Improving the Device Performance of CZTSSe Thin-Film Solar Cells via Indium Doping.

Cation incorporation emerges as a promising approach for improving the performance of the kesterite Cu2ZnSn(S,Se)4 (CZTSSe) device. Herein, we report indium (In) doping using the chemical bath deposition (CBD) technique to enhance the optoelectronic properties of CZTSSe thin-film solar cells (TFSCs). To incorporate a small amount of the In element into the CZTSSe absorber thin films, an ultrathin (<10 nm) layer of In2S3 is deposited on soft-annealed precursor (Zn-Sn-Cu) thin films prior to the sulfo-selenization process. The successful doping of In improved crystal growth and promoted the formation of larger grains. Furthermore, the CZTSSe TFSCs fabricated with In doping exhibited improved device performance. In particular, the In-CZTSSe-2-based device showed an improved power conversion efficiency (PCE) of 9.53%, open-circuit voltage (Voc) of 486 mV, and fill factor (FF) of 61% compared to the undoped device. Moreover, the small amount of In incorporated into the CZTSSe absorber demonstrated reduced nonradiative recombination, improved carrier separation, and enhanced carrier transport properties. This study suggests a simple and effective way to incorporate In to achieve high efficiency and low Voc loss.

Thermodynamics of Azo Dye Adsorption on a Newly Synthesized Titania-Doped Silica Aerogel by Cogelation: A Comparative Investigation with Silica Aerogels and Activated Charcoal.

The adsorption isotherms of azo dyes on a newly synthesized titania-doped silica (TdS) aerogel compared to silica aerogels and activated charcoal (AC) are systematically investigated. Monolithic TdS aerogels were synthesized by the cogelation process followed by supercritical drying of tetraethyl orthosilicate (TEOS) as a gel precursor and titanium(IV) isopropoxide (TTIP) as a metal complex precursor for co-polymerization in ethanol solvent. An acid-base catalyst was used for the hydrolysis and condensation of TEOS and TTIP. The effect of Ti4+ doping in a silica aerogel on the mesoporous structure and the adsorption capacity of methylene blue (MB) and crystal violet (CV) dyes were evaluated from the UV-vis absorption spectra. In order to compare the adsorption isotherms, the surface areas of silica and TdS aerogels were first normalized with respect to AC, as adsorption is a surface phenomenon. The azo dye equilibrium adsorption data were analyzed using different isotherm equations and found to follow the Langmuir adsorption isotherm. The maximum monolayer adsorption capacities for the adsorbent TdS aerogel normalized with the AC of the Langmuir isotherm are 131.58 and 159.89 mg/g for MB and CV dyes, respectively. From the Langmuir curve fitting, the Q max value of the TdS aerogel was found to increase by 1.22-fold compared to AC, while it increased 1.25-1.53-fold compared to the silica aerogel. After four cycles, regeneration efficiency values for MB and CV dyes are about 84 and 80%, respectively. The study demonstrates the excellent potential and recovery rate of silica and TdS aerogel adsorbents in removing dyes from wastewater. The pore volume and average pore size of the new aerogel, TdS, were found to be lower than those of the silica aerogel. Thus, a new TdS aerogel with a high capacity of adsorption of azo dyes is successfully achieved.

Status review of nickel phosphides for hybrid supercapacitors.

Transition metal phosphides are a new class of materials that have attracted enormous attention as a potential electrode for supercapacitors (SCs) compared to metal oxides/hydroxides and metal sulfides due to their strong redox-active behaviour, good electrical conductivity, layered structure, low cost, and high chemical and thermal stability. Recently, several efforts have been made to develop nickel phosphides (NixPy) (NPs) for high-performance SCs. The electrochemical properties of NPs can be easily tuned by several innovative approaches, such as heteroatom doping, defect engineering, and developing a hollow architecture. The prospects of NPs as a positive electrode in hybrid SCs are summarized to understand the material's practical relevance. Finally, the challenges and perspectives are provided for the development of high-performance NPs for SCs. The thorough elucidation of the structure-property-performance relationship offers a guide for developing NP-based next-generation energy-storage devices.

Terbium-Doped and Dual-Passivated γ-CsPb(I1- x Brx )3 Inorganic Perovskite Solar Cells with Improved Air Thermal Stability and High Efficiency.

