Analysis of optical dispersion parameters and electrochromic properties of manganese-doped Co 3 O 4 dendrite structured thin films

Nebulized spray pyrolysis method was employed to deposit pristine and manganese (Mn) -doped Co3O4 thin films for different Mn concentrations (4, 6 and 8 at.%). The structural properties revealed that the obtained films show predominant orientation along (311) plane and significant peak shift was observed upon an increase in Mn doping confirms the substitution of Mn in Co3O4 lattice. The pristine Co3O4 film shows clustered grains and dendrite patterns appearing with the increase in Mn content as evident from SEM studies. The optical dispersion parameters of the prepared films of pristine and Mn doped Co3O4 films were determined from UV transmission spectra. The phase purity and elemental analysis of the films revealed single phase with better stoichiometric films were obtained. The XPS core level spectra of 6 at.% Mn doped Co3O4 films exhibited the presence of two different oxidation states (Mn2+ and Mn3+). The electrical resistivity of the films decreased with increase in Mn dopant concentration was observed from linear four probe method. The Co3O4 film deposited using 6 at.% of Mn exhibited a maximum optical modulation of 35% and coloration efficiency of 29 cm2/C

Solvent volume-driven CuInAlS2 nanoflake counter electrode for effective electrocatalytic tri-iodide reduction in dye-sensitized solar cells

The influence of solvent volume on the properties of CuInAlS2 (CIAS) thin films deposited using simple and cost-effective nebulizer spray technique is studied. The polycrystalline CIAS thin films with tetragonal structure have been observed from the XRD results. SEM images show nanoflake-like structure on the film surface. The elemental presence and its chemical composition were examined by XPS and EDS. The deposited CIAS film for different solvent volume exhibited p-type semiconductor. Cyclic voltammetry, electrochemical impedance spectroscopy, and Tafel polarization measurements demonstrated that CIAS counter electrodes are capable of tri-iodide reduction process. The performances of photocurrent density-voltage for the CIAS CE exhibited the maximum efficiency of 2.55% with the short-circuit current density of 7.22 mA cm−2

Solvent volume dependent physical properties and electrocatalytic ability of nebulizer spray deposited CuInGaS 2 counter electrode for dye-sensitized solar cells

CuInGaS2 (CIGS) thin films were coated using nebulizer spray technique for different solvent volumes (10, 30, 50 and 70 ml) at the substrate temperature of 350 °C. The structural, optical and electrical properties were studied for the prepared CIGS thin films. CIGS thin films exhibited tetragonal structure and the maximum crystallite size was calculated for the film deposited using 50 ml solvent volume. The surface morphology of CIGS thin films was analyzed from scanning electron microscopy and atomic force microscopy studies. The electrical parameters of CIGS thin films such as resistivity, carrier concentration and mobility were examined using four probe method and Hall measurements. Electrocatalytic activities of the CIGS films towards redox couple (I−/I3−) were analyzed by cyclic voltammograms, electrochemical impedance spectroscopy, and Tafel polarization measurements. The high photocurrent efficiency was obtained for the CIGS counter electrode prepared using 50 ml solvent volume

Low-cost and eco-friendly nebulizer spray coated CuInAlS 2 counter electrode for dye-sensitized solar cells

CuInAlS2 thin films for different substrate temperatures were deposited by a novel nebulizer spray technique. The polycrystalline CIAS thin film exhibited tetragonal structure with the preferential orientation of (1 1 2) plane. Nanoflakes were observed from the surface morphology of CIAS film. The peak position of core level spectra confirms the presence of CuInAlS2 from XPS analysis. The absorbance spectra and optical band gap were observed from the optical property. The activation energy, carrier concentration, hole mobility and resistivity were determined by linear four probe and Hall effect measurements. The CIAS film was used as a counter electrode (CE) in dye-sensitized solar cells (DSSCs) and is characterized by cyclic voltammetry, electrochemical impedance spectroscopy and Tafel measurements. DSSC fabricated with the CIAS CE achieved the photo conversion efficiency of about 2.55%

Facile preparation of hierarchical nanostructured CuInS2 counter electrodes for dye-sensitized solar cells

