Fabrication of TiO2/Ag/Ag2O Nanoparticles to Enhance the Photocatalytic Activity of Degussa P25 Titania

2016 ◽  
Vol 69 (1) ◽  
pp. 41 ◽  
Author(s):  
Safyan A. Khan ◽  
Shahid Ali ◽  
Manzar Sohail ◽  
Mohamed A. Morsy ◽  
Zain H. Yamani
Keyword(s):  
Chemical Reduction ◽  
Visible Region ◽  
Spherical Shape ◽  
Ag Nps ◽  
X Ray ◽  
Transmission Electron ◽  
Silver Nps ◽  
Degussa P25 ◽  
Average Size ◽  
Ag2o Nanoparticles

A simple chemical reduction approach was used to synthesize Ag nanoparticles (NPs) over a reputed photocatalyst, Degussa P25 (TiO2). Silver doping extended the P25 absorption wavelength from the ultraviolet to the visible region. The synthesized silver NPs (Ag NPs) were of spherical shape and had an average size of ~4.6 nm. In the next stage, Ag NPs were partially oxidized by treatment with hydrogen peroxide. The resulting P25/Ag/Ag2O nanocomposites were characterized by X-ray powder diffraction, transmission electron microscopy, energy dispersive X-ray analysis, Brunauer–Emmett–Teller analysis, and UV-visible spectroscopy. The photocatalytic activities of the P25, P25/Ag, and P25/Ag/Ag2O catalysts were investigated for the degradation of non-biodegradable dyes, methylene blue and rhodamine 6G. The P25/Ag/Ag2O nanocomposite exhibited better photodegradation activity than P25, as well as the commonly used Ag3PO4, under visible light irradiation.

Synthesis and Characterization of SiO2@Y2MoO6:Eu3+ Core–Shell Structured Spherical Phosphors by Sol–Gel Process

2016 ◽  
Vol 16 (4) ◽  
pp. 3914-3920 ◽  
Author(s):  
G. Z Li ◽  
F. H Liu ◽  
Z. S Chu ◽  
D. M Wu ◽  
L. B Yang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Annealing Temperature ◽  
Uv Light ◽  
Sol Gel ◽  
Spherical Shape ◽  
Core Shell ◽  
X Ray ◽  
Transmission Electron ◽  
Sol Gel Process ◽  
Average Size

SiO2@Y2MoO6:Eu3+ core–shell phosphors were prepared by the sol–gel process. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), field emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectra (EDS), transmission electron microscopy (TEM), photoluminescence (PL) spectra as well as kinetic decays were used to characterize the resulting SiO2@Y2MoO6:Eu3+ core–shell phosphors. The XRD results demonstrated that the Y2MoO6:Eu3+ layers on the SiO2 spheres crystallized after being annealed at 700 °C and the crystallinity increased with raising the annealing temperature. The obtained core–shell phosphors have spherical shape with narrow size distribution (average size ca. 640 nm), non-agglomeration, and smooth surface. The thickness of the Y2MoO6:Eu3+ shells on the SiO2 cores could be easily tailored by varying the number of deposition cycles (70 nm for four deposition cycles). The Eu3+ shows a strong PL emission (dominated by 5D0–7F2 red emission at 614 nm) under the excitation of 347 nm UV light. The PL intensity of Eu3+ increases with increasing the annealing temperature and the number of coating cycles.

scholarly journals Structural and optical investigation of CdSe quantum dots

2013 ◽  
Vol 8 (2) ◽  
pp. 83-88
Author(s):  
Neupane Dipesh
Keyword(s):  
Quantum Dots ◽  
Large Scale ◽  
Room Temperature ◽  
Spherical Shape ◽  
Cdse Quantum Dots ◽  
Optical Investigation ◽  
X Ray ◽  
Transmission Electron ◽  
Engineering And Technology ◽  
Average Size

CdSe semiconducting Quantum dots were prepared by a chemical method at a room temperature. X-ray powder diffraction and transmission electron microscope measurements conformed a hexagonal cubic crystalline phase of Cdse semiconducting Quantum dots of about 15 nm average size with nearly spherical shape. The absorption and photoluminescence spectra of the CdSe quantum dots were strongly shown blue shifted due to size quantization. The present study describes a simultaneous and highly reproducible large scale synthesis of highly luminescent CdSe Quantum dots. Kathmandu University Journal of Science, Engineering and Technology Vol. 8, No. II, December, 2012, 83-88 DOI: http://dx.doi.org/10.3126/kuset.v8i2.7329

scholarly journals Sonochemical Synthesis, Characterization, and Photocatalytic Activity of N-Doped TiO2Nanocrystals with Mesoporous Structure