Realizing photoactive and thermodynamically stable all-inorganic perovskite solar cells (PSCs) remains a challenging task within halide perovskite photovoltaic (PV) research. Here, a dual strategy for realizing efficient inorganic mixed halide perovskite PV devices based on a terbium-doped solar absorber, that is, CsPb1- x Tbx I2 Br, is reported, which undertakes a bulk and surface passivation treatment in the form of CsPb1- x Tbx I2 Br quantum dots, to maintain a photoactive γ-phase under ambient conditions and with significantly improved operational stability. Devices fabricated from these air-processed perovskite thin films exhibit an air-stable power conversion efficiency (PCE) that reaches 17.51% (small-area devices) with negligible hysteresis and maintains >90% of the initial efficiency when operating for 600 h under harsh environmental conditions, stemming from the combined effects of the dual-protection strategy. This approach is further examined within large-area PSC modules (19.8 cm2 active area) to realize 10.94% PCE and >30 days ambient stability, as well as within low-bandgap γ-CsPb0.95 Tb0.05 I2.5 Br0.5 (Eg  = 1.73 eV) materials, yielding 19.01% (18.43% certified) PCE.

Bio-mimetic synthesis of catalytically active nano-silver using Bos taurus (A-2) urine.

Herein we have synthesized silver nanoparticles (Ag NPs) using liquid metabolic waste of Bos taurus (A-2 type) urine. Various bio-molecules present in cow urine, are effectively used to reduce silver (Ag) ions into silver nanoparticles in one step. This is bio-inspired electron transfer to Ag ion for the formation of base Ag metal and is fairly prompt and facile. These nanoparticles act as a positive catalyst for various organic transformation reactions. The structural, morphological, and optical properties of the as-synthesized Ag NPs are widely characterized by X-ray diffraction spectroscopy, ultraviolet-visible spectroscopy, scanning electron microscope, Fourier transmission infra-red spectroscopy, and atomic force microscopy. The as-synthesized bio-mimetic Ag NPs show potential activity for several reduction reactions of nitro groups. The Ag NPs were also used for degradation of hazardous dyes such as Methylene blue and Crystal violet with good degradation rate constant.

Study of solvent variation on controlled synthesis of different nanostructured NiCo2O4 thin films for supercapacitive application.

The present investigation deals with controlled synthesis of nanostructured NiCo2O4 thin films directly on stainless steel substrates by facile and economical chemical bath deposition technique, without adding a surfactant or a binder. The consequences of different compositions of solvents on morphological and electrochemical properties have been studied systematically. We used different solvent composition as Double Distilled Water (DDW), DDW:Ethanol (1:1) and DDW: N, N dimethylformamide (1:1). The films have been named as NCO-W for DDW, NCO-WE for DDW: Ethanol (1:1) solvent and NCO-WD for DDW: N, N dimethylformamide (1:1) solvent. The morphologies of NiCo2O4 thin films modify substantially with change in a solvent. NCO-W exhibited the spikes of Crossandra infundibuliformis like nanostructures. The NCO-WE favored the formation of uniformly distributed leaf-like nanostructure whereas NCO-WD showed randomly oriented nanoplates all over the surface area. The Electrochemical performance of these NiCo2O4 thin films were studied using cyclic voltammetry, chronopotentiometry, and electrochemical impedance spectroscopy techniques. The NCO-W, NCO-WE and NCO-WD electrodes showed specific capacitance values of 271, 553 and 140 F/g respectively at the current density of 0.5 mA/cm2 and excellent capacitance retention of 90%, 91% and 80% after 2000 cycles for NCO-W, NCO-WE and NCO-WD samples respectively. This result reveals that NiCo2O4 is a prominent electrode material for supercapacitor application.

Sustainable approach to almond skin mediated synthesis of tunable selenium microstructures for coating cotton fabric to impart specific antibacterial activity.

