Thermoelectric properties of Ag-doped n-type (Bi2Te3)0.9-(Bi2−xAgxSe3)0.1 (x=0-0.4) alloys prepared by spark plasma sintering

Ag-doped n-type (Bi₂Te₃)_0.9-(Bi_2−xAg_xSe₃)_0.1 (x=0-0.4) alloys were prepared by spark plasma sintering and their physical properties evaluated. When at low Ag content (x=0.05), the temperature dependence of the lattice thermal conductivity follows the trend of (Bi₂Te₃)_0.9-(Bi₂Se₃)_0.1; while at higher Ag content, a relatively rapid reduction above 400 K can be observed due possibly to the enhancement of scattering of phonons by the increased defects. The Seebeck coefficient increases with Ag content, with some loss of electrical conductivity, but the maximum dimensionless figure of merit ZT can be obtained to be 0.86 for the alloy with x=0.4 at 505 K, about 0.2 higher than that of the alloy (Bi₂Te₃)_0.9-(Bi₂Se₃)_0.1 without Ag-doping.     

Thermoelectric properties of Cu-doped n-type (Bi2Te3)0.9–(Bi2−xCuxSe3)0.1(x=0–0.2) alloys

n-Type (Bi₂Te₃)_0.9–(Bi_2−xCu_xSe₃)_0.1 (x=0–0.2) alloys with Cu substitution for Bi were prepared by spark plasma-sintering technique and their structural and thermoelectric properties were evaluated. Rietveld analysis reveals that approximate 9.0% of Bi atomic sites are occupied by Cu atoms and less than 4.0 wt% second phase Cu_2.86Te₂ precipitated in the Cu-doped parent alloys. Measurements show that an introduction of a small amount of Cu (x0.1) can reduce the lattice thermal conductivity (κ_L), and improve the electrical conductivity and Seebeck coefficient. An optimal dimensionless figure of merit (ZT) value of 0.98 is obtained for x=0.1 at 417 K, which is obviously higher than those of Cu-free Bi₂Se_0.3Te_2.7 (ZT=0.66) and Ag-doped alloys (ZT=0.86) prepared by the same technologies.     

Bi2WO6量子点(QDs)修饰Bi2MoO6-xF2x异质结的构筑及其催化活性增强机理

采用简单沉积-沉淀法合成了Bi₂WO₆@Bi₂MoO_6-xF_2x（BWO/BMO6-xF2x）异质结,借助XRD、XPS、TEM、SEM、EDS、UV-Vis-DRS、PC和EIS等测试技术对其组成、形貌、光吸收特性和光电化学性能等进行系统表征,并以模型污染物罗丹明B（RhB）的光催化降解作为探针反应来评价Bi₂WO₆@Bi₂MoO_6-xF_2x异质结的光催化活性增强机制。形貌分析表明,所得Bi₂MoO₆微球由大量厚度为20~50 nm的纳米片组成;FE-SEM和HR-TEM分析表明,尺寸约为10 nm的Bi₂WO₆量子点均匀沉积在Bi₂MoO_6-xF_2x微球表面,形成新颖的Bi₂WO₆@Bi₂MoO_6-xF_2x异质结;与纯Bi₂MoO₆或者Bi₂WO₆相比,1∶1Bi₂WO₆@Bi₂MoO_6-xF_2x异质结表现出更好的光催化活性和光电流性质,其对RhB光催化降解的表观速率常数分别为纯BMO和BWO的6.4和11.6倍。PC和EIS图谱分析表明,Bi₂WO₆量子点表面沉积显著提高Bi₂MoO_6-xF_2x光生电子/空穴的分离效率和迁移速率;活性物种捕获实验证明了·O₂^-和h⁺是主要的活性物种。根据实验结果,探讨了F^-掺杂和Bi₂WO₆量子点之间的协同效应对Bi₂MoO₆的光催化活性的影响机制。     

