Influence of the Al-Doped ZnO Sputter-Deposition Temperature on Cu(In,Ga)Se2 Solar Cell Performance.

Heterojunction Cu(In,Ga)Se2 (CIGS) solar cells comprise a substrate/Mo/CIGS/CdS/i-ZnO/ZnO:Al. Here, Al-doped zinc oxide (AZO) films were deposited by magnetron sputtering, and the substrate temperature was optimized for CIGS solar cells with two types of CIGS light absorbers with different material properties fabricated by three-stage co-evaporation and two-step metallization followed by sulfurization after selenization (SAS). The microstructure and optoelectronic properties of the AZO thin films fabricated at different substrate temperatures (150-550 °C) were analyzed along with their effects on the CIGS solar cell performance. X-ray diffraction results confirmed that all the deposited AZO films have a hexagonal wurtzite crystal structure regardless of substrate temperature. The optical and electrical properties of the AZO films improved significantly with increasing substrate temperature. Photovoltaic performances of the two types of CIGS solar cells were influenced by changes in the AZO substrate temperature. For the three-stage co-evaporated CIGS cell, as the sputter-deposition temperature of the AZO layer was raised from 150 °C to 550 °C, the efficiencies of CIGS devices decreased monotonically, which suggests the optimum AZO deposition temperature is 150 °C. In contrast, the cell efficiency of CIGS devices fabricated using the two-step SAS-processed CIGS absorbers improved with increasing the AZO deposition temperature from 150 to 350 °C. However, the rise in AZO deposition temperature to 550 °C decreased the cell efficiency, indicating that the optimum AZO deposition temperature was 350 °C. The findings of this study provide insights for the efficient fabrication of CIGS solar cells considering the correlation between CIGS absorber characteristics and AZO layer deposition temperature.

Synthesis and Characterization of Cu2ZnSnSe4 by Non-Vacuum Method for Photovoltaic Applications.

Wet ball milling was used for the synthesis of Cu2ZnSnSe4 (CZTSe) nanoparticles with a kesterite structure. The prepared nanoparticles were used for ink formulation. Surfactants and binders were added to improve the ink stability, prevent agglomeration, and enhance ink adhesion. The films deposited via spin coating were annealed at different temperatures using a rapid thermal processing system in the presence of selenium powder in an inert environment. Analytical techniques, such as X-ray diffraction, Raman spectroscopy, and Fourier-transform infrared spectroscopy, were used to confirm the formation of CZTSe nanoparticles with a single-phase, crystalline kesterite structure. Field-emission scanning electron microscopy and energy-dispersive X-ray spectroscopy were used to study the surface morphology and chemical composition of the thin films before and after annealing, with and without the sodium solution. The optoelectrical properties were investigated using ultraviolet-visible spectroscopy and Hall measurements. All the prepared CZTSe thin films exhibited a p-type nature with an optical bandgap in the range of 0.82-1.02 eV. The open-circuit voltage and fill factor of the CZTSe-based devices increased from 266 to 335 mV and from 37.79% to 44.19%, respectively, indicating a decrease in the number of recombination centers after Na incorporation.

Polyaniline-wrapped MnMoO4 as an active catalyst for hydrogen production by electrochemical water splitting.

Developing efficient, low-cost, and environment-friendly electrocatalysts for hydrogen generation is critical for lowering energy usage in electrochemical water splitting. Moreover, for commercialization, fabricating cost-efficient, earth-abundant electrocatalysts with superior characteristics is of urgent need. Towards this endeavor, we report the synthesis of PANI-MnMoO4 nanocomposites using a hydrothermal approach and an in situ polymerization method with various concentrations of MnMoO4. The fabricated nanocomposite electrocatalyst exhibits bifunctional electrocatalytic activity towards the oxygen evolution reaction (OER) and the hydrogen evolution reaction (HER) at a lower overpotential of 410 mV at 30 mA cm-2 and 155 mV at 10 mA cm-2, respectively in an alkaline electrolyte. Furthermore, while showing overall water splitting (OWS) performance, the optimized PM-10 (PANI-MnMoO4) electrode reveals the most outstanding OWS performance with a lower cell voltage of 1.65 V (vs. RHE) at a current density of 50 mA cm-2 with an excellent long-term cell resilience of 24 h.

Fabrication of Cu2ZnSnS4 Light Absorber Using a Cost-Effective Mechanochemical Method for Photovoltaic Applications.

In the present study, we adopt an easy and cost-effective route for preparing Cu2ZnSnS4 (CZTS)-absorber nanoparticles by a mechanochemical method using non-toxic and environmentally benign solvents (butanol, methyl ethyl ketone, and ethanol). The gram-scale synthesis of absorber nanoparticles was achieved in a non-hazardous, zero-waste process without using high-vacuum equipment. The effects of annealing and Na incorporation on the properties of spin-coated CZTS thin films were scrutinized. The deposited samples showed kesterite crystal structure and single phase. The morphological results revealed an improvement in the surface morphology after annealing. The optical bandgaps of the thin films lied in the range of 1.50-1.57 eV with p-type nature. Finally, photovoltaic devices were fabricated, and their cell performance parameters were studied. An efficiency of 0.16% was observed. The present study provides a potential route for the cost-effective fabrication of CZTS-based photovoltaic devices.

Fundamental Aspects and Comprehensive Review on Physical Properties of Chemically Grown Tin-Based Binary Sulfides.