Currently, the synthesis of nanostructured inorganic materials with tunable morphology is still a great challenge. In this study, almond skin extract was employed for the biogenic synthesis of selenium nanoparticles with tunable morphologies such as rods and brooms. The effects of various synthesis parameters on morphologies were investigated using UV-Visible spectroscopy and scanning electron microscopy (SEM) which indicated that selenium brooms (SeBrs) were best synthesized using almond skin extract and optimized conditions of SeO2, ascorbic acid, pH, incubation temperature and time. Based on these results, the mechanism of SeBrs synthesis is proposed as having involved four stages such as nucleation, self-assembly, Ostwald ripening, and decomposition. Further, the test of antibacterial activity together with minimum inhibitory concentrations and minimum bactericidal concentrations indicated the selective, specific and good activity against B. subtilis. In addition, in situ coating of SeBrs on cotton fabric and its investigation by SEM demonstrated successful coating. Evident from plate-based assay and study of growth kinetics, coated fabric exhibited excellent anti-B. subtilis activity which demonstrated that biogenic SeBrs can be employed to coat cotton fabrics that can be used in operation theatres to reduce the episodes of Bacillus related Bacteraemia.

In2O3 nanocapsules for rapid photodegradation of crystal violet dye under sunlight.

We report, a shape controlled novel synthesis of Indium oxide (In2O3) nanocapsule using biogenic reflux method. The In2O3 samples were obtained through optimization of the concentration of sodium citrate, which played a significant role to tune the size of nanocapsules. All synthesized In2O3 samples were characterized by using X-ray diffraction (XRD), infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and selected area electron diffraction (SAED). The morphological study reflects the effect of sodium citrate on the size of nanocapsules and confirms the formation of nanocapsules in the range of 50 nm. Furthermore, the photocatalytic activity of In2O3 nanocapsules based photocatalyst was carried out for the degradation of Crystal Violet (CV) dye under natural sunlight illumination. The experiment revealed that the In2O3 nanocapsule efficiently degrades 90% of CV within 180 min. This effort recommends the synthesis of In2O3 nanocapsule based photocatalyst for rapid degradation of CV under natural sunlight illumination.

Quantum Dot Based Solar Cells: Role of Nanoarchitectures, Perovskite Quantum Dots, and Charge-Transporting Layers.

Quantum dot solar cells (QDSCs) are attractive technology for commercialization, owing to various advantages, such as cost effectiveness, and require relatively simple device fabrication processes. The properties of semiconductor quantum dots (QDs), such as band gap energy, optical absorption, and carrier transport, can be effectively tuned by modulating their size and shape. Two types of architectures of QDSCs have been developed: 1) photoelectric cells (PECs) fabricated from QDs sensitized on nanostructured TiO2 , and 2) photovoltaic cells fabricated from a Schottky junction and heterojunction. Different types of semiconductor QDs, such as a secondary, ternary, quaternary, and perovskite semiconductors, are used for the advancement of QDSCs. The major challenge in QDSCs is the presence of defects in QDs, which lead to recombination reactions and thereby limit the overall performance of the device. To tackle this problem, several strategies, such as the implementation of a passivation layer over the QD layer and the preparation of core-shell structures, have been developed. This review covers aspects of QDSCs that are essential to understand for further improvement in this field and their commercialization.

Ru-Loaded mesoporous WO3 microflowers for dual applications: enhanced H2S sensing and sunlight-driven photocatalysis.

We report a facile synthesis of Ru-loaded WO3 marigold structures through a hydrothermal route and their bidirectional applications as enhanced H2S gas sensors and efficient sunlight-driven photocatalysts. The developed hierarchical marigold structures provide effective gas diffusion channels via a well-aligned mesoporous framework, resulting in remarkable enhancement in the sensing response to H2S. The temperature and gas concentration dependence on the sensing properties reveals that Ru loading not only improves the sensing response, but also lowers the operating temperature of the sensor from 275 to 200 °C. The 0.5 wt% Ru-loaded WO3 shows selective response towards H2S, which is 45 times higher (142) than that of pristine WO3 (3.16) sensor, whereas the 0.25 wt% Ru-loaded WO3 exhibits the highest photocatalytic activity, as shown by the degradation of rhodamine B (RhB) under natural sunlight. The gas sensing and photocatalytic properties are explained through the role of Ru and the structural and morphological properties of the developed material.

Symmetric supercapacitor: Sulphurized graphene and ionic liquid.

