Bimetallic Alloy of Fe2O3-Ag Nanoparticles: Characterization and Structural Modeling

2016 ◽  
Vol 1816 ◽  
Author(s):  
A. Ruíz-Baltazar ◽  
R. Esparza ◽  
J.L López-Miranda ◽  
G. Rosas ◽  
R. Pérez

ABSTRACTThe synthesis of Fe3O4-Ag bimetallic nanoparticles by chemical reduction was carried out. Fe nanoparticles were obtained using Fe (III) Chloride hexahydrate (FeCl3•6H2O) as precursor and sodium borohydride (NaBH4) as reducing agent, subsequently, a solution of silver nitrate (AgNO3) was added to the reaction. The synthesis methodology employed in this case, is a modification of chemical reduction method. Through this procedure has been possible simplify the synthesis route used to obtain bimetallic systems such as Fe3O4-Ag. Particles with semi-spherical morphology were observed. High-resolution transmission electron microscopy (HREM), ultraviolet visible spectroscopy (UV-is) and quasi-elastic light scattering (QELS) techniques were employed for the structural characterization of Fe3O4-Ag nanostructures. Some models presented describe and prove the formation of the Fe3O4-Ag alloy type structures.

2015 ◽  
Vol 2015 ◽  
pp. 1-6 ◽  
Author(s):  
Alvaro Ruíz-Baltazar ◽  
Simón Yobanny Reyes-López ◽  
Rodrigo Esparza ◽  
Miriam Estévez ◽  
Ángel Hernández-Martínez ◽  
...  

The synthesis ofα-Fe2O3-Ag bimetallic nanoparticles using a novel and simplified route is presented in this work. These hybrid nanoparticles were produced using a modification of the chemical reduction method by sodium borohydride (NaBH4). Fe(III) chloride hexahydrate (FeCl3·6H2O) and silver nitrate (AgNO3) as precursors were employed. Particles with semispherical morphology and dumbbell configuration were observed. High-resolution transmission electron microscopy (HRTEM) technique reveals the structure of the dumbbell-likeα-Fe2O3-Ag nanoparticles. Some theoretical models further confirm the formation of theα-Fe2O3-Ag structures. Analysis by cyclic voltammetry reveals an interesting catalytic behavior which is associated with the combination of the individual properties of the Ag andα-Fe2O3nanoparticles.


MRS Advances ◽  
2017 ◽  
Vol 2 (50) ◽  
pp. 2857-2863 ◽  
Author(s):  
A. Santoveña ◽  
C. Rodriguez-Proenza ◽  
J.A. Maya-Cornejo ◽  
A. Ruiz-Baltazar ◽  
D. Bahena ◽  
...  

ABSTRACTBimetallic nanoparticles are of special interest for their potential applications to fuel cells, among the bimetallic systems, AuPd bimetallic nanoparticles have received great interest as they can be widely used as effective catalysts for various electrochemical reactions. Monodisperse AgPd alloy nanoparticles were synthesized by polyol method using silver nitrate and potassium tetrachloropalladate(II) in ethylene glycol as the reducing agent at 160 °C. Structural, compositional and electrochemical characterizations of synthesized bimetallic nanoparticles were investigated. High-angle annular dark field scanning/transmission electron microscopy (HAADF-STEM) images and parallel beam X-ray diffraction (XRD) of the bimetallic nanoparticles were obtained. XRD and the contrast of the HAADF-STEM images show that the bimetallic nanoparticles have an alloy structure. Cyclic voltammetry was carried out in order to confirm the electrochemical responses of the AgPd/C electrocatalysts for methanol oxidation. Thanks to the narrow size distribution of the AgPd alloy bimetallic nanoparticles (9.15 nm) the supported AgPd/C electrocatalysts have high catalytic activity toward methanol electro-oxidation.


2004 ◽  
Vol 818 ◽  
Author(s):  
Ru-Shi Liu ◽  
Hau-Ming Chen ◽  
Shu-Fen Hu

AbstractA systematic study is reported about the amount-dependent morphology change in a series of Au-Pt bimetallic nanoparticles synthesized using chemical reduction. The amount of Au precursor is kept constant throughout whole series of compounds to obtain fixed Au core size (∼7.5 nm). The Au/Pt ratio is varied from 1/1 to 1/4 in order to synthesize Pt shell layer of different thickness. We observed a remarkable shift of surface plasmon band around 410 nm. With the aid of high resolution transmission electron microscope (HRTEM) and energy-dispersive spectrometer (EDS), the composition of shell layer is found to be Pt enriched Au-Pt alloy. As the amount of Pt increases, the Pt clusters formed a string-like shape on the surface of nanoparticles. The average diameter of these Pt clusters is about 2 nm. This special structure may exhibit unique catalytic property.


2011 ◽  
Vol 2011 ◽  
pp. 1-5 ◽  
Author(s):  
Manuel Ramos ◽  
Domingo A. Ferrer ◽  
Russell R. Chianelli ◽  
Victor Correa ◽  
Joseph Serrano-Matos ◽  
...  

Bimetallic nanoparticles are important because they possess catalytic and electronic properties with potential applications in medicine, electronics, and chemical industries. A galvanic replacement reaction synthesis has been used in this research to form bimetallic nanoparticles. The complete description of the synthesis consists of using the chemical reduction of metallic silver nitrite (AgNO3) and gold-III chloride hydrate (HAuCl) salt precursors. The nanoparticles display round shapes, as revealed by high-resolution transmission electron microscope (HRTEM). In order to better understand the colloidal structure, it was necessary to employ computational models which involved the simulations of HRTEM images.


