钛酸钠纳米线制备TiO_2纳米线的反应条件

结合离子交换-高温烧结法,由钛酸钠纳米线制备了TiO_2纳米线。通过XRD、Uv-vis漫反射和SEM等测试手段,探讨离子交换时间和高温烧结温度对制备TiO_2纳米线的影响,并以甲基橙为目标污染物测试其光催化性能。结果表明:离子交换时间越长越有利于钛酸纳米线的形成,离子交换48h时钛酸钠纳米线基本转换成为钛酸纳米线;过低的烧结温度不利于TiO_2纳米线的形成,烧结温度650℃时钛酸纳米线基本分解成为TiO_2纳米线;钛酸钠纳米线几乎没有光催化性能,而TiO_2纳米线具有很强的光催化性能。     

两步水热法制备还原氧化石墨烯/纳米TiO_2复合材料及其光催化性能

为研究由还原氧化石墨烯(RGO)和具有高活性晶面的TiO_2组成的复合材料的制备方法及其光催化性能,首先采用两步水热法制备了RGO/纳米TiO_2复合材料:第1步为合成暴露高活性晶面的纳米TiO_2;第2步为将合成的纳米TiO_2与氧化石墨烯(GO)复合,形成RGO/纳米TiO_2复合材料。然后,利用XRD、SEM、X射线光电子能谱仪和紫外-可见漫反射光谱等手段对制备的暴露不同晶面的纳米TiO_2和RGO/纳米TiO_2复合材料进行了表征,评价了其光催化性能。结果表明:在水热法的第1步中,通过调节HF的浓度能可控制备出具有高活性的(001)和(101)晶面的纳米TiO_2,氟原子在纳米TiO_2中以物理吸附态和化学结合态这2种形态存在;在第2步后,GO与纳米TiO_2复合形成RGO/纳米TiO_2复合材料,同时在此过程中GO被转化成RGO。在紫外光照射下,两步水热法合成的RGO/纳米TiO_2复合材料具有很好的光催化性能,明显优于商用TiO_2(P25)和纳米TiO_2的。RGO/纳米TiO_2复合材料的光催化性能有明显的提高,RGO和TiO_2暴露的晶面对光催化活性有影响。     

TiO_2-Al_2O_3负载型催化剂的制备及其光催化性能

以钛酸四丁酯和氢氧化钠为反应物,采用两步水热法制备TiO2纳米线,并将其原位负载于Al2O3载体上,研究它们对甲基橙的光催化降解性能。结果表明,锐钛矿相TiO2主要呈纳米线和八面体状负载在Al2O3载体上,当TiO2负载质量分数为30%,焙烧温度为400℃,催化剂用量为1.332 0 g/L时,TiO2-Al2O3负载型催化剂光催化降解甲基橙的性能最佳,光照5 h后,甲基橙在紫外和太阳光下的降解率分别达到58.9%和55.6%。相同实验条件下,TiO2-Al2O3负载型催化剂对甲基橙的降解率比单纯TiO2提高了35.1%。     

Cu/TiO2 纳米线的制备及其光催化性能

以P25粉体为原料,采用水热法合成了TiO2 纳米线,通过NaBH4还原CuCl2溶液,在TiO2纳米线的表面负载了Cu纳米颗粒.利用透射电镜(TEM)、X射线光电子能谱(XPS)和紫外-可见光谱(UV-Vis)对产物进行了表征.结果表明,Cu纳米粒子均匀分散在纳米线表面,并且该Cu/TiO2纳米线在可见光区域表现出较强的吸收性能.光催化降解酸性红3R染料溶液测试表明,在TiO2纳米线表面负载Cu纳米颗粒对提高其催化性能具有积极作用.     

水热法制备Sb_2Te_3纳米线及其性能表征

在450K,pH值为11的条件下,以SbCl3,和Na2TeO3粉体为原料,用水热法制备了Sb2Te3纳米线。X-射线衍射(XRD)分析表明,所制的的材料为Sb2Te3,透射电镜(TEM)观察到Sb2Te3纳米线直径约为20nm,长度在200~600nm之间,并且自然平行密排成六边形纳米片状;然而在450K,pH值为13的条件下,制备出的产物则为完整的纳米片。扫描电镜(TEM)分析发现纳米线延(015)方向生长。差热测试得到Sb2Te3纳米线的熔点为727.5K。红外光谱的进一步研究表明,由Sb2Te3纳米线编织成的纳米片结构要优于整体生长成的纳米片,并就Sb2Te3纳米线的生长机理进行了初步推测。     

