ZnO/CdS/Ag复合光催化剂的制备及其催化和抗菌性能

先用水热反应合成六方晶相CdS多层级花状微球并在其表面生长ZnO纳米棒形成均匀的ZnO/CdS复合结构,然后用光还原法将Ag纳米颗粒负载于ZnO纳米棒制备出ZnO/CdS/Ag三元半导体光催化剂,对其进行扫描电镜和透射电镜观察、光电性能测试、活性基团捕获实验以及光催化降解和抗菌性能测试,研究其对亚甲基蓝(MB)的降解和抗菌性能。结果表明：ZnO纳米棒均匀生长在CdS微球表面,CdS晶体没有明显裸露,Ag纳米粒子负载在ZnO纳米棒的表面;ZnO/CdS/Ag三元复合光催化剂有良好的可见光响应、较低的阻抗和较高的光电流密度;ZnO/CdS/Ag复合光催化剂能同时产生羟基和超氧自由基等活性氧基团;ZnO/CdS/Ag三元复合光催化剂对亚甲基蓝(MB)的30 min降解率高于90%;0.25 mg/mL的ZnO/CdS/Ag对革兰氏阴性菌(大肠杆菌)的灭菌率高于96%,对革兰氏阳性菌(金黄色葡萄球菌)能完全灭除。     

The rapid detection for methane of ZnO porous nanoflakes with the decoration of Ag nanoparticles

Realizing the real-time detection of CH₄ is important for the safety of human life. A facile hydrothermal method was used to synthesize Ag nanoparticles-decorated ZnO porous nanoflakes (PNFs) in this study. The characterization results confirmed that Ag nanoparticles had been decorated in ZnO nanoflakes with the thickness of ~10 nm. The gas-sensing properties of Ag-decorated ZnO nanoflakes were also investigated. While the gas-sensing performances of ZnO were remarkably improved by decorating Ag nanoparticles on the surface of ZnO nanoflakes, the response of the Ag-decorated ZnO sensor to 3000 ppm CH₄ is almost 1.3 times as high as that of pristine ZnO sensor. The obtained Ag/ZnO sensor exhibits better long-term stability and shorter response recovery time (5/38 s) in the comparison with pristine ZnO, demonstrating the possibility for the actual detection of CH₄. The enhanced CH₄ sensing performance can be attributed to the synergism between the unique hierarchical porous structure and the sensitizing actions utilized by the Ag nanoparticles.     

Numerical calculation of plasmonic field absorption enhancement in CdSe-quantum dot sensitized ZnO nanorods by Ag nanoparticle periodic arrays

Plasmonic field absorption enhancement (PFAE) of Ag nanoparticles (Ag NPs) periodic arrays in CdSe-quantum dot (QD) sensitized ZnO nanorods was numerically investigated by the three-dimensional finite difference time domain (FDTD). The Ag NPs with spherical morphology were found to have an optimum PFAE compared to other Ag NP morphologies such as cubic and pyramidal. The results also showed that PFAE intensity in CdSe-QD-sensitized ZnO nanorods is increased with the reduction of Ag NP diameter until 10 nm and decreases thereafter. Moreover, the optimum density of spherical Ag NPs for optimum PFAE was observed as 20%. PFAE in CdSe-QD-sensitized ZnO nanorods is improved with increasing space between ZnO nanorods until 180 nm and reduces thereafter. Finally, the results showed that PFAE of Ag NPs for the high distance between ZnO nanorods is dependent on radiation angle; while for the low distance between ZnO nanorods it is free of radiation angle.     

Facile preparation of Ag/ZnO nanoparticles via photoreduction

Ag/ZnO nanoparticles can be obtained via photocatalytic reduction of silver nitrate at ZnO nanorods when a solution of AgNO₃ and nanorods ZnO suspended in ethyleneglycol is exposed to daylight. The mean size of the deposited sphere like Ag particles is about 5 nm. However, some of the particles can be as large as 20 nm. The ZnO nanorods were pre-prepared by basic precipitation from zinc acetate di-hydrate in the ionic liquid 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)amide. They are about 50–300 nm in length and 10–50 nm in width. Transmission electron microscopy (TEM), energy-dispersive X-ray analysis (EDS), X-ray powder diffraction (XRD), UV–Vis spectroscopy, X-ray photoelectron spectroscopy (XPS), and photoluminescence (PL) were used to characterize the resulting Ag/ZnO nanocomposites.     

