Ternary nanocomposites of CdS/WO3/g-C3N4 for hydrogen production.

The sustainable rise in global warming and the consumption of fossil fuels considerably contribute to energy and environmental issues. To address these issues, semiconductor heterostructures can be used to generate clean energy sources as alternative energy sources and to reduce environmental impacts. Herein, we report the synthesis of a ternary semiconductor of the CdS/WO3/g-C3N4 (i.e. C-CNW) nanostructured composite for hydrogen production and dye degradation under visible-light irradiation. The structural properties of the prepared materials were studied using a series of investigational analyses. The 3C-CNW nanostructure photocatalyst exhibited faster malachite green (MG) dye photodegradation within 105 min and the highest hydrogen production rate is 868.23 µmol g-1 h-1 under visible light illumination. Moreover, the photocatalytic hydrogen production of the 3C-CNW nanostructure photocatalyst with various scavengers was analyzed. Its higher photocatalytic activity is ascribed to the Z-scheme mechanism, which induces rapid diffusion of photoinduced charges within the ternary photocatalyst with its optical bandgap. This proposed strategy is useful to improve photocatalysts that play a role in mitigating energy and environmental issues.

InVO4 nanosheets decorated with ZnWO4 nanorods: A novel composite and its enhanced photocatalytic performance under solar light.

InVO4 is the most attractive inorganic new-generation material for advanced scientific research, especially in the fields of energy and environmental science. In theory, this stable, non-toxic, energy-efficient metal vanadate semiconductor is expected to exhibit significant catalytic activity owing to its narrow bandgap energy. However, this has not been achieved in practice because of its inherent defects in terms of the separation and migration of charge carriers. In fact, the exploration of this material is still in its infancy, and more research is needed to improve its efficiency and speed up its commercialization. Band gap engineering using heterojunction formation offers better results than other methods, such as morphological variations and doping efforts. In this context, the present study offers a significant solution substantiated by experimental results. This includes the successful synthesis of a novel nanocomposite of InVO4 nanosheets decorated with ZnWO4 nanorods with a unique improved light absorption ability. Three composites with 26.48-33.85 nm crystal sizes and 11.74-19.98 m2/g surface area were prepared with tailor-made bandgap energies in the range of 2.52-2.97 eV. Furthermore, they produced high photoexcitation currents with low EIS resistance with respect to their constituents. The as-prepared InVO4-based novel catalyst almost completely (98.33%) decomposed tetracycline (TC) antibiotic in just 90 min, proving its high efficacy. The enhanced performance of the novel catalyst is 7.6 times that of InVO4 and 10 times that of ZnWO4. Moreover, the catalyst intake was significantly small (15 mg/100 mL TC solution).

Heterostructured 2D/2D ZnIn2S4/g-C3N4 nanohybrids for photocatalytic degradation of antibiotic sulfamethoxazole and photoelectrochemical properties.

In recent years, antibiotic drugs have been extensively used owing to increased industrial growth, and this has created issues related to drinking water and a green environment. Different techniques have been used to resolve these issues, among which heterogeneous photocatalysis has been widely explored for the elimination of toxic compounds from wastewater resources. In this study, ZnIn2S4, g-C3N4, and ZnIn2S4/g-C3N4 hybrid heterostructured composites are synthesized via hydrothermal method and used these (i) for the removal of antibiotic sulfamethoxazole pollutant and (ii) photoelectrochemical water oxidation. The nanomaterials were characterized using X-ray diffraction, Scanning electron microscopy, transmission electron microscopy, and UV-vis spectroscopy. The developed hybrid heterostructured composites were able to degrade sulfamethoxazole pollutants as well as offer improved photoelectrochemical properties compared to pristine samples. The catalytic performance of the materials developed under visible light irradiation was greatly improved for the degradation of the antibiotic drug up to 89.4% in 2 h. Moreover, the hybrid heterostructured photoelectrode showed a better photocurrent density (8.68 mA/cm2) and exhibited ∼19.2 and 29.9 times greater photocurrent density than the pristine photoelectrodes. Such a considerably increased catalytic activity was attributed to the active separation of charge carriers and transmission. The study offers an innovative approach to develop effective catalysts, and for the degradation of sulfamethoxazole as well as the PEC properties for hydrogen production.

