Investigation of structural, optical, and electrical properties of regioregular poly(3-hexylthiophene)/fullerene blend nanocomposites for organic solar cells

We investigated the influence of thermal annealing on the structural and optical properties of two variations of organic nanocomposite materials; 1) poly [3-hexylthiophene] and [6,6]-phenyl C₆₁ butyric acid methyl ester ( P3HT:PC₆₁BM), and 2) poly [3-hexylthiophene] and [6,6]-phenyl C₇₁ butyric acid methyl ester) (P3HT:PC₇₁BM). The evolution of surface roughness and morphology was investigated using atomic force microscopy while device electrical properties were investigated by measuring current-voltage (I-V) characteristics. Upon thermal treatment, results show that P3HT:PC₇₁BM nanocomposites produce a more homogeneous mixture of finer grain size than P3HT:PC₆₁BM. Furthermore, stronger optical absorption in the visible region is observed in P3HT:PC₇₁BM compared to P3HT:PC₆₁BM. Since optical absorption is closely related to film crystallinity, it is inferred that P3HT:PC₇₁BM composites undergo more extensive crystallization upon annealing. Photoluminescence spectra of both P3HT:PC₆₁BM and P3HT:PC₇₁BM nanocomposites (dissolved in chlorobenzene) show that each has excellent quenching effects. I-V characteristic curves show that P3HT:PC₇₁BM registers higher current density under AM 1.5 illumination than does P3HT:PC₆₁BM. For the devices described in this paper having active areas of approximately 12 mm², efficiency is approximately 33% better for C₇₁-based solar cells than that observed for devices made using C₆₁ fullerene.     

Effect of annealing of poly(3-hexylthiophene)/fullerene bulk heterojunction composites on structural and optical properties

Composite films of P3HT/PCBM-(poly[3-2,5-diyl]/[6,6]-phenyl C₆₁ butyric acid methyl ester) are widely used as an active layer in plastic solar cells. We have studied the influence of thermal annealing on nano-structural and optical properties of thin spin-coated P3HT/PCBM-films. Their structural properties were studied by X-ray diffraction in grazing incidence geometry. It was found that the crystallinity of the investigated films is drastically increased upon annealing. Furthermore, the anisotropic dielectric function of such films was determined by spectroscopic ellipsometry. Significant changes were observed both in parallel and perpendicular components of the dielectric function after annealing. These changes were attributed to the formation of crystalline domains upon annealing.     

Approach to a block polymer precursor from poly(3-hexylthiophene) nitroxide-mediated in situ polymerization for stabilization of poly(3-hexylthiophene)/ZnO hybrid solar cells

A cross-linked block copolymer poly(3-hexylthiophene)-b-poly(zinc dimethacrylate) (P3HT-b-PZn(MA)₂), which acted as precursor for the preparation of poly(3-hexylthiophene)/ZnO (P3HT/ZnO) hybrid film by in-situ hydrolysis, was rationally designed and synthesized via nitroxide-mediated in-situ polymerization of zinc methacrylate (Zn(MA)₂) using poly(3-hexylthiophene) alkoxyamine (P3HT-TIPNO) as macroinitiator for the purpose of stabilizing the P3HT/ZnO hybrid solar cells. The cross-linking was confirmed by the insolubility of the film in organic solvents and Fourier-transform infrared experiment. With the function of the cross-linked template, the diffusion of ZnO nanoparticles prepared by in-situ hydrolysis could be lowered to suppress the formation of large aggregations, which favored the formation of a better and more stable interpenetrating network and provided more heterojunction interfaces for exciton dissociation. As a result, the inverted device based on cross-linked P3HT/ZnO hybrid film obtained by in situ hydrolyzing P3HT-b-PZn(MA)₂ block copolymer yielded a power conversion efficiency of 0.45% under AM 1.5G illumination from a calibrated solar simulator with an intensity of 100 mW/cm², and the deterioration of the photoconversion performance was suppressed in the hybrid solar cells with the cross-linked P3HT/ZnO compared to cells with non-cross-linked P3HT/ZnO obtained by in situ hydrolyzing P3HT-TIPNO/Zn(MA)₂ blend film.     

Understanding the effect of surface chemistry on charge generation and transport in poly (3-hexylthiophene)/CdSe hybrid solar cells

For hybrid solar cells, interfacial chemistry is one of the most critical factors for good device performance. We have demonstrated that the size of the surface ligands and the dispersion of nanoparticles in the solvent and in the polymer are important criteria in obtaining optimized device performance. The size of the ligands will affect the charge transport at the particle/particle and particle/polymer interfaces and the chemical structures of the ligands will determine their compatibility with the solvent and polymer. Hence other than pyridine, 2-thiophenemethylamine also showed good potential as ligand replacement for poly(3-hexylthiophene)/CdSe hybrid solar cells. With the right ligand combination, we have shown that the power conversion efficiency improved by a factor of 6 after ligand exchange.     