Symmetric supercapacitor is advanced over simple supercapacitor device due to their stability over a large potential window and high energy density. Graphene is a desired candidate for supercapacitor application since it has a high surface area, good electronic conductivity and high electro chemical stability. There is a pragmatic use of ionic liquid electrolyte for supercapacitor due to its stability over a large potential window, good ionic conductivity and eco-friendly nature. For high performance supercapacitor, the interaction between ionic liquid electrolyte and graphene are crucial for better charge transportation. In respect of this, a three-dimensional (3D) nanoporous honeycomb shaped sulfur embedded graphene (S-graphene) has been synthesized by simple chemical method. Here, the fabrication of high performance symmetric supercapacitor is done by using S-graphene as an electrode and [BMIM-PF6] as an electrolyte. The particular architecture of S-graphene benefited to reduce the ion diffusion resistance, providing the large surface area for charge transportation and efficient charge storage. The S-graphene and ionic liquid-based symmetric supercapacitor device showed the large potential window of 3.2 V with high energy density 124 Wh kg-1 at 0.2 A g-1 constant applied current density. Furthermore, this device shows good cycling performance (stability) with a capacitive retention of 95% over 20,000 cycles at a higher current density of 2 A g-1.

Nanoarchitectures in dye-sensitized solar cells: metal oxides, oxide perovskites and carbon-based materials.

Dye-sensitized solar cells (DSSCs) have aroused great interest and been regarded as a potential renewable energy resource among the third-generation solar cell technologies to fulfill the 21st century global energy demand. DSSCs have notable advantages such as low cost, easy fabrication process and being eco-friendly in nature. The progress of DSSCs over the last 20 years has been nearly constant due to some limitations, like poor long-term stability, narrow absorption spectrum, charge carrier transportation and collection losses and poor charge transfer mechanism for regeneration of dye molecules. The main challenge for the scientific community is to improve the performance of DSSCs by using different approaches, like finding new electrode materials with suitable nanoarchitectures, dyes in composition with promising semiconductors and metal quantum dot fluorescent dyes, and cost-effective hole transporting materials (HTMs). This review focuses on DSSC photo-physics, which includes charge separation, effective transportation, collection and recombination processes. Different nanostructured materials, including metal oxides, oxide perovskites and carbon-based composites, have been studied for photoanodes, and counter electrodes, which are crucial to achieve DSSC devices with higher efficiency and better stability.

Aqueous-Solution-Processed Cu2ZnSn(S,Se)4 Thin-Film Solar Cells via an Improved Successive Ion-Layer-Adsorption-Reaction Sequence.

A facile improved successive ionic-layer adsorption and reaction (SILAR) sequence is described for the fabrication of Cu2ZnSn(S,Se)4 (CZTSSe) thin-film solar cells (TFSCs) via the selenization of a precursor film. The precursor films were fabricated using a modified SILAR sequence to overcome compositional inhomogeneity due to different adsorptivities of the cations (Cu+, Sn4+, and Zn2+) in a single cationic bath. Rapid thermal annealing of the precursor films under S and Se vapor atmospheres led to the formation of carbon-free Cu2ZnSnS4 (CZTS) and CZTSSe absorber layers, respectively, with single large-grained layers. The best devices based on CZTS and CZTSSe absorber layers showed total area (∼0.30 cm2) power conversion efficiencies (PCEs) of 1.96 and 3.74%, respectively, which are notably the first-demonstrated efficiencies using a modified SILAR sequence. Detailed diode analyses of these solar cells revealed that a high shunt conductance (G sh), reverse saturation current density (J o), and ideality factor (n d) significantly affected the PCE, open-circuit voltage (V oc), and fill factor (FF), whereas the short-circuit current density (J sc) was dominated by the series resistance (R s) and G sh. However, the diode analyses combined with the compositional and interface microstructural analyses shed light on further improvements to the device efficiency. The facile layer-by-layer growth of the kesterite CZTS-based thin films in aqueous solution provides a great promise as an environmentally benign pathway to fabricate a variety of multielement-component compounds with high compositional homogeneities.

A Simple Aqueous Precursor Solution Processing of Earth-Abundant Cu2SnS3 Absorbers for Thin-Film Solar Cells.