2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
Tiekun Jia ◽  
Fang Fu ◽  
Junwei Zhao ◽  
Jian Chen ◽  
Xiaofeng Wang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Region ◽  
Nitrogen Adsorption ◽  
Mesoporous Structure ◽  
Diffuse Reflection Spectroscopy ◽  
X Ray ◽  
Transmission Electron ◽  
Average Size ◽  
Adsorption Desorption

N-Doped TiO2nanocrystals were synthesized via a simple sonochemical route, using titanium tetrachloride, aqueous ammonia, and urea as starting materials. The as-synthesized samples were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM) equipped with an energy dispersion X-ray spectrometer (EDS), transmission electron microscopy (TEM), UV-vis diffuse reflection spectroscopy, Raman spectroscopy, and nitrogen adsorption-desorption isotherms. The results of TEM and nitrogen adsorption-desorption showed that the average size and specific surface area of the as-synthesized nanocrystals are 10 nm and 107.2 m2/g, respectively. Raman spectral characterization combined with the results of XRD and EDS revealed that N dopant ions were successfully doped into TiO2. Compared with pure TiO2, the adsorption band edge of N-doped TiO2samples exhibited an obvious red shift to visible region. The photocatalytic activities were evaluated by the degradation of Rhodamine B (RhB) under visible light, and the results showed that the N-doped TiO2sample synthesized by an optimal amount of urea exhibited excellent photocatalytic activity due to its special mesoporous structure and the incorporation of nitrogen dopant ions.

Formation of Platinum Nanodendrites Embedded Organic Insulator for Memory Application

2014 ◽  
Vol 1024 ◽  
pp. 44-47 ◽  
Author(s):  
Nur Syafinaz Ridhuan ◽  
Nabil Iman Muzzafaruddin ◽  
Abdul Razak Khairunisak ◽  
K.C. Aw
Keyword(s):  
Electron Microscope ◽  
Transmission Electron Microscope ◽  
Reduction Method ◽  
Chemical Reduction ◽  
Chemical Reduction Method ◽  
Growth Duration ◽  
X Ray ◽  
Transmission Electron ◽  
Average Size ◽  
Memory Characteristics

This work describes the formation of platinum nanodendrites (PtNDs) using the chemical reduction method. The PtNDs were formed with varying concentration of K2PtCl4 precursor (5-20 mM) and growth duration (8-16 min). The optimum concentration of K2PtCl4 was 15 mM whereby high crystalline nanodendrites with an average size of 118 nm were produced. Aggregation of nanodendrites occurred when the growth duration was prolonged to more than 12 minutes. The morphology and size of PtNDs were characterized by using a transmission electron microscope (TEM), high resolution transmission electron microscope (HRTEM) and X-ray diffractometer (XRD). Additionally, the memory characteristics of PtNDs embedded in polymethylsilsesquioxanes (PMSSQ)/Si with gold electrodes were studied in this work. PtNDs played a role as charge-trapped sites and showed good memory effect when embedded in PMSSQ. Optimum memory properties of PMSSQ-embedded PtNDs were obtained for PtNDs synthesized with 15 mM K2PtCl4 concentration at 12 min of growth duration with 170 electrons trapped per PtNDs and Vth of 2.8 V.

scholarly journals FusariumAntifungal Activities of Copper Nanoparticles Synthesized by a Chemical Reduction Method

2016 ◽  
Vol 2016 ◽  
pp. 1-7 ◽  
Author(s):  
Pham Van Viet ◽  
Hai Thi Nguyen ◽  
Thi Minh Cao ◽  
Le Van Hieu
Keyword(s):  
Copper Nanoparticles ◽  
Reduction Method ◽  
Chemical Reduction ◽  
Fungal Growth ◽  
Spherical Shape ◽  
Xrd Analysis ◽  
Chemical Reduction Method ◽  
Transmission Electron ◽  
Ft Ir ◽  
Average Size

We report on the process of synthesizing copper nanoparticles (Cu Nps) for a short reactive time by chemical reduction method with a support of CTAB reductive agent. Their properties were determined by ultraviolet-visible (UV-Vis) absorption spectrum, the X-ray (XRD) analysis, Fourier transform infrared spectroscopy (FT-IR), and Transmission Electron Microscopy (TEM) images. The antifungal activity of Cu Nps was evaluated by testing againstFusariumsp. The Cu Nps were obtained with the average size in the range of 20–50 nm having spherical shape. The survey shows that when Cu Nps were used at 450 ppm concentration in 9-day incubation, 93.98% of fungal growth was inhibited.