Fabrication of InVO4/SnWO4 heterostructured photocatalyst for efficient photocatalytic degradation of tetracycline under visible light.

In the present study, novel InVO4/SnWO4 nanocomposites with different concentrations of SnWO4 were successfully prepared using a facile hydrothermal technique and investigated employing a wide range of analytical methods for efficient photocatalytic degradation of tetracycline (TC). X-ray diffraction analysis showed the presence of the orthorhombic phases of both InVO4 and SnWO4 in the composite catalyst. Dispersion of SnWO4 nanoplates over the InVO4 nanosheets enhanced the synergistic interactions, improving the separation of charge carriers and their transfer. Furthermore, the formation of heterostructure expanded the absorption range and promoted visible light harvesting. The TC degradation efficiency of InVO4/SnWO4 nanocomposite (5 mg loading of SnWO4) reached 97.13% in 80 min under visible light, with the kinetic rate constants 5.51 and 7.63 times greater than those of pure InVO4 and SnWO4, respectively. Additionally, the scavenger results proved that hydroxyl radicals and holes played a significant role in the photodegradation of TC. Furthermore, the electrochemical impedance spectroscopy (EIS) and transient photocurrent response analysis showed enhanced e-/h+ partition efficiency. Thus, the formation of heterostructure with strong synergistic interactions can effectively transfer the excited charge carriers and shorten the reunion rate. Accordingly, the InVO4/SnWO4 nanocomposites exhibited remarkable photocatalytic performance due to the increased number of charge carriers on the surface.

Hydrothermally derived Cr-doped SnO2 nanoflakes for enhanced photocatalytic and photoelectrochemical water oxidation performance under visible light irradiation.

Photocatalytic dye degradation is a method of environmental degradation that is commonly used to eliminate various pollutants produced by pharmaceutical and textile industries. Herein, pure and chromium (Cr)-doped SnO2 nanoflakes were synthesized using a simple facile hydrothermal method and photocatalytic properties were studied under visible light illumination. In addition, photoelectrochemical (PEC) water oxidation properties were also studied using the prepared samples. Doping of transition metal ions introduces structural defects, which narrow the band gap of host sample, resulting in high catalytic activity. The synthesized doped SnO2 displayed a rutile tetragonal crystal phase with a nanoflakes-like surface morphology having no other contaminations. The optical band gap of Cr-doped SnO2 nanoflakes was significantly reduced (2.48 eV) over the pure sample (3.32 eV), due to successful incorporation of Cr ions into the host lattice. Furthermore, the dye removal efficiency of these nanoflakes was investigated for methyl orange (MO) and tetracycline (TC) organic contaminations. The Cr-doped SnO2 nanoflakes exhibited superior photodegradation with 87.8% and 90.6% dye removal efficiency, within 90 min of light illumination. PEC water oxidation analysis showed that the doped photoelectrode achieved enhanced photocurrent density and showed a higher photocurrent density (1.08 mA cm-2) over that of the undoped electrode (0.60 mA cm-2). Electrochemical impedance spectroscopy (EIS) showed that doped electrodes exhibited lesser charge resistance than the pure electrode. The synthesized Cr-doped SnO2 nanoflakes are suitable for water oxidation and photodegradation of organic pollutants. Thus, we strongly believe that the obtained results in this report will continue to provide new opportunities for the improvement of effective visible light photocatalysts for industrial wastewater treatment and water splitting for H2 generation.

Cobalt-doped V2O5 hexagonal nanosheets for superior photocatalytic toxic pollutants degradation, Cr (VI) reduction, and photoelectrochemical water oxidation performance.