A simple and eco-friendly method of solution processing of Cu2SnS3 (CTS) absorbers using an aqueous precursor solution is presented. The precursor solution was prepared by mixing metal salts into a mixture of water and ethanol (5:1) with monoethanolamine as an additive at room temperature. Nearly carbon-free CTS films were formed by multispin coating the precursor solution and heat treating in air followed by rapid thermal annealing in S vapor atmosphere at various temperatures. Exploring the role of the annealing temperature in the phase, composition, and morphological evolution is essential for obtaining highly efficient CTS-based thin film solar cells (TFSCs). Investigations of CTS absorber layers annealed at various temperatures revealed that the annealing temperature plays an important role in further improving device properties and efficiency. A substantial improvement in device efficiency occurred only at the critical annealing temperature, which produces a compact and void-free microstructure with large grains and high crystallinity as a pure-phase absorber layer. Finally, at an annealing temperature of 600 °C, the CTS thin film exhibited structural, compositional, and microstructural isotropy by yielding a reproducible power conversion efficiency of 1.80%. Interestingly, CTS TFSCs exhibited good stability when stored in an air atmosphere without encapsulation at room temperature for 3 months, whereas the performance degraded slightly when subjected to accelerated aging at 80 °C for 100 h under normal laboratory conditions.

In situ processed gold nanoparticle-embedded TiO2 nanofibers enabling plasmonic perovskite solar cells to exceed 14% conversion efficiency.

We have demonstrated organometallic perovskite solar cells (PSCs) based on Au decorated TiO2 nanofibers and methylammonium lead iodide (MAPbI3). A power conversion efficiency of 14.92% was achieved, which is significantly higher than that of conventional mesoporous (mp) TiO2, as well as TiO2 nanofiber-based devices. The present synthetic process provides new opportunities for the development of efficient plasmonic PSCs based on metal oxide nanofibers. Solar cells based on these architectures exhibit a short-circuit current density J(SC) of 21.63 ± 0.36 mA cm(-2), V(OC) of 0.986 ± 0.01 V and fill factor of 70% ± 3%, which provide a power conversion efficiency of 14.92% ± 0.33% under standard AM 1.5 conditions. The results of time-resolved photoluminescence (TRPL) spectroscopy and solid-state impedance spectroscopy (ssIS) revealed that PSCs based on Au-decorated TiO2 nanofibers exhibit a low recombination rate. The present results are much higher than those for reported PSCs based on a Au@TiO2 electron-transporting layer (ETL).

High performing smart electrochromic device based on honeycomb nanostructured h-WO3 thin films: hydrothermal assisted synthesis.

Herein, we report honeycomb nanostructured single crystalline hexagonal WO(3) (h-WO(3)) thin films in order to improve electrochromic performance. In the present investigation, honeycomb nanostructured WO(3) with different unit size and nanowire array with highly nanocrystalline frameworks have been synthesized via a hydrothermal technique. The influence of hydrothermal reaction time on the honeycomb unit cells, crystallite size, lithium ion diffusion coefficient and switching time for coloration/bleaching were studied systematically. The electrochromic study reveals that the honeycomb unit cell size has a significant impact on the electrochromic performance. Small unit cells in the honeycomb lead to large optical modulation and fast switching response. A large optical modulation in the visible spectral region (60.74% at λ = 630 nm) at a potential of -1.2 V with fast switching time (4.29 s for coloration and 3.38 s for bleaching) and high coloration efficiency (87.23 cm(2) C(-1)) is observed in the honeycomb WO(3) thin films with a unit cell diameter of 1.7 µm. The variation in color on reduction of WO(3) with applied potential has been plotted on an xy-chromaticity diagram and the color space coordinate shows the transition from a colorless to deep blue state.

From nanocorals to nanorods to nanoflowers nanoarchitecture for efficient dye-sensitized solar cells at relatively low film thickness: All Hydrothermal Process.