Bi2WO6量子点(QDs)修饰Bi2MoO6-xF2x异质结的构筑及其催化活性增强机理

采用简单沉积-沉淀法合成了Bi_2WO_6@Bi_2MoO_(6-x)F_(2x)(BWO/BMO_(6-x)F_(2x))异质结,借助XRD、XPS、TEM、SEM、EDS、UV-Vis-DRS、PC和EIS等测试技术对其组成、形貌、光吸收特性和光电化学性能等进行系统表征,并以模型污染物罗丹明B(Rh B)的光催化降解作为探针反应来评价Bi_2WO_6@Bi_2MoO_(6-x)F_(2x)异质结的光催化活性增强机制。形貌分析表明,所得Bi_2MoO_6微球由大量厚度为20~50 nm的纳米片组成;FE-SEM和HR-TEM分析表明,尺寸约为10 nm的Bi_2WO_6量子点均匀沉积在Bi_2MoO_(6-x)F_(2x)微球表面,形成新颖的Bi_2WO_6@Bi_2MoO_(6-x)F_(2x)异质结;与纯Bi_2MoO_6或者Bi_2WO_6相比,1∶1Bi_2WO_6@Bi_2MoO_(6-x)F_(2x)异质结表现出更好的光催化活性和光电流性质,其对RhB光催化降解的表观速率常数分别为纯BMO和BWO的6.4和11.6倍。PC和EIS图谱分析表明,Bi_2WO_6量子点表面沉积显著提高Bi_2MoO_(6-x)F_(2x)光生电子/空穴的分离效率和迁移速率;活性物种捕获实验证明了·O_2~-和h~+是主要的活性物种。根据实验结果,探讨了F-掺杂和Bi_2WO_6量子点之间的协同效应对Bi_2MoO_6的光催化活性的影响机制。     

A TEM, XRD, and crystal chemical investigation of oxygen/vacancy ordering in (Ba1−xLax)2In2O5+x, 0x0.6

A careful TEM and XRD study of the (Ba_1−xLa_x)₂In₂O_5+x, 0x0.6, ‘defect-perovskite’-type solid solution has been carried out. A well-defined structural phase transition is shown to occur between x=0.1 and 0.2 from the orthorhombic brownmillerite structure type on the low x side to a multiple twinned, tetragonal 1×1×2 perovskite-related superstructure phase on the high x side at x=0.2. This phase transition correlates with an important phase transition previously observed in electrical conductivity versus temperature measurements. The existence of additional satellite reflections close to the regions of reciprocal space was found to be typical of all (Ba_1−xLa_x)₂In₂O_5+x specimens, although their intensity relative to the parent Bragg reflections systematically reduces as x increases. As x increases beyond 0.2, the -type satellite reflections initially become weaker and rather more diffuse for x=0.3 before splitting into pairs of rather weak and somewhat diffuse incommensurate satellite reflections for x=0.4 and beyond. An interpretation in terms of oxygen vacancy ordering and associated structural relaxation is given. Additional structured diffuse scattering is also observed and a tentative explanation in terms of Ba/La ordering and associated local strain distortions put forward.     

固溶体Bi_2Mo_(1-x)W_xO_6的水热合成及光催化性能

采用水热法,在较低温度下合成了系列Bi2Mo1-xWxO6固溶体。结果表明,W的替代抑制了固溶体的晶粒生长,导致了较小的晶粒尺寸。随着x的增加,红外光谱中840cm-1处M-O键的振动频率νM-O有规律地向低频率方向移动,表明Mo6+离子逐步被W6+替代,生成了无限互溶的固溶体。光吸收性能研究表明,随着W6+逐步替代Mo6+,带隙出现了先降后升的趋势,x=0.4时带隙最小。而固溶体的光催化性能随着x的增加,出现了先增后减的趋势,x=0.4时光催化活性最高。此外,含W样品的光催化活性高于Bi2MoO6。这与固溶体的带隙、带结构和晶粒尺寸变化有关。     