TiO_2纳米颗粒/纳米棒阵列复合薄膜的制备及其光电催化性能

以金属钛箔为钛源,采用双氧水和盐酸体系,通过水热法制备合成TiO2纳米棒阵列薄膜,并通过调节双氧水和盐酸的用量,调控TiO2纳米棒阵列薄膜的微观形貌和物相构成。结合溶剂挥发自组装法将TiO2纳米颗粒引入纳米棒阵列中,得到复合型TiO2光催化剂。以亚甲基蓝为模拟污染物,考察TiO2复合薄膜的光催化活性。通过扫描电镜(SEM)和X射线衍射(XRD)测试对TiO2复合薄膜的物相和表面形貌等进行了表征,并采用电化学交流阻抗法(EIS)分析其表面电荷转移特性。TiO2纳米颗粒/纳米棒阵列复合薄膜在光电协同条件下,展示出高的光电催化活性。     

简单两步法制备载银TiO_2纳米管

简单两步法制备载Ag的TiO2纳米管。采用溶胶-凝胶结合水热法制备TiO2纳米管(TiNT),利用传统的"银镜反应",得到表面载Ag的TiO2纳米管(Ag-TiNT)。利用X射线衍射(XRD)、高分辨率透射电镜(TEM)、电子衍射能谱(EDS)对产物进行了表征。结果表明,Ag粒子均匀地分散在纳米管的外表面。从UV-Vis吸收光谱上可以观察到,载银的TiO2纳米管在可见光区域的吸收有了明显提高。     

水热法合成高纯TiO_2(B)纳米线及其锂电性能的研究

以钛酸丁酯为钛源,采用水热法合成了高纯度的TiO2(B)纳米线。用X射线衍射(XRD),扫描电镜(SEM),透射电镜(TEM)以及激光拉曼光谱仪(Raman)对其晶体结构、形貌和纯度进行了表征与分析,并对其锂离子电池性能进行了测试。结果表明,通过该方法得到的一维TiO2(B)纳米线纯度达到了93.2%。该材料表现出了优异的电化学性能,在0.2C下首次放电比容量达254.8 mAh/g,且循环性能良好,100次循环后容量损失只有约7.84%。     

MS(M=Cd或Zn)纳米粒子负载TiO_2纳米线的制备及可见光催化性能

以具有层状结构的钛酸盐纳米线、CdCl2或ZnSO4及硫代乙酰胺为原料,采用两步水热合成法制备了高温稳定的六方相CdS或低温稳定的立方相ZnS纳米粒子负载的TiO2纳米线复合材料。首先,CdCl2或ZnSO4与钛酸盐纳米线在水热条件下进行离子交换制得含Cd2+或Zn2+的钛酸盐纳米线;然后,在硫代乙酰胺溶液中于160℃下直接处理含Cd2+或Zn2+的钛酸盐纳米线就可获得负载有硫化物纳米粒子的TiO2复合纳米线。它们在酸浸后,TiO2纳米线的表面仍存在少量硫化物纳米粒子。通过测试酸浸后样品、纯TiO2纳米线和商用P25对亚甲基蓝水溶液的可见光催化降解实验结果证实,含CdS纳米粒子样品的光催化活性最高。     

银负载TiO_2纳米线/石墨烯的制备及光催化应用

采用二步水热法和光照还原法制备了银负载TiO2纳米线/石墨烯(GR/TiO2NW/Ag)复合材料,并对其进行了表征,结果表明:Ag纳米颗粒修饰的TiO2NW分布于石墨烯表面,TiO2NW为锐钛矿晶型,光生电子和空穴复合效率降低。并研究了GR/TiO2NW/Ag复合材料在紫外光下降解双酚A废水的光催化性能,实验结果表明,GR/TiO2NW/Ag对双酚A的降解效果明显优于TiO2。40min内,GR/TiO2NW/Ag在紫外光照下对双酚A降解率达到100%。     

Synthesis and optical absorption property of ordered macroporous titania film doped with Ag nanoparticles

Ordered macroporous anatase titania films doped with Ag nanoparticles (NPs) were synthesized by infiltrating titania sol into the interstitial voids of polystyrene colloidal sphere templates, removing the templates, immersing the films in a silver nitrate solution, and subsequently reducing in hydrogen atmosphere. Ag NPs were distributed uniformly within the macropores of the anatase titania film. Both the macroporous titania films doped with Ag NPs and those without doping have a blue-shift compared with that of the sol–gel derived titania film. Except for the plasma resonance absorption of Ag NPs, the macroporous titania film doped with Ag NPs also has a red-shift compared with the undoped sample. The macroporous titania film doped with Ag NPs have potential applications in the fields of optics, gas sensors, and catalysis.     

