Innate cation sensitivity in a semiconducting polymer

Water- gated organic thin film transistors (OTFTs) using the hole transporting semiconducting polymer, poly(2,5-bis(3-hexadecylthiophen-2-yl)thieno[3,2-b]thiophene) (PBTTT), show an innate response of their threshold voltage to the addition of divalent metal cations to the gating water, without deliberately introducing an ion- sensitive component. A similar threshold response is shown for several divalent cations, but is absent for monovalent cations. Response is absent for transistors using the inorganic semiconductor ZnO, or the similar organic semiconductor poly(3-hexylthiophene) (rrP3HT), instead of PBTTT. We assign innate cation sensitivity to residues of the organometallic Pd(0) complex used as catalyst in PBTTT synthesis which bears strong resemblance to typical metal chelating agents. Organometallic Pd(0) residues are absent from ZnO, and also from rrP3HT which is polymerised with a different type of catalyst. However, when Pd(0) complex is deliberately added to rrP3HT casting solutions, resulting OTFTs also display threshold response to a divalent cation

A water-gated organic thin film transistor as a sensor for water-borne amines

The p-type semiconducting polymer Poly(2,5-bis(3-hexadecylthiophen-2-yl)thieno[3,2-b]thiophene) (PBTTT) displays innate sensitivity to water-borne amines. We demonstrate this with the help of water- gated PBTTT thin film transistors (TFTs). When octylamine is added to the gating water, TFTs respond with a significantly reduced saturated drain current. Underlying TFT drift is minimised by initial conditioning, and remaining drift can be accounted for by normalising current response to the current level under purge immediately before exposure. Normalised current response vs. amine concentration is reproducible between different transistors, and can be modelled by a Langmuir surface adsorption isotherm, which suggests physisorption of analyte at the PBTTT surface, rather than bulk penetration. Same PBTTT transistors do not respond to 1- octanol, confirming the specific affinity between amines and thiophene- based organic semiconductors

Fabrication of Effective Co-SnO₂/SGCN Photocatalysts for the Removal of Organic Pollutants and Pathogen Inactivation

Substantial improvement is needed in efficient and affordable decolorization and disinfection methods to solve the issues caused by dyes and harmful bacteria in water and wastewater. This work involves the photocatalytic degradation of methylene blue (MB) as well as gram-negative and gram-positive bacteria by cobalt-doped tin oxide (Co-SnO2) nanoparticles (NPs) and Co-SnO2/SGCN (sulfur-doped graphitic carbon nitride) nanocomposites (NCs) under sunlight. The coprecipitation approach was used to synthesize the photocatalysts. Maximum methylene blue (MB) photocatalytic degradation was seen with the 7% Co-SnO2 NPs compared to other (1, 3, 5, and 9 wt.%) Co-SnO2 NPs. The 7% Co-SnO2 NPs were then homogenized with different amounts (10, 30, 50, and 70 weight %) of sulfur-doped graphitic carbon nitride (SGCN) to develop Co-SnO2/SGCN heterostructures with the most significant degree of MB degradation. The synthesized samples were identified by modern characterization methods such as FT-IR, SEM, EDX, UV-visible, and XRD spectroscopies. The Co-SnO2/50% SGCN composites showed a significant increase in MB degradation and degraded 96% of MB after 150 min of sunlight irradiation. Both gram-negative (E. coli) and gram-positive (B. subtiles) bacterial strains were subjected to antibacterial activity. All samples were shown to have vigorous antibacterial activity against gram-positive and gram-negative bacteria, but the Co-SnO2/50% SGCN composites exhibited the maximum bactericidal action. Thus, the proposed NC is an efficient organic/inorganic photocatalyst that is recyclable and stable without lowering efficiency. Hence, Co-SnO2/50% SGCNNC has the potential to be employed in water treatment as a dual-functional material that simultaneously removes organic pollutants and eradicates bacteria

Design and Experimental Studies on a Single Slope Solar Still for Water Desalination

Gulf countries experience an imbalance between water supply and demand, which leads to a dramatic decline in the amount of groundwater. Solar energy for water desalination is an attractive option in this region, where the climate is sunny all year. A very basic solar device called a single basin solar still is commonly used to convert available seawater into drinkable water. The issue of producing drinking water may be resolved by using this technique, but because of its low productivity, it is rarely used. The experiments were carried out on a south-facing, single slope solar still with a 23-degree inclination of the condensing cover from October to November 2022, on different days for different water depths. According to the findings, the solar still with 4 cm of depth (as compared to 5, 6, and 7 cm) exhibited the maximum water productivity (2.680 L/day) with an efficiency of 30%. When the solar still was equipped with an external mirror, the temperature in the basin was raised, and water productivity increased to 3.075 L/day with an improved efficiency of 35%. Further, the effects of wind velocity, ambient temperature, inner glass temperature, and intensity of solar radiation on daily productivity have been studied