白钨矿结构BiVO4的水热合成及其可见光催化性能

以Bi(NO3)3·5H2O和NH4VO3为原材料,采用水热法合成了BiVO4可见光催化材料,并采用XRD、SEM和UV-Vis等对合成产物的物相结构、形貌、光吸收性能以及光催化性能进行了研究。研究表明,反应体系的pH值对合成产物的物相结构具有重要的影响,在酸性和弱碱性条件下可获得具有不规则纳米片状形貌的单斜白钨矿结构BiVO4晶体。合成产物对波长小于525nm的光具有强烈的吸收。水热条件的不同直接影响着产物对甲基橙溶液的可见光催化降解性能,在Bi∶V比例为1∶1,同时pH值为3.08并于160℃下水热处理1h所合成的BiVO4晶体对甲基橙溶液具有最佳的可见光催化活性。     

大孔TiO_2-ZnO复合纳米材料的制备及其性能

采用溶胶-凝胶法和胶态晶体模板法,制备了大孔TiO2-ZnO复合纳米材料。其晶相结构和形貌特征采用X射线粉末衍射(XRD)、透视电子显微镜(TEM)进行了表征,并以甲基橙为降解对象,对其光催化活性进行了研究。结果表明,采用无皂乳液聚合法得到的聚苯乙烯(PS)微球粒径均匀,为900nm。以紧密堆积的PS胶态晶体为模板,制得的TiO2-ZnO复合纳米材料的大孔孔径约为900nm,孔壁厚度约为20nm。XRD结果显示,材料中的TiO2为锐钛矿型。光催化降解结果表明,大孔TiO2-ZnO复合纳米材料对甲基橙降解1.5h后降解率可达91.3%,与普通的TiO2-ZnO纳米粉体材料相比提高了11.2%.     

膜厚对Ag-TiO2薄膜光学性能和光催化性能影响的研究

采用电子束沉积方法制备了Ag-TiO₂光催化剂 ,采用电子扫描显微镜(SEM)、X射线衍射仪(XRD)、透 射电镜(TEM)、紫外-可见(UV-Vis)光谱仪和原子力显微镜(AFM)等手段对薄膜的形貌、物 相 组成,吸收光谱和粗糙度进 行了表征。利用太阳光,以甲基橙(MO)为模拟污染物,考察光催化剂的光催化活性,探讨了薄 膜厚度对光催化 效率的影响。结果表明,在300℃温度下,所形成的薄膜 为无定形结构 ;当薄膜厚为570nm时,降解40days后,MO的降 解率达到55%。     

锐钛型纳米TiO_2光催化性能的研究

以TiCl4为原料,采用沸腾回流强迫水解法制备纳米TiO2,用XRD、TEM对粉体进行表征。采用甲基橙溶液进行光催化降解试验,研究了TiO2的煅烧温度、添加量以及溶液的初始pH值对光催化性能的影响。实验结果表明,当溶液pH=2,TiO2煅烧温度为600℃,添加量为0.8 g/L,光催化75 min甲基橙的脱色率为90.87%。     

银纳米颗粒修饰TiO2薄膜的结构,光学及光催化性能

采用电子束沉积技术在石英玻璃、硅片基板上沉积了TiO₂薄膜,利用热蒸发技术在TiO₂薄膜表面沉积了不同厚度的Ag膜,研究了Ag膜厚度对TiO₂薄膜结构、形貌、光学和光催化 性能的影响。利 用紫外-可见分光光度计(UV-VIS)、X射线衍射仪(XRD)、冷场发射电子显微镜(SEM)对沉积 后的薄膜分别 进行光学、结构、形貌分析。利用能谱仪测定了元素成分及含量。用光催化降解亚甲基橙(M O)的速率评 价了合成的Ag-TiO₂的光催化性能。结果表明:Ag纳米粒子在TiO₂表面均匀分布;制备 的Ag修饰多孔TiO₂纳米薄膜具有优异的光催化性能。测试结果表明:在250 ℃下制备的T iO₂薄膜为无定形结构;随着Ag膜厚度 的增加,样品的光催化活性提高。当Ag膜厚度为3.7 nm时,光催化活 性最高;与纯TiO₂相比,Ag-TiO₂具有更高的光催化活性。     