The worldwide energy calamity and ecological disturbances demand materials that can remove harmful contaminants from the polluted water. Recently, semiconductor-based catalytic dye removal has created much consideration due to its high efficacy and eco-friendly contaminated water treatment processes. Vanadium oxide (V2O5) has attracted superior attention as a catalyst due to its robust oxidation power, chemical inertness, and stability against photodegradation. In this study, pristine and cobalt (Co)-doped V2O5 samples were synthesized by solvothermal method and examined for their photo-degradation activity and photoelectrochemical (PEC) water oxidation properties. The orthorhombic crystal phase was confirmed by X-ray diffraction (XRD), hexagonal-shaped morphology was observed by scanning electron microscope (SEM) and reduced optical band gap (2.01 eV) was noticed for doped V2O5 catalyst compared to the pristine (2.20 eV) catalyst. The doped V2O5 catalyst exhibited enhanced photodegradation of crystal violet CV (92.7%) and Cr (VI) reduction (90.5%) after 100 min of light irradiation. The doped photocatalyst exhibited approximately 2.1 and 1.9-fold enhancement of photodegradation of CV and Cr(VI) reduction, respectively. The doped electrode showed improved photocurrent density (0.54 mA/cm-2) compared to pristine electrode (0.12 mA/cm-2). Moreover, the doped electrode showed reduced charge-transfer resistance and enhanced charge-transfer properties compared to those of the pristine electrode. Hence, the prepared hexagonal-shaped V2O5 is a suitable material for the elimination of environmental contaminants from the polluted water as well as water splitting for hydrogen generation.

Enhancing Electrochemical Performance with g-C3N4/CeO2 Binary Electrode Material.

An innovative form of 2D/0D g-C3N4/CeO2 nanostructure was synthesized using a simple precursor decomposition process. The 2D g-C3N4 directs the growth of 0D CeO2 quantum dots, while also promoting good dispersion of CeO2QDs. This 2D/0D nanostructure shows a capacitance of 202.5 F/g and notable rate capability and stability, outperforming the g-C3N4 electrode, reflecting the state-of-the-art g-C3N4 binary electrodes. The binary combination of materials also enables an asymmetric device (g-C3N4/CeO2QDs//AC) to deliver the highest energy density (9.25 Wh/kg) and power density (900 W/kg). The superior rate capacity and stability endorsed the quantum structural merits of CeO2QDs and layered g-C3N4, which offer more accessible sites for ion transport. These results suggest that the g-C3N4/CeO2QDs nanostructure is a promising electrode material for energy storage devices.

High-Throughput Strategies for the Design, Discovery, and Analysis of Bismuth-Based Photocatalysts.

Bismuth-based nanostructures (BBNs) have attracted extensive research attention due to their tremendous development in the fields of photocatalysis and electro-catalysis. BBNs are considered potential photocatalysts because of their easily tuned electronic properties by changing their chemical composition, surface morphology, crystal structure, and band energies. However, their photocatalytic performance is not satisfactory yet, which limits their use in practical applications. To date, the charge carrier behavior of surface-engineered bismuth-based nanostructured photocatalysts has been under study to harness abundant solar energy for pollutant degradation and water splitting. Therefore, in this review, photocatalytic concepts and surface engineering for improving charge transport and the separation of available photocatalysts are first introduced. Afterward, the different strategies mainly implemented for the improvement of the photocatalytic activity are considered, including different synthetic approaches, the engineering of nanostructures, the influence of phase structure, and the active species produced from heterojunctions. Photocatalytic enhancement via the surface plasmon resonance effect is also examined and the photocatalytic performance of the bismuth-based photocatalytic mechanism is elucidated and discussed in detail, considering the different semiconductor junctions. Based on recent reports, current challenges and future directions for designing and developing bismuth-based nanostructured photocatalysts for enhanced photoactivity and stability are summarized.

g-C3N4 nanosheets functionalized yttrium-doped ZrO2 nanoparticles for efficient photocatalytic Cr(VI) reduction and energy storage applications.