Pressure Dependence of the Lattice Distortion in Perovskite La0.5−xBixCa0.5MnO3 (x=0.1, 0.15, 0.2)

The in situ behavior of distorted perovskite La_0.5−xBi_xCa_0.5MnO₃ (x=0.1, 0.15, 0.2) under high pressure has been studied by energy-dispersive X-ray diffraction in a diamond anvil cell. An abnormal change of the 202–040 d-spacing ascribed to the disappearance of the distortion mode Q₂ in the MnO₆ octahedra is observed at 1.2, 1.4, and 1.6 GPa, respectively, and it results in a reduction of the Jahn–Teller distortion commonly existing in the manganites. Effect of the unique 6s² long-pair character of the Bi³⁺ ion on the pressure dependence of the lattice distortion is discussed.     

Preparation and characterization of lithium ion-conducting glass-ceramics in the Li1 + xCrxGe2 − x(PO4)3 system

Li₂O–Cr₂O₃–GeO₂–P₂O₅ based glasses were synthesized by a conventional melt-quenching method and successfully converted into glass-ceramics through heat treatment. Experimental results of DTA, XRD, ac impedance techniques and FESEM indicated that Li_1.4Cr_0.4Ge_1.6(PO₄)₃ glass-ceramics treated at 900 °C for 12 h in the Li_1 + xCr_xGe_2 − x(PO₄)₃ (x = 0–0.8) system exhibited the best glass stability against crystallization and the highest ambient conductivity value of 6.81 × 10⁻⁴ S/cm with an activation energy as low as 26.9 kJ/mol. In addition, the Li_1.4Cr_0.4Ge_1.6(PO₄)₃ glass-ceramics displayed good chemical stability against lithium metal at room temperature. The good thermal and chemical stability, excellent conducting property, easy preparation and low cost make it promising to be used as solid-state electrolytes for all-solid-state lithium batteries.     

用于NO_x低温下吸附还原的CoO_x/CeO_2二元氧化物的制备

研究了以多孔二氧化硅微球和活性炭为载体制备NOx吸附/还原催化剂的方法,摸索了最佳Ce/Co物质的量的比例。采用低温氮吸附方法测定了样品的BET比表面和孔容,利用XRD方法表征了样品中所掺杂的金属元素的晶型。研究发现:当nCe/nCo=75/25时,材料获得最佳NOx吸附能力,当以多孔二氧化硅微球作载体时,材料对于NOx的吸附主要来自CoOx和CeO2的二元氧化物;当以活性炭作为载体时,活性炭参与了NOx的吸附,因此其吸附容量大大提高。对NOx的吸附机理进行了探讨,并研究了样品的NH3还原性质。     

Analysis of thermo-magnetic fluctuations above the glass-transition temperature in Bi1.6Pb0.5Sr2−xEuxCa1.1Cu2.1O8+δ (0.000 ≤ x ≤ 0.180) system

The resistivity of Bi_1.6Pb_0.5Sr_2−xEu_xCa_1.1Cu_2.1O_8+δ (0.000 ≤ x ≤ 0.180) superconductor has been measured as a function of temperature and magnetic field. The resistivity shows a glassy behavior even at higher temperatures and magnetic fields for the Eu-doped samples as compared with the Eu free sample. The values of glass-transition temperature [T_g], magnetic field dependent activation energy [U₀(B)] and the temperature and magnetic field dependent activation energy [U₀(B,T)] are found to be maximum for optimal doping levels (x = 0.135) which shows that the flux lines are effectively pinned in this sample. Also for temperatures below the superconducting transition temperature (T_C), a scaling of measured resistivity curves in magnetic field (B = 0.4 and 0.8 T) is obtained and this scaling is quite useful for better understanding of the behavior of the flux vortices in high temperature superconductors.     

