scholarly journals Flexible transparent electrodes based on silver nanowires synthesized via a simple method

2017 ◽  
Vol 4 (9) ◽  
pp. 170756 ◽  
Author(s):  
De Li ◽  
Tao Han ◽  
Lei Zhang ◽  
Huai Zhang ◽  
Hui Chen

Silver nanowires (Ag NWs) with the length of approximately 60 µm and the diameter of approximately 300 nm are prepared via a simple, cost-effective, high-yield and eco-friendly procedure under a high molar concentration ratio of silver nitrate (AgNO 3 ) solution to poly(vinyl pyrrolidone) solution. The pre-synthesized Ag NWs were analysed by scanning electron microscopy, X-ray diffraction and UV–visible spectrophotometer. Furthermore, the as-prepared silver nanowires were roll-coated on the surfaces of the polyethylene terephthalate (PET) substrates. By optimizing the concentration of silver nanowire solution, the flexible Ag NW/PET transparent electrodes with a sheet resistance of 3.8 Ω sq −1 at a transmittance of 70% can be fabricated. The results reported in this paper provide a basis for optimizing the growth of silver nanowires and performances of transparent electrodes.

2016 ◽  
Vol 2016 ◽  
pp. 1-8 ◽  
Author(s):  
Mohammad Taghi Satoungar ◽  
Hamed Azizi ◽  
Saeid Fattahi ◽  
Mohammad Khajeh Mehrizi ◽  
Hedieh Fallahi

Synthesis and characterization of multiple crystalline silver nanowires (NWs) with uniform diameters were carried out by using 1,2-propandiol and ethylene glycol (EG) as comediated solvents and FeCl3as mediated agent in the presence of poly(vinyl pyrrolidone) (PVP). Experimental data and structural characterizations revealed that AgNWs have evolved from the multiple crystalline seeds initially generated by reduction of AgNO3with EG and 1,2-propandiol followed by reducing Fe(III) to Fe(II) which in turn reacts with and removes adsorbed atomic oxygen from the surfaces of silver seeds. In addition, uniform silver nanowires were obtained by using FeCl2and AlCl3as mediated agents in EG solution. Field emission scanning electron microscopy (FESEM) and transmission electron microscopy (TEM) showed uniform nanowires in both diameter and length. UV-Vis spectra showed adsorption peaks confirming the formation of nanowires. X-ray diffraction (XRD) patterns displayed the final product with high crystallinity and purity. In this study, a growth mechanism for forming AgNWs was proposed and a comparison between different mediated agents was carried out.


Materials ◽  
2021 ◽  
Vol 14 (9) ◽  
pp. 2219
Author(s):  
Xiaopeng Li ◽  
Jiayue Zhou ◽  
Dejun Yan ◽  
Yong Peng ◽  
Yong Wang ◽  
...  

In this paper, silver nanowires (AgNWs) with a diameter of 40 nm and a length of 45 μm were dispersed into an ethanol solution to prepare AgNW solutions with concentrations of 1, 2, and 3 mg/mL, respectively. The AgNW solutions were then deposited on a glass substrate using spin-coating at 1000, 2000, and 3000 rpm for 45 s, respectively, to prepare transparent electrodes. The results showed that the distribution of AgNWs on the substrate increased in density with the increase in the AgNW solution concentration and the decrease in spin speed. The effect of concentration on the distribution of AgNWs was greater than that of the spin speed. The transmittance of each electrode was between 84.19% and 88.12% at 550 nm, the average sheet resistance was between 20.09 and 358.11 Ω/sq, the highest figure of merit (FoM) was 104.42, and the lowest haze value was 1.48%. The electrode prepared at 1000 rpm with a concentration of 2 mg/mL and that prepared at 3000 rpm with a concentration of 3 mg/mL were very similar in terms of the average sheet resistance, transmittance at 550 nm, FoM, and haze value; thus, these two electrodes could be considered equivalent. The haze value of the electrode was positively correlated with the spin speed at low concentration, but that relationship became inverse as the concentration rose. For the AgNWs used in this experiment with an aspect ratio of 1125, the concentration of the AgNW solution should reach at least 2 mg/mL to ensure that the FoM of the electrode is greater than 35.