Tyrosine-assisted preparation of Ag/ZnO nanocomposites with enhanced photocatalytic performance and synergistic antibacterial activities

In this paper, Ag/ZnO metal-semiconductor nanocomposites were prepared through a facile one-pot hydrothermal method with the assistance of tyrosine. The synthesized samples were structurally characterized by x-ray diffraction, scanning electron microscope, transmission electron microscope and x-ray photoelectron spectroscopy. It was shown that the added tyrosine served both as a shape conductor for the formation of ZnO faceted nanorods and as a reducing agent of Ag(+) ions. In the reaction process, the complexation of Ag(+) with NH(3) and OH(-) decreased the redox potential of Ag(+)/Ag, which prevented the formation of isolated Ag nanoparticles in solution. The prepared Ag/ZnO nanocomposites showed potential applications in photodegradation of organic dye pollutants and destruction of bacteria.     

One-pot synthesis of ZnO/Ag nanospheres with enhanced photocatalytic activity

ZnO/Ag composite nanospheres with an average diameter of about 440 nm, were synthesized through a facile one-pot solvothermal reaction, using a kind of biomolecular sodium alginate as template, H₂O and diethanolamine as solvents, followed by the assembly of ZnO and Ag nanoparticles in-situly produced. The composite spheres were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and energy disperse X-ray spectrum. Moreover, the results showed that the as-made ZnO/Ag assembled nanospheres exhibited better photocatalytic performance than the pure ZnO nanoparticles and this one-pot synthesis method has great potential to be extended for the synthesis of other metallic oxide/metal spheres.     

Optical studies of ZnO/Ag nanojunctions

Ag/ZnO nano-hetero-junctions were synthesized by an electrochemical route. The optical absorption spectroscopy and photoluminescence studies reveal the reaction mechanism at the junction. Optical absorption spectra indicate presence of well-defined ZnO excitonic feature along with the Ag surface plasmon absorption feature at 400 nm. Moreover, ZnO green photoluminescence appears on junction formation with Ag. Detailed analysis of emission and excitation processes indicate that efficient charge transfer is taking place from ZnO to Ag. Ag is also responsible for creation of levels in the HOMO-LUMO gap of ZnO. This finding may be of relevance so far as p-type doping in ZnO is concerned.     

MOF衍生的多孔ZnO/C、Ag/ZnO/C复合材料光催化性能研究

以金属有机骨架(MOF-5)为前驱体, 通过高温热处理和湿化学法获得ZnO/C和Ag/ZnO/C两种光催化复合材料。采用X 射线衍射(XRD)、扫描电子显微镜(SEM)、X射线能谱(EDS)和紫外-可见分光漫反射(UV-Vis DRS)等方法对所得样品的晶体结构、形貌特征、组成及光谱特性进行了表征。结果显示, 高温热处理保留了MOF-5的原始结构。ZnO/C比表面积为390 m²/g, 载银后比表面积仍达232 m²/g, 负载的银颗粒尺寸约30 nm。光催化降解实验表明ZnO/C和Ag/ZnO/C复合材料对亚甲基蓝(MB)都具有很高的降解效率, 均优于商业TiO₂。Ag/ZnO/C的光催化性能更好, 且具有较好的重复利用和稳定性。因此, 适度的高温碳化和掺杂贵金属是获得优良光催化性能的根本原因。     

Potentiometric cholesterol biosensor based on ZnO nanorods chemically grown on Ag wire

An electrochemical biosensor based on ZnO nanorods for potentiometric cholesterol determination is proposed. Hexagon-shaped ZnO nanorods were directly grown on a silver wire having a diameter of 250 μm using low temperature aqueous chemical approach that produced ZnO nanorods with a diameter of 125-250 nm and a length of ~ 1 μm. Cholesterol oxidase (ChOx) was immobilized by a physical adsorption method onto ZnO nanorods. The electrochemical response of the ChOx/ZnO/Ag biosensor against a standard reference electrode (Ag/AgCl) was investigated as a logarithmic function of the cholesterol concentration (1 × 10⁻⁶ M to 1 × 10⁻² M) showing good linearity with a sensitivity of 35.2 mV per decade and the stable output signal was attained at around 10 s.     

Electrodeposition of template free hierarchical ZnO nanorod arrays via a chloride medium

We have successfully grown template and buffer free ZnO nanorod films via chloride medium by controlling bath temperature in a simple and cost effective electrochemical deposition method. Thin films of ZnO nano-rods were obtained by applying a potential of ?0.75 V by employing Ag/AgCl reference electrode for 4 h of deposition time. The CV measurements were carried out to determine potential required to deposit ZnO nanorod films whereas chronoamperometry studies were carried out to investigate current and time required to deposit ZnO nanorod films. The formation of ZnO nanorod has been confirmed by scanning electron microscopy (SEM) and Raman spectroscopy. Low angle XRD analysis confirms that ZnO nanorod films have preferred orientation along (101) direction with hexagonal wurtzite crystal structure. The SEM micrographs show nice surface morphology with uniform, dense and highly crystalline hexagonal ZnO nanorods formation. Bath temperature has a little influence on the orientation of nanorods but has a great impact on their aspect ratio. Increase in bath temperature show improvement in crystallinity, increase in diameter and uniform distribution of nanorods. Compositional analysis shows that the amount of oxygen is ~49.35 % and that of Zn is ~50.65 %. The optical band gap values were found to be 3.19 and 3.26 eV for ZnO nanorods prepared at bath temperature 70 and 80 °C respectively. These results indicate that by controlling the bath temperature band gap of ZnO nanorods can be tailored. The obtained results suggest that it is possible to synthesize ZnO nanorod films by a simple, cost effective electrodeposition process which can be useful for opto-electronic devices fabrication.     