Novel g-C3N4 functionalized yttrium-doped ZrO2 hybrid heterostructured (g-YZr) nanoparticles have been synthesized to investigate photocatalytic Cr(VI) reduction as well as electrochemical energy storage applications. The nanoparticles have been characterized to examine their structural, optical, and photocatalytic properties. XRD confirmed the incorporation of dopant ions and heterostructure development between g-C3N4 and doped ZrO2. When g-C3N4 was doped with ZrO2, the ability of light adsorption was greatly enhanced due to the narrow band gap. The distinctive structure of g-YZr exhibited outstanding photocatalytic Cr(VI) reduction owing to its superior surface area, which greatly prevented the charge carriers' recombination rate and exhibited superior photocatalytic performance within 90 min of solar light irradiation. Furthermore, these catalysts demonstrated similar catalytic Cr(VI) reduction activity following four repeatability tests, indicating the exceptional structural stability of g-YZr catalysts. The electrochemical performance of the electrodes revealed that g-YZr exhibited superior specific capacitance over the other electrodes owing to extra energetic sites and robust synergic effect. Enhanced specific capacitance and long cyclic stability of the hybrid heterostructures displayed their usefulness for energy storage applications.

SnO2 Quantum Dots Distributed along V2O5 Nanobelts for Utilization as a High-Capacity Storage Hybrid Material in Li-Ion Batteries.

In this study, the facile synthesis of SnO2 quantum dot (QD)-garnished V2O5 nanobelts exhibiting significantly enhanced reversible capacity and outstanding cyclic stability for Li+ storage was achieved. Electrochemical impedance analysis revealed strong charge transfer kinetics related to that of V2O5 nanobelts. The SnO2 QD-garnished V2O5 nanobelts exhibited the highest discharge capacity of ca. 760 mAhg-1 at a density of 441 mAg-1 between the voltage ranges of 0.0 to 3.0 V, while the pristine V2O5 nanobelts samples recorded a discharge capacity of ca. 403 mAhg-1. The high capacity of QD-garnished nanobelts was achieved as an outcome of their huge surface area of 50.49 m2g-1 and improved electronic conductivity. Therefore, the as-presented SnO2 QD-garnished V2O5 nanobelts synthesis strategy could produce an ideal material for application in high-performance Li-ion batteries.

Enhanced solar-light-driven photocatalytic properties of novel Z-scheme binary BiPO4 nanorods anchored onto NiFe2O4 nanoplates: Efficient removal of toxic organic pollutants.

Global environmental problems have been increasing with the growth of the world economy and have become a crucial issue. To replace fossil fuels, sustainable and eco-friendly catalysts are required for the removal of organic pollutants. In this study, nickel ferrite (NiFe2O4) was prepared using a simple wet-chemical synthesis, followed by calcination; bismuth phosphate (BiPO4) was also prepared using a hydrothermal method. Further, NiFe2O4/BiPO4 nanocomposites were prepared using a hydrothermal technique. Numerous characterization studies, such as structural, morphology, surface area, optical, photoluminescence, and photoelectrochemical investigations, were used to analyze NiFe2O4/BiPO4 nanocomposites. The morphology analysis indicated a successful decoration of BiPO4 nanorods on the surface of NiFe2O4 nanoplate. Further, the bandgap of the NiFe2O4/BiPO4 nanocomposites was modified owing to the formation of a heterostructure. The as-prepared NiFe2O4/BiPO4 nanocomposite exhibited promising properties to be used as a novel heterostructure for tetracycline (TC) and Rhodamine B (RhB) removal. The NiFe2O4/BiPO4 nanocomposite degrades TC (98%) and RhB (99%) pollutants upon solar-light irradiation within 100 and 60 min, respectively. Moreover, the trapping experiments confirmed the Z-scheme approach of the prepared nanocomposites. The efficient separation and transfer of photogenerated electron-hole pairs rendered by the heterostructure were confirmed by utilizing electrochemical impedance spectroscopy, photocurrent experiments, and photoluminescence. Mott-Schottky measurements were used determine the positions of the conduction and valence bands of the samples, and the detailed mechanism of photocatalytic degradation of toxic pollutants was projected and discussed.

