Green Synthesis of Pristine and Ag-Doped TiO2 and Investigation of Their Performance as Photoanodes in Dye-Sensitized Solar Cells.

Dye-sensitized solar cells (DSSCs) have emerged as a potential candidate for third-generation thin film solar energy conversion systems because of their outstanding optoelectronic properties, cost-effectiveness, environmental friendliness, and easy manufacturing process. The electron transport layer is one of the most essential components in DSSCs since it plays a crucial role in the device's greatest performance. Silver ions as a dopant have drawn attention in DSSC device applications because of their stability under ambient conditions, decreased charge recombination, increased efficient charge transfer, and optical, structural, and electrochemical properties. Because of these concepts, herein, we report the synthesis of pristine TiO2 using a novel green modified solvothermal simplistic method. Additionally, the prepared semiconductor nanomaterials, Ag-doped TiO2 with percentages of 1, 2, 3, and 4%, were used as photoanodes to enhance the device's performance. The obtained nanomaterials were characterized using XRD, FTIR, FE-SEM, EDS, and UV-vis techniques. The average crystallite size for pristine TiO2 and Ag-doped TiO2 with percentages of 1, 2, 3, and 4% was found to be 13 nm by using the highest intensity peaks in the XRD spectra. The Ag-doped TiO2 nanomaterials exhibited excellent photovoltaic activity as compared to pristine TiO2. The incorporation of Ag could assist in successful charge transport and minimize the charge recombination process. The DSSCs showed a Jsc of 8.336 mA/cm2, a Voc of 698 mV, and an FF of 0.422 with a power conversion efficiency (PCE) of 2.45% at a Ag concentration of 4% under illumination of 100 mW/cm2 power with N719 dye, indicating an important improvement when compared to 2% Ag-doped (PCE of 0.97%) and pristine TiO2 (PCE of 0.62%).

Understanding charge carrier dynamics in a P3HT:FLR blend.

In organic semiconductors, optical absorption is pivotal for the performance of optoelectronic devices. The absorption by the semiconductors generates excitons which dissociate into free charge carriers, resulting in energy conversion. Although high performance has been achieved in non-fullerene organic solar cells, their charge generation behavior is far from being well understood. Keeping this in view, we have employed optical spectroscopic tools to study the charge generation mechanism in FLR (1,6,7,10-tetramethylfluoranthene) as a non-fullerene electron acceptor blended with P3HT (poly(3-hexylthiophene)) as an electron donor in five different solvents. Through steady state UV-visible and photoluminescence spectroscopy, we provide a basic understanding of charge transport by enlightening the influence of solvents on the aggregation behavior and exciton bandwidth. Furthermore, for the first time, by employing ultrafast vis-NIR transient absorption spectroscopy, we address the ultrafast charge generation and charge separation mechanism with systematic variation in solvent polarity by incorporating the time evolution of the transient species under various pump-probe wavelengths in the range of 450 nm to 1600 nm. For the different excitation wavelengths, the lifetime kinetics have been depicted by their multiexponential fits. The results show a fast decay term at a lifetime of a few picoseconds (ps) (∼1 to 5 ps) and a slow decay term at a lifetime of ∼500 ps. The charge generation in the P3HT:FLR blend proceeds on a ps time scale, which implies good intermixing of the components. It is clearly established that the non-halogenated solvents influence this aggregation behavior and higher conjugation lengths with higher photoluminescence quenching contribute to the higher charge generation. The enhanced polaron population in P3HT with the addition of FLR illustrates the importance of this acceptor material in the blend because a good solvent-material combination is essential to enhance the charge generation. As such, this comprehensive study explicitly shows the role of FLR as an emerging efficient non-fullerene acceptor for further improving the performance of devices.

Electro-analytical investigation of potential induced degradation in mc-silicon solar cells: case of sodium ion induced inductive loop.

Potential induced degradation of the shunt type (PID-s) in multi-crystalline silicon (mc-Si) solar cells is becoming critical for performance reduction of solar panels in large scale photovoltaic (PV) power plants. In this article PID-s has been investigated by applying high voltage stress on mc-Si solar cells for their degradation and recovery and results have been explained on the basis of DC and AC characterization. The efficiency decreases drastically from 15.7% to 2.9% due to a high voltage stress of -800 V at 85 °C for 48 hours, which is attributed to a reduction in shunt resistance and an increase in depletion and diffusion capacitances. The reduction in electrical performance due to PID-s has been further explained by morphological, structural and elemental analysis. Observed negative capacitance behaviour in impedance spectra of mc-Si solar cells after PID-s has been attributed to structural deformation caused by potential induced migration of sodium ions (Na+) into mc-Si. The structural deformation induced by potential induced migration of Na+ ions has been confirmed by using non-destructive and lattice strain sensitive micro-Raman spectroscopy. The obtained experimental results have been correlated with existing theoretical understanding of p-n junction solar cells to explain the consequences of PID-s.

Investigating the influence of charge transport on the performance of PTB7:PC71BM based organic solar cells.

A key challenge for researchers in the field of organic solar cells (OSCs) is to develop a physical model for a device that correctly describes the charge carrier transport phenomenon. In this article, an analytical study on the charge carrier transport phenomenon in an OSC is reported, which expresses a balance between free charge carrier generation and recombination in low mobility PTB7:PC71BM blend layers. First, the current density-voltage (J-V) data for the fabricated OSC were extracted from experiments by varying the incident power light intensity (IPL) and then analysis through theoretical simulation was used to quantify the dominant interface recombination parameters limiting the device's performance. It was found that although the generation of free charge carriers increased at higher IPL values, the performance of the device remained low due to poor electrical transport properties which resulted in a considerable accumulation of generated charge carriers in the active layer. Therefore, it has become important to work out the complex relation between charge carrier mobility, exciton-recombination dynamics and the overall electrical performance parameters in a single framework. This article explains the influence of incident power light intensity and charge carrier mobility on performance parameters, which limits the power conversion efficiency (PCE) of the OSC. The presented analysis could be helpful in optimizing the architecture of future devices to increase the PCE of OSCs.