Effect of thermal annealing treatment on structural, electrical and optical properties of transparent sol-gel ZnO thin films

Effect of thermal annealing in different ambients on the structural, electrical and optical properties of the sol-gel derived ZnO thin films are studied. XRD results show that the annealed ZnO films with wurtzite structure are randomly oriented. Crystallite size, carrier concentration, resistivity and mobility are found to be dependent on the annealing temperature. The change in carrier concentration is discussed with respect to the removal of adsorbed oxygen from the grain boundaries. The highest carrier concentration and lowest resistivity are 8 × 10¹⁸ cm⁻³ and 2.25 × 10⁻¹ Ω cm, respectively, for the film annealed at 500 °C in vacuum. The annealed films are highly transparent with average transmission exceeding 80% in the wavelength region of 400-800 nm. In all three ambients, the optical band gap value does not change much below 500 °C temperature while above this temperature band gap value decreases for nitrogen and air and increases for vacuum.     

Magnetic, optical and structural property studies of Mn-doped ZnO nanosheets

We report the synthesis of pure and Mn doped ZnO in the form of nanosheets using a simple and single step procedure involving a microwave assisted chemical method. As prepared Mn-doped ZnO nanosheets were characterized using X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), ultra violet-visible (UV-Vis), Raman spectroscopy and magnetization measurements. The structural studies using XRD and TEM revealed the absence of Mn-related secondary phases and showed that Mn-doped ZnO comprise a single phase nature with wurtzite structure. FESEM and TEM micrographs show that the average diameter of Mn-ZnO assembled nanosheets is about approximately 50 nm, and the length of a Mn-doped ZnO nanosheet building block which is made up of thin mutilayered sheets is around approximately 300 nm. Concerning the Raman scattering spectra, the shift in peak position of E2 (high) mode toward low frequencies due to the Mn doping could be explained well by means of the spatial correlation model. Magnetic measurements showed that Mn-doped ZnO nanosheets exhibit ferromagnetic ordering at or above room temperature.     

Magnetic, optical and structural studies on Ag doped ZnO nanoparticles

The influences of annealing effects have been explored on the crystallinity, morphology, optical and magnetic properties of Ag–ZnO nanostructures prepared by a simple sol–gel method. X-ray powder diffraction, scanning electron microscope, high resolution transmission electron microscope (HRTEM), vibrating sample magnetometer and photoluminescence spectroscopy (PL) have been used to characterize the crystal structures, surface morphology, magnetic and optical properties of the pure ZnO and Ag–ZnO nanostructures respectively. The synthesized Ag–ZnO nanostructures are found to have hexagonal wurtzite crystal structures and their grain size increases while lattice strain decreases on annealing. From HRTEM observation, it is found that the annealed samples show nanorod like structures with Ag nanoparticles (NPs) embedded on the surface. Due to annealing effect, Ag–ZnO shows higher saturation magnetization at room temperature.     

Structure-dependent optical and electrical transport properties of nanostructured Al-doped ZnO

The structure-property relation of nanostructured Al-doped ZnO thin films has been investigated in detail through a systematic variation of structure and morphology, with particular emphasis on how they affect optical and electrical properties. A variety of structures, ranging from compact polycrystalline films to mesoporous, hierarchically organized cluster assemblies, are grown by pulsed laser deposition at room temperature at different oxygen pressures. We investigate the dependence of functional properties on structure and morphology and show how the correlation between electrical and optical properties can be studied to evaluate energy gap, conduction band effective mass and transport mechanisms. Understanding these properties opens up opportunities for specific applications in photovoltaic devices, where optimized combinations of conductivity, transparency and light scattering are required.     

Hydrothermal derived nanostructure rare earth (Er,Yb)-doped ZnO: structural,optical and electrical properties

The structural, optical and electrical properties of undoped and rare-earth (Er, Yb) doped zinc oxide (ZnO) nanopowder samples synthesized by hydrothermal method were investigated. The obtained samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy-dispersive spectroscopy. The optical properties of undoped and rare-earth (Er, Yb) doped ZnO were carried out with UV–visible diffuse reflectance spectroscopy techniques. XRD results reveal that Yb and Er doped ZnO nanopowders have single phase hexagonal (Wurtzite) structure without any impurities. SEM analysis indicate that dopants with different radii affected the surface morphology of ZnO nanostructures. The optical band gap of all samples were calculated from UV–Vis diffuse reflectance spectroscopy data. We have obtained band gap values of undoped, Er and Yb doped ZnO as 3.24, 3.23, 3.22 eV, respectively. Electrical characterization of the samples were made in the 280–350 K temperature range using Van der Pauw method based on Hall effect measurement. The carrier concentrations decreased for both Er and Yb doping while the Hall mobility and electrical resistivity increased with Yb, Er doping compared to undoped ZnO nanopowder at room temperature. The temperature dependent resistivity measurements of Er doped ZnO showed a metal–semiconductor transition at about 295 K, while Yb doped ZnO showed characteristic semiconductor behavior.     