2012 ◽  
Vol 1372 ◽  
Author(s):  
A. Ruíz-Baltazar ◽  
Claudia López ◽  
R. Pérez ◽  
G. Rosas

ABSTRACTDifferent synthesis methods has been employed to produce nanoparticles, however, chemical reduction method offer a effective route to obtained sizes nanoparticles controlled and morphologies very well defined. Iron nanoparticles were synthesized by chemical reduction using sodium borohydride (SB) NaBH4, Fe (III) Chloride hexahydrate (FeCl3·6H2O) as starting metallic salt (MS) and Poly-vinyl pyrrolidone (PVP) as surfactant agent. The nanoparticles have been characterized by transmission electron microscopy (TEM) and UV-Vis spectroscopy.


2013 ◽  
Vol 760-762 ◽  
pp. 750-754
Author(s):  
Li Min Lu ◽  
Ou Zhang ◽  
Tao Nie ◽  
Jing Kun Xu ◽  
Kai Xin Zhang ◽  
...  

PtAu bimetallic nanoparticles (NPs) were successfully synthesized on single-stranded DNA functionalized graphene nanomaterials (ss-DNA/GR) via a simple chemical reduction method. The nanocomposites (PtAu/ss-DNA/GR) were characterized by transmission electron microscopy (TEM), energy-dispersive X-ray spectrometer (EDS) and electrochemical techniques. Then a sensitive dopamine (DA) sensor was fabricated based on PtAu/ss-DNA/GR nanocomposites modified glassy carbon electrode (GCE). The results of electrochemical experiments demonstrated that the sensor exhibited excellent electrocatalytic activity to the oxidation of DA. The sensor displayed wide linear detection range from 8.0×10-8 to 1.0×10-5 M and 1.0×10-5 to 5.0×10-5 M and a low detection limit of 1.0×10-8 M (S/N = 3). In addition, the sensor also showed high selectivity, good reproducibility and stability for DA detection. Thus, it is considered to be an ideal candidate for practical application.


MRS Advances ◽  
2016 ◽  
Vol 1 (36) ◽  
pp. 2525-2530
Author(s):  
Judith Tanori ◽  
Diana Vargas-Hernández ◽  
Elisa Martínez-Barbosa ◽  
Raúl Borja-Urby ◽  
Arturo García-Bórquez ◽  
...  

ABSTRACTSelf-assembling systems of amphiphilic molecules display structures similar to those of biomineralization natural systems. This allows to somehow mimic nature to synthesize nanomaterials with low polidispersity and with diverse morphologies. In this work we describe the synthesis and characterization of gold-copper, silver-copper, and gold-silver bimetallic nanoparticles by chemical reduction in self-assembling systems of two surfactants. The nanoparticles were characterized by Transmission Electron Microscopy and UV-Vis spectroscopy. We have prepared a composite material using mesoporous silica as support of the AuAg bimetallic nanoparticles. The system was used in photocatalysis experiments for water remediation applications. Our results show that the AuAg/SBA15 composite material degrades methyl orange in water from 17 ppm to 4 ppm in 30 minutes.


Nanomaterials ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 1499
Author(s):  
Angelina Pavlets ◽  
Anastasia Alekseenko ◽  
Vladislav Menshchikov ◽  
Sergey Belenov ◽  
Vadim Volochaev ◽  
...  

A carbon supported PtCux/C catalyst, which demonstrates high activity in the oxygen electroreduction and methanol electrooxidation reactions in acidic media, has been obtained using a method of chemical reduction of Pt (IV) and Cu (2+) in the liquid phase. It has been found that the potential range of the preliminary voltammetric activation of the PtCux/C catalyst has a significant effect on the de-alloyed material activity in the oxygen electroreduction reaction (ORR). High-resolution transmission electron microscopy (HRTEM) demonstrates that there are differences in the structures of the as-prepared material and the materials activated in different potential ranges. In this case, there is practically no difference in the composition of the PtCux-y/C materials obtained after activation in different conditions. The main reason for the established effect, apparently, is the reorganized features of the bimetallic nanoparticles’ surface structure, which depend on the value of the limiting anodic potential in the activation process. The effect of the activation conditions on the catalyst’s activity in the methanol electrooxidation reaction is less pronounced.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Jien Ye ◽  
Yi Wang ◽  
Qiao Xu ◽  
Hanxin Wu ◽  
Jianhao Tong ◽  
...  

AbstractPassivation of nanoscale zerovalent iron hinders its efficiency in water treatment, and loading another catalytic metal has been found to improve the efficiency significantly. In this study, Cu/Fe bimetallic nanoparticles were prepared by liquid-phase chemical reduction for removal of hexavalent chromium (Cr(VI)) from wastewater. Synthesized bimetallic nanoparticles were characterized by transmission electron microscopy, Brunauer–Emmet–Teller isotherm, and X-ray diffraction. The results showed that Cu loading can significantly enhance the removal efficiency of Cr(VI) by 29.3% to 84.0%, and the optimal Cu loading rate was 3% (wt%). The removal efficiency decreased with increasing initial pH and Cr(VI) concentration. The removal of Cr(VI) was better fitted by pseudo-second-order model than pseudo-first-order model. Thermodynamic analysis revealed that the Cr(VI) removal was spontaneous and endothermic, and the increase of reaction temperature facilitated the process. X-ray photoelectron spectroscopy (XPS) analysis indicated that Cr(VI) was completely reduced to Cr(III) and precipitated on the particle surface as hydroxylated Cr(OH)3 and CrxFe1−x(OH)3 coprecipitation. Our work could be beneficial for the application of iron-based nanomaterials in remediation of wastewater.


Materials ◽  
2021 ◽  
Vol 14 (9) ◽  
pp. 2326
Author(s):  
Entesar Ali Ganash ◽  
Reem Mohammad Altuwirqi

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.


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