2012 ◽  
Vol 268-270 ◽  
pp. 580-583 ◽  
Author(s):  
Yong Tang Jia ◽  
Cui Wu ◽  
Feng Chun Dong ◽  
Gang Huang ◽  
Xian Hua Zeng

The composite nanofiber membranes of poly (ε-caprolactone)/poly(vinyl pyrrolidone) (PCL/PVP) containing silver nanoparticles were prepared by electrospinning method. The morphology of composite nanofibers was characterized by scanning electron microscopy (SEM). The silver nanoparticles on the electrospun fibers were characterized by X-Ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The contact angle and water uptake of PCL/PVP/Ag nanofiber membranes were measured. The SEM photos indicated that the average diameter of the fibers was significantly decreased with the addition of silver nanoparticles. The X-Ray images showed that Ag nanoparticles were distributed on the surface of nanofiber membranes. When the PVP mole ratio was higher than 15%, the nanofiber membranes showed good hydrophilic property. The PCL/PVP/Ag nanofiber membranes could be applied to prepare wound dressing.


2018 ◽  
Vol 928 ◽  
pp. 106-112 ◽  
Author(s):  
Abdallah Yousef Mohammed Ali ◽  
Ahmed H. El-Shazly ◽  
M.F. Elkady ◽  
S.E. AbdElhafez

The prime purpose of the current study was to investigate the consequence of surfactant on the kinematic viscosity, thermal conductivity, and stability of MgO-oil based nanofluid. Magnesia (MgO) nanoparticles were prepared by the wet chemical method. Structural and morphological analysis of synthesized nanoparticles were performed via X-ray diffraction (XRD) and Transmission electron microscope (TEM). Subsequently, nanofluid was prepared at a solid concentration of 0.025% in presence of various surfactants with the aid of ultrasonic technique. The impact of the different surfactants (Cetyl Trimethyl Ammonium Bromide (CTAB), Poly Vinyl Pyrrolidone (PVP), Poly Vinyl Alcohol (PVA), and Oleic Acid) on the nanofluid stability was tested. It was evident that CTAB and PVA surfactants establish the most stable prepared MgO-oil based nanofluid. The experiments revealed that the maximum UV–Vis absorbance of the solution corresponds to the dispersion of CTAB in the base fluid.


2002 ◽  
Vol 14 (11) ◽  
pp. 4736-4745 ◽  
Author(s):  
Yugang Sun ◽  
Yadong Yin ◽  
Brian T. Mayers ◽  
Thurston Herricks ◽  
Younan Xia

2012 ◽  
Vol 2012 ◽  
pp. 1-11 ◽  
Author(s):  
Mahmoud Goodarz Naseri ◽  
Elias B. Saion ◽  
Ahmad Kamali

This study reports the simple synthesis of MFe2O4 (where M=Zn, Mn, and Co) nanoparticles by a thermal treatment method, followed by calcination at various temperatures from 723 to 873 K. Poly(vinyl pyrrolidone) (PVP) was used as a capping agent to stabilize the particles and prevent them from agglomeration. The characterization studies were conducted by X-ray diffraction (XRD) and transmission electron microscopy (TEM). The average particle sizes were obtained by TEM images, which were in good agreement with the XRD results. Fourier transform infrared spectroscopy (FT-IR) confirmed the presence of metal oxide bands for all the calcined samples. Magnetic properties were demonstrated by a vibrating sample magnetometer (VSM), which displayed that the calcined samples exhibited superparamagnetic and ferromagnetic behaviors.