The rapid research progress in tin-based binary sulfides (SnxSy = o-SnS, c-SnS, SnS2, and Sn2S3) by the solution process has opened a new path not only for photovoltaics to generate clean energy at ultra-low costs but also for photocatalytic and thermoelectric applications. Fascinated by their prosperous developments, a fundamental understanding of the SnxSy thin film growth with respect to the deposition parameters is necessary to enhance the film quality and device performance. Therefore, the present review article initially delivers all-inclusive information such as structural characteristics, optical characteristics, and electrical characteristics of SnxSy. Next, an overview of the chemical bath deposition of SnxSy thin films and the influence of each deposition parameter on the growth and physical properties of SnxSy are interestingly outlined.

Synthesis and Characterization of π-SnS Nanoparticles and Corresponding Thin Films.

Tin sulfide polymorph (π-SnS) nanoparticles exhibit promising optoelectrical characteristics for photovoltaic and hydrogen production performance, mainly because of the possibility of tuning their properties by adjusting the synthesis conditions. This study demonstrates a chemical approach to synthesize π-SnS nanoparticles and the engineering of their properties by altering the Sn precursor concentration (from 0.04 M to 0.20 M). X-ray diffraction and Raman studies confirmed the presence of pure cubic SnS phase nanoparticles with good crystallinity. SEM images indicated the group of cloudy shaped grains, and XPS results confirmed the presence of Sn and S in the synthesized nanoparticles. Optical studies revealed that the estimated energy bandgap values of the as-synthesized π-SnS nanoparticles varied from 1.52 to 1.68 eV. This work highlights the effects of the Sn precursor concentration on the properties of the π-SnS nanoparticles and describes the bandgap engineering process. Optimized π-SnS nanoparticles were used to deposit nanocrystalline π-SnS thin films using the drop-casting technique, and their physical properties were improved by annealing (300 °C for 2 h).

RGO/WO3 hierarchical architectures for improved H2S sensing and highly efficient solar-driving photo-degradation of RhB dye.

Surface area and surface active sites are two important key parameters in enhancing the gas sensing as well as photocatalytic properties of the parent material. With this motivation, herein, we report a facile synthesis of Reduced Graphene Oxide/Tungsten Oxide RGO/WO3 hierarchical nanostructures via simple hydrothermal route, and their validation in accomplishment of improved H2S sensing and highly efficient solar driven photo-degradation of RhB Dye. The self-made RGO using modified Hummer's method, is utilized to develop the RGO/WO3 nanocomposites with 0.15, 0.3 and 0.5 wt% of RGO in WO3 matrix. As-developed nanocomposites were analyzed using various physicochemical techniques such as XRD, FE-SEM, TEM/HRTEM, and EDAX. The creation of hierarchic marigold frameworks culminated in a well affiliated mesoporous system, offering efficient gas delivery networks, leading to a significant increase in sensing response to H2S. The optimized sensor (RGO/WO3 with 0.3 wt% loading) exhibited selective response towards H2S, which is ~ 13 times higher (Ra/Rg = 22.9) than pristine WO3 (Ra/Rg = 1.78) sensor. Looking at bi-directional application, graphene platform boosted the photocatalytic activity (94% degradation of Rhodamine B dye in 210 min) under natural sunlight. The RGO's role in increasing the active surface and surface area is clarified by the H2S gas response analysis and solar-driven photo-degradation of RhB dye solution. The outcome of this study provides the new insights to RGO/WO3 based nanocomposites' research spreadsheet, in view of multidisciplinary applications.

Improvement of Vacuum Free Hybrid Photovoltaic Performance Based on a Well-Aligned ZnO Nanorod and WO3 as a Carrier Transport Layer.

Well-aligned zinc oxide nanorods (WA-ZnO Nrods) with different lengths were synthesized and the effects of the growth times on the optical, morphological, and electrical properties of the WA-ZnO Nrods were examined. We also investigated the application of WA-ZnO Nrods as an electron transport layer (ETL) and tungsten trioxide (WO3) as a hole transport layer (HTL) to vacuum free hybrid photovoltaic (HPV) performance. The eutectic gallium-indium (EGaIn) alloy was used as a top electrode coated using a brush-painting method. A device with the structure of indium tin oxide (ITO)/WA-ZnO Nrods/(P3HT:PCBM)/WO3/EGaIn was optimized and fabricated. The maximum power conversion efficiency (PCE) was ~4.5%. Improvement of the device performance indicates that the well-aligned ZnO Nrods and WO3 can effectively be applied as charge carrier transport layer for vacuum free hybrid (HPV).

Bright luminescence from pure DNA-curcumin-based phosphors for bio hybrid light-emitting diodes.

Recently, significant advances have occurred in the development of phosphors for bio hybrid light-emitting diodes (Bio-HLEDs), which have created brighter, metal-free, rare-earth phosphor-free, eco-friendly, and cost-competitive features for visible light emission. Here, we demonstrate an original approach using bioinspired phosphors in Bio-HLEDs based on natural deoxyribonucleic acid (DNA)-curcumin complexes with cetyltrimethylammonium (CTMA) in bio-crystalline form. The curcumin chromophore was bound to the DNA double helix structure as observed using field emission tunnelling electron microscopy (FE-TEM). Efficient luminescence occurred due to tightly bound curcumin chromophore to DNA duplex. Bio-HLED shows low luminous drop rate of 0.0551 s(-1). Moreover, the solid bio-crystals confined the activating bright luminescence with a quantum yield of 62%, thereby overcoming aggregation-induced quenching effect. The results of this study herald the development of commercially viable large-scale hybrid light applications that are environmentally benign.