scholarly journals Synthesis and Characterization of Sr-Doped ZnSe Nanoparticles for Catalytic and Biological Activities

Water ◽  
2021 ◽  
Vol 13 (16) ◽  
pp. 2189
Author(s):  
V. Beena ◽  
S. L. Rayar ◽  
S. Ajitha ◽  
Awais Ahmad ◽  
Munirah D. Albaqami ◽  
...  

The development of cost-effective and ecofriendly approaches toward water purification and antibacterial activity is a hot research topic in this era. Purposely, strontium-doped zinc selenide (Sr-doped ZnSe) nanoparticles, with different molar ratios of Sr2+ cations (0.01, 0.05, and 0.1), were prepared via the co-precipitation method, in which sodium borohydride (NaBH4) and 2-mercaptoethanol were employed as reducing and stabilizing agents, respectively. The ZnSe cubic structure expanded by Sr2+ cations was indicated by X-ray diffraction (XRD) analysis. The absorption of the chemical compounds on the surface was observed via Fourier transform infrared (FT-IR) spectroscopy. The optical orientation was measured by ultraviolet–visible diffused reflectance spectroscopy (UV-DRS) analysis. The surface area, morphology, and elemental purity were analyzed using field emission scanning electron microscopy (FE-SEM), high-resolution transmission electron microscopy (HR-TEM), and energy-dispersive spectroscopy (EDS) analyses. The oxidation state and valency of the synthesized nanoparticles were analyzed using X-ray photoelectron spectroscopy (XPS). Sr-doped ZnSe nanoparticles were investigated for photocatalytic degradation of methyl orange (MO), and their antibacterial potential was investigated against different bacterial strains. The antibacterial activity examined against Staphylococcus aureus and Escherichia coli implied the excellent biological activity of the nanoparticles. Moreover, the Sr-doped ZnSe nanoparticles were evaluated by the successful degradation of methyl orange under visible light irradiation. Therefore, Sr-doped ZnSe nanoparticles have tremendous potential in biological and water remediation fields.

2019 ◽  
Vol 26 (1) ◽  
pp. 104-113 ◽  
Author(s):  
Xian-sheng Wang ◽  
Yu-duo Zhang ◽  
Qiao-chu Wang ◽  
Bo Dong ◽  
Yan-jia Wang ◽  
...  

AbstractZnO is modified by Cu2O by the process of precipitation and calcination. X-ray diffraction has shown that Cu2O/ZnO catalysts are made of highly purified cubic Cu2O and hexagonal ZnO. Scanning electron microscopy and transmission electron microscopy have shown that ZnO adhered to the surface of Cu2O. Due to the doping of Cu2O, the absorption range of the Cu2O/ZnO catalyst is shifted from the ultraviolet to the visible region due to diffuse reflection. X-ray photoelectron spectroscopy and photoluminescence spectra have confirmed that there is a substantial interaction between the two phases of the resultant catalyst. The degradation efficiency of Cu2O/ZnO on methyl orange solution is obviously enhanced compared to Cu2O and ZnO. The maximum degradation efficiency is 98%. The degradation efficiency is affected by the pH of the solution and initial concentration. After three rounds of recycling, the degradation rate is almost same. This shows a consistent performance of Cu2O/ZnO. The increase in catalytic ability is related to the lattice interaction caused by the doping of Cu2O.


2011 ◽  
Vol 197-198 ◽  
pp. 919-925 ◽  
Author(s):  
Min Wang ◽  
Qiong Liu

Silver (Ag+) doped iron (III) vanadate (FeVO4) samples are prepared by the precipitation method and then characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), and X-ray photoelectron spectroscopy(XPS). The photocatalytic activity under visible light is evaluated by photocatalytic degradation of methyl orange (MO) in the solution. The results show that both FeVO4 and Ag+ doped FeVO4 samples are triclinic, the later have different surface morphology, and some needle-shaped materials appear in the later. From XPS, there are more Fe2+ ions in Ag+ doped FeVO4 sample than that in FeVO4 one without Ag+. It indicates that Ag+ doping can increase the density of the surface oxygen vacancies of catalysts, which can act as electron traps promoting the electron-hole separation and then increase the photo-activity. The decoloration rate after Ag+ doping against methyl orange solution can reach about 81%, and be more about 20% than that of pure FeVO4.


2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Sasikala Sundar ◽  
V. Ganesh

