高电位CuV_2O_6正极材料在热电池中的应用

采用固相法以CuO粉末和V2O5粉末为原料制备α-CuV2O6粉末,用X射线衍射分析(XRD)、差热分析(DTA)和粒度分析方法对铜钒氧材料进行了表征,并对其作为热电池正极材料的电化学行为进行了研究。电化学性能测试表明,制备的α-CuV2O6电极单体电池具有较高的放电电压和较大的放电比容量。     

WO3/BiVO4 composite photoelectrode prepared by improved auto-combustion method for highly efficient water splitting

We report on the improvement in the water splitting efficiency of a WO₃/BiVO₄ composite photoelectrode by the application of an improved auto-combustion method to the preparation of porous BiVO₄ thin films. The unique feature of this preparation method is the addition of both NH₄NO₃, as a strong oxidizing agent, and an organic additive into BiVO₄ precursor solution. The local decomposition heat of the organic additive and oxidizing agent created a porous film with small, highly crystalline BiVO₄ particles. The photoelectrode has many advantages over existing ones, such as the high light-harvesting efficiency (LHE), a single BiVO₄ phase, the facile access of the holes to the photoelectrode/electrolyte interface, and the ease of water and oxygen diffusion. The maximum incident photon-to-current efficiency (IPCE) was estimated to be 64% (at 440 nm, 1.23 V vs. RHE) and the applied bias photon-tocurrent efficiency (ABPE) reached as high as 1.28%. This ABPE value is highest among all oxide semiconductor photoelectrodes reported previously, except for the case of a stacking photoelectrode system.     

Effect of Eu3+-doping on morphology and fluorescent properties of neodymium vanadate nanorod-arrays

Tetragonal structural (t-NdVO₄) nanorod-arrays were fabricated by simple one-pot hydrothermal method. The phase, morphology and microstructure of NdVO₄ were characterized by X-ray diffractometer, scanning electron microscope (SEM), transmission electron microscope (TEM), dispersive X-ray spectrometer (EDS) and selected area electron diffraction (SAED) techniques. t-NdVO₄ nanorods are single-crystalline with a length of 100 nm and a diameter of 25 nm, which grow orientally along the direction of (112) crystalline plane and self-assemble to form nanorod-arrays. The results show that Eu³⁺-doping interrupts the formation of NdVO₄ nanorod-arrays, and then leads to the red-shift of the strongest luminescence emission of Nd³⁺ transition from ⁴D_3/2 state to ⁴I_11/2 and decreases its intensity of the fluorescence emission at 400 nm sharply. The research results have some reference values to optimize the photoluminescence performance of rare earth vanadates.     

Construction of BiVO4 nanosheets@WO3 arrays heterojunction photoanodes by versatile phase transformation strategy

A versatile phase transformation strategy was proposed to synthesize novel BiVO₄ nanosheets (NSs)@WO₃ nanorod (NR) and nanoplate (NP) arrays films. The strategy was carried out by following a three-step hydrothermal process (WO₃→WO₃/Bi₂WO₆→WO₃/BiVO₄). According to the characterization results, plenty of BiVO₄ NSs grew well on the surface of WO₃ NR and NP arrays films, thus forming the WO₃/BiVO₄ heterojunction structure. The prepared WO₃/BiVO₄ heterojunction films were used as the photoanodes for the photoelectrochemical (PEC) water splitting. As indicated by the results, the photoanodes exhibited an excellent PEC activity. The photocurrent densities of the WO₃/BiVO₄ NR and NP photoanodes at 1.23 V (vs RHE) without cocatalyst under visible light illumination reached up to about 1.56 and 1.20 mA/cm^brespectively.     

铝酸钠溶液中钒酸盐的析出行为研究

以氧化铝生产流程中氢氧化铝的洗涤液为原料,研究了苛性碱浓度、反应温度及反应时间对溶液中钒酸盐析出情况的影响。结果表明,钒酸盐的析出率随苛性碱浓度的升高和反应时间的延长而增大,随反应温度的升高而减小。当铝酸钠溶液的苛性碱浓度为200g/L、反应温度为30℃、反应时间为72h时,溶液中的钒元素可减少60%以上。结晶析出的钒酸盐主要为钒酸钠和偏钒酸钠,其晶体结构为八面体。     