Low-energy bead-milling dispersions of rod-type titania nanoparticles and their optical properties

The low-energy dispersion of nanomaterials in the bead-milling process is examined. The effect of milling parameters including bead size, rotation speed, and milling time on the dispersibility of fragile rod-type titanium dioxide nanoparticles is investigated. From experimental data obtained for the morphological, optical, and crystalline properties of dispersed nanoparticles, an unbroken primary particle dispersion in colloidal suspension was obtained only by conducting the bead-milling process using the optimum milling parameters. Deviation from the optimum conditions (i.e., higher rotation speed and larger bead size) causes re-agglomeration phenomena, produces smaller and ellipsoidal particles, and worsens crystallinity and physicochemical properties, especially the refractive index, of the dispersed nanoparticles. We also found that decreases in refractive index induced by the milling process are related to collisions forming broken particles and the amorphous phase on the surface of the particles. In addition, the present low-energy dispersion method is prospective for industrial applications, confirming almost no impurity (from breakage of the beads) was apparent in the final product.     

Preparation and optical properties of titania/epoxy nanocomposite coatings

This work reports the preparation of TiO₂/Epoxy nanocomposites coatings with high refractive index and optical transparency. Highly dispersed titania nanoparticles were synthesized by sol-gel method at room temperature. The TiO₂ nanoparticles can be dispersed directly into the polymer without the use of organic surfactant. Nanocomposite coating with refractive index of 1.668 can be obtained by adding 30 wt% TiO₂ nanoparticles into the polymer matrix. All coatings with different amount of TiO₂ exhibit excellent optical transparency of more than 90%. Although higher refractive index of the nanocomposite can be obtained by increasing the content of TiO₂ nanoparticles, cracks also appear in the surface of the hybrid coating.     

TiO2纳米管上负载纳米铁的制备及其光电性能研究

采用阳极氧化法在钛金属表面制备出致密有序的TiO2纳米管阵列,分别利用磁控溅射和电子束辐照沉积技术在其上沉积Fe纳米颗粒以提高其光电性能。利用场发射扫描电镜观察两种不同技术制备的TiO2纳米管阵列负载纳米Fe结构的表面形貌。研究比较了不同制备方法得到的样品在紫外光和可见光照射下的光电效应。     

Tailoring of optical and electrical properties of PMMA by incorporation of Ag nanoparticles

Silver–poly(methyl methacrylate) (Ag–PMMA) nanocomposite films were prepared via ex situ chemical route by employing sodium borohydride (\(\hbox {NaBH}_{4}\)) as a reducing agent. In this study, PVP-stabilized Ag nanoparticles were prepared and mixed with PMMA solution. Optical and structural characterizations of resulting nanocomposite films were performed using UV–visible spectroscopy, transmission electron microscopy (TEM) and scanning electron microscopy (SEM). Characteristic surface plasmon resonance (SPR) peak of Ag nanoparticles was observed at about 3.04 eV (408 nm) in absorption spectra of Ag–PMMA nanocomposite films. TEM micrograph revealed that the spherical Ag nanoparticles with an average diameter of 5.4\(\,\pm \,\)2.5 nm are embedded in PMMA. In Raman spectra, besides shifting of vibrational bands, enhancement in intensity of Raman signal with incorporation of Ag nanoparticles was observed. Current (I)–voltage (V) measurements revealed that conductivity of PMMA increased with increasing concentration of Ag nanoparticles. Analysis of I–V data further disclosed that at voltage <2 V, ohmic conduction mechanism is the dominant mechanism, while at voltage >2 V Poole–Frenkel is the dominant conduction mechanism. Urbach’s energy, the measure of disorder, increased from 0.40 eV for PMMA to 1.11 eV for Ag–PMMA nanocomposite films containing 0.039 wt% of Ag nanoparticles.     

