ca位上Ba掺杂效应研究

用固态反应法制备了具有单相结构的La_0.5Ca_0.5-xBa_xMnO₃系列样品,其结构随Ba含量增加由立方晶系转变为典型的正交晶系．零场下输运性质实验表明,在较低掺杂量时,系统在整个温区显示半导体型导电特征,而当掺杂量超过0.14时,系统发生由半导体到金属的转变,且转变的温度随掺杂量增加而移向高温瑞．基于对实验结果的分析,就Ca位上Ba掺杂所起的作用进行了初步探讨．     

真空烧结对SrTiO3功能陶瓷性能的影响

采用真空烧结替代气氛烧结制备SrTiO3陶瓷材料,获得了既具有电容效应又具有良好压敏效应性能的SrTiO3复合功能陶瓷元件.在此基础上探讨了Nb2O5和La2赴O3作为单、双施主掺杂对SrTiO3功能陶瓷半导化、电性能及显微结构的影响.研究结果表明,双施主掺杂不仅可以促进SrTiO3功能陶瓷半导化,而且对显微结构有重要的影响.在x(Nb2O5);x(La2O3)0.6:0.2时可获得性能较好的半导体材料.相比于气氛烧结工艺,真空烧结同样可以得到性能优良的SrTiO3功能陶瓷材料.     

Dielectric and piezoelectric properties in the lead-free system Na0.5K0.5NbO3-BiScO3-LiTaO3

Phase relations, dielectric and piezoelectric properties are reported for the ternary system 98%[(1 - x) (Na(0.5)K(0.5)NbO(3))-x(LiTaO(3))]-2%[BiScO(3)] for compositions x ≤ 10 mol% LiTaO(3). The phase content at room-temperature changed from mixed phase, monoclinic + tetragonal, for unmodified 98%(Na(0.5)K(0.5)NbO(3))-2%(BiScO(3)), to tetragonal phase for compositions >2 mol% LiTaO(3). Curie peaks at 360 to 370°C were observed for all compositions, but peaks became diffuse at x ≥ 3 mol%, and two dielectric peaks, at 370 and 470°C, were observed for 5 mol% LiTaO(3). Phase segregation, and finite size affects associated with the core-shell structure, account for the occurrence of two dielectric peaks in 5 mol% LiTaO(3), and diffuse dielectric behavior. The value of d(33) piezoelectric charge coefficient increased from ~160 pC/N for 0 mol% LiTaO(3) to 205 to 214 pC/N for 1 to 2 mol% LiTaO3 solid solutions, before falling sharply at 3 mol% LiTaO(3). TEM-EDX analysis revealed core-shell grain structures with segregation of Bi, Sc, and Ta in the outer ~100-nm shell of the 5 mol% LT sample.     

Preparation of poly(acrylic)/SiO2/EuL3 x 2H2O, hybrid thin films from monodispersed colloidal silica

In this study, poly(acrylic)/SiO2/EuL3 x 2H2O hybrid thin films were prepared from various acrylic monomers (MMA and EDMA/TMPTA), lanthanide metal complexes (EuL3 x 2H2O, L = pyridine carboxylic acid), and monodispersed colloidal silica with a coupling agent, 3-(trimethoxysilyl)propyl methacrylate (MSMA). It is a combination of the sol-gel reaction, thermal polymerization, and spin coating. The silica content in the hybrid thin films is fixed at 20 wt%, and the EuL3 x 2H2O content is varied from 0.01 g to 0.07 g. FTIR and EA analysis confirms the chemical structure of the prepared EuL3 x 2H2O and poly(acrylic)/SiO2/EuL3 x 2H2O hybrid thin films. UV-Vis spectra and n&k analysis shows that the hybrid thin film has good transparency in visible light. The refractive index of hybrid thin films can be effectively controlled through the EuL3 x 2H2O content. The PL spectra shows that the strongest emission peak occurs at 615 nm and the emission intensity increases to the peak maximum at an EuL3 x 2H2O content of 0.05 g. Both TGA and PL analysis show that the prepared hybrid thin films from the crosslinked acrylic polymer moiety have much better film uniformity, thermal stability, and fluorescence properties. The TEM diagram shows that the MSMA/SiO2/EuL3 x 2H2O particles with a size 15-20 nm are well dispersed in the reaction solution. The SEM diagram shows that the particle distribution in the prepared hybrid thin films is uniform and no phase separation is observed. Finally, AFM analysis indicates that the prepared hybrid thin films have an excellent surface planarity.     