水热法制备BiVO_4及其光催化性能研究

采用水热反应法并改变反应条件制备不同形貌和晶体结构的BiVO4可见光催化剂,并探讨不同形貌BiVO4的形成机制及其光催化活性的影响因素。借助X-射线衍射（XRD）、扫描电子显微镜（SEM）及固体紫外-可见漫反射光谱（DRS）对产品进行表征,并在可见光（λ〉420 nm）照射下考察其降解亚甲基蓝（MB）的光催化性能。结果表明,高温更有利于单斜型钒酸铋的生成,反应初始pH值对钒酸铋的形貌影响较大。反应过程中,前驱液中的颗粒通过溶解再结晶、定向聚集自组装、熟化过程最终形成不同形貌的钒酸铋颗粒。钒酸铋的光催化降解速率主要受其晶粒粒径和晶体微观应变的影响,晶粒粒径越大,微观应变越小,结晶度越好,降解速率越高。     

新型钒酸盐混晶Nd∶Gd_(0.42)Y_(0.58)VO_4/Cr~(4+)∶YAG被动调Q锁模特性研究

研究了Nd∶Gd0.42Y0.58VO4混晶的激光运转特性。采用Cr4+∶YAG晶体作为被动可饱和吸收体,实现了Nd∶Gd0.42Y0.58VO4混晶的调Q锁模激光运转。实验测量了不同Cr4+∶YAG初始透过率情况下激光器的输出特性。在Cr4+∶YAG初始透过率T0=86.3%,输出镜透过率T=10%时,调Q锁模运转阈值为2.8 W,随着抽运功率的增加,调制深度逐渐加大。采用透过率T=20%的输出镜,注入抽运功率10.3 W时,调Q锁模深度约为70%,相应的脉冲包络重复频率为40 kHz,半高宽度为25 ns,平均输出功率为2.58 W,光-光转换效率为25%。     

无铅低熔玻璃的研究及其进展

随着欧盟RoHS绿色指令的颁布和人类环保意识的增强，低熔点玻璃无铅化已越来越受到人们的重视。概述了无铅低熔玻璃的国内外研究现状，对无铅硼酸盐、磷酸盐、钒酸盐玻璃等体系的组成以及物化性能进行了较为全面的介绍，并分析了无铅低熔玻璃今后发展的难点和趋势。     

Synthesis of manganese vanadate nanobelts and their visible light photocatalytic activity for methylene blue

Manganese vanadate nanobelts have been synthesised by a simple hydrothermal process using polymer polyvinyl pyrrolidone as the surfactant by adjusting the pH value. The X-ray diffraction, selected area electron diffraction and the high-resolution transmission electron microscopy (TEM) show that the manganese vanadate nanobelts are composed of a single crystalline monoclinic Mn₂V₂O₇ phase. Scanning electron microscopy and TEM observations show that the thickness, width and length of the nanobelts are 20 nm, 350 nm–1 μm and several dozens to several hundreds of micrometres, respectively. The photocatalytic activities of the manganese vanadate nanobelts have been evaluated by the photocatalytic degradation of methylene blue (MB) in an aqueous solution as a model pollutant under the solar light irradiation. After 4 h of the irradiation by the solar light, the MB solution with the volume of 10 mL and the concentration of 10 mg·mL^?1 can be totally degraded using 10 mg manganese vanadate nanobelts.     

Structures of sodium vanadate solution under different conditions

Combined with Fourier transform infrared spectroscopy(FTIR) analysis of sodium vanadate solution,the relationship between conductivity and structure was investigated by measuring the electric conductivity of the solution under different alkali concentrations and molar ratios of NaOH to V_2O_5. Results suggest that the polymerization vanadium acid radical ions gradually transform into monomer with the solution diluting. When the solution is diluted to a certain extent,only the vanadium acid radical ion with V-OH chemical bond exists in the solution. At NaOH concentration of below 105.21 g·L^-1,the vanadate anions mainly exist in the form of vanadium acid radical ion with V-OH chemical bond and the ion transference number is approximately from 0.58 to 0.82. In the medium NaOH concentration range of 105.21-117.03 g·L^-1, the vanadate anions mostly exist in the form of vanadium acid radical ion with V-OH and V-O-V chemical bonds and the ion transference number is approximately 3.29. At NaOH concentration of above 117.03 g·L^-1, vanadate anions exist in the form of vanadium acid radical ion with V-OH and V-O-V chemical bonds.