Room temperature solid-state synthesis and ethanol sensing properties of sea-urchin-like ZnO nanostructures

ZnO gas-sensing materials were prepared by one-step solid-state reaction at room temperature. X-ray diffraction (XRD) and field-emission scanning electron microscopy (FE-SEM) were used to characterize the hierarchal ZnO nanocrystals. The results indicate that ZnO clusters are assembled with nanosheets when no surface-active agent is present. When surface-active agent PEG-10000 was added, sea-urchin-like ZnO are assembled from ZnO nodules. The rods have an average diameter of 33 nm and length of about 100 nm. The primary gas-sensing results show that sea-urchin-like ZnO have good gas sensitivity to ethanol vapor.     

Plasmonic ZnO/Ag Embedded Structures as Collecting Layers for Photogenerating Electrons in Solar Hydrogen Generation Photoelectrodes

A new fabrication strategy in which Ag plasmonics are embedded in the interface between ZnO nanorods and a conducting substrate is experimentally demonstrated using a femtosecond‐laser (fs‐laser)‐induced plasmonic ZnO/Ag photoelectrodes. This fs‐laser fabrication technique can be applied to generate patternable plasmonic nanostructures for improving their effectiveness in hydrogen generation. Plasmonic ZnO/Ag nanostructure photoelectrodes show an increase in the photocurrent of a ZnO nanorod photoelectrodes by higher than 85% at 0.5 V. Both localized surface plasmon resonance in metal nanoparticles and plasmon polaritons propagating at the metal/semiconductor interface are available for improving the capture of sunlight and collecting charge carriers. Furthermore, in‐situ X‐ray absorption spectroscopy is performed to monitor the plasmonic‐generating electromagnetic field upon the interface between ZnO/Ag nanostructures. This can reveal induced vacancies on the conduction band of ZnO, which allow effective separation of charge carriers and improves the efficiency of hydrogen generation. Plasmon‐induced effects enhance the photoresponse simultaneously, by improving optical absorbance and facilitating the separation of charge carriers.     

A selective ethanol gas sensor based on spray-derived Ag–ZnO thin films

A simple and cost-effective spray pyrolysis technique was employed to synthesize silver-doped zinc oxide (Ag–ZnO) thin films on the glass substrates from aqueous solutions of zinc acetate and silver nitrate precursors at 450 °C. The effects of Ag doping on structural, morphological, and gas-sensing properties of films were examined. The X-ray diffraction spectra of the Ag–ZnO films showed the polycrystalline nature having hexagonal crystal structure. Scanning electron microscopy (SEM) images of the pure ZnO films revealed the uniform distribution of the spherical grains (~80 nm size). Tiny Ag nanoparticles are clearly visualized in the SEM of Ag–ZnO films. The investigation of the effect of Ag doping on the gas-sensing properties of the Ag–ZnO revealed that the 15 % Ag-doped ZnO sample has the highest gas sensitivity (85 %) and excessive Ag doping in ZnO degraded the gas sensitivity. A possible mechanism of Ag–ZnO-based sensor sensitivity to the target gas is also proposed.     

A facile low-cost synthesis of ZnO nanorods via a solid-state reaction at low temperature

ZnO nanorods have been prepared via a solid-state reaction between anhydrous zinc sulfate and sodium hydroxide in the absence of surfactant and template at relatively low temperature. The products were characterized by XRD, XPS and TEM. The influence of Zn²⁺/OH⁻ ratio on the size and morphology of the as-prepared ZnO samples has been studied, and the experimental results showed that when Zn²⁺/OH⁻ ratio was 1:4, good rod-like morphology with the diameter of 30–50 nm and length of ca. 600 nm can be obtained. Finally, the mechanism for the ZnO nanorods developed in the reaction system has been explained.     

