Interfacial electronic modulation of NiCo decorated nano-flowered MoS2 on carbonized wood as a remarkable bifunctional electrocatalyst for boosting overall water splitting.

The development of a cost-effective and efficient bifunctional electrode for overall water splitting holds significant importance in accelerating the sustainable advancement of hydrogen energy. The present study involved a bifunctional catalytic electrode was prepared by loading NiCo-modified 1T/2H MoS2 onto carbonized wood (NiCo-MoS2-CW) using the hydrothermal and electrodeposition techniques. The XPS analysis revealed that NiCo-modified MoS2 exhibited a weak electron characteristic, which facilitated the ionization of H2O and significantly enhanced the Volmer step. The XPS analysis unveiled that NiCo-modified MoS2 displayed a weak electron characteristic, thereby promoting the ionization of H2O and substantially augmenting the Volmer step. The electrocatalytic performance of the NiCo-MoS2-CW in 1.0 M KOH is remarkably impressive, exhibiting minimal overpotentials of only 64 mV (10 mA cm-2) and 216 mV (50 mA cm-2) for the hydrogen evolution reaction and oxygen evolution reaction, respectively. The NiCo-MoS2-CW || NiCo-MoS2-CW electrolytic cell can achieve a cell voltage of only 1.69 V to achieve a current density of 50 mA cm-2. Overall, this study proposes a potential approach to improve the catalytic efficiency of overall water splitting by modulating the interfacial electronic properties of MoS2.

MoS2high temperature sensitive element with a single Si3N4protective layer.

Temperature sensors find extensive applications in industrial production, defense, and military sectors. However, conventional temperature sensors are limited to operating temperatures below 200°C and are unsuitable for detecting extremely high temperatures. In this paper, a method for thermal protection of molybdenum disulfide (MoS2) films is proposed and a MoS2 high temperature sensor is prepared. By depositing a monolayer of Si3N4 onto MoS2, not only is the issue of high-temperature oxidation effectively addressed, but also the contamination by impurities that could potentially compromise the performance of MoS2 is prevented. Moreover, the width of the Schottky barrier of metal/MoS2 is reduced by using PECVD deposition of 400 nm Si3N4 to form an ohmic contact, which improves the electrical performance of the device by three orders of magnitude. The sensor exhibits a positive temperature coefficient measurement range of 25 to 550°C, with a maximum temperature coefficient of resistance (TCR) of 0.32%·°C-1. The thermal protection method proposed in this paper provides a new idea for the fabrication of high-temperature sensors, which is expected to be applied in the high-temperature field. .

H2O2 Self-Supplied MoS2/CaO2 Nanozyme Hydrogel with Near-Infrared Photothermal Synergetic Cascade Peroxidase-Like Activity for Wound Disinfection.

In wound healing and clinical anti-infection therapy, the current feasibility of nanocatalysts is extremely limited because of inadequate reactive oxygen species (ROS) generation. Herein, a novel H2O2 self-supplying nanocomposite (M/C/AEK) consists of molybdenum disulfide (MoS2) decorated with calcium peroxide (CaO2) prepared at ambient temperature and encapsulated in AEK hydrogel. In the presence of H2O2 and poly(vinyl pyrrolidone) (PVP), CaO2 nanoclusters, ≈30 nm, are anchored on the MoS2 surface. MoS2/CaO2 can induce both a cascaded peroxidase (POD)-like and catalase (CAT)-like catalytic activity to produce toxic hydroxyl radicals through self-supplied H2O2 and O2 responsive to the faintly acidic environment of acute wounds. The POD-like activity is increased under acidic compared with neutral conditions, allowing selective treatment of acute, slightly acidic wounds while avoiding the side effects of high-concentration antibacterial agents on normal tissues. The high near-infrared photothermal effect synergistically with POD-like/CAT-like activity of MoS2/CaO2 boosts the production of more ROS to eradicate Staphylococcus aureus and Escherichia coli bacteria (98.6% and 98.9%) effectively and selectively stimulate wound healing. The porous M/C/AEK hydrogel in the wound microenvironment can efficiently capture bacteria, and its Ca2+ ions and keratin stimulate healing, revealing excellent potential in advanced wound care and infection control therapies.