Z-scheme binary 1D ZnWO4 nanorods decorated 2D NiFe2O4 nanoplates as photocatalysts for high efficiency photocatalytic degradation of toxic organic pollutants from wastewater.

In this study, dimensionally coupled Z-scheme binary nanocomposites from two-dimensional (2D) NiFe2O4 nanoplates and one-dimensional (1D) ZnWO4 nanorods are prepared for efficient degradation of an antibiotic tetracycline (TC) and organic dye rhodamine B (RhB) under solar illumination. NiFe2O4/ZnWO4 nanocomposites were synthesized by a simple and ecological in-situ hydrothermal method without the use of surfactants. Structural and morphological studies revealed the formation of heterostructure and 1D ZnWO4 nanorods were uniformly distributed over the surface of NiFe2O4 nanoplates. Light-harvesting capability was improved and optimized by loading with different amounts of ZnWO4. Photoluminescence analysis demonstrated inhibited nature of the recombination of photo-excited charge carriers in the nanocomposites. Photocatalytic experiments revealed that the nanocomposite exhibited improved Z-scheme electron-transfer for the degradation of TC under solar illumination. In particular, NFZW-20 nanocomposite demonstrated superior photocatalytic degradation of TC of approximately 98% within 105 min. Furthermore, their photocatalytic performance was investigated by RhB dye under the solar irradiation to achieve 98% of degradation of RhB in 70 min. Improved photocatalytic activities are attributed to the Z-scheme electron-transfer mechanism, which could enhance the superior ability of light absorption and reduced recombination rate of the photogenerated charge carriers.

ZnO nanosheets-decorated Bi2WO6 nanolayers as efficient photocatalysts for the removal of toxic environmental pollutants and photoelectrochemical solar water oxidation.

Herein we report the fabrication of novel Bi2WO6/ZnO heterostructured hybrids for organic contaminant degradation from wastewater and photoelectrochemical (PEC) water splitting upon solar illumination. The Bi2WO6/ZnO photocatalysts were synthesized using a simple and eco-friendly hydrothermal process without the support of any surfactants. From the photocatalytic experiments, heterostructured Bi2WO6/ZnO nanohybrid catalysts exhibited considerably better photocatalytic performance for rhodamine B (RhB) degradation under solar illumination. The BWZ-20 nanocomposite demonstrated superior photodegradation of RhB dye up to 99% in about 50 min. Furthermore, BWZ-20 photoelectrode showeda lower charge-transfer resistance than other samples prepared, suggesting its suitability for PEC water splitting. The photocurrent densities of Bi2WO6/ZnO photoelectrodes were evaluated under the solar irradiation. The BWZ-20 photoelectrode exhibited a significant photocurrent density (0.45 × 10-3A/cm2) at +0.3 V vs. Ag/AgCl, which was~1036-times higher than that of pure Bi2WO6, and ~4.8-times greater than the pure ZnO. Such improved photocatalytic and PEC activities are mainly attributed to the formation of an interface between ZnO and Bi2WO6, superior light absorption ability, low charge-transfer resistance, remarkable production of charge carriers, easy migration of charges, and suppression of the recombination of photogenerated charge carriers.

Steady-state protein focusing in carrier ampholyte based isoelectric focusing: Part I-Analytical solution.

The determination of an analytical solution to find the steady-state protein concentration distribution in IEF is very challenging due to the nonlinear coupling between mass and charge conservation equations. In this study, approximate analytical solutions are obtained for steady-state protein distribution in carrier ampholyte based IEF. Similar to the work of Svensson, the final concentration profile for proteins is assumed to be Gaussian, but appropriate expressions are presented in order to obtain the effective electric field and pH gradient in the focused protein band region. Analytical results are found from iterative solutions of a system of coupled algebraic equations using only several iterations for IEF separation of three plasma proteins: albumin, cardiac troponin I, and hemoglobin. The analytical results are compared with numerically predicted results for IEF, showing excellent agreement. Analytically obtained electric field and ionic conductivity distributions show significant deviation from their nominal values, which is essential in finding the protein focusing behavior at isoelectric points. These analytical solutions can be used to determine steady-state protein concentration distribution for experiment design of IEF considering any number of proteins and ampholytes. Moreover, the model presented herein can be used to find the conductivity, electric field, and pH field.