Nb掺杂浓度对SrTiO3的电子结构和光学性能的影响

用第一性原理计算不同Nb掺杂浓度的n型Nb掺杂SrTiO3,研究了Nb掺杂浓度对SrTiO3的形成焓、电子结构和光学性能的影响.在Nb掺杂SrTiO3中Nb替位Ti原子,与实验结果一致.Nb掺杂SrTiO3的费米能级进入导带底部,Nb掺杂SrTiO3呈现n型半导体特征.从微观角度分析了Nb掺杂浓度对导电性的影响,1.11at％ Nb掺杂SrTiO3在可见光范围有强吸收,是一种有潜在应用的光催化材料;而1.67at％和2.5at％Nb掺杂SrTiO3是潜在的透明导电材料.     

Synthesis and photoelectric properties of V3O7 x H2O and V3O7, nanobelts

V3O7 x H2O nanobelts have been synthesized via a hydrothermal route. Monoclinic V3O7, nanobelts could be obtained by thermal decomposition of V3O7 x H2O nanobelts at 400 degrees C. The synthesized products were characterized by X-ray diffraction, scanning electron microscopy, and transmission electron microscopy. It was found that the V3O7 x H2O is of orthorhombic phase and single crystalline nanobelts with width of 100-500 nm and length up to 100 microm. The formation mechanism of the V3O7 x H2O nanobelts was discussed. Light sensitivity in exposure to a simulated sunlight in different intensity and biases have been investigated on the electrode made from the V3O7 x H2O and V3O7, nanobelts. The results show that the photocurrent intensity of the V3O7 nanobelts is much larger than that of the V3O7 x H2O nanobelts. The fast current response has been observed under alternative control of light on and off at 2 s interval.     

Experimental and DFT Studies of Au Deposition Over WO3/g-C3N4 Z-Scheme Heterojunction

A typical Z-scheme system is composed of two photocatalysts which generate two sets of charge carriers and split water into H2 and O2 at different locations.Scientists are struggling to enhance the efficiencies of these systems by maximizing their light absorption,engineering more stable redox couples,and discovering new O2 and H2 evolutions co-catalysts.In this work,Au decorated WO3/g-C3N4 Z-scheme nanocomposites are fabricated via wet-chemical and photo-deposition methods.The nanocomposites are utilized in photocatalysis for H2 production and 2,4-dichlorophenol(2,4-DCP)degradation.It is investigated that the optimized 4Au/6%WO3/CN nanocomposite is highly efficient for production of 69.9 and 307.3μmol h−1 g−1 H2 gas,respectively,under visible-light(λ>420 nm)and UV–visible illumination.Further,the fabricated 4Au/6%WO3/CN nanocomposite is significant(i.e.,100%degradation in 2 h)for 2,4-DCP degradation under visible light and highly stable in photocatalysis.A significant 4.17%quantum efficiency is recorded for H2 production at wavelength 420 nm.This enhanced performance is attributed to the improved charge separation and the surface plasmon resonance effect of Au nanoparticles.Solid-state density functional theory simulations are performed to countercheck and validate our experimental data.Positive surface formation energy,high charge transfer,and strong non-bonding interaction via electrostatic forces confirm the stability of 4Au/6%WO3/CN interface.     

Synthesis and Characterization of LiNi0.85Co0.15-xAlxO2 as Cathode Materials for Lithium-ion Batteries

LiNi0.85CO0.15-xAlxO2 samples （x=0.025, 0.05 and 0.10） were prepared by solid state reaction at 725℃ for 24 h from LiOH-H2O, Ni2O3, Co2O3 and Al（OH）3 under oxygen flow. Layered LiNiO2 simultaneously doped by Co-Al has been tried to improve the cathode performance. The results showed that substitution of optimum amount Al and Co for the Ni in LiNiO2 definitely had some beneficial effect on increasing the capacity and cycling behavior. When increasing x in LiNio.85CO0.15-xAlxO2, the initial discharge capacity decreased and its cyclability increased. Compromising high specific capacity and good cyclability, the optimum x in LiNi0.85Co0.15-xAlxO2 was x=0.05. As a consequence, LiNi0.85Co0.15-xAlxO2 had the first discharge capacity of 186.2 mAh/g and a capacity of 180.1 mAh/g after 10 cycles. Differential capacity vs voltage curves indicated that the co-doped LiNiO2 showed suppression of the phase transitions as compared with LiNiO2.     