Indirect-To-Direct Bandgap Crossover and Room-Temperature Valley Polarization of Multilayer MoS2 Achieved by Electrochemical Intercalation.

Monolayer (1L) group VI transition metal dichalcogenides (TMDs) exhibit broken inversion symmetry and strong spin-orbit coupling, offering promising applications in optoelectronics and valleytronics. Despite their direct bandgap, high absorption coefficient, and spin-valley locking in K or K' valleys, the ultra-short valley lifetime limits their room-temperature applications. In contrast, multilayer TMDs, with more absorptive layers, sacrifice the direct bandgap and valley polarization upon gaining inversion symmetry from the bilayer structure. It is demonstrated that multilayer molybdenum disulfide (MoS2) can maintain 1) a structure with broken inversion symmetry and strong spin-orbit coupling, 2) a direct bandgap with high photoluminescence (PL) intensity, and 3) stable valley polarization up to room temperature. Through the intercalation of organic 1-ethyl-3-methylimidazolium (EMIM+) ions, multilayer MoS2 not only exhibits layer decoupling but also benefits from an electron doping effect. This results in a hundredfold increase in PL intensity and stable valley polarization, achieving 55% and 16% degrees of valley polarization at 3 K and room temperature, respectively. The persistent valley polarization at room temperature, due to interlayer decoupling and trion dominance facilitated by a gate-free method, opens up potential applications in valley-selective optoelectronics and valley transistors.

Understanding Iron-Doping Modulating Domain Orientation and Improving the Device Performance of Monolayer Molybdenum Disulfide.

Domain orientation modulation and controlled doping of two-dimensional (2D) transition-metal dichalcogenides (TMDCs) are two pivotal tasks for synthesizing wafer-scale single crystals and boosting device performances. However, realizing two such targets and uncovering internal physical mechanisms remain daunting challenges. We develop an accurate Fe doping strategy, which enables domain orientation control and electron mobility improvement of monolayer MoS2. By tuning of the Fe dopant dosages, parallel steps with different heights are formed, which induce edge-nucleation of unidirectionally aligned monolayer MoS2. In parallel, Fe doping induces the down shift of the conduction band minimum of monolayer MoS2 and matches well with the work function of an electrode, which reduces Schottky barrier height and delivers ultralow contact resistance (561 Ω µm) and excellent electron mobility (37.5 cm2 V-1 s-1). The modulation mechanism is clarified by combining theory calculations and electronic structure characterizations. This work hereby provides a new paradigm for synthesizing wafer-scale 2D TMDC single crystals and constructing high-performance devices.

Micron-Scale Vertical MoS2/Porous g-C3N4 Piezocatalyst via a Precursor's Supramolecular Self-Template Architecture: Degradation and Hydrogen Evolution.

Piezocatalysis can effectively harvest various kinds of mechanical energy with high entropy from the environment and drive some redox reactions without light irradiation, where MoS2- and g-C3N4-based piezocatalysts are recent research hotspots. This study constructs an architecture of ordered melamine hydrochloride-cyanuric acid/MoO42- supramolecular precursor via self-assembly, serving as a self-template for in situ tight growth of vertically aligned micron-scale MoS2 on porous foam-like g-C3N4(CMx) under S vapor with a bioinspired rooting and sprouting-like process. Experiments, DFT calculations, and finite element simulations collectively confirm the high piezoresponse of the CMx with high exposure of active sites and enhanced mechanical energy collection. The vertical interfaces and built-in electric fields in the composite induce efficient charge carrier separation and transfer. The optimized CM0.77 efficiently degrades various organic dyes and antibiotic under dark ultrasound [rhodamine B (RhB): 0.47 s-1, methyl orange (MO): 0.05 s-1, methylene blue (MB): 0.21 s-1, and tetracycline hydrochloride (TC): 0.03 s-1] and achieves hydrogen evolution (2431 µmol·g-1·h-1). Under simulated water flow (10 L/min), the expanded CM0.77/Al2O3 porous foam ceramic (CM/alumina ceramic) purifier device degrades 95% of 400 mL of RhB within 25 min. The developed ordered vertical MoS2/g-C3N4 piezocatalyst demonstrates rapid pollutant degradation and efficient hydrogen evolution under water flow and ultrasound, providing new insights for constructing multidimensional piezoelectric composites for environmental remediation and clean energy production.