CuInS2 (CIS) thin films have been synthesized onto the glass substrates for different solvent volumes (10, 30, 50 and 70 ml) by nebulizer spray technique. The effect of solvent volume on the structural, morphological, compositional, optical and electrical properties of CIS thin films has been investigated. X-ray diffraction patterns suggest that the obtained CIS films are polycrystalline with the tetragonal structure. The surface morphology of the prepared CIS films purely depends on the solvent volume. The elemental quantitative investigation and the stoichiometric ratio of the CIS thin films were verified from XPS and EDS. High absorbance with the optical band gap of 1.13 eV was obtained at the higher solvent volume. All the deposited CIS thin films exhibited p-type semiconducting behavior with the high electrical conductivity and carrier concentration. CIS thin films deposited onto the FTO substrate were used as a counter electrode (CE) in dye-sensitized solar cells. CIS CEs possessed high electrocatalytic behavior and fast electron charge transfer at the CE/electrolyte interface. The CIS CE prepared using 50 ml solvent volume generated high energy conversion efficiency of about 3.25%

Facile Fabrication of Ultrafine Copper Nanoparticles in Organic Solvent

A facile chemical reduction method has been developed to fabricate ultrafine copper nanoparticles whose sizes can be controlled down to ca. 1 nm by using poly(N-vinylpyrrolidone) (PVP) as the stabilizer and sodium borohyrdride as the reducing agent in an alkaline ethylene glycol (EG) solvent. Transmission electron microscopy (TEM) results and UV–vis absorption spectra demonstrated that the as-prepared particles were well monodispersed, mostly composed of pure metallic Cu nanocrystals and extremely stable over extended period of simply sealed storage

A Rapid Synthesis of Oriented Palladium Nanoparticles by UV Irradiation

Palladium nanoparticles of average size around 8 nm have been synthesized rapidly by UV irradiation of mixture of palladium chloride and potassium oxalate solutions. A rod-shaped palladium oxalate complex has been observed as an intermediate. In the absence of potassium oxalate, no Pd nanoparticles have been observed. The synthesized Pd nanoparticles have been characterized by powder X-ray diffraction (XRD), transmission electron microscopy (TEM), selective area electron diffraction and energy dispersive analysis by X-rays (EDAX) analyses. XRD analysis indicates the preferential orientation of catalytically active {111} planes in Pd nanoparticles. A plausible mechanism has been proposed for the formation of anisotropic Pd nanoparticles

2D nanosheet molybdenum disulphide (MoS2) modified electrodes explored towards the hydrogen evolution reaction

We explore the use of two-dimensional (2D) MoS2 nanosheets as an electro-catalyst for the Hydrogen Evolution Reaction (HER). Using four commonly employed commercially available carbon based electrode support materials, namely edge plane pyrolytic graphite (EPPG), glassy carbon (GC), boron-doped diamond (BDD) and screen-printed graphite electrodes (SPE), we critically evaluate the reported electro-catalytic performance of unmodified and MoS2 modified electrodes towards the HER. Surprisingly, current literature focuses almost exclusively on the use of GC as an underling support electrode upon which HER materials are immobilised. 2D MoS2 nanosheet modified electrodes are found to exhibit a coverage dependant electrocatalytic effect towards the HER. Modification of the supporting electrode surface with an optimal mass of 2D MoS2 nanosheets results in a lowering of the HER onset potential by ca. 0.33, 0.57, 0.29 and 0.31 V at EPPG, GC, SPE and BDD electrodes compared to their unmodified counterparts respectively. The lowering of the HER onset potential is associated with each supporting electrodes individual electron transfer kinetics/properties. The effect of MoS2 coverage is also explored. We reveal that its ability to catalyse the HER is dependent on the mass deposited until a critical mass of 2D MoS2 nanosheets is achieved, after which its electrocatalytic benefits and/or surface stability curtail. The active surface site density and turn over frequency for the 2D MoS2 nanosheets is determined, characterised and found to be dependent on both the coverage of 2D MoS2 nanosheets and the underlying/supporting substrate. This work is essential for those designing, fabricating and consequently electrochemically testing 2D nanosheet materials for the HER