Zero-dimensional graphene quantum dots (GQDs) consist of single- or few-layer graphene with a size less than 20 nm and stand for a new type of QDs with unique properties combining the graphene nature and size-resulted quantum effects. GQDs possess unique optical and electronic properties, and in particular possess a band-gap less than 2.0 eV because of quantum confinement and edge effects. In this study, we investigated the performance of DSSCs using different thicknesses of ZnO nanoparticles as a photo-anode and GQDs as a green photosensitizer. The current voltage (I-V) test results indicate that the performance of DSSCs is improved by increasing the thickness of the photo-anode and the thickness of 40 μm shows the highest efficiency for DSSC device based on ZnO nanoparticles photo-anodes. The DSSC using ZnO nanoparticles as a photo-anode with thickness of 40 μm shows almost same efficiency when we replaced N-719 with GQDs which is confirmed that using GQDs as an alternative to ruthenium based dyes is a new approach for DSSCs.
Laser ablation-based nanoparticle synthesis in solution is rapidly becoming popular, particularly for potential biomedical and life science applications. This method promises one pot synthesis and concomitant bio-functionalization, is devoid of toxic chemicals, does not require complicated apparatus, can be combined with natural stabilizers, is directly biocompatible, and has high particle size uniformity. Size control and reduction is generally determined by the laser settings; that the size and size distribution scales with laser fluence is well described. Conversely, the effect of the laser repetition rate on the final nanoparticle product in laser ablation is less well-documented, especially in the presence of stabilizers. Here, the influence of the laser repetition rate during laser ablation synthesis of silver nanoparticles in the presence of starch as a stabilizer was investigated. The increment of the repetition rate does not negatively influence the ablation efficiency, but rather shows increased productivity, causes a red-shift in the plasmon resonance peak of the silver-starch nanoparticles, an increase in mean particle size and size distribution, and a distinct lack of agglomerate formation. Optimal results were achieved at 10 Hz repetition rate, with a mean particle size of ~10 nm and a bandwidth of ~6 nm 'full width at half maximum' (FWHM). Stability measurements showed no significant changes in mean particle size or agglomeration or even flocculation. However, zeta potential measurements showed that optimal double layer charge is achieved at 30 Hz. Consequently, Ag-NP synthesis via the laser ablation synthesis in solution (LASiS) method in starch solution seems to be a trade-off between small size and narrow size distributions and inherent and long-term stability.
In this paper a template-free precipitation method was used as an easy and low cost way to synthesize Ag2S semiconductor nanoparticles. The Kramers-Kronig method (K-K) and classical dispersion theory was applied to calculate the optical constants of the prepared samples, such as the reflective index n(ω) and dielectric constant ε(ω) in Far-infrared regime.
A template-free precipitation method was used as a simple and low cost method for preparation of CeO2 nanoparticles. The structure and morphology of the prepared nanoparticle samples were studied in detail using X-ray diffraction, Raman spectroscopy and Scanning Electron Microscopy (SEM) measurements. The whole powder pattern modelling (WPPM) method was applied on XRD data to accurately measure the crystalline domain size and their size distribution. The average crystalline domain diameter was found to be 5.2 nm, with a very narrow size distribution. UV-visible absorbance spectrum was used to calculate the optical energy band gap of the prepared CeO2 nanoparticles. The FT-IR spectrum of prepared CeO2 nanoparticles showed absorption bands at 400 cm(-1) to 450 cm(-1) regime, which correspond to CeO2 stretching vibration. The dielectric constant (εr) and dielectric loss (tan δ) values of sintered CeO2 compact consolidated from prepared nanoparticles were measured at different temperatures in the range from 298 K (room temperature) to 623 K, and at different frequencies from 1 kHz to 1 MHz.
Since the turn of the 21st century, water pollution has been a major issue, and most of the pollution is generated by dyes. Adsorption is one of the most commonly used dye-removal methods from aqueous solution. Magnetic-particle integration in the water-treatment industry is gaining considerable attention because of its outstanding physical and chemical properties. Magnetic-particle adsorption technology shows promising and effective outcomes for wastewater treatment owing to the presence of magnetic material in the adsorbents that can facilitate separation through the application of an external magnetic field. Meanwhile, the introduction of activated carbon (AC) derived from various materials into a magnetic material can lead to efficient organic-dye removal. Therefore, this combination can provide an economical, efficient, and environmentally friendly water-purification process. Although activated carbon from low-cost and abundant materials has considerable potential in the water-treatment industry, the widespread applications of adsorption technology are limited by adsorbent recovery and separation after treatment. This work specifically and comprehensively describes the use of a combination of a magnetic material and an activated carbon material for dye adsorption in wastewater treatment. The literature survey in this mini-review provides evidence of the potential use of these magnetic adsorbents, as well as their magnetic separation and recovery. Future directions and challenges of magnetic activated carbon in wastewater treatment are also discussed in this paper.
Ternary nanocomposites synergistically combine the material characteristics of three materials, altering the desired charge storage properties such as electrical conductivity, redox states, and surface area. Therefore, to improve the energy synergistic of SnO2, TiO2, and three-dimensional graphene, herein, we report a facile hydrothermal technique to synthesize a ternary nanocomposite of three-dimensional graphene-tin oxide-titanium dioxide (3DG-SnO2-TiO2). The synthesized ternary nanocomposite was characterized using material characterization techniques such as XRD, Raman spectroscopy, FTIR spectroscopy, FESEM, and EDXS. The surface area and porosity of the material were studied using Brunauer-Emmett-Teller (BET) studies. XRD studies showed the crystalline nature of the characteristic peaks of the individual materials, and FESEM studies revealed the deposition of SnO2-TiO2 on 3DG. The BET results show that incorporating 3DG into the SnO2-TiO2 binary nanocomposite increased its surface area compared to the binary composite. A three-electrode system compared the electrochemical performances of both the binary and ternary composites as a battery-type supercapacitor electrode in different molar KOH (1, 3, and 6 M) electrolytes. It was determined that the ternary nanocomposite electrode in 6 M KOH delivered a maximum specific capacitance of 232.7 C g-1 at 1 A g-1. An asymmetric supercapacitor (ASC) was fabricated based on 3DG-SnO2-TiO2 as a positive electrode and commercial activated carbon as a negative electrode (3DG-SnO2-TiO2//AC). The ASC delivered a maximum energy density of 28.6 Wh kg-1 at a power density of 367.7 W kg-1. Furthermore, the device delivered a superior cycling stability of ∼97% after 5000 cycles, showing its prospects as a commercial ASC electrode.