Non-thermal plasma assisted CO2 conversion to CO: Influence of non-catalytic glass packing materials

The current research is focused on the decomposition of carbon dioxide (CO2) into carbon monoxide (CO) and oxygen (O2) in a non-thermal plasma reactor using dielectric barrier discharge (DBD) at ambient conditions. Pure CO2 was injected into the DBD reactor at a flow rate of 30 mL min-1, and the voltage was varied between 16 kV to 22 kV. The filamentary micro discharges generated during plasma has a significant effect on CO2 conversion. The effect of packing materials on CO2 conversion was investigated by packing non-catalytic materials such as quartz wool, glass capillary, glass wool, and glass beads in the discharge zone of the DBD reactor. Among the studied packing materials, quartz wool exhibited a maximum CO2 conversion of 9.3 % at a discharge power of 2.0 W and specific energy input (SEI) of 4.0 J mL-1. However, glass capillary exhibited the highest energy efficiency of 1.2 mmol kJ-1 at an SEI of 3.5 J mL-1

CuInS2 Nanosheet Arrays with a MoS2 Heterojunction as a Photocathode for PEC Water Splitting

Developing cost-effective noble metal-free co-catalysts as alternatives to platinum group metals is an impeccable strategy to enhance photoelectrochemical (PEC) water splitting. In this report, we successfully fabricated CuInS2 nanosheet array-based photocathode modified with CdS and co-catalyst MoS2 in a green approach to improve water splitting under solar irradiation. The visible light absorption of the modified hybrid photocathode (CIS/CdS/MoS2) was significantly enhanced due to introducing CdS and MoS2. Photoluminescence, impedance spectroscopy, and Mott-Schottky analysis depicted improved separation of excited electron-hole pairs, minimized resistance of charge transfer, and increased excited-state charge carrier concentration, resulting in increased photocurrent. Typical results indicated that composite photoelectrodes delivered higher photocurrent (−1.75 mA/cm2 at 0 V vs RHE) and HC-STH conversion efficiency (0.42% at 0.49 V vs RHE) than those of CIS and CIS/CdS photoelectrodes. This improved PEC performance is accredited to the synergetic impact of CdS in charge generation and transfer and MoS2 as a cocatalyst with active surface sites for proton reduction. This study not only reveals the promising nature of CuInS2-based light absorber photocathodes for solar energy utilization but also recommends the use of MoS2 as a cocatalyst for the proton reduction reactions for widespread applications in solar to hydrogen conversion

Emerging Copper-Based Semiconducting Materials for Photocathodic Applications in Solar Driven Water Splitting

Hydrogen production through solar-driven water splitting is a promising approach and an alternative to the conventional steam reforming of natural gas and coal gasification. The growing energy demand and environmental degradation through carbon-emitting fossil fuels urge a transition in the usage of non-renewable to renewable sources of energy. The photocathodes in a photoelectrochemical (PEC) water-splitting cell are essential for the direct evolution of hydrogen. Among the known photocathodes, Cu-based p-type semiconducting materials are the most promising photo-absorber materials owing to their low-cost, low toxicity, natural abundance, suitable bandgaps, and favorable band edges for reduction. Moreover, the chemical stability and the rate of recombination significantly limit the longevity, the PEC performance, and practical applicability of Cu-based photocathodes. To overcome these problems, it is critical to have a thorough understanding of the constraints, improvement strategies, and an assessment of current developments in order to construct and design highly stable and efficient photocathodes. Here, in this review we have summarized the development of Cu-based metal oxide and sulfide photocathodes with the significant operational challenges and strategies that have successfully been employed to enhance the PEC performance. Furthermore, the emphasis is placed on recent reports and future perspectives regarding emerging challenges

Recent trends in photoelectrochemical water splitting: the role of cocatalysts

Environmental degradation due to the carbon emissions from burning fossil fuels has triggered the need for sustainable and renewable energy. Hydrogen has the potential to meet the global energy requirement due to its high energy density; moreover, it is also clean burning. Photoelectrochemical (PEC) water splitting is a method that generates hydrogen from water by using solar radiation. Despite the advantages of PEC water splitting, its applications are limited by poor efficiency due to the recombination of charge carriers, high overpotential, and sluggish reaction kinetics. The synergistic effect of using different strategies with cocatalyst decoration is promising to enhance efficiency and stability. Transition metal-based cocatalysts are known to improve PEC efficiency by reducing the barrier to charge transfer. Recent developments in novel cocatalyst design have led to significant advances in the fundamental understanding of improved reaction kinetics and the mechanism of hydrogen evolution. To highlight key important advances in the understanding of surface reactions, this review provides a detailed outline of very recent reports on novel PEC system design engineering with cocatalysts. More importantly, the role of cocatalysts in surface passivation and photovoltage, and photocurrent enhancement are highlighted. Finally, some challenges and potential opportunities for designing efficient cocatalysts are discussed