Steady-state protein focusing in carrier ampholyte-based isoelectric focusing: Part II-validation and case studies.

In this study, we systematically investigate the validity and applicability of an analytical model developed for carrier ampholyte-based isoelectric focusing (IEF). Three different IEF cases are considered in order to evaluate the efficacy of the approximate analytical results by comparison with high-resolution computer simulations. In the first case, three proteins are separated in a narrow pH range (6-9) by using 50 carrier ampholytes. In the second and third cases, the separation of proteins is studied in broad pH range (3-10) IEF by using 100 carrier ampholytes. Results obtained from the approximate analytical models are in very good agreement with the numerical results for IEF separation of cardiac troponin I, albumin, and hemoglobin in both narrow and broad pH ranges. The sensitivity of the analytical model is also tested for different initial mass ratios of proteins to ampholytes. No appreciable differences are observed between the approximate analytical and numerical results within the mass ratio range studied. The effect of a nominal electric field and/or a nominal pH gradient on protein focusing is also examined to demonstrate the effectiveness of the analytical model. Our results indicate that the use of both nominal electric field and pH gradient will result in erroneous peak concentrations for proteins. Finally, we describe the limitations of the approximate analytical solutions.

Efficient algorithm for simulation of isoelectric focusing.

IEF simulation is an effective tool to investigate the transport phenomena and separation performance as well as to design IEF microchip. However, multidimensional IEF simulations are computationally intensive as one has to solve a large number of mass conservation equations for ampholytes to simulate a realistic case. In this study, a parallel scheme for a 2D IEF simulation is developed to reduce the computational time. The calculation time for each equation is analyzed to identify which procedure is suitable for parallelization. As expected, simultaneous solution of mass conservation equations of ampholytes is identified as the computational hot spot, and the computational time can be significantly reduced by parallelizing the solution procedure for that. Moreover, to optimize the computing time, electric potential behavior during transient state is investigated. It is found that for a straight channel the transient variation of electric potential along the channel is negligible in a narrow pH range (5∼8) IEF. Thus the charge conservation equation is solved for the first time step only, and the electric potential obtain from that is used for subsequent calculations. IEF simulations are carried out using this algorithm for separation of cardiac troponin I from serum albumin in a pH range of 5-8 using 192 biprotic ampholytes. Significant reduction in simulation time is achieved using the parallel algorithm. We also study the effect of number of ampholytes to form the pH gradient and its effect in the focusing and separation behavior of cardiac troponin I and albumin. Our results show that, at the completion of separation phase, the pH profile is stepwise for lower number of ampholytes, but becomes smooth as the number of ampholytes increases. Numerical results also show that higher protein concentration can be obtained using higher number of ampholytes.

Electrochemical immunosensing of tumor markers.

The rising incidence and mortality rates of cancer have led to a growing need for precise and prompt early diagnostic approaches to effectively combat this disease. However, traditional methods employed for detecting tumor cells, such as histopathological and immunological techniques, are often associated with complex procedures, high analytical expenses, elevated false positive rates, and a dependence on experienced personnel. Tracking tumor markers is recognized as one of the most effective approaches for early detection and prognosis of cancer. While onco-biomarkers can also be produced in normal circumstances, their concentration is significantly elevated when tumors are present. By monitoring the levels of these markers, healthcare professionals can obtain valuable insights into the presence, progression, and response to treatment of cancer, aiding in timely diagnosis and effective management. This review aims to provide researchers with a comprehensive overview of the recent advancements in tumor markers using electrochemical immunosensors. By highlighting the latest developments in this field, researchers can gain a general understanding of the progress made in the utilization of electrochemical immunosensors for detecting tumor markers. Furthermore, this review also discusses the current limitations associated with electrochemical immunosensors and offers insights into paving the way for further improvements and advancements in this area of research.

