Synthesis of InP and InAs quantum rods using Indium Acetate and Myristic acid

2004 ◽  
Vol 848 ◽  
Author(s):  
Itzhak Shweky ◽  
Assaf Aharoni ◽  
Taleb Mokari ◽  
Moshe Nadler ◽  
Eli Rothenberg ◽  
...  

ABSTRACTThe development of solution based synthesis approaches for preparing nanocrystals of III-V semiconductor presents a significant & important challenge especially with relation to shape control to achieve rod growth. To this end, a novel approach for synthesis of soluble semiconductor quantum rods using metal nanoparticles to direct and catalyze one-dimensional growth is developed. The synthesis method is useful in particular for III-V semiconductor with cubic lattice, where the utilization of surfactant-controlled rod-growth is not easily realized. The growth takes place via the solution–liquid–solid (SLS) mechanism where proper precursors are injected into a coordinating solvent as we reported in earlier work for InAs nanorods. Herein, we report the synthesis of high quality InP nanorods using Indium Acetate and myristic acid with gold nanoparticles as the catalysts in the SLS growth mode. A similar route was successfully developed for the growth of InAs nanorods. We find that the amount of Au catalyst in the reaction is an important parameter to achieving shape control. Transmission electron microscope (TEM) images of InP and InAs nanocrystals revealed that the crystals are mostly rod-shaped. XRD measurements, absorption spectra were preformed for the nanorods characterization.

2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
Abdullah Khalil ◽  
Mustapha Jouiad ◽  
Marwan Khraisheh ◽  
Raed Hashaikeh

A novel approach for synthesizing copper oxide (CuO) nanoparticles (NPs) through electrospinning is reported. The approach is based on producing rough and discontinuous electrospun nanofibers from a precursor based on copper acetate salt and polyvinyl alcohol (PVA) polymer. Selectively removing the polymeric phase from the fibers produced highly rough CuO nanofibers, which were composed of NPs that are weakly held together in a one-dimensional (1D) manner. Sonication in a suitable liquid under controlled conditions completely disintegrated the nanofibers into NPs, resulting in the formation of uniform CuO NPs suspension. Aberration corrected high resolution transmission electron microscope (HRTEM) showed that the obtained NPs are highly crystalline and nearly sphere-like with a diameter of 30 to 70 nm. Thus, electrospinning, which is a low cost and industrially scalable technique, can also be employed for economic and large scale synthesis of NPs.


2019 ◽  
Author(s):  
Chem Int

This research work presents a facile and green route for synthesis silver sulfide (Ag2SNPs) nanoparticles from silver nitrate (AgNO3) and sodium sulfide nonahydrate (Na2S.9H2O) in the presence of rosemary leaves aqueous extract at ambient temperature (27 oC). Structural and morphological properties of Ag2SNPs nanoparticles were analyzed by X-ray diffraction (XRD) and transmission electron microscopy (TEM). The surface Plasmon resonance for Ag2SNPs was obtained around 355 nm. Ag2SNPs was spherical in shape with an effective diameter size of 14 nm. Our novel approach represents a promising and effective method to large scale synthesis of eco-friendly antibacterial activity silver sulfide nanoparticles.


Author(s):  
Zhibin Liu ◽  
Keda Ding ◽  
Zhifu Liu ◽  
Faqiang Zhang ◽  
Huarong Zeng ◽  
...  

2021 ◽  
Vol 5 (1) ◽  
Author(s):  
Tushar Gupta ◽  
Kenan Elibol ◽  
Stefan Hummel ◽  
Michael Stöger-Pollach ◽  
Clemens Mangler ◽  
...  

AbstractTwo-dimensional (2D) antimony (Sb, “antimonene”) is of interest in electronics and batteries. Sb however exhibits a large allotropic structural diversity, which is also influenced by its support. Thus, Sb heterostructure formation is key in 2D Sb integration. Particularly, 2D Sb/graphene interfaces are important. We thus study here few-layered 2D Sb/graphene heterostructures with atomic resolution (scanning) transmission electron microscopy. We find two Sb morphologies to coexist: first, a 2D morphology of layered β-Sb with β-Sb(001)||graphene(001) texture. Second, one-dimensional Sb nanowires which can be matched to β-Sb[2-21]⊥graphene(001) and are closely related to cubic Sb(001)||graphene(001). Importantly, both Sb morphologies show rotational van-der-Waals epitaxy with graphene. Both are resilient against oxidation, although superficial Sb-oxide formation merits consideration, including epitaxial Sb2O3(111)/β-Sb(001) heterostructures. Exact Sb growth behavior depends on processing and substrate properties including, notably, the support underneath the graphene. Our work elucidates the rich phase and epitaxy landscape in 2D Sb and 2D Sb/graphene heterostructures.