The metastable Ni7±xS6, and mixed Ni6±x(S1−ySey)5, phases

The closely related, narrowly non-stoichiometric, metastable as well as thermodynamically stable “phases” in the metal-rich part of the Ni–S phase diagram near the nominal composition Ni_7±xS₆ have been carefully re-investigated via electron diffraction and transmission electron microscope imaging. Two quite distinct polymorphs have been identified, a minority incommensurate interface-modulated polymorph and a (heavily twinned) majority I1a1, a=2a_p, b=2b_p, c=−a_p+c_p superstructure (of an underlying Bmmb, a_p3.3, b_p16.4, c_p11.3 Å parent structure) polymorph. The incommensurate polymorph is shown to be very closely related to the only known polymorph of Ni_6±xSe₅ and is rapidly stabilized to room temperature upon doping of the sulfide compounds with selenium.     

Synthesis and characterization of the new pyrochlore Bi1.5Sb1.5−xNbxMnO7 solid solution

The solid solution with formula Bi_1.5Sb_1.5−xNb_xMnO₇ has been synthesized using the ceramic method at 1000 °C. This solid solution was crystallized in the pyrohlore structure in cubic lattice with Fd-3 m space group. The cell parameter increases linearly with increase in the niobium concentration. The magnetic susceptibility measurements achieved between 4 and 300 K show a paramagnetic behaviour with an effective moment 5.84 μ_β for Bi_1.5Sb_1.5MnO₇ compound (x = 0) and 5.61 μ_B for Bi_1.5Nb_1.5MnO₇ compound (x = 1.5) indicating “ + 2” oxidation state for manganese ion. The electric conductivity measured using the complex impedance spectroscopy method put in evidence an increase of the electric conductivity with the temperature, and the antimony compound is slightly more conductor than the niobium compound; results indicate electronic conductivity with semi-conducting behaviour.     

室温电化学沉积Ba1-xCaxMoO4多晶固溶体薄膜

近年发展起来的制备功能薄膜的电化学沉积技术,是软溶液工艺路线(Soft Solution Processing简记为SSP)中的重要技术[1]。与传统的薄膜制备技术相比,电化学沉积技术在反应控制、形貌控制、沉积速度、能量消耗、环境影响、薄膜晶化以及沉积设备等方面都有较明显的优势,同时避免了     

NixCo3-xO4表面修饰对CdSe/TiO2纳米管阵列光电化学氧化水活性的影响

利用氨挥发诱导法在CdSe/TiO2纳米管阵列表面负载一层NixCo3-xO4。采用SEM、XRD、XPS、UV-Vis对样品进行表征,通过线性扫描伏安法测定光阳极的释氧电势来评价其光电水氧化活性。结果表明:表面NixCo3-xO4是尖晶石结构;相对于CdSe/TiO2纳米管阵列光阳极,NixCo3-xO4/CdSe/TiO2光阳极能将光电氧化水的过电势降低430 mV。Ni离子的引入使得NixCo3-xO4表面富含三价阳离子(Ni3+,Co3+),从而促进CdSe/TiO2光阳极光电水氧化的进行。     

Effect of strontium substitution on the activity of La2?xSrxNiO4 (x = 0.0–1.2) in NO decomposition

The aim of this work is to study the effect of Sr substitution on the redox properties and catalytic activity of La_2−x Sr _x NiO₄ (x = 0.0–1.2) for NO decomposition. Results suggest that the x = 0.6 sample shows the highest activity. The characterization (TPD, TPR, etc.) of samples indicates that the x = 0.6 sample possesses suitable abilities in both oxidation and reduction, which facilitates the proceeding of oxygen desorption and NO adsorption. At temperature below 700°C, the oxygen desorption is difficult, and is the rate-determining step of NO decomposition. With the increase of reaction temperature (T > 700°C), the oxygen desorption is favorable and, the active adsorption of NO on the active site (NO + V _o + Ni²⁺ → NO⁻-Ni³⁺) turns out to be the rate-determining step. The existence of oxygen vacancy is the prerequisite condition for NO decomposition, but its quantity does not relate much to the activity. Supported by the National Hi-Tech Research and Development Program of China (863 Program)(Grant No. 2004CB 719502) and the National Natural Science Foundation of China (Grant No. 20177022)     