Three-Dimensional Flexible SnO2@Hard Carbon@MoS2@Soft Carbon Fiber Film Anode toward Ultrafast and Stable Sodium Storage.

Developing flexible electrodes for the application in sodium-ion batteries (SIBs) has received great attention and has been still challenging due to their merits of additive-free, lightweight, and high energy density. In this work, a free-standing 3D flexible SIB anode with the composition of SnO2@hard carbon@MoS2@soft carbon is designed and successfully synthesized. This electrode combines the energy storage advantages and hybrid sodium storage mechanisms of each material, manifested in the enhanced flexibility, specific capacity, conductivity, rate, cycling performances, etc. Based on the synergistic effects, it exhibits much higher specific capacity than SnO2 carbon nanofibers, as well as more excellent cycling performance (250 mA h g-1 after 500 cycles at 1 A g-1) than MoS2 nanospheres (32 mA h g-1). In addition, relevant kinetic mechanisms are also expounded with the aid of theoretical calculation. This work provides a feasible and advantageous strategy for constructing high-performance and flexible energy storage electrodes based on hybrid mechanisms and synergistic effects.

Ruthenium atoms anchored on oxygen-modified molybdenum disulfide with strong interfacial coupling as efficient and stable catalysts for lithium-oxygen batteries.

Rechargeable non-aqueous lithium-oxygen batteries (LOBs) have garnered increasing attention owing to their high theoretical energy density. However, their slow cathodic kinetics hinder efficient battery reactions. Nanoscale catalysts can effectively enhance electrocatalytic activity and atomic utilization efficiency. However, the agglomeration of nanoscale catalysts (such as cluster and single atoms) during continuous discharge/charge cycles leads to decreased electrochemical performance and poor cyclic stability. Herein, the ruthenium (Ru) atomic sites anchored on an O-doped molybdenum disulfide (O-MoS2) catalyst (designated as Ru/O-MoS2) was fabricated using a facile impregnation and calcination method. Strong Ru-O coupling between Ru atoms and the O-MoS2 substrate optimizes the localized electronic structure, resulting in improved electrochemical performance and enhanced resistance to Ostwald ripening. When employed as a cathode catalyst for LOBs, Ru/O-MoS2 catalyst exhibits a high reversible specific capacity (18700.5 (±59.8) mAh g-1), good rate capability, and enhanced long-term stability (115 cycles, 1200 h). This study encourages facile and efficient strategies for the development of effective and stable electrocatalysts for use in LOBs.

Two-Dimensional Layered Nano-MoS2 Induces Earthworm Immune Cell Apoptosis by Regulating Lysosomal Maintenance and Function: Toward Unbiased Screening and Validation of Suspicious Pathways.

Molybdenum-based nanosheets (NSMoS2) are increasingly applied in various fields and undergoing relevant risk evaluations on subjectively hypothesized toxicity pathways. However, risk assessment should be unbiased and focus on appropriate end points to avoid biased prescreening. Here, we developed an adverse biological outcome screening strategy based on nontargeted functional protein profiles in earthworm (Eisenia fetida) immune cells exposed to NSMoS2 and their ionic counterpart (Na2MoO4). Through this framework, the apoptosis-related processes with distinct mechanisms were rapidly identified and thoroughly validated phenotypically. Specifically, upon exposure to 50 µg Mo/mL Na2MoO4, cellular signaling and energy homeostasis were disrupted within the transcription-translation biological chain. The autophagic pathway was activated, which, together with energy deprivation, phenotypically induced significant autophagy that ultimately led to apoptosis. In contrast, NSMoS2, tested at the same concentration, caused a reprogramming of apoptotic gene and protein expressions. Transcriptome plasticity facilitated the endocytic-adaptive transcriptional profile characterized by cytoskeleton remodeling and lysosome organization/movement under NSMoS2 exposure. Subcellular dynamics further revealed NSMoS2-induced lysosomal damage with a time-sensitive physiological window, ultimately mediating apoptosis. These findings provide a mechanistic and visual understanding of the distinct risk profile of NSMoS2 compared to molybdate, highlighting the importance of integrating nontargeted screening and phenotypic validation in early risk warning.

