scholarly journals Preparation and Studies of Electrodeposited CuSe Thin Films

2017 ◽  
Vol 6 (2) ◽  
pp. 107
Author(s):  
A. Kassim ◽  
Z. Zainal ◽  
N. Saravanan ◽  
R. Vikneshwari ◽  
S. Malathi

Cathodic electrodeposition in the presence of sodium dodecyl-sulphate in aqueous solution was used to prepare CuSe thin film deposited on titanium substrates. The effect of deposition potential, concentration<br />and deposition time were studied to determine the optimum condition for the electrodeposition process. The films were characterized by X-ray diffractrometry. Scanning electron microscopy was used to study<br />the morphology of the deposits. The photoresponse of the films prepared was analysed using linear sweep voltammetry in the presence of sodium thiosulphate.

2011 ◽  
Vol 311-313 ◽  
pp. 477-480
Author(s):  
Zhi Ai Yang ◽  
Li Jin Feng ◽  
Xia Wang ◽  
Rong Ma ◽  
Jian Ping Sun ◽  
...  

Subscript textThe Co3O4 nanocubes were synthesized by hydrothermal process. The products are characterized in detail by multiform techniques: scanning electron microscopy, transmission electron microscopy, X-ray diffraction, and energy-dispersive X-ray analysis. The results show that the products are uniform nanocubes with an average crystallite size about 20-40 nm. Electrocatalytic property of the prepared Co3O4 nanocubes was characterized by linear sweep voltammetry. LSV results indicate that Co3O4 nanocubes exhibit a remarkable electrocatalytic activity for the H2O2 reduction.


2013 ◽  
Vol 2013 ◽  
pp. 1-7 ◽  
Author(s):  
Bizuneh Workie ◽  
Brian E. McCandless ◽  
Zewdu Gebeyehu

We have studied electrophoretic deposition of AlN from its suspension in acetylacetone with I2as an additive. AlN powder with particle size <10 μm is dispersed to produce a positive charge and deposited on the cathode by applying fields greater than 10 V/cm between the electrodes. X-ray diffraction and FTIR studies indicate that the AlN before and after deposition has the same composition and structure. An increase in the amount of AlN in the suspension, the deposition potential, and the deposition time results in a linear increase in the weight of the AlN deposited. Electrophoretic deposition from 10 g/L AlN suspension shows an initial increase in the weight of AlN deposited with the concentration of I2, and the weight of AlN decreases after reaching a maximum at 0.20 g/L I2.


2011 ◽  
Vol 56 (11) ◽  
pp. 4344-4350 ◽  
Author(s):  
Ts. Dobrovolska ◽  
I. Krastev ◽  
B.M. Jović ◽  
V.D. Jović ◽  
G. Beck ◽  
...  

Electrochem ◽  
2021 ◽  
Vol 2 (1) ◽  
pp. 83-94
Author(s):  
Elisabetta Petrucci ◽  
Monica Orsini ◽  
Francesco Porcelli ◽  
Serena De Santis ◽  
Giovanni Sotgiu

Ruthenium oxide (RuOx) thin films were spin coated by thermal decomposition of alcoholic solutions of RuCl3 on titanium foils and subsequently annealed at 400 °C. The effect of spin coating parameters, such as spinning speed, volume, and molar concentration of the precursor as well as the number of deposits, on the morphology and electrochemical performance of the electrodes was investigated. The films were characterized by scanning electron microscopy (SEM) equipped with energy-dispersive X-ray spectroscopy (EDX), cyclic voltammetry (CV) with and without chloride, and linear sweep voltammetry (LSV). The prepared materials were also compared to drop cast films and spin-coated films obtained by adopting low-temperature intermediate treatments. The results indicate that even dispersion of the oxide layer was always achieved. By tuning the spin coating parameters, it was possible to obtain different electrochemical responses. The most influential parameter is the number of deposits, while the concentration of the precursor salt and the rotation speed were less relevant, under the adopted conditions.


Polymers ◽  
2021 ◽  
Vol 13 (2) ◽  
pp. 190
Author(s):  
Razik Djara ◽  
Marie-Agnès Lacour ◽  
Abdelhafid Merzouki ◽  
Julien Cambedouzou ◽  
David Cornu ◽  
...  

The breakthrough in water electrolysis technology for the sustainable production of H2, considered as a future fuel, is currently hampered by the development of tough electrocatalytic materials. We report a new strategy of fabricating conducting polymer-derived nanostructured materials to accelerate the electrocatalytic hydrogen evolution reaction (HER), oxygen evolution reaction (OER), and water splitting. Extended physical (XRD, scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX)) and electrochemical (cyclic voltammetry (CV), linear sweep voltammetry (LSV), electrochemical impedance spectroscopy (EIS)) methods were merged to precisely characterize the as-synthesized iridium and ruthenium modified polyaniline (PANI) materials and interrogate their efficiency. The presence of Ir(+III) cations during polymerization leads to the formation of Ir metal nanoparticles, while Ru(+III) induces the formation of RuO2 oxide nanoparticles by thermal treatment; they are therefore methods for the on-demand production of oxide or metal nanostructured electrocatalysts. The findings from using 0.5 M H2SO4 highlight an ultrafast electrochemical kinetic of the material PANI-Ir for HER (36 − 0 = 36 mV overpotential to reach 10 mA cm−2 at 21 mV dec−1), and of PANI-Ru for OER (1.47 − 1.23 = 240 mV overpotential to reach 10 mA cm−2 at 47 mV dec−1), resulting in an efficient water splitting exactly at its thermoneutral cell voltage of 1.45 V, and satisfactory durability (96 h).