Highly efficient photodegradation of toxic organic pollutants using Cu-doped V2O5 nanosheets under visible light.

Photodegradation of organic pollutants using metal oxides has shown extraordinary promise owing to the catalytic efficacy, low cost, less noxiousness, and good chemical constancy. In this research, pure and transition metal ions (Cu)-doped V2O5 nanosheets were synthesized and investigated for their photocatalytic efficiency using methyl blue (MB) and rhodamine B (RhB) organic dye pollutants under visible light irradiation. The orthorhombic crystal phase was confirmed by XRD analysis, which exhibited a stable phase upon incorporating Cu dopant ions. Optical properties were examined using optical absorption spectroscopy, while a reduced band gap was observed in the doped V2O5 nanosheets over the undoped sample. EIS analysis confirmed lower charge resistance in doped V2O5 nanosheets. The Cu dopant incorporation into the host matrix considerably enhanced photodegradation efficiency for MB and RhB impurities under light illumination. The improvement in catalytic efficacy is attributed to dopant ions that can separate photoinduced charge carriers and the quick movement of the charge. Moreover, comparatively lesser crystalline size, improved specific surface area, and hydroxyl group onto the catalyst surface are quite advantageous to offer better photocatalytic activity of Cu-doped V2O5 nanosheets.

Enriched photocatalytic and photoelectrochemical activities of a 2D/0D g-C3N4/CeO2 nanostructure.

Sunlight-powered photocatalysts made from CeO2 nanosized particles and g-C3N4 nanostructures were produced through a thermal decomposition process with urea and cerium nitrate hexahydrate. The preparation of g-C3N4, CeO2, and a binary nanostructured g-C3N4/CeO2 photocatalyst was done through a facile thermal decomposition method. The structural properties were analyzed using powder X-ray diffraction, scanning electron microscopy, high-resolution transmission electron microscopy, energy dispersive X-ray spectroscopy, and X-ray photoelectron spectroscopy (XPS). Photocatalyst properties were characterized by using crystal violet (CV), a UV-Vis spectrophotometer, photocurrent and electron impedance spectroscopy (EIS). The structural and morphological analyses revealed that the g-C3N4/CeO2 nanostructures significantly enhanced the photoactivity for CV dye degradation under simulated sunlight, with a degradation rate of 94.5% after 105 min, compared to 82.5% for pure g-C3N4 and 45% for pure CeO2. This improvement was attributed to the noticeable visible light absorption and remarkable charge separation abilities of the nanostructures. Additionally, the g-C3N4/CeO2 nanostructures showed notable PEC performance under simulated sunlight. This study presents an easy and efficient method for producing g-C3N4 photocatalysts decorated with semiconductor materials and provides insights for designing nanostructures for photocatalytic and energy applications.

Recent Advances and Strategies in MXene-Based Electrodes for Supercapacitors: Applications, Challenges and Future Prospects.

With the growing demand for technologies to sustain high energy consumption, supercapacitors are gaining prominence as efficient energy storage solutions beyond conventional batteries. MXene-based electrodes have gained recognition as a promising material for supercapacitor applications because of their superior electrical conductivity, extensive surface area, and chemical stability. This review provides a comprehensive analysis of the recent progress and strategies in the development of MXene-based electrodes for supercapacitors. It covers various synthesis methods, characterization techniques, and performance parameters of these electrodes. The review also highlights the current challenges and limitations, including scalability and stability issues, and suggests potential solutions. The future outlooks and directions for further research in this field are also discussed, including the creation of new synthesis methods and the exploration of novel applications. The aim of the review is to offer a current and up-to-date understanding of the state-of-the-art in MXene-based electrodes for supercapacitors and to stimulate further research in the field.