Growth,structural, optical,DFT, thermal and dielectric studies of N-Benzyl-3-nitroaniline (B3NA): a promising nonlinear optical crystal

The non-linear optical material N-Benzyl-3-nitroaniline was synthesized and grown through an aqueous solution using a low temperature solution growth technique. This conforming monoclinic crystal structure with the P2₁ space group was established by the characterization study of single crystal X-ray diffraction. A powder X-ray diffraction analysis was performed to confirm crystalline nature. As one of the functioning groups of nitro-aniline revealed using the Fourier transform infrared spectrum and the prominent spectral band seen at 3404 cm^?1 is caused by stretching vibrations of the N–H group. The lower cut-off wavelength of the ultra violet-visible absorption and emission spectrum was found to be about 320 nm as the excitation of fluorescence and the emission of blue and red colors are expected at 459 nm and 688 nm. To determine the difference in energy between HOMO and LUMO by 9.6258, using the B3LYP/6-311G++ (d,p) method. The time-based DFT technique was used to calculate the first-order hyperpolarization (β)?=?1.214?×?10^–30 esu. Thermo gravimetric and differential thermal analysis measurements were used to determine the crystal’s moisturing toughness up to 282.87 °C. The relative dielectric constant changes with frequency. Kurtz Perry’s method confirmed 1.66 times the efficiency of second harmonic generation to this present crystal comparing KDP crystal. This data shows that there is a significant amount of promise that is used in optoelectronic materials.

     

Thickness dependence of structural, electrical and optical properties of sprayed ZnO:Cu films

ZnO:Cu thin films have been deposited by spray pyrolysis techniques within two different (450 °C and 500 °C) substrate temperatures. The structural properties of ZnO:Cu thin films have been investigated by X-ray diffraction techniques. The X-ray diffraction spectra showed that ZnO:Cu thin films are polycrystalline with the hexagonal structure and show a good c-axis orientation perpendicular to the substrate. The most preferential orientation is along the (002) direction for all spray deposited ZnO:Cu films together with orientations in the (100) and (101) planes also being abundant. Some parameters of the films were calculated and correlated with the film thickness for two different substrate temperatures. The optical properties of ZnO:Cu thin films have been investigated by UV/VIS spectrometer and the band gap values were found to be ranging from 3.29 eV to 3.46 eV.     

Role of defects in tailoring structural, electrical and optical properties of ZnO

In this short topical review, a brief account of the evolution of defects due to controlled changes in polycrystalline zinc oxide has been presented. X-ray diffraction, Positron annihilation spectroscopy and optical absorption spectroscopy has been employed to understand various defective states of ZnO. Thermogravimetric analysis, room temperature resistivity and photoluminescence measurements (just mentioned) have been used to throw more light on this topic. A coherent scenario in the light of previous works in this field has been discussed. At the end discussion on the magnetic studies on ZnO-based systems has been added in short.     

Poly(BCB)/Au-nanoparticles hybrid film modified electrode: Preparation, characterization and its application as a non-enzymatic sensor

We report electrochemical preparation and characterization of poly-brilliant cresyl blue (Poly(BCB))/gold nanoparticles (Au-NPs) modified electrode. The Poly(BCB)/Au-NPs modified electrode has been used as an electrochemical sensor for the detection of hydrogen peroxide (H₂O₂) at lower potential (− 0.2 V). The Poly(BCB)/Au-NPs film was characterized by scanning electron microscopy, Uv-visible spectroscopy (Uv-vis) and cyclic voltammetry. We have observed that, Au-NPs attached glassy carbon electrode (Au-NPs/GCE) significantly enhanced the polymerization of BCB compared to bare GCE. The Poly(BCB) film was irreversibly attached onto the Au-NPs modified electrode, the resulting hybrid film modified electrode was electrochemically active in the pH range from 2 to 11. Attachment of Poly(BCB)/Au-NPs hybrid film on the electrode surface was confirmed by Uv-vis spectra. In addition, electrocatalytic properties of the Poly(BCB)/Au-NPs/GCE towards reduction of H₂O₂ have been investigated, and it was found that the sensitivity, reduction potential as well as the corresponding detection limit were improved as compared to the voltammetric response of the Poly(BCB)/GCE and Au-NPs/GCE. Based on this study, a non-enzymatic electrochemical sensor for the determination of H₂O₂ has been reported. Moreover, analysis of commercial H₂O₂ samples was performed using the proposed method and satisfactory results were obtained.     