Electrochemical Investigation of TLR4/MD-2-Immobilized Polyaniline and Hollow Polyaniline Nanofibers:Toward Real-Time Triaging of Gram-Negative Bacteria Responsible for Delayed Wound Healing

Detecting gram -ve bacterial colonies is crucial in address-ing the clinical challenges associated with chronic wounds and delayed healing. These bacteria can exacerbate wound conditions, hindering natural healing and potentially leading to infections. The electrochemical sensing platform presented in this study serves as a valuable tool for healthcare professionals to make timely and targeted treatment decisions. Toward this, we developed a cost-effective electrochemical sensing platform leveraging the TLR4/MD-2 complex to detect gram -ve bacterial colonies. Our biosensors were meticulously fashioned using polyaniline (PANi) and hollow PANi (HPANi) nanofibers. Notably, the HPANi-based sensors, owing to their distinctive hollow structure, facilitated amplified responses under comparable experimental conditions compared with PANi-based counterparts. The designed sensing platform demonstrated exceptional accuracy in identifying Escherichia coli (gram -ve), showcasing a theoretical detection limit of 0.215 CFU/mL for PANi and a remarkably improved 0.14 CFU/mL for HPANi. These sensors displayed outstanding selectivity for gram -ve bacteria, even amidst gram +ve bacteria and fungi. Moreover, our platform demonstrated remarkable sensitivity, yielding 3.04 ((ΔR/R)/CFU/mL)/cm2 for the HPANi-based sensor, surpassing the performance of the PANi-based sensor at 1.98 ((ΔR/R)/CFU/mL)/cm2.</p

Mn-doped ZnO microspheres prepared by solution combustion synthesis for room temperature NH3 sensing

Despite being the most favorable ammonia (NH3) gas sensors, metal oxide semiconductors fail to deliver high selectivity and room temperature (RT) sensing. Tuning the metal oxide with doping is an attractive way of overcoming these disadvantages. Herein, we report Mn-doped ZnO microspheres as promising sensors for highly sensitive and selective RT sensing of NH3. ZnO and 2 wt% Mn-doped ZnO microspheres were synthesized by a low-cost and fast solution combustion synthesis, and their structure, morphology, and gas sensing properties were investigated. Mn-doping resulted in a change in the lattice parameters, an increase in the oxygen vacancies, and surface acidity of ZnO as confirmed by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and Temperature programmed desorption (TPD), respectively. Mn-doped ZnO showed a response (Ra/Rg) of 20.2 in 100 ppm NH3, which is significantly higher than ZnO. The sensor showed high selectivity, three times higher than that of ZnO, and good stability. Improvement in the sensing performance of Mn-doped ZnO is attributed to the increase in the defects and surface acidity with Mn-doping. © 2022 The Author(s

Enhanced electrical and photocatalytic activities in Na0.5Bi0.5TiO3 through structural modulation by using anatase and rutile phases of TiO2

his paper deals with an in-depth analysis on the role of the microstructure phase of titanium dioxide (TiO2) precursor in sodium bismuth titanate (Na0.5Bi0.5TiO3, hereafter represented as NBT) ceramics prepared through the hydrothermal method. The comparison of the grain size, microstructure, crystal structure, and electrical properties of the NBT ceramics is carried out using anatase and rutile TiO2. NBT ceramics with anatase TiO2 (denoted by NBTA) displayed superior dielectric and ferro/piezoelectric properties along with the additional functionality in terms of photocatalysis. Systematic studies of functional properties such as piezoelectric, ferroelectric, and dielectric stressed the far-reaching influence of effects on grain size. The mechanisms and functional properties of grain quantitative effects are also discussed. Grain boundaries volume fraction increment has decreased the dielectric peak but increased the diffusiveness in the case of the NBT with rutile TiO2 precursor (denoted as NBTR). Similarly, elastic stiffness increment restricts the movement of the domain wall and led to a decrement in remnant polarization along with an increase in the values of the corresponding piezoelectric coefficient in fine-grain NBTR samples