Antibiotics ◽  
2021 ◽  
Vol 10 (6) ◽  
pp. 678
Author(s):  
Abdallah S. Abdelsattar ◽  
Rana Nofal ◽  
Salsabil Makky ◽  
Anan Safwat ◽  
Amera Taha ◽  
...  

The emergence and evolution of antibiotic-resistant bacteria is considered a public health concern. Salmonella is one of the most common pathogens that cause high mortality and morbidity rates in humans, animals, and poultry annually. In this work, we developed a combination of silver nanoparticles (AgNPs) with bacteriophage (phage) as an antimicrobial agent to control microbial growth. The synthesized AgNPs with propolis were characterized by testing their color change from transparent to deep brown by transmission electron microscopy (TEM) and Fourier-Transform Infrared Spectroscopy (FTIR). The phage ZCSE2 was found to be stable when combined with AgNPs. Both minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) were evaluated for AgNPs, phage, and their combination. The results indicated that MIC and MBC values were equal to 23 µg/mL against Salmonella bacteria at a concentration of 107 CFU/mL. The combination of 0.4× MIC from AgNPs and phage with Multiplicity of Infection (MOI) 0.1 showed an inhibitory effect. This combination of AgNPs and phage offers a prospect of nanoparticles with significantly enhanced antibacterial properties and therapeutic performance.


Catalysts ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. 640
Author(s):  
Hideaki Sasaki ◽  
Keisuke Sakamoto ◽  
Masami Mori ◽  
Tatsuaki Sakamoto

CeO2-based solid solutions in which Pd partially substitutes for Ce attract considerable attention, owing to their high catalytic performances. In this study, the solid solution (Ce1−xPdxO2−δ) with a high Pd content (x ~ 0.2) was synthesized through co-precipitation under oxidative conditions using molten nitrate, and its structure and thermal decomposition were examined. The characteristics of the solid solution, such as the change in a lattice constant, inhibition of sintering, and ionic states, were examined using X-ray diffraction (XRD), scanning electron microscopy–energy-dispersive X-ray spectroscopy (SEM−EDS), transmission electron microscopy (TEM)−EDS, and X-ray photoelectron spectroscopy (XPS). The synthesis method proposed in this study appears suitable for the easy preparation of CeO2 solid solutions with a high Pd content.


2019 ◽  
Vol 19 (01) ◽  
pp. 1950003
Author(s):  
P. R. Ghutepatil ◽  
S. H. Pawar

In this paper, uniform and superparamagnetic nanoparticles have been prepared using one-step polyol synthesis method. Structural, morphological and magnetic properties of obtained MnFe2O4 nanoparticles have been investigated by using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), field emission scanning electron microscope (FE-SEM), transmission electron microscopy (TEM), vibrating sample magnetometry (VSM) and thermogravimetric analysis (TGA) techniques. Structural investigation showed that the average crystallite size of obtained nanoparticles was about 10[Formula: see text]nm. Magnetic study revealed that the nanoparticles were superparamagnetic at room temperature with magnetization 67[Formula: see text]emu/g at room temperature. The self-heating characteristics of synthesized MnFe2O4 nanoparticles were studied by applying external AC magnetic field of 167.6 to 335.2[Formula: see text]Oe at a fixed frequency of 265[Formula: see text]kHz. The SAR values of MnFe2O4 nanoparticles were calculated for 2, 5, 10[Formula: see text]mg[Formula: see text]mL[Formula: see text] concentrations and it is observed that the threshold hyperthermia temperature is achieved for all concentrations.


2020 ◽  
Vol 302 ◽  
pp. 123-134
Author(s):  
Thammanoon Kapanya ◽  
Chanchana Thanachayanont ◽  
Adisorn Tuantranont ◽  
Thapanee Sarakonsri

Synthesis routes of CoSb3 need a long reaction time, especially at high temperature and-/or high pressure. Although the modified polyol process assisted with microwave radiation can be used to solve these problems, it used the excess amount of Sb ion. Therefore, this study aimed to solve this drawback by retarding the rate of reduction. The different microwave times (0, 1, and 3 min) were investigated to find out the shortest heating duration for preparing CoSb3 nanoparticles. Te-doped and Sn-doped CoSb3 were synthesized to investigate the benefit of this synthesis method for increasing the solubility limit of Te and Sn in the CoSb3 structure. The phase and microstructure of the synthesized products were characterized by using x-ray diffraction (XRD), scanning electron microscope (SEM) and transmission electron microscope (TEM). The results showed that the high crystalline phase of CoSb3 (JCPDS: 78-0977) without any metallic impurity phases product was successfully synthesized in 3 minutes for a heating time at normal pressure, non-excessive addition of Sb ion precursor, and low temperature. The XRD results of Te-doped and Sn-doped CoSb3 products exhibited poor crystalline phase and hard to exactly identify. In SEM and TEM results, the CoSb3 powder consisted of very tiny spherical-like particles around 10 nanometers attaching together even at different microwave time similar to Te-doped/Sn-doped samples.


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