ZnO/SnO_2,SnO_2/ZnO UPF复合膜的制备及气敏特性研究

用直流气体放电活化反应蒸发沉积技术在普通玻璃基片上制备了ZnO／SnO2及SnO2／ZnO超微粒子（UPF）双层复合薄膜。样品经扫描电子显微镜（SEM）和X射线衍射仪分析，结论为超微粒子的复合薄膜。同时提出了最佳制备工艺。气敏测试结果表明：ZnO／SnO2及SnO2／ZnOUPF复合膜较单层ZnO及SnO2UPF表现出优良的选择性，其灵敏度和最佳工作温度也得到相应的改善。     

A novel route to ZnO nanorods with small diameters of 20 nm

The ZnO nanorods with small diameters of 20 nm were prepared successfully by an easy “in situ consumed template” route. In the synthesis, Zn(Ac)₂ were used as Zn source and dodecanethiol (DT) was used as coordinated agents in ethanol solvent. The samples were characterized detailed by XRD, TEM and IR techniques. The results indicated that the ZnO rods were uniform in diameters with good crystallinity. Time-dependent experiments indicated that the ZnO rods are grown within the Zn–DT complex (a complex composed of Zn and DT) that was formed at the beginning of the reaction. With prolonging the reaction time, the Zn–DT “template” was gradually in situ consumed and transformed into ZnO, and finally, the ZnO nanorods with diameters of 20 nm were obtained. The method here provides the new route for ZnO nanorods with small diameters.     

Premelting behavior and interfacial reaction of the Sn/Cu and Sn/Ag soldering systems during the reflow process

The early interfacial reaction and premelting characteristics of the Sn/Cu and Sn/Ag soldering systems, and the formation and morphology transition of interfacial intermetallic compounds in the two systems during the reflow soldering process were investigated by using a differential scanning calorimeter. Results show that the initial interfacial eutectic reaction arising from atomic interdiffusion in solid-state Sn/Cu and Sn/Ag systems results in the premelting at each interface of the two systems at a temperature 4.9 and 10.6?°C respectively lower than the actual melting point of pure tin, and consequently both of the Sn/Cu and Sn/Ag soldering systems exhibit morphology change of the intermetallic compound (IMC) as the solder experiences a transition from solid-state to liquid-state in a very small temperature range. The change in the interfacial energy between the solid (or liquid) Sn-rich phase and IMC phase is the essential factor leading to the morphology transition of the interfacial IMC in the Sn/Cu and Sn/Ag soldering systems.     

Spectral properties of nanoengineered Ag/Au bilayer rods fabricated by electron beam lithography

Ag/Au bimetallic nanoparticles possess the combinatory advantages of Au and Ag nanoparticles and can also be utilized to tune the properties of localized surface plasmon resonance. Ag/Au bilayer nanorods were prepared by electron beam lithography, and their spectral properties were investigated. Compared with Ag monolayer nanorods, Ag/Au bilayer nanorods show broader localized surface plasmon resonance bands, and the longitudinal mode and transverse mode localized surface plasmon bands show blueshift and redshift, respectively. The maximum near-field intensity of the longitudinal mode of the Ag/Au nanorod is less than half that of the Ag/Au nanorod without gold layer. Shape-induced modification of Ag/Au bilayer nanorods on their spectral properties was also discussed.     

Facile synthesis of Ag/ZnO microstructures with enhanced photocatalytic activity

In this paper, we developed a facile low-temperature solution route to prepare radical-shaped ZnO microprisms and to deposit metal silver on the surface of ZnO to form Ag/ZnO microstructures. The samples were characterized using X-ray powder diffraction (XRD), scanning electron microscopy (SEM), and photoluminescence (PL) spectroscopy. Experimental results show that the deposition of metal Ag nanospecies can be achieved successfully by simply aging the solution at 75 °C, and the radical-shaped microstructures of ZnO are well maintained. The Ag/ZnO microstructures exhibit much lower PL emission intensity and much higher photocatalytic activity than those of radical-shaped ZnO microprisms.     

Enhanced luminescence of Ag-decorated ZnO nanorods

Ag-decorated ZnO nanorods were synthesized by thermal evaporation of a mixture of ZnO and graphite powders at 900 °C followed by wet Ag coating and thermal annealing. The ZnO nanorods had a rod-like morphology with a relatively uniform width and length. The widths and lengths of the nanorods ranged from 50 to 300 nm and up to a few hundred micrometers, respectively. The diameters of the Ag particles on the nanorods ranged from 10 to 100 nm. The dependence of the photoluminescence properties of Ag-decorated ZnO nanorods on the postannealing atmosphere was examined. Annealing resulted in an increase and decrease in the near band edge (NBE) and deep level (DL) emission intensities of Ag-coated ZnO nanorods, respectively, whereas both the NBE and DL emission intensities of uncoated ZnO nanorods were increased by annealing. The intensity ratio of NBE emission to DL emission of the Ag-coated ZnO nanorods was increased ~15-fold by hydrogen annealing. The underlying mechanism for NBE emission enhancement and DL emission suppression of Ag-coated ZnO nanorods by postannealing is discussed based on the surface plasmon resonance effect of Ag.