2000 ◽  
Vol 15 (11) ◽  
pp. 2408-2413 ◽  
Author(s):  
D. Yang ◽  
R. F. Frindt

Layered MnPS3 and CdPS3 powders were used to prepare M1−xK2xPS3/poly(ethylene glycol) (PEG) and M1−xK2xPS3/poly(vinyl pyrrolidone) (PVP) (M = Cd, Mn) intercalation nanocomposites. The structure of these compounds was studied by x-ray diffraction. The host layers in Cd0.8K0.4PS3 (PEG)2.0 and Mn0.8K0.4PS3(PEG)2.0 nanocomposites were 3-dimensional crystals with a monoclinic unit cell. The in-plane spacings were slightly expanded from original monoclinic MPS3 (0.2% for CdPS3 and 0.5% for MnPS3), while the inter-layer spacing was expanded by 8.87 Å for Cd0.8K0.4PS3(PEG)2.0 and 8.86 Å for Mn0.8K0.4PS3(PEG)2.0. The Cd0.8K0.4PS3(PVP)1.1 and Mn0.8K0.4PS3(PVP)1.1 nanocomposites, on the other hand, had an expanded interlayer spacing of about 30 Å and the diffraction patterns contained only (00l) and (hk0) peaks, and no mixed (hkl) peaks were observed. The (hk0) peaks were 2-dimensional, with strongly asymmetric line shapes, and there was excellent agreement with pattern calculations for single molecular layers. This demonstrated that the host layers in Cd0.8K0.4PS3(PVP)1.1 and Mn0.8K0.4PS3(PVP)1.1 nanocomposites were tubostratically stacked layered systems.


2014 ◽  
Vol 11 (2) ◽  
pp. 153-158
Author(s):  
H Ananda ◽  
T Urs ◽  
Y Prakash ◽  
K Hemalatha ◽  
H Somashekarappa ◽  
...  

Microstructural studies on FeCl3 doped Hydroxypropyl methyl cellulose (HPMC)/Poly vinyl pyrrolidone (PVP) blend films were carried out using X-Ray diffraction studies. The XRD data revealed that the crystalline regions of the HPMC/PVP blend film decreases up to a certain percentage of FeCl3 and then increases. Electrical conductivity studies on these doped films suggest complex formation due to doping which affects microstructure and also ac conductivity of polymer films. All these results were analyzed and explained on the basis of micro structural modification of HPMC/PVP blends as function of dopant concentration.


2021 ◽  
Vol 5 (1) ◽  
pp. 1-6
Author(s):  
Bazvand M

Due to the growing demand for energy as well as the depletion of shallow land reservoirs, it sounds more important to utilize deep sea reservoirs. Due to their special conditions, drilling and production of these reservoirs face more problems. The science that helps us avoiding problems during operation is called flow assurance. One of the important issues in flow assurance is to prevent formation of gas hydrates. One of gas hydrates preventing methods is to use of inhibitors. Using of inhibitors is a cost- effective and eco-friendly method; so, it is used more nowadays. This paper introduces a new hydrate inhibitor that has been developed from the modification of one of the most widely used inhibitors present in the industry, Poly Vinyl Pyrrolidone, to improve its efficiency. The main structure of the paper is about what is the gas hydrate and its prevention methods. Finally, compare different inhibitors with new one. The results show that hydrate formation time for all polymers is approximately the same, while a half of new inhibitor in compare with amount of others inhibitors causes the same results. This matter shows a double efficiency, and this means a saving of double Polymer consumption.


2020 ◽  
Vol 170 ◽  
pp. 01018
Author(s):  
Nishigandh Pande ◽  
Adinath Jambhale ◽  
Dipika Jaspal ◽  
Jalinder Ambekar ◽  
Himanshu Patil

The synthesis of cost-effective and safe polymeric nanocomposite materials has been a subject of interest and study for material science researchers. Poly (N-Methyl Aniline) –Li nanocomposite has been synthesized by a one-pot in-situ method and has been explored as an electrolyte in the battery. Poly (N-Methyl Aniline)-Li nanocomposite prepared, has been characterized by UV-visible, FTIR, FE-SEM, X-ray diffraction techniques. A mechanism of interaction of lithiumion with nitrogen at the imine site has been proposed. The charge-discharge process of poly (N-Methyl Aniline) –Li nanocomposite, when used in the battery, has been discussed.


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