scholarly journals Facile Synthesis of Carboxymethyl Cellulose Coated Core/Shell SiO2@Cu Nanoparticles and Their Antifungal Activity against Phytophthora capsici

Polymers ◽  
2021 ◽  
Vol 13 (6) ◽  
pp. 888
Author(s):  
Nguyen Thi Thanh Hai ◽  
Nguyen Duc Cuong ◽  
Nguyen Tran Quyen ◽  
Nguyen Quoc Hien ◽  
Tran Thi Dieu Hien ◽  
...  
Keyword(s):  
Antifungal Activity ◽  
Carboxymethyl Cellulose ◽  
Chemical Reduction ◽  
Low Cost ◽  
Phytophthora Capsici ◽  
Reduction Process ◽  
Spherical Shape ◽  
Core Shell ◽  
Cu Nanoparticles ◽  
Average Size

Cu nanoparticles are a potential material for creating novel alternative antimicrobial products due to their unique antibacterial/antifungal properties, stability, dispersion, low cost and abundance as well as being economical and ecofriendly. In this work, carboxymethyl cellulose coated core/shell SiO2@Cu nanoparticles (NPs) were synthesized by a simple and effective chemical reduction process. The initial SiO2 NPs, which were prepared from rice husk ash, were coated by a copper ultrathin film using hydrazine and carboxymethyl cellulose (CMC) as reducing agent and stable agent, respectively. The core/shell SiO2@Cu nanoparticles with an average size of ~19 nm were surrounded by CMC. The results indicated that the SiO2@Cu@CMC suspension was a homogenous morphology with a spherical shape, regular dispersion and good stability. Furthermore, the multicomponent SiO2@Cu@CMC NPs showed good antifungal activity against Phytophthora capsici (P. capsici). The novel Cu NPs-based multicomponent suspension is a key compound in the development of new fungicides for the control of the Phytophthora disease.

scholarly journals Size Control of Synthesized Silver Nanoparticles by Simultaneous Chemical Reduction and Laser Fragmentation in Origanum majorana Extract: Antibacterial Application

Materials ◽  
2021 ◽  
Vol 14 (9) ◽  
pp. 2326
Author(s):  
Entesar Ali Ganash ◽  
Reem Mohammad Altuwirqi
Keyword(s):  
Silver Nanoparticles ◽  
Irradiation Time ◽  
Chemical Reduction ◽  
Size Control ◽  
Reduction Process ◽  
Laser Wavelength ◽  
X Ray Diffraction ◽  
Ag Nps ◽  
Transmission Electron ◽  
Origanum Majorana

In this work, silver nanoparticles (Ag NPs) were synthesized using a chemical reduction approach and a pulsed laser fragmentation in liquid (PLFL) technique, simultaneously. A laser wavelength of 532 nm was focused on the as produced Ag NPs, suspended in an Origanum majorana extract solution, with the aim of controlling their size. The effect of liquid medium concentration and irradiation time on the properties of the fabricated NPs was studied. While the X-ray diffraction (XRD) pattern confirmed the existence of Ag NPs, the UV–Vis spectrophotometry showed a significant absorption peak at about 420 nm, which is attributed to the characteristic surface plasmon resonance (SPR) peak of the obtained Ag NPs. By increasing the irradiation time and the Origanum majora extract concentration, the SPR peak shifted toward a shorter wavelength. This shift indicates a reduction in the NPs’ size. The effect of PLFL on size reduction was clearly revealed from the transmission electron microscopy images. The PLFL technique, depending on experimental parameters, reduced the size of the obtained Ag NPs to less than 10 nm. The mean zeta potential of the fabricated Ag NPs was found to be greater than −30 mV, signifying their stability. The Ag NPs were also found to effectively inhibit bacterial activity. The PLFL technique has proved to be a powerful method for controlling the size of NPs when it is simultaneously associated with a chemical reduction process.

scholarly journals Enhanced Photocatalytic Activity of Cu2O Cabbage/RGO Nanocomposites under Visible Light Irradiation

Polymers ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 1712
Author(s):  
Appusamy Muthukrishnaraj ◽  
Salma Ahmed Al-Zahrani ◽  
Ahmed Al Otaibi ◽  
Semmedu Selvaraj Kalaivani ◽  
Ayyar Manikandan ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Thermo Gravimetric Analysis ◽  
Visible Region ◽  
Catalytic Performance ◽  
Precipitation Method ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Dye Pollutants ◽  
Transmission Electron