Antifungal efficiency of corona pretreated polyester and polyamide fabrics loaded with Ag nanoparticles

This study discusses the possibility of using the corona (electric discharge at atmospheric pressure) treatment for fiber surface activation that can facilitate the loading of Ag nanoparticles (NPs) from colloids onto the polyester and polyamide fabrics and thus enhance their antifungal activity against Candida albicans. The laundering durability of achieved effects and the influence of dyeing of fabrics with disperse dyes on their antifungal efficiency were studied. The morphology of fibers loaded with Ag nanoparticles was characterized by SEM whereas X-ray photoelectron spectroscopy was used for the evaluation of surface chemical changes. Corona pretreated polyester and polyamide fabrics loaded with Ag nanoparticles showed better antifungal properties compared to untreated fabrics. The advantage of corona treated fabrics became even more prominent after washing test, particularly for polyester fabrics. Antifungal efficiency of polyester and polyamide fabrics loaded with Ag nanoparticles were almost unaffected by dyeing process.     

咔唑和二氰基蒽掺杂纳米粒子的制备及光学性质

以蓝光染料咔唑为电子给体,黄光染料9,10-二氰基蒽为电子受体,采用再沉淀法制备了咔唑和二氰基蒽等摩尔掺杂的纳米粒子。掺杂纳米粒子与纯咔唑聚集体或二氰基蒽聚集体的形貌和发射光颜色明显不同,说明咔唑和二氰基蒽很好的掺杂到一起。吸收光谱表明咔唑和二氰基蒽在掺杂纳米粒子中没有形成电荷转移复合物,荧光发射光谱和荧光寿命表明咔唑和二氰基蒽在掺杂纳米粒子中形成激基复合物,激基复合物的出现使得掺杂纳米粒子的发射光颜色为橙色。     

载Ag/Cu纳米粒子多孔聚丙烯腈复合纤维膜的制备及其抑菌性

金属纳米粒子因其独特的物理化学性能,在催化、抑菌、水污染处理和生物医学等领域表现出巨大的应用前景。但是金属纳米粒子在制备和使用过程中容易发生团聚而影响其性能。因此,提高金属纳米粒子的稳定性,对提升其应用性能具有重大意义。本文在以聚丙烯腈(PAN)为基体,聚乙烯吡咯烷酮(PVP)为致孔剂,基于静电纺丝技术制得多孔聚丙烯腈纳米纤维(PPAN NFs)的基础上,通过浸渍沉积法分别制备出负载银纳米粒子(Ag NPs)复合纳米纤维(Ag-PPAN NFs)和负载铜纳米粒子(Cu NPs)复合纳米纤维(Cu-PPAN NFs)。在利用FESEM、EDS、XRD等方法对制备纤维膜的形貌和结构进行表征的基础上,通过抑菌圈法和FESEM观察经复合纳米纤维处理前后的细菌形貌来研究Ag-PPAN NFs和Cu-PPAN NFs对大肠杆菌、金黄色葡萄球菌和白色念球菌的抑菌性能。研究结果发现：PPAN NFs可有效解决Ag NPs和Cu NPs在制备和使用过程中易于聚集的问题,制得的复合纳米纤维对大肠杆菌、金黄色葡萄球菌和白色念球菌具有一定的抗菌活性,可成为一种新型的抗菌纤维材料。     

Preparation, characterization and photocatalytic performance of Nd-doped titania nanoparticles with mesostructure

Nd³⁺-doped titania nanoparticles with mesostructures were synthesized via hydrothermal process by using cetyltrimethylammonium bromide (CTAB) as directing and pore-forming agent. The obtained materials were characterized by XRD, nitrogen adsorption-desorption, TEM and DRS. The existence of neodymium ion affect significantly the phase transition of the amorphous to anatase, and the band-gap energy was reduced because of the defect energy level induced by the 4f atomic orbital of Nd³⁺ with the optimal content of 1.5 at.% Nd. Density functional theory calculations can explain the band-gap narrowing. The maximum photocatalytic activity corresponds to the 0.5 at.% Nd³⁺-doped anatase nanopowders with mesostructures, which is higher than that of undoped samples.     

Influence of the interaction between two Ag nanoparticles on optical properties of Ag/PGMEA nanocomposite materials

We report local electric field calculations in Ag/PGMEA nanocomposite materials using the dipole discrete approximation. We employ calculation and simulation to show that the nanoparticle radius and the interparticle distance could control and tune the surface plasmon resonances, which influence the extinction spectra and the near-field enhancement of Ag/PGMEA nanostructures. With decreasing interparticle distance, the near-field coupling between particles will induce the shift of surface plasmon resonance peak and improve the near-field intensity. With increasing radius (r), the resonance wavelength peak is red-shifted because of the interaction between two Ag nanoparticles. At 449 nm, the highest near-field enhancement factor obtained in the center of the gap was 30.5 for two interacting Ag nanoparticles of r = 11 nm with a gap of 5 nm.