尖晶石型LiMn2-xInxO4(x=0，0.01，0.02，0.05)的合成及电化学性能研究

以醋酸锰、氢氧化锂和三氧化二铟为原料,以柠檬酸为配位剂,采用溶胶-凝胶法制备了掺杂In的尖晶石LiMn2-xInxO4(x=0,0.01,0.02,0.05),采用XRD、SEM对目标材料进行了结构和形貌表征,采用恒流充放电、循环伏安(CV)以及交流阻抗(EIS)谱测试对材料进行了电化学性能表征,考察了不同In掺杂量对材料性能的影响。结果表明,当In掺杂量为1%时,LiMn1.99In0.01O4样品具有纯的尖晶石锰酸锂结构,在0.5C和3.4～4.35 V电压范围条件下,LiMn1.99In0.01O4的初始放电容量为119.9 mAh.g-1,经过1C 30次,2C 30次,再0.5C 5次循环后,其放电容量保持率为84.9%,显示了良好的电化学性能。掺杂1%的In的样品比未掺杂的样品具有更优的高温循环稳定性能。     

Bismuth coordinance in dilute alloys of the noncrystalline Se100−xBix system

The glass transition temperature, T_g, and the coordination peak of the radial distribution function, obtained from electron diffraction experiments, are studied for amorphous thin films of the Se_100−xBi_x system (x ≤ 8) prepared by vacuum evaporation. The controversial problem of the coordination of Bi in these alloys is raised. The T_g data versus composition are analyzed by means of a simple analytic model. All results can be interpreted by assuming that the average coordination of Bi for the more dilute portions of the system is four, as opposed to the expected value of three, and three when x is greater than 5.     

Synthesis and properties of the Co7Se8−xSx and Ni7Se8−xSx solid solutions

We report the synthesis and elementary properties of the Co₇Se_8−xS_x (x=0-8) and Ni₇Se_8−xS_x (x=0-7) solid solutions. Both systems form a NiAs-type structure with metal vacancies. In general, the lattice parameters decrease with increasing x, but in the Ni₇Se_8−xS_x system c increases on going from x=5 to 7. Magnetic susceptibility measurements show that all samples exhibit temperature-independent paramagnetism from 25-250 K. Samples within the Co₇Se_8−xS_x system, as well as Ni₇Se₈ and Ni₇SeS₇, were found to be poor metals with resistivities of ∼0.20 and ∼0.06 mΩ cm at 300 K, respectively. The Sommerfeld constant (γ) was determined from specific heat measurements to be ∼13 mJ/mol_CoK² and ∼7 mJ/mol_NiK² for Co₇Se_8−xS_x and Ni₇Se_8−xS_x, respectively.     

正极材料Li(Ni0.5Mn0.5)1-xMxO2 (M=Ti，Al；x=0，0.02)电化学行为的比较研究

0IntroductionMany efforts have been made to develop newmaterials as an alternative to LiCoO2due to the rela-tively high cost and toxicity of Co.Much attention hasbeen paid to layered structure cathode materials suchas LiMnO2and LiNiO2due to their lower co…     

Metal-organic deposition of YBa2Cu3Ox and Bi2Sr2Ca1Cu2Ox films on various substrates starting from different fluorine-free metallorganic compounds

YBa₂Cu₃O_x (Y-123) and Bi₂Sr₂Ca₁Cu₂O_x (Bi-2212) films on various substrates have been prepared by Metal-Organic Deposition starting from different metallorganic fluorine-free compounds and using a very simple instrumentation. The processing conditions include a rapid pyrolysis step in air and an annealing step in oxygen for Y-123 and in air for Bi-2212. The films obtained have been characterized by X-ray diffraction (XRD) and the formation of a superconducting phase of Y-123 or Bi-2212 was confirmed measuring the critical temperature (T _c) with Ac-susceptibility and resistive measurements. Microstructure and final cationic ratios have been studied by scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS).