SnS2 Nanoparticles and Thin Film for Application as an Adsorbent and Photovoltaic Buffer.

Energy consumption and environmental pollution are major issues faced by the world. The present study introduces a single solution using SnS2 for these two major global problems. SnS2 nanoparticles and thin films were explored as an adsorbent to remove organic toxic materials (Rhodamine B (RhB)) from water and an alternative to the toxic cadmium sulfide (CdS) buffer for thin-film solar cells, respectively. Primary characterization tools such as X-ray photoelectron spectroscopy (XPS), Raman, X-ray diffraction (XRD), and UV-Vis-NIR spectroscopy were used to analyze the SnS2 nanoparticles and thin films. At a reaction time of 180 min, 0.4 g/L of SnS2 nanoparticles showed the highest adsorption capacity of 85% for RhB (10 ppm), indicating that SnS2 is an appropriate adsorbent. The fabricated Cu(In,Ga)Se2 (CIGS) device with SnS2 as a buffer showed a conversion efficiency (~5.1%) close to that (~7.5%) of a device fabricated with the conventional CdS buffer, suggesting that SnS2 has potential as an alternative buffer.

Nanostructurally engineered TiO2 embedded Mentha aquatica biowaste derived carbon for supercapacitor applications.

The invention of cost-effective, clean, and eco-friendly energy storage technology has been capturing a lot of worldwide interest. Herein, biogenically synthesized TiO2 nanoparticles (NPs) were ultrasonically coupled with biomass-derived activated carbon (BAC) to obtain composite (denoted as TiO2@BAC). With the inspiration of nature, Mentha Aquatica leaves extract was employed for biogenic preparation of TiO2 NPs, and residual solid waste (SW) after extract was subsequently utilized for BAC. It is noteworthy that, this unique intensive method does not require any harmful or toxic chemicals and solvents, and no secondary waste is generated. TEM analysis of TiO2@BAC revealed spherical morphology of TiO2 NPs (average size âˆ¼ 18 nm) that were accumulated on nanosheets. Raman, XRD, and XPS manifested the successful construction of TiO2@BAC. The electrochemical performance of the as-synthesized BAC, TiO2 NPs, and TiO2@BAC electrodes was tested towards supercapacitor applications. Notably, the TiO2@BAC electrode exhibited capacitance of 149 F/g at a current density of 1 A/g, which is approximately twice than that of the bare TiO2 electrode (76 F/g) along with excellent capacitance restoration of ∼99%. The TiO2@BAC electrode further revealed outstanding cyclic stability, exhibiting capacitance retention of ∼90% (at 5 A/g) after 10,000 charge/discharge cycles. Furthermore, the TiO2@BAC electrode delivered optimal specific energy density (6.96 Wh/kg) and large power density (2.07 kW/kg at 10 A/g). Moreover, the TiO2@BAC delivers an excellent restoration and retention performances of ∼100 and ∼95% (after 10,000 cycles) at 1 A/g with ∼98% coulombic efficiency in symmetric configuration (maximum cell voltage of 1.2 V).

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).

Performance of Graphene-CdS Hybrid Nanocomposite Thin Film for Applications in Cu(In,Ga)Se2 Solar Cell and H2 Production.

A graphene-cadmium sulfide (Gr-CdS) nanocomposite was prepared by a chemical solution method, and its material properties were characterized by several analysis techniques. The synthesized pure CdS nanoparticles (NPs) and Gr-CdS nanocomposites were confirmed to have a stoichiometric atomic ratio (Cd/S = 1:1). The Cd 3d and S 2p peaks of the Gr-CdS nanocomposite appeared at lower binding energies compared to those of the pure CdS NPs according to X-ray photoelectron spectroscopy analyses. The formation of the Gr-CdS nanocomposite was also evidenced by the structural analysis using Raman spectroscopy and X-ray diffraction. Transmission electron microscopy confirmed that CdS NPs were uniformly distributed on the graphene sheets. The absorption spectra of both the Gr-CdS nanocomposite and pure CdS NPs thin films showed an absorption edge at 550 nm related to the energy band gap of CdS (~2.42 eV). The Cu(In,Ga)Se2 thin film photovoltaic device with Gr-CdS nanocomposite buffer layer showed a higher electrical conversion efficiency than that with pure CdS NPs thin film buffer layer. In addition, the water splitting efficiency of the Gr-CdS nanocomposite was almost three times higher than that of pure CdS NPs.