2020 ◽  
Vol 58 (7) ◽  
pp. 447-452
Author(s):  
Ikgyu Kim ◽  
Kwangbae Kim ◽  
Ohsung Song

A stripping solution with thiourea, iron(III) sulfate, and sodium dodecyl sulfate(SDS) was employed to strip Ni-based 14 karat white gold alloys, and the formation of the NiS byproduct and elimination of passivation were investigated in the presence of 0.0-0.2 g/L SDS. White gold alloy samples with a flat shape were cast by gypsum investment and were stripped using the prepared stripping solution. Subsequently, the surface morphology, elimination of the passivation layer, weight loss, microstructure, elemental composition, and electrochemical properties of the samples were analyzed by optical microscopy, Raman spectroscopy, precision scale, scanning electron microscopy, energy dispersive X-ray spectroscopy, and linear sweep voltammetry, respectively. It was found that passivation layers of the as-cast samples were removed by the suggested stripping solution. Upon the addition of SDS, the stripped sample showed a bright silver color without NiS, while the sample showed a dark tarnished appearance due to NiS formation without SDS. The weight loss ratio decreased with increasing SDS content and stabilized at 0.2 % for SDS concentrations exceeding 0.15 g/L, and the sample showed a uniformly etched microstructure. EDS results showed that NiS was formed without SDS addition, while linear sweep voltammetry results indicated that NiS formation was restrained upon SDS addition because SDS suppresses the formation of formamidine disulfide from thiourea. Thus, the suggested thiourea stripping with SDS addition was successfully applied to Ni-based 14 karat white gold alloys.


2019 ◽  
Vol 2019 ◽  
pp. 1-5
Author(s):  
Assamen Ayalew Ejigu

In this study, we have successfully deposited n-type Cu2O triangular nanopyramids on Si by employing ion beam sputter deposition with an Ar : O2 ratio of 9 : 1 at a substrate temperature of 450°C. Scanning electron microscopy measurements showed attractively triangular nanopyramids of ∼500 nm edge and height lengths. Both X-ray diffraction and Raman spectroscopy characterizations showed the structures were single-phase polycrystalline Cu2O, and the room-temperature photoluminescence investigation showed interestingly green and blue exciton luminescence emissions. All Mott—Schottky, linear sweep voltammetry, and photocurrent measurements indicated that the conductivity of the Cu2O pyramids is of n-type.


2004 ◽  
Vol 19 (2) ◽  
pp. 429-438 ◽  
Author(s):  
Todd M. McEvoy ◽  
Keith J. Stevenson

The cathodic electrodeposition of molybdenum oxide thin films prepared from aqueous solutions containing iso-polymolybdates and peroxo-polymolybdates is described. Chronocoulometry, x-ray photoelectron spectroscopy, spectroelectrochemistry, and electrochemical quartz crystal microgravimetry were used to establish corresponding reaction mechanisms for films grown at different deposition potentials. Electrodeposition from acidified iso-polymolybdate solutions proceeds by the reduction of molybdic acid, whereas deposition from aqueous peroxo-based solutions involves the graded reduction of several solution components, primarily comprising molybdic acid and peroxo-polymolybdates. Careful regulation of the deposition potential allows for controlled growth of distinct molybdenum oxide compositions producing films with varied water content and valency.


2018 ◽  
Vol 233 (1) ◽  
pp. 105-116
Author(s):  
Christoph Seitz ◽  
Sebastian Werner ◽  
Roland Marschall ◽  
Bernd M. Smarsly

Abstract Copper oxide (CuO) nanofibres are utilised to sense the toxic and abrasive gas hydrogen sulfide (H2S) in the ppm (parts per million) range. The detection by CuO is based on a significant increase in the conductance upon the formation of CuS, and is thereby selective and sensitive towards H2S. Nanofibres outperform thin films of CuO by compensating the volumetric stress which occurs during sensing. Here, sensors are presented exhibiting up to 600 cycles of sensing and regeneration. To get further insights into the degradation of the fibres upon the reaction with H2S the sensors were analysed by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), resistance and linear sweep voltammetry (LSV) measurements before and after cycling. SEM and TEM revealed a drastic change in morphology of the CuO fibres resulting in an undefined aggregate of nanoparticles after 600 cycles. Resistance and LSV measurements showed that the contacting and the measurement process itself are crucial factors for optimising long-term use of CuO-based H2S sensors.


2021 ◽  
Vol 12 (6) ◽  
pp. 7715-7724

Copper (II) oxide (Cu2O) has attracted much interest as a semiconductor material for solar cell applications. Here we report the synthesis of Cu2O, thin films through an economical and simple electrodeposition method at low duration (10 min) by linear sweep voltammetry (LSV) method at 50 °C bath temperature, with the use of citric acid as a complexing agent. The influence of pH value (pH = 9.5, 10.5, 11.5, and 12.5) on structural, morphological, and optical properties of the synthesized Cu2O thin films onto copper substrate was investigated. The synthesized Cu2O thin films have been characterized using various techniques like X-ray diffraction (XRD), Raman spectroscopy, Scanning Electron Microscopy (SEM-EDX), UV-vis spectrophotometry. The X-ray diffraction showed that the deposited thin films at pH= 9.5, 10.5, 11.5 matched well with the cubic (Pn-3m) structure and showed an improvement of the crystallinity near the value pH=10.5. Raman spectroscopy confirms the cubic structure of the synthesized thin film. Thin films show a high absorption coefficient in the visible spectra, and the calculated band gap energy value is near 1.8 eV.


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