Towards the utilization of Cu2O nanomaterial for the degradation of industrial dye pollutants such as methylene blue and methyl orange, the graphene-incorporated Cu2O nanocomposites (GCC) were developed via a precipitation method. Using Hummers method, the grapheme oxide (GO) was initially synthesized. The varying weight percentages (1–4 wt %) of GO was incorporated along with the precipitation of Cu2O catalyst. Various characterization techniques such as Fourier-transform infra-red (FT-IR), X-ray diffraction (XRD), UV–visible diffused reflectance (UV-DRS), Raman spectroscopy, thermo gravimetric analysis (TGA), energy-dispersive X-ray analysis (EDX), and electro chemical impedance (EIS) were followed for characterization. The cabbage-like morphology of the developed Cu2O and its composites were ascertained from field-emission scanning electron microscopy (FESEM) and high-resolution transmission electron microscopy (HR-TEM). In addition, the growth mechanism was also proposed. The results infer that 2 wt % GO-incorporated Cu2O composites shows the highest value of degradation efficiency (97.9% and 96.1%) for MB and MO at 160 and 220 min, respectively. Further, its catalytic performance over visible region (red shift) was also enhanced to an appreciable extent, when compared with that of other samples.

The effect of silver concentration and calcination temperature on structural and optical properties of ZnO:Ag nanoparticles

2015 ◽  
Vol 29 (01) ◽  
pp. 1450254 ◽  
Author(s):  
M. Shayani Rad ◽  
A. Kompany ◽  
A. Khorsand Zak ◽  
M. E. Abrishami
Keyword(s):  
Calcination Temperature ◽  
Sol Gel ◽  
Visible Emission ◽  
X Ray Diffraction ◽  
Ag Nps ◽  
Zno Nps ◽  
Calcination Temperatures ◽  
Transmission Electron ◽  
Xrd Patterns ◽  
Average Size

Pure and silver added zinc oxide nanoparticles ( ZnO -NPs and ZnO : Ag -NPs) were synthesized through a modified sol–gel method. The prepared samples were characterized using X-ray diffraction (XRD), transmission electron microscopy (TEM) and photoluminescence (PL) spectroscopy. In the XRD patterns, silver diffracted peaks were also observed for the samples synthesized at different calcination temperatures of 500°C, 700°C, 900°C except 1100°C, in addition to ZnO . TEM images indicated that the average size of ZnO : Ag -NPs increases with the amount of Ag concentration. The PL spectra of the samples revealed that the increase of Ag concentration results in the increase of the visible emission intensity, whereas by increasing the calcination temperature the intensity of visible emission of the samples decreases.

Well-Aligned Graphene Oxide Nanosheets Decorated with Zinc Oxide Nanocrystals for High Performance Photocatalytic Application

2015 ◽  
Vol 14 (03) ◽  
pp. 1550007 ◽  
Author(s):  
K. Kaviyarasu ◽  
C. Maria Magdalane ◽  
E. Manikandan ◽  
M. Jayachandran ◽  
R. Ladchumananandasivam ◽  
...  
Keyword(s):  
Zinc Oxide ◽  
Graphene Oxide ◽  
High Performance ◽  
Chemical Reduction ◽  
Visible Region ◽  
Single Layer ◽  
Single Layer Graphene ◽  
Graphene Oxides ◽  
X Ray ◽  
Nanoscale Structures

Graphene oxide (GO) nanosheets modified with zinc oxide nanocrystals were achieved by a green wet-chemical approach. As-obtained products were characterized by XRD, Raman spectra, XPS, HR-TEM, EDS, PL and Photocatalytic studies. XRD studies indicate that the GO nanosheet have the same crystal structure found in hexagonal form of ZnO . The enhanced Raman spectrum of 2D bands confirmed formation of single layer graphene oxides. The gradual photocatalytic reduction of the GO nanosheet in the GO : ZnO suspension of ethanol was studied by using X-ray photoelectron (XPS) spectroscopy. The nanoscale structures were observed and confirmed using high resolution transmission electron microscopy (HR-TEM). The evolution of the elemental composition, especially the various numbers of layers were determined from energy dispersive X-ray spectra (EDS). PL properties of GO : ZnO nanosheet were found to be dependent on the growth condition and the resultant morphology revealed that GO nanosheet were highly transparent in the visible region. The photocatalytic performance of GO : ZnO nanocomposites was performed under UV irradiation. Therefore, the ZnO nanocrystals in the GO : ZnO composite could be applied in gradual chemical reduction and consequently tuning the electrical conductivity of the graphene oxide nanosheet.

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