纳米Cu2O粉体的室温固相合成及其光催化性能

以硫酸铜、氢氧化钠、葡萄糖为原料,室温固相合成了纳米氧化亚铜粉体;利用X-射线衍射(XRD)和透射电子显微镜(TEM)对所得氧化亚铜粉体进行了表征;研究了在紫外光和太阳光下,所得氧化亚铜粉对甲基橙溶液的光催化降解效果.结果表明,所得产物为氧化亚铜,粒径为10～20nm,在紫外光和日光下均有较好的催化性能.     

基于石墨毡生长的镍钴基化合物电极的双功能电催化性能

以先水热后硫化的方法制备出基于石墨毡基底的镍钴基化合物(NiCo2O4/GF和NiCo2 S4/GF)电极,探究不同水热温度对电极的催化特性的影响.通过扫描电子显微镜(SEM)、能量色散X射线光谱仪(EDS)、X射线衍射仪(XRD)和X射线光电子能谱仪(XPS)对样品表面形貌、结构、晶向及元素分布进行分析.通过循环伏安...     

自组装Fe_2O_3超薄圆饼的制备及其可见光催化性能

采用水热法成功制备出厚度约为6 nm、直径为(90±10)nm的Fe_2O_3超薄圆饼结构。通过X射线衍射仪(XRD)、扫描电子显微镜(SEM)、透射电子显微镜(TEM)、BrunauerEmmett-Teller (BET)和紫外可见光分光光度计(UV-Vis)等测量手段分别对样品的结构、形貌、比表面积和光电性能进行表征,结果表明:Fe_2O_3超薄圆饼结构由平均直径为5.5 nm,比表面积高达256.2 m~2·g~(-1)的超细Fe_2O_3纳米颗粒组装而成,超细Fe_2O_3纳米颗粒的组装造成其颗粒间存在较多间隙,这就使Fe_2O_3超薄圆饼的最终产物上具有大量的活性位点,为其光催化应用提供了良好的条件。在可见光照射下,材料对罗丹明B、刚果红和甲基橙三种不同类型染料分子的光催化实验结果表明,由(001)裸露晶面为主导的Fe_2O_3超薄圆饼对阳离子型的染料分子具有优异的可见光催化性能。     

种子辅助化学法合成ZnO纳米棒及其表征

低温条件下(95℃),采用ZnO种子辅助化学反应法,成功制备了宏量直、细的ZnO纳米棒;用X射线衍射(XRD)、扫描电子显微镜(SEM)、透射电子显微镜(TEM)等分析手段对纳米棒的结构和形貌进行了表征;同时还对ZnO纳米棒的形成机理作了分析;并以ZnO纳米棒作为光催化荆,对甲基橙(MO)溶液进行了光催化实验.结果表明,ZnO与Zn源的摩尔比对ZnO纳米棒的形貌影响很大,PVA通过空间位阻效应控制ZnO纳米棒的长度,ZnO纳米棒有较好的光催化活性.     

Bi_2O_3/TiO_2纳米复合物的微波合成及光催化性质

以硝酸铋和硫酸钛为原料,通过直接投料微波辐射水解合成法制备了掺铋TiO2纳米复合物,并用XRD、TEM进行了表征。结果表明,直接投料摩尔比为1∶10掺铋TiO2纳米复合物,经500℃热处理后晶型为锐钛矿型,粒径为6～10nm。以催化降解甲基橙来考察其光催化活性,结果表明所制备的纳米复合物是一个好的催化剂。研究了Bi3+的掺杂量、热处理温度、催化剂用量对掺铋TiO2纳米复合物光催化性能的影响。当催化剂用量为1g/L时,2mg/L的甲基橙溶液在紫外光辐射30min后,降解率达到97%。该复合物对甲基橙溶液的光催化降解符合一级动力学方程。     