Abstract Magnetic nanoparticles of iron oxide (γ-Fe2O3) have been prepared using bio-assisted method and their application in the field of biosensors is demonstrated. Particularly in this work, different nanostructures of γ-Fe2O3 namely nanospheres (NS), nanograsses (NG) and nanowires (NW) are prepared using a bio-surfactant namely Furostanol Saponin (FS) present in Fenugreek seeds extract through co-precipitation method by following “green” route. Three distinct morphologies of iron oxide nanostructures possessing the same crystal structure, magnetic properties, and varied size distribution are prepared and characterized. The resultant materials are analyzed using field emission scanning electron microscopy, transmission electron microscopy, powder X-ray diffraction, X-ray photoelectron spectroscopy, vibrating sample magnetometer and Fourier transform infrared spectroscopy. Moreover, the effect of reaction time and concentration of FS on the resultant morphologies of γ-Fe2O3 nanostructures are systematically investigated. Among different shapes, NWs and NSs of γ-Fe2O3 are found to exhibit better sensing behaviour for both the individual and simultaneous electrochemical detection of most popular biomarkers namely dopamine (DA) and uric acid (UA). Electrochemical studies reveal that γ-Fe2O3 NWs showed better sensing characteristics than γ-Fe2O3 NSs and NGs in terms of distinguishable voltammetric signals for DA and UA with enhanced oxidation current values. Differential pulse voltammetric studies exhibit linear dependence on DA and UA concentrations in the range of 0.15–75 µM and 5 μM – 0.15 mM respectively. The detection limit values for DA and UA are determined to be 150 nM and 5 µM. In addition γ-Fe2O3 NWs modified electrode showed higher sensitivity, reduced overpotential along with good selectivity towards the determination of DA and UA even in the presence of other common interferents. Thus the proposed biosensor electrode is very easy to fabricate, eco-friendly, cheaper and possesses higher surface area suggesting the unique structural patterns of γ-Fe2O3 nanostructures to be a promising candidate for electrochemical bio-sensing and biomedical applications.


2012 ◽  
Vol 624 ◽  
pp. 88-93 ◽  
Author(s):  
En Lei Qi ◽  
Ben Niu ◽  
Shi Lei Zhang ◽  
Jie Qiang Wang

CeO2 nanobundles were obtained by the microwave homogeneous precipitation method using cerium nitrate and urea as raw materials. Ag nanoparticles were obtained by the microwave solvolthermal method using silver nitrate, PVP and ethanol as raw materials. Nanostructured Ag/CeO2 was prepared by the impregnation method. The products were characterized by X-ray diffraction, SEM, TEM, UV-vis spectrum, BET. The photocatalytic properties of CeO2 and Ag/CeO2 nanomaterials were evaluated by degradation of methyl orange. The results show that the photocatalytic degradation of modified cerium oxide modified by nano silver on methyl orange is significantly improved. For the Ag (0.1 wt%)/CeO2 material, the degradation rate on methyl orange is up to 83.2% under visible light irradiation for 1h. The catalytic activity of nanostructured Ag (0.1 wt%)/CeO2 in dye decolorization is substantially higher than the standard reference TiO2 P25.


2007 ◽  
Vol 280-283 ◽  
pp. 305-310
Author(s):  
Tao Yan ◽  
Xiao Lin Liu ◽  
Jian Feng Chen

The sensitivity of CuO dispersed on fluorite-type oxide, namely CeO2 was studied in this work. Mixed oxide sample of nanostructured CuxCe1-xO2-y of various composition were generated by step chemical precipitation method. Distinct copper species were identified as a function of copper content by X-ray photoelectron spectroscopy, X-ray powder diffraction, the special surface areas, transmission electron microscopy, scanning electron microscopy analysis, and sensing properties to CO. It was found that only small amounts of copper are sufficient to promote the sensitivity of CeO2 by several orders of magnitude, which excessive amounts of copper (Cu/(Cu+Ce)>0.12) are detrimental to the sensing properties of nanocompositions. The possible causes for this behavior are also discussed.


2014 ◽  
Vol 1004-1005 ◽  
pp. 962-966
Author(s):  
Lu Sheng Chen ◽  
Huan Shuang Zhang ◽  
Shu Lian Liu ◽  
Wen Hua Song ◽  
Chao Liu ◽  
...  

In this work, samarium and antimony (Sm–Sb) codoped tin oxide (SnO2) films have been successfully prepared on titanium (Ti) substrate by a facile sol gel method. The samples were characterized by X–ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The composite film materials were used as anode for the electro-degradation of methyl orange solution. Two effective factors of electro–catalytic properties namely, the content of Sm in the SnO2 samples and the calcination temperature, have been optimized based on the electro-degradation experiments. A moderately calcination temperature of 873 K and 1.0% Sm doping owned the best performance. The smaller grain sizes and optical band gap of the SnO2 by introduction of the Sm improved electro-catalytic activity.


2012 ◽  
Vol 624 ◽  
pp. 67-71
Author(s):  
Si Qin Zhao ◽  
Hong Liang Wan ◽  
S. Asuha

Nanowires of sodium titanate, TiO2 and Eu3+/TiO2 were synthesized by hydrothermal method, and their microstructure, optical properties and valence states of exterior elements were characterized by X-ray powder diffraction (XRD), scanning electron microscopy(SEM), X-ray photoelectron spectroscopy (XPS) and UV-Vis diffuse reflectance spectroscopy techniques. At the same time, the photocatalytic activities of the materials for degradation of methyl orange under visible-light irradiation were also investigated. The results showed the formation of nanowires of sodium titanate with average crystallite sizes of 50-200 nm and in lengths from several microns to several dozens microns, and its chemical formula was determined to be Na2Ti3O7. TiO2 and Eu3+ /TiO2nanowires were prepared from the Na2Ti3O7 nanowires via ion exchange (i.e., with H+ and Eu3+ ions) and high temperature sintering processes. These three kinds of nanowires showed different photocatalytic activities for degradation of methyl orange. Na2Ti3O7 nanowire did not show any photocatalytic activity for methyl orange degradation, while TiO2 nanowire was superior to Na2Ti3O7 nanowire; and, Eu3+/ TiO2 nanowire possessed the highest photocatalytic activity.