Ni_(0.5)Zn_(0.5)Fe_2O_4铁氧体的制备及其电磁损耗性能

以Zn(NO3)2.6H2O、Ni(NO3)2.6H2O和Fe(NO3)3.9H2O及柠檬酸为原料,采用溶胶-凝胶法制备前驱体,在1 200℃下煅烧3 h合成ZnFe2O4和Ni0.5Zn0.5Fe2O4铁氧体粉体。利用差热分析、X射线衍射、扫描电镜、透射电镜和红外光谱等测试手段对产物进行分析和表征。结果表明:ZnFe2O4和Ni0.5Zn0.5Fe2O4属于立方晶系尖晶石结构,结晶完整,晶粒大小在100 nm左右。在0.2~1.8 GHz的频率下对产品进行了电磁损耗性能测试,发现Ni0.5Zn0.5Fe2O4具有较好的电磁损耗特性。     

Influence of Ag-doping in La0.5Sr0.5CoO3 on Its Structural and Magnetic Properties

The structural and magnetic properties of the mixed valent cobaltites La_0.5Sr_0.5?x Ag _x CoO₃ (0≤x≤0.15) with perovskite structure have been investigated. X-ray diffraction (XRD) analysis using Rietveld refinement shows that all our samples crystallize in the orthorhombic structure with $R\overline{3}c$ space group. Although the unit cell volume remains almost constant, the Co–O bond length and the Co–O–Co bond angle are sensitive to the Ag addition. All our studied samples undergo a paramagnetic-ferromagnetic transition with decreasing temperature. The zero field cooled (ZFC) and field cooled (FC) magnetization curves at 50 mT of La_0.5Sr_0.5CoO₃ (x=0) sample exhibits thermomagnetic irreversibility indicating frustration and competition of both antiferromagnetic and ferromagnetic interactions. It is suggested that Co³⁺ ions are in the intermediate spin state but Co⁴⁺ ions stay in a mixture of intermediate and high spin states. Ag addition leads to dramatic changes in magnetic properties. An interesting result has been obtained for La_0.5Sr_0.4Ag_0.1CoO₃, where the ZFC and FC curves coincide. For La_0.5Sr_0.35Ag_0.15CoO₃ (x=0.15) sample, the observed thermomagnetic irreversibility is much higher than that observed in x=0 sample. Hysteresis loops were recorded for x=0, 0.05, 0.1, and 0.15. The coercitive field is found to increase with Ag content reaching 0.26 T for x=0.15 whereas the remanent magnetization decreases.     

PbS插层K4Nb6O17复合物的制备及其光催化制氢活性

采用固相法合成层状半导体K4Nb6O17,通过层间离子交换反应、胺插入反应以及硫化反应制备了纳米PbS插层的K4Nb6O17复合光催化剂(记作K4Nb6O17/PbS).利用X射线衍射(XRD),场发射扫描电镜(SEM),X射线荧光光谱仪(XRF),紫外可见漫反射(UV-Vis)和分子荧光光谱(PL)等技术对其进行表征.考察了催化剂在Na2SO3和Na2S为牺牲剂的光催化制氢活性.结果表明,PbS的插层拓展了K4Nb6O17对可见光的响应,催化制氢活性也有明显提高.在紫外光和可见光下3 h产氢量分别达到123.94和0.66 mmol/(g cat).最后讨论了插层复合催化剂光生电荷转移的机理.     

Synthesis of (CrxV1−x )2O3 fine particles by a laser-induced vapor-phase reaction and their crystal structure

Single-phase crystalline fine particles of (CrxV1–x)2O3 have been synthesized by a vapor-phase explosive reaction of a gas mixture of CrO2Cl2 + VOCl3 + H2 + O2 induced by a single laser pulse. The distribution of particle size was uniform with a mean particle size of 80 nm. Lattice constants of (CrxV1–x)2O3 (x=0–1) were accurately determined by the whole-powder-pattern decomposition (WPPD) method. A sharp increase in the a axis-length and a sharp decrease in the c axis-length of the hexagonal unit cell of the oxide (x=0.03) have been observed. The crystal structures of (CrxV1–x)2O3 (x=0.15, 0.5, 0.7) were studied by Rietveld analysis.     

掺杂(Fe、Nb)SrTiO3晶界组成的电子能量损失谱(EELS)分析

采用高空间分辨率扫描透射电镜（STEM）对掺杂（Fe^3 、Nb^5 ）SrTiO3晶界进行了观察，并利用采集的电子能量损失谱（EELS）对晶界组成进行了分析，结果表明，掺杂Fe的SrTiO3陶瓷晶界存在1nm左右的非晶膜，同晶体内部相比晶界缺Sr；三叉晶界为钛基玻璃相，Ti、O及Fe含量明显高于晶界，掺Nb的SrTiO3陶瓷晶界同晶粒相比同样缺Sr，三叉晶界主要以SiO2非晶相为主，Fe^3 、Nb^5 对Ti^4 的替位及在晶界的偏析引起SrTiO3晶格畸变是导致晶界组成变化的主要原因。