Formation and Electrical Interfacing of Nanocrystal-Molecule Nanostructures

2009 ◽  
Vol 1154 ◽  
Author(s):  
Claire Barrett ◽  
Gaëtan Lévêque ◽  
Hugh Doyle ◽  
Donocadh P Lydon ◽  
Gareth Redmond ◽  
...  

AbstractThe formation of nanocrystal-molecule-nanocrystal nanostructures via controlled mixing of Au nanocrystals and bifunctional Re linkers is reported. UV-visible absorbance data, coupled with histogram analysis of nanostructures measured using Scanning Electron Microscopy has shown a characteristic optical response at wavelengths close to 600 nm following formation of dimer and trimer nanostructures. Directed assembly processes based on dielectrophoretic trapping have also been developed for electrical interfacing of these nanostructures between top-down nanoelectrode pairs for electrical characterization.

2019 ◽  
Vol 824 ◽  
pp. 163-167
Author(s):  
Pema Dechen ◽  
Ekasith Somsook

In this report, synthesis and characterization of gold nanoparticles (AuNPs) from gold leaf by electrolysis in two different media (gel and paper) in presence of sodium chloride (NaCl), glucose (C6H12O6) and polyvinyl pyrrolidone (PVP) at room temperature were investigated. Graphite was used as two electrodes, NaCl was used as an electrolyte, C6H12O6 was used as reducing agent and PVP was used as stabilizer to control the aggregation of the nanoparticles. UV-Visible spectroscopy (UV-Vis) and scanning electron microscopy (SEM) were used to confirm the characteristics and morphologies of the synthesized AuNPs.


2018 ◽  
Author(s):  
H.H. Yap ◽  
C.K. Oh

Abstract The ability to expose a huge kerf/PCM (Process Control Monitor) test structure at the same level is limited from top down finger polishing. Also, in Scanning Electron Microscopy (SEM) the electron beam (e-beam) shift for electron beam absorbed current (EBAC) analysis is not able to cover the whole structure. The recently implemented technique described herein combines the focus ion beam (FIB) chemical enhanced milling method with EBAC analysis to stop the polishing at the upper layer and split the EBAC analysis into portions from the test structure. These help to improve the area of interest (AOI) evenness and enable the extension of the EBAC analysis.


2021 ◽  
Vol 43 (1) ◽  
pp. 14-14
Author(s):  
Fazal Akbar Jan Fazal Akbar Jan ◽  
Muhammad Aamir Muhammad Aamir ◽  
Naimat Ullah and Husaain Gulab Naimat Ullah and Husaain Gulab

The synthesized oxide (SnO2) nanoparticles by sol-gel method were characterized using UV-Visible spectroscopy (UV-Vis), Fourier Transform Infrared spectroscopy (FTIR), X-rays diffraction(XRD) and Scanning electron microscopy(SEM). Using X-rays diffraction analysis different parameter were calculated such as crystallite size, d-spacing, dislocation density, number of unit cell, cell volume, morphological index, micro strain and instrumental broadening. The average particle size was 28.396 nm. Scanning electron microscopy revealed that SnO2 nanopartcles are uniformly distributed. Optical properties such as band gap (energy gap = 3.6 eV) was calculated from UV-Visible spectroscopy. The characterized particles were used as photocatalyst for the degradation of Eosin dye in aqueous solution under UV light. The effect of different parameters i.e irradiation time, initial dye concentration, pH of the medium and catalyst weight on percent degradation was also studied. Mmaximum dye degradation was found at 220 minutes time interval that was 92 % using 10 ppm solution. At pH 5 the degradation of dye was found to be 94%. The catalyst dose of 0.06 g was found to be the optimum weight for the best photo catalytic degradation of Eosin Y.


2021 ◽  
Vol 43 (1) ◽  
pp. 14-14
Author(s):  
Fazal Akbar Jan Fazal Akbar Jan ◽  
Muhammad Aamir Muhammad Aamir ◽  
Naimat Ullah and Husaain Gulab Naimat Ullah and Husaain Gulab

The synthesized oxide (SnO2) nanoparticles by sol-gel method were characterized using UV-Visible spectroscopy (UV-Vis), Fourier Transform Infrared spectroscopy (FTIR), X-rays diffraction(XRD) and Scanning electron microscopy(SEM). Using X-rays diffraction analysis different parameter were calculated such as crystallite size, d-spacing, dislocation density, number of unit cell, cell volume, morphological index, micro strain and instrumental broadening. The average particle size was 28.396 nm. Scanning electron microscopy revealed that SnO2 nanopartcles are uniformly distributed. Optical properties such as band gap (energy gap = 3.6 eV) was calculated from UV-Visible spectroscopy. The characterized particles were used as photocatalyst for the degradation of Eosin dye in aqueous solution under UV light. The effect of different parameters i.e irradiation time, initial dye concentration, pH of the medium and catalyst weight on percent degradation was also studied. Mmaximum dye degradation was found at 220 minutes time interval that was 92 % using 10 ppm solution. At pH 5 the degradation of dye was found to be 94%. The catalyst dose of 0.06 g was found to be the optimum weight for the best photo catalytic degradation of Eosin Y.


2015 ◽  
Vol 30 ◽  
pp. 106-115 ◽  
Author(s):  
Soheila Honary ◽  
Hamed Barabadi ◽  
Pouneh Ebrahimi ◽  
Farzaneh Naghibi ◽  
Ahad Alizadeh

This study aimed to biosynthesize and optimize the process of iron oxide nanoparticles producing by Penicilliumwaksmanii isolated from soil by employing mathematical methodology. The synthesized nanoparticles were formed with fairly well-defined dimensions with good monodispersity determined by SEM (Scanning Electron Microscopy), AFM (Atomic Force Microscopy), DLS (Dynamic Light Scattering), UV-Visible spectroscopy, zeta potential, polydispersity index (PDI) and correlogram of nanoparticles. The effects of different factors such as pH, temperature and concentration of FeCl3 on the particle size were investigated by Box-Behnken experimental design. The R2 value was calculated to be 0.9992 indicating the accuracy and ability of the polynomial model.


2020 ◽  
Vol 10 (8) ◽  
pp. 1300-1307
Author(s):  
Zigong Chang ◽  
Haiyun Jiang ◽  
Ruomei Wu ◽  
Weili Zhang ◽  
Hui Zeng ◽  
...  

The film of PEDOT was prepared in this study via electrochemical polymerization using EDOT as monomer in LiClO4/PC solution. The effects on the properties of the film were surveyed including the deposition voltage and deposition time. The morphology of the film was observed by scanning electron microscopy. The electrochromic kinetics was analyzed by combination of electrochemical workstation and UV-Visible spectrophotometer such as the transmittance, transmittance contrast, coloring efficiency and the response time. The results indicated the film presents a coral shape despites of the deposition voltage and the deposition time. In case of the application as electrochromic film, the optimal process condition is 1.3 V and 24 s. The corresponding transmittance is 82.77% in fade state. The transmittance contrast is 17.87%, and the coloring efficiency is about 117.92 cm2/C, the response time is 0.52 s.


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