NANO ◽  
2017 ◽  
Vol 12 (05) ◽  
pp. 1750054 ◽  
Author(s):  
Aijia Wei ◽  
Wen Li ◽  
Lihui Zhang ◽  
Xiaohui Li ◽  
Xue Bai ◽  
...  

Zn[Formula: see text] and F[Formula: see text] ions are successfully used to modify pure Li4Ti5O[Formula: see text] via a co-precipitation method followed by calcination at 400[Formula: see text]C for 5[Formula: see text]h in an Ar atmosphere in order to further investigate the reaction mechanism of the fluoride modification process. Zn[Formula: see text] and F[Formula: see text] co-modified Li4Ti5O[Formula: see text] samples are characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and electrochemical measurements. After the modification process, no ZnF2 coating layer is formed on the surface of Li4Ti5O[Formula: see text], instead, F[Formula: see text] ions react with Li4Ti5O[Formula: see text] to generate a new phase, composed of a small amount of anatase TiO2, rutile TiO2, LiF, and Zn[Formula: see text] ions are suspected to form a ZnO coating layer on Li4Ti5O[Formula: see text] particles. The electrolyte reduction decomposition is suppressed in Zn[Formula: see text] and F[Formula: see text] co-modified Li4Ti5O[Formula: see text] due to the ZnO coating layer. 1[Formula: see text]wt.% Zn[Formula: see text] and F[Formula: see text] co-modified Li4Ti5O[Formula: see text] exhibits the best rate capability, which leads to a charge capacity of 236.7, 227.8, 222.1, 202.7, 188.9 and 150.7[Formula: see text]mAh g[Formula: see text] at 0.2C, 0.5C, 1C, 3C, 5C and 10C, respectively, between 0[Formula: see text]V and 3[Formula: see text]V. Furthermore, 1[Formula: see text]wt.% Zn[Formula: see text] and F[Formula: see text] co-modified Li4Ti5O[Formula: see text] exhibits 96.0% charge capacity retention at 3C rate after 200 cycles, which is significantly higher than that of pure Li4Ti5O[Formula: see text] (78.4%).


2016 ◽  
Vol 73 (7) ◽  
pp. 1746-1755 ◽  
Author(s):  
Roushan Khoshnavazi ◽  
Shler Fereydouni ◽  
Leila Bahrami

The synergistic effect of polyoxometalate (POM) and metal-doped TiO2 (metal = Zr, Y and Ce) was examined, to fabricate nanocomposites with enhanced photocatalytic activities toward the degradation of methyl orange (MO), as a model textile dye. A series of new nanocomposites, containing different loading amounts of H9Na3[WZn3(H2O)2(ZnW9O34)2].24H2O (HZnW) (10–30%) on each of the metal-doped TiO2 nanoparticles, were synthesized using impregnation method. The morphology and crystal phase of the as-prepared nanocomposites were investigated by various characterization techniques: Fourier transform infrared spectroscopy, scanning electron microscopy, transmission electron microscopy, X-ray diffraction, energy-dispersive X-ray analysis and diffuse reflectance spectroscopy, indicating that the HZnW and metal-doped TiO2 had been successfully incorporated into the nanocomposite structure. The effects of parameters such as loading amount of HZnW, catalyst dose, pH and initial concentration of dye solution were investigated on the degradation kinetics and it was interestingly found that the prepared nanocomposites could efficiently degrade the MO dye in 5–7 min under UV light irradiation. The best results were obtained for the HZnW-Zr-TiO2 among the different nanocomposites. Also, control studies showed the superior photocatalytic properties of composites compared to that of the individual components. The facile preparation and their improved photocatalytic activities suggest that these materials can have a promising future for water and wastewater purifications.


Author(s):  
Fengfeng Li ◽  
Mingxi Zhang ◽  
Jin Wang ◽  
Yongfeng Cai ◽  
Dushao Zhao ◽  
...  

Abstract In this work, we fabricate a highly efficient photocatalytic AgBr/Ag2CO3 heterojunction through the co-precipitation method. The obtained samples were characterized by means of X-ray diffraction, scanning electron microscopy, transmission electron microscopy, ultraviolet-visible diffuse reflectance spectra and X-ray photoelectron spectroscopy. The photocatalytic activities of obtained samples can be assessed by visible light (λ ≥ 400 nm) degradation of rhodamine B solution. X-ray diffraction revealed that the crystallinity of the AgBr/Ag2CO3heterojunction was significantly higher than pure AgBr and Ag2CO3. Moreover, the AgBr/ Ag2CO3 heterojunction prepared at pH = 6 has the best photocatalytic performance, it can raise the degradation degree of rhodamine B over 95% at 20 min. Finally, a possible photocatalytic mechanism is discussed.


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