Simple and low temperature hydrothermal process is employed to synthesize exotic nanostructures of TiO2. The nanostructures are obtained merely by changing the nature of the precursors and processing parameters. The chloride and isopropoxide salts of titanium are used to grow high quality thin films comprising anatase nanocorals, rutile nanorods and rutile nanoflowers respectively. A novel route of addition of room temperature ionic liquid (RTIL) is used to synthesize hitherto unexplored nano-morphologies. The Bronsted Acidic Ionic Liquid [BAIL] 0.01 M, 1: 3-ethoxycarbonylethyl-1-methyl-imidazolium chloride [CMIM][HSO4] RTIL directed growth of TiO2 flowers with bunch of aligned nanorods are obtained. The structural, optical and morphological properties of hydrothermally grown TiO2 samples are studied with the different characterization techniques. The influence of these exotic nano-morphologies on the performance of dye sensitized solar cells (DSSCs) is investigated in detail. It is found that [CMIM][HSO4] can facilitate the formation of novel nanoflower morphology with uniform, dense, and collectively aligned in regular petal like oriented TiO2 nanorods and hence improves the dye adsorption and the photovoltaic performance of DSSCs, typically in short-circuit photocurrent and power conversion efficiency. A best power conversion efficiency of 6.63% has been achieved on a DSSC based on nanoflowers (TNF) film obtained from a [CMIM][HSO4] solution.

Low-cost electrospun highly crystalline kesterite Cu2ZnSnS4 nanofiber counter electrodes for efficient dye-sensitized solar cells.

In the present investigation, kesterite Cu2ZnSnS4 (CZTS) nanofibers were obtained by electrospinning process using polyvinylpyrrolidone (PVP) and cellulose acetate (CA) solvent separately. The synthesized CZTS nanofibers were characterized using thermogravimetric analysis (TGA), optical absorption, X-ray powder diffraction (XRD), field-emission scanning electron microscopy (FESEM), micro-Raman spectroscopy, high-resolution transmission electron microscopy (HRTEM), and X-ray photoelectron spectroscopy (XPS). Our results showed that the PVP synthesized CZTS nanofibers are a single crystalline while CA assisted CZTS nanofibers are polycrystalline in nature. The optical properties demonstrated that the prepared nanofibers have strong absorption in 300-550 nm range with band gap energy of 1.5 eV. The X-ray and micro-Raman analysis revealed that synthesised nanofibers showing pure phase kesterite CZTS. Further the synthesized CZTS nanofibers were used as counter electrodes for dye-sensitized solar cells (DSSCs). Our results indicate that, PVP-CZTS and CA-CZTS counter electrode based DSSC shows 3.10% and 3.90% respectively. The detailed interfaces of these counter electrodes and DSSCs were analyzed by electrochemical impedance spectroscopic (EIS) measurements for analysis of such high power conversion efficiency. The present study will be helpful for alternative counter electrode for Pt counter electrodes in DSSCs application. We believe that our synthetic method will be helpful for low-cost and efficient thin film photovoltaic technology.

Surfactant free most probable TiO2 nanostructures via hydrothermal and its dye sensitized solar cell properties.

Tailoring the nano-morphology and nano-architecture of titanium dioxide (TiO2) is the most important task in the third generation solar cells (Dye sensitized solar cells/Quantum dot sensitized solar cells) (DSSCs/QDSSCs). In this article we present complete study of surfactant free synthesis of TiO2 nanostructures by a simple and promising hydrothermal route. The plethora of nanostructures like nanoparticles clusters, 1D tetragonal nanorods, 3D dendrites containing nanorods having <30 nm diameter and 3D hollow urchin like have been synthesized. These nanostructures possess effective large surface area and thus useful in DSSCs. In the present work, 7.16% power conversion efficiency has been demonstrated for 3D dendritic hollow urchin like morphology. Our synthetic strategy provides an effective solution for surfactant free synthesis of efficient TiO2 nanoarchitectures.

Chemically grown vertically aligned 1D ZnO nanorods with CdS coating for efficient quantum dot sensitized solar cells (QDSSC): a controlled synthesis route.

In the present article, vertically aligned ZnO nanorod arrays were synthesized by an aqueous chemical growth (ACG) route on a fluoride doped tin oxide (FTO) coated glass substrate. These nanorods were further sensitized with cadmium sulfide (CdS) quantum dots (QDs) by a successive ionic layer adsorption and reaction (SILAR) technique. The synthesized CdS coated ZnO nanorods were characterized for their structural and morphological properties with X-ray diffraction (XRD), high resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS) and field emission scanning electron microscopy (FESEM). Finally, prepared CdS coated 1D ZnO photoelectrodes were tested for their photoelectrochemical performance. Our results show that the sample deposited after 40 SILAR cycles shows 5.61 mA cm(-2) short current density (JSC) with η = 1.61% power conversion efficiency.