Investigating the Role of Substrate Tin Diffusion on Hematite Based Photoelectrochemical Water Splitting System.

Hematite (α-Fe2O3) nanostructures have been extensively studied as photo-anodes for the conversion of sunlight into chemical fuels by water splitting. A number of factors limit the photo-activity of pristine hematite nanostructures, including poor electrical conductivity and long penetration depth of light. Previous studies have shown that use of tin (Sn) as an n-type dopant can substantially enhance the photoactivity of hematite photoanodes by modifying their morphological, optical and electrical properties. This article presents impedance spectroscopic investigation of interplay between Sn-doping and the photoanode performance for photoelectrochemical water splitting using hematite nanostructure. Mott-Schottky measurements show that the Sn dopant serves as electron donor and increases the donor density of Sn-doped α-Fe2O3 nanostructured layer to 2.39 × 1019 cm-3. Photoelectrochemical impedance spectroscopy shows efficient photogenerated charge transfer from hematite to electrolyte in Sn-doped α-Fe2O3 nanostructure. The Sn-doped α-Fe2O3 nanostructure exhibit a photocurrent density of 1.2 mA/cm2 at 1.4 V versus RHE electrode.

Revealing the correlation between charge carrier recombination and extraction in an organic solar cell under varying illumination intensity.

The design and fabrication of better excitonic solar cells are the need of the hour for futuristic energy solutions. This designing needs a better understanding of the charge transport properties of excitonic solar cells. One of the popular methods of understanding the charge transport properties is the analysis of the J-V characteristics of a device through theoretical simulation at varied illumination intensity. Herein, a J-V characteristic of a polymer:fullerene based bulk heterojunction (BHJ) organic solar cells (OSCs) of structure ITO/PEDOT:PSS (∼40 nm)/PTB7:PC71BM (∼100 nm)/Al (∼120 nm) is analyzed using one- and two-diode models at varied illumination intensity in the range of 0.1-2.33 Sun. It was found that the double diode model is better with respect to the single diode model and can explain the J-V characteristics of the OSCs correctly. Further, the recombination mechanism is investigated thoroughly and it was observed that fill factor (FF) is in the range of 62.5%-41.4% for the corresponding values of the recombination-to-extraction ratio (θ) varying from 0.001 to 0.023. These findings are attributed to the change in charge transport mechanism from trap-assisted to bimolecular recombination with the variation of illumination intensity.

In Vitro Evaluation of Carbachol and Endothelin on Contractility of Colonic Smooth Muscle in Hirschsprung's Disease.

Background: The hypomotility of colon observed in Hirschsprung's disease (HD) has been attributed to congenital aganglionosis only. So far, it is not clear whether the contractility of colonic smooth muscle in this condition is altered or not. Therefore, the present study attempted to understand the contractile status of colonic segments of HD patients by examining carbachol and endothelin (ET-1) evoked colonic smooth muscle contractions in vitro . Methods: Contractile responses were recorded from strips of colonic segments obtained from HD patients, using organ bath preparations. Cholinergic agonist carbachol and ET-1 along with their antagonists were used to evoke contractile responses. Thereafter, the samples were histopathologically confirmed for HD. Results: Colonic strips of HD did not show any spontaneous contractions but responded to carbachol and ET-1 to a lesser extent. In HD, response of carbachol was blocked by atropine and hexamethonium by nearly 73% and 50% respectively. ET-1 induced contractile responses were blocked by ET-A and ET-B antagonist up to 40%, signifying the possible role of ET-A and ET-B receptors in HD colon contractility. Conclusion: As evidenced by lack of spontaneous contractions and impaired carbachol and ET-1-induced contractile responses, it is concluded that, in addition to aganglionosis, decreased contractility of colonic smooth muscle may contribute to hypomotility observed in patients with HD.

Recombination kinetics in a silicon solar cell at low concentration: electro-analytical characterization of space-charge and quasi-neutral regions.

The present work reports a detailed electro-analytical framework for studying commercially available mono-crystalline silicon solar cells under varying illumination conditions to explore their application in the up-and-coming field of low concentration photovoltaics (LCPVs). The effect of low concentration illumination (>1-12 suns) on performance indicating parameters, i.e., short circuit current, open circuit voltage, fill factor, efficiency and ideality factor, was investigated using DC characterization. The same framework can be used for AC characterization in order to explore diffusion capacitance, transition capacitance, diffusion resistance and recombination kinetics under varying illumination. Recent developments in the impedance spectroscopy technique have broadened its horizon and have allowed its use in addressing unexplored material and performance aspects of mono-crystalline Si solar cells under non-equilibrium conditions. The obtained DC and AC experimental results are coupled with theoretical treatment to demonstrate the characteristic features of charge recombination in the space-charge region and the quasi-neutral region.

Plasmon enhanced light trapping to improve efficiency of dye-sensitized solar cell.

Photoelectric conversion efficiency of a dye-sensitized solar cell was improved by trapping more light into the absorbing region using Ag nanoparticle. Improved light transmission is observed experimentally in silver nanoparticle coated FTO glass. The size of Ag nanoparticle is estimated as 110 nm by comparing theoretical results with experimental data. The transmission data is used to explore the effect on electrical parameters of dye-sensitized solar cell using theoretical model. Plasmon enhanced DSSC showed increased efficiency of 11.76% under AM1.5 solar spectrum compared with 10.86% for a DSSC without Ag nanoparticles.