SnO2纳米棒阵列的制备及光学、场发射性能研究

采用简单的一步水热法直接在不锈钢基底上制备了不同形貌的SnO2纳米棒阵列。利用X射线衍射（XRD）,扫描电镜（SEM）、透射电镜（TEM）、 分光光度计、场发射装置对材料的结构、形貌、光致发光谱和场发射特性进行了表征。XRD结果表明不锈钢基底上制备的样品为四方晶系金红石结构。SEM和TEM结果表明不同的反应条件下都能够在基底上大面积的垂直生长单晶SnO2纳米棒阵列,但是形貌和尺寸发生了改变（A:针尖状,B:铅笔状）。室温下的光致发光光谱（PL）表明两种样品在367、392、419 nm处分别存在较强的发射峰,并且紫外光峰强与可见光峰强比值较大,说明样品的结晶质量较好。场发射测试结果表明:两种样品的场发射都是通过电子隧道效应进行的,且样品A的场发射性能优于样品B。     

Microwave assisted synthesis of ZnO nanoparticles in ionic liquid [Bmim]cl and their photocatalytic investigation

In this study, ZnO nanoparticles were synthesized based on the chemical reaction of zinc acetate and NaOH in ionic liquid 1-butyl-3-methylimidazolium chloride ([Bmim]Cl) under microwave irradiation. The prepared ZnO were characterized by utilizing various techniques such as X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), UV–Vis spectroscopy, FT-IR spectroscopy, and BET method. XRD pattern reveals the produced ZnO has hexagonal structure and the images of SEM and TEM also reveal it consists of nanoparticles with an average size between 15 and 25 nm. The role of the ionic liquid on morphology of ZnO was investigated. For this purpose, a control ZnO sample was prepared without using any [Bmim]Cl. Photocatalytic properties of the synthesized ZnO on degradation of malachite green dye as model pollutant was investigated. The effect of various parameters such as pH, concentration of the dye and catalyst on the degradation of malachite green was investigated. In order to explore the mechanism of photocatalytic degradation of malachite green, scavenger addition method has been employed. It is found that hydroxide radicals are main reactive species for the degradation.     

在家用微波炉中合成四针状ZnO

将锌粉和石墨粉以一定比例混合放入家用微波炉中,在微波辐照下燃烧生成了白色松软的ZnO膜,将此薄膜用扫描电子显微镜(SEM)、能量损失谱(EDS)、透射电子显微镜(TEM)和X射线衍射光谱(XRD)分析其成分和形貌。结果显示,该ZnO为单晶四针状晶须,晶须直径为20~50nm,分析了它的生长机理并测试其场发射特性,得到该ZnO的开启场强较低为3.88V/μm,相应的电流密度为10μA/cm2,在场强为5.7V/μm时达到最大发射电流密度为0.39mA/cm2。     

竹叶状ZnS纳米带的生成与表征

通过无催化物理热蒸发ZnS粉末的方法成功地制备了一种新颖的竹叶状ZnS纳米带。X射线衍射分析和扫描电镜透射电子显微镜,用来对ZnS生长物进行表征,检测显示,所制得的竹叶状纳米带的厚度50～100nm,度宽500～600nm,长度数十微米。透射电镜和选区电子衍射花样表明,制备的纳米带是单晶六角纤锌矿结构。样品的光学性能显示在424nm处有一个强烈的蓝光发射,这种发射是由于氧空位和其他表面态造成的。同时对纳米带的生长机制作了论述。     

Greener Electrochemical Synthesis of High Quality Graphene Nanosheets Directly from Pencil and its SPR Sensing Application

A green, simple, and cost effective electrochemical method to synthesize pure graphene oxide (GO) and graphene nanosheets (GNs) using pencil in ionic liquid medium is reported. The morphology and microstructure of prepared GNs and GO are examined using scanning electron microscopy (SEM), transmission electron microscopy (TEM), atomic force microscopy (AFM), X‐ray diffraction (XRD), and Raman spectroscopy; the experiments confirm the formation of high quality graphene. The synthesized GO is used for the real‐time and label‐free surface plasmon resonance (SPR) sensing of the biological warfare agent Salmonella typhi.     