On the structural, morphological, optical and electrical properties of sol-gel deposited ZnO:In films

Indium-doped zinc oxide thin films deposition was performed by the sol-gel technique using homogeneous and stable solutions of zinc acetate 2-hydrate and indium chloride in ethanol. Films were spin coated onto glass substrates. After drying and after a heat treatment at 450 °C, highly transparent (80%-90%) films were obtained. The effect on the structural, morphological, optical and electrical thin films properties of the dopant concentration was investigated. The temperature dependencies of the electrical conductivity under vacuum and in open atmosphere were analysed and discussed.     

Effect of thickness on the structural, electrical and optical properties of ZnO films

A series of ZnO films of different thickness have been deposited on glass substrates using sol-gel technique by varying the number of spin coatings and the effect of film thickness on the structural, electrical and optical properties have been investigated. The XRD results indicate that the full width at half maximum (FWHM) of the (0 0 2) diffraction peak and the strain along c-axis are decreased as the film is grown up to a thickness of 300 nm. Above 300 nm, the strain again becomes appreciable. The surface morphology shows that the grains become more uniform and bigger in size as the film thickness increases. Electrical result shows that although ZnO film with thickness of around 260 nm has the highest resistivity but is better for current conduction. The excitonic nature in the absorption spectrum becomes prominent for a film with thickness of around 260 nm. The band gap increases and then decreases as the film grows thicker.     

Effects of substrate temperature on structural, electrical and optical properties of As-doped ZnO films

As-doped ZnO films were prepared by co-sputtering ZnO and Zn₃As₂ targets on glass substrates at various temperatures from 250 to 500 °C. The effects of substrate temperature on structural, electrical and optical properties of the films were investigated. The films grown at temperatures from 250 to 400 °C were c-axis oriented and those deposited above 400 °C exhibited poor crystallinity. Hall measurement showed that p-type ZnO:As films were prepared at different temperatures. With increasing the substrate temperature from 250 to 500 °C, the optical band gap (E_g) first decreased, and then increased. The E_g changes upon the substrate temperature were due to the effect of substrate temperature on the crystallinity of ZnO films.     

Investigations on structural, optical and electrical properties of p-type ZnO nanorods using hydrothermal method

Undoped and doped ZnO nanorods were grown from an aqueous solution at low temperature (90 °C) on sapphire (100) substrates coated with ZnO thin film annealed in air at 550 °C for 1 h. X-ray diffraction results show that these nanorods have wurtzite type structure, and they are oriented in the c-axis direction. The optical properties are examined by room temperature micro photoluminescence and Raman scattering analysis which confirm that the nanorods exhibit good optical and electrical properties. A strong enhancement of multiple-phonon Raman scattering process with longitudinal optical phonon overtone up to fifth order was observed. It is found that the thin film coating of ZnO plays an important role in the c-axis oriented growth of undoped and doped ZnO nanorods due to good lattice match between the thin film and nanorods.     

Synthesis,structural, thermal and optical studies of rare earth coordinated complex: Tb(Sal)3Phen

Complexes of salicylic acid (Sal) and 1,10-phenanthroline (Phen) were synthesized coordinated with terbium ion (Tb³⁺) in crystalline phases. The structural characterizations of the lanthanide complex were made using FT-IR, NMR (¹H and ¹³C) and XRD techniques. These measurements confirm the formation of Tb(Sal)₃Phen complex structure. The thermal aspects of the complex were examined using DTA and TGA techniques. An enhancement in luminescence intensity of Tb³⁺ ion bands were observed in Tb(Sal)₃Phen complex as compared to TbCl₃ crystals on 355 nm laser excitation. Enhancement is reported due to the efficient energy transfer process from Sal to Tb³⁺ ions. This is also confirmed by the time resolved photoluminescence spectroscopy with increase in lifetime of Tb³⁺ ions due to encapsulation in Sal/Phen network. Our system in itself can be a deserving candidate for luminescent solar collector material when coupled with solar cells.     

Poly(anthranilic acid)/multi-walled carbon nanotube composites: spectral, morphological, and electrical properties

In this research article, we have described the synthesis of acid (HCl)-doped poly(anthranilic acid) (PAA) with carboxylic groups containing multi-walled carbon nanotubes (c-MWNTs) via in situ polymerization. Anthranilic acid monomers were adsorbed on the surface of MWNTs and polymerized to form PAA/c-MWNT composites. The structure of PAA/c-MWNT composites was characterized by UV–vis spectra, Fourier transform infrared spectroscopy, nuclear magnetic resonance, and X-ray diffraction patterns. Scanning electron microscopy and transmission electron microscopy images showed that both the thinner fibrous phase and the larger block phase could be observed. The individual fibrous phases had diameters of about 100 nm, and therefore, must be the carbon nanotubes (diameter 10–20 nm) coated by a PAA layer. The electrical conductivities of PAA/c-MWNT increased with the increase of c-MWNT content.