Integrated p-n Junctions for Efficient Solar Water Splitting upon TiO2/CdS/BiSbS3 Ternary Hybrids for Improved Hydrogen Evolution and Mechanistic Insights

The development of efficient and novel p-n heterojunctions for photoelectrochemical (PEC) water splitting is still a challenging problem. We have demonstrated the complementary nature of (p-type) BiSbS3 as a sensitizer when coupled with (n-type) TiO2/CdS to improve the photocatalytic activity and solar to hydrogen conversion efficiency. The as-prepared p-n heterojunction TiO2/CdS/BiSbS3 exhibits good visible light harvesting capacity and high charge separation over the binary heterojunction, which are confirmed by photoluminescence (PL) and electrical impedance spectroscopy (EIS). The ternary heterojunction produces higher H-2 than the binary systems TiO2/CdS and TiO2/BiSbS3. This ternary heterojunction system displayed the highest photocurrent density of 5 mA center dot cm(-2) at 1.23 V vs. reversible hydrogen electrode (RHE) in neutral conditions, and STH of 3.8% at 0.52 V vs. RHE is observed. The improved photocatalytic response was due to the favorable energy band positions of CdS and BiSbS3. This study highlights the p-n junction made up of TiO2/CdS/BiSbS3, which promises efficient charge formation, separation, and suppression of charge recombination for improved PEC water splitting efficiency. Further, no appreciable loss of activity was observed for the photoanode over 2500 s. Band alignment and interfaces mechanisms have been studied as well

Synthesis, optoelectronic properties and applications of halide perovskites

Halide perovskites have emerged as a class of most promising and cost-effective semiconductor materials for next generation photoluminescent, electroluminescent and photovoltaic devices. These perovskites have high optical absorption coefficients and exhibit narrow-band bright photoluminescence, in addition to their halide-dependent tuneable bandgaps, low exciton binding energies, and long-range carrier diffusion. These properties make these perovskites superior to classical semiconductors such as silicon. Most importantly, the simple synthesis of perovskites in the form of high quality films, single crystals, nanocrystals and quantum dots has attracted newcomers to develop novel perovskites with unique optoelectronic properties for optical and photovoltaic applications. Here, we comprehensively review recent advances in the synthesis and optoelectronic properties of films, microcrystals, nanocrystals and quantum dots of lead halide and lead-free halide perovskites. Followed by the classification of synthesis, we address the ensemble and single particle properties of perovskites from the viewpoints of the confinement and transport of charge carriers or excitons. Further, we correlate the charge carrier properties of perovskite films, microcrystals, nanocrystals and quantum dots with the crystal structure and size, halide composition, temperature, and pressure. Finally, we illustrate the emerging applications of perovskites to solar cells, LEDs, and lasers, and discuss the ongoing challenges in the field

Physicochemical process of non-thermal plasma at gas-liquid interface and synergistic effect of plasma with catalyst

An atmospheric-pressure plasma jet (APPJ) was directly irradiated at a gas-liquid interface under ambient conditions. The reactive oxygen species (ROS) like hydroxyl radicals (•OH), hydrogen peroxide (H2O2) and ozone (O3) and also reactive nitrogen species (RNS) such as nitrogen oxides (NOx) and nitric acid (HNO3) formed during the plasma discharge were quantified under various experimental parameters. In a chemical dosimetry method, terephthalic acid (TA) was employed for the quantification of •OH and titanium sulfate was used to quantify the H2O2. Quantitative determination of NO3− was carried out by using Ion chromatography (IC). The changes in the solution pH were studied during the plasma treatment. Strong acidification along with the production of dominant reactive nitrogen species and ozone formation were observed with air. The effect of various gases, gas flow rate, various applied voltage and catalyst were studied to optimize the experimental conditions for the best performance. The influence of catalyst Fe2+ salt, TiO2 on the formation of reactive species were studied. The efficiency of the plasma device for the degradation of crystal violet (CV) was also investigated with TiO2 and Fe2+ salt. © 2022 Korean Physical Societ