ZnO纳米晶须的形态控制及其结构表征

采用激光分子束外延法先在Si(111)衬底上制备Zn薄膜,在不同的氧气体积流量和生长温度下,用热蒸发法在镀有Zn薄膜的Si(111)衬底上制备了不同形貌的ZnO纳米晶须。分别用X射线衍射(XRD)、扫描电子显微镜(SEM)、透射电子显微镜(TEM)和高分辨透射电子显微镜(HRTEM)对样品的成分、微结构和形貌进行了表征。Zn薄膜在高温下被氧化,并为晶体生长提供均匀的成核点,有利于形成一定大小和数量的ZnO晶核。研究结果表明,氧气体积流量和生长温度对ZnO纳米晶须的形貌有一定的影响。     

基于ZnO纳米片/纳米球复合结构光阳极的染料敏化太阳电池

将电沉积和溶剂热方法制备的ZnO纳米片阵列和ZnO纳米球组装成ZnO纳米片/纳米球复合结构光阳极,并应用 透射电镜(TEM)、扫描电镜(SEM)、X射线衍射仪(XRD)对合成产物的形貌和晶相进行表征.染料敏化太阳电池性能测试表 明,与单一光阳极结构的ZnO纳米片基电池相比,基于更大比表面积和更强光散射效应的ZnO纳米片...     

Synthesis and characterization of lead selenide nanostructure through simple sonochemical method in the presence of novel precursor

In the present study, PbSe nanostructures have been synthesized by using [bis(salicylate)lead(II)]; [Pb(Hsal)₂] as lead precursor in the presence of sonochemical method in aqueous solution. Besides, the effects of reaction time, ultrasonic power, and surfactant on the morphology and particle size of products were studied by SEM images. It was found out that the size and morphology of the products were greatly influenced by these parameters. The XRD studies indicated the production of pure cubic PbSe nanostructures could only happen in the presence of ultrasonic radiation. The average diameter of the PbSe nanostructures was 12 nm. Products were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), photoluminescence (PL) and EDX analysis.     

One-step, solid-state reaction to ZnO nanoparticles in the presence of ionic liquid

ZnO nanoparticles have been synthesized in ionic liquids (1-butyl-3-methylimidazolium chloride, [BMIM]Cl) by one-step solid-state reaction at room temperature for short time. The structure and morphology of the products were characterized by means of X-ray powder diffraction (XRD), scanning electron microscope (SEM) and transmission electron microscopy (TEM), whose results indicated that the sample was spherical in morphology with diameters of 15–20 nm. The room temperature photoluminescence spectra (PL) showed strong and broad green light emission. In addition, [BMIM]Cl could be collected and reused for subsequent reactions. This method provides a facile, one-step and low-cost route for the synthesis of nanostructures of metal oxides with potential photo-catalysis.     

Solvothermal synthesis of Bi2O3/BiVO4 heterojunction with enhanced visible-light photocatalytic performances

Novel, three-dimensional, flower-like Bi2O3/BiVO4 heterojunction photocatalysts have been prepared by the combination of homogeneous precipitation and two-step solvothermal method followed by thermal solution of NaOH etching process. The as-obtained samples were fully characterized by X-ray diffraction, scanning electron microscopy, energy dispersive X-ray analysis, Brunauer-Emmett-Teller surface area, and UV-vis diffusereflectance spectroscopy in detail. The crystallinity, microstructure, specific surface area, optical property and photocatalytic activity of samples greatly changed depending on solvothermal reaction time. The photocatalytic activities of samples were evaluated on the degradation of methyl orange (MO) under visible-light irradiation. The Bi2O3/BiVO4 exhibited much higher photocatalytic activities than pure BiVO4 and conventional TiO2 (P25). The result revealed that the three-dimensional heterojunction played a critical role in the separation of the electron and hole pairs and enhancement of the interfacial charge transfer efficiency, which was responsible for the enhanced photocatalytic activity.