Integrated triple signal amplification strategy for ultrasensitive electrochemical detection of gastric cancer-related microRNA utilizing MoS2-based nanozyme, hybridization chain reaction, and horseradish peroxidase.

Early diagnosis and treatment of gastric cancer (GC) play a vital role in improving efficacy, reducing mortality and prolonging patients' lives. Given the importance of early detection of gastric cancer, an electrochemical biosensor was developed for the ultrasensitive detection of miR-19b-3p by integrating MoS2-based nanozymes, hybridization chain reaction (HCR) with enzyme catalyzed reaction. The as-prepared MoS2-based nanocomposites were used as substrate materials to construct nanoprobes, which can simultaneously load probe DNA and HCR initiator for signal amplification. Moreover, the MoS2-based nanocomposites are also employed as nanozymes to amplify electrochemical response. The presence of miR-19b-3p induced the assembly of MoS2-based nanoprobes on the electrode surface, which can activate in-situ HCR reaction to load a large number of horseradish peroxidase (HRP) for signal amplification. Coupling with the co-catalytic ability of HRP and MoS2-based nanozymes, the designed electrochemical biosensor can detect as low as 0.7 aM miR-19b-3p. More importantly, this biosensor can efficiently analyze miR-19b-3p in clinical samples from healthy people and gastric cancer patients due to its excellent sensitivity and selectivity, suggesting that this biosensor has a potential application in early diagnosis of disease.

Gate modulation of barrier height of unipolar vertically stacked monolayer ReS2/MoS2 heterojunction.

This study investigates vertically stacked CVD grown ReS2/MoS2 unipolar heterostructure device as Field Effect Transistor (FET) device wherein ReS2 on top acts as drain and MoS2 at bottom acts as source. The electrical measurements of ReS2/MoS2 FET device were carried out and variation in Ids (drain current) Vs Vds (drain voltage) for different Vgs (gate voltage) revealing the n-type device characteristics. Furthermore, the threshold voltage was calculated at the gate bias voltage corresponding to maximum transconductance (gm) value which is ~ 12 V. The mobility of the proposed ReS2/MoS2 heterojunction FET device was calculated as 60.97 cm2 V-1 s-1. The band structure of the fabricated vDW heterostructure was extracted utilizing ultraviolet photoelectron spectroscopy and the UV-visible spectroscopy revealing the formation of 2D electron gas (2DEG) at the ReS2/MoS2 interface which explains the high carrier mobility of the fabricated FET. The field effect behavior is studied by the modulation of the barrier height across heterojunction and detailed explanation is presented in terms of the charge transport across the heterojunction.

Enhanced Raman Scattering in CVD-Grown MoS2/Ag Nanoparticle Hybrids.

Surface-Enhanced Raman Spectroscopy (SERS) is a powerful, non-destructive technique for enhancing molecular spectra, first discovered in 1974. This study investigates the enhancement of Raman signals from single- and few-layer molybdenum disulfide (MoS2) when interacting with silver nanoparticles. We synthesized a MoS2 membrane primarily consisting of monolayers and bilayers through a wet chemical vapor deposition method using metal salts. The silver nanoparticles were either directly grown on the MoS2 membrane or placed beneath it. Raman measurements revealed a significant increase in signal intensity from the MoS2 membrane on the silver nanoparticles, attributed to localized surface plasmon resonances that facilitate SERS. Our results indicate that dichalcogenide/plasmonic systems have promising applications in the semiconductor industry.

Enhancing the Performance of MoS2 Field-Effect Transistors Using Self-Assembled Monolayers: A Promising Strategy to Alleviate Dielectric Layer Scattering and Improve Device Performance.

Field-effect transistors (FETs) based on two-dimensional molybdenum disulfide (2D-MoS2) have great potential in electronic and optoelectronic applications, but the performances of these devices still face challenges such as scattering at the contact interface, which results in reduced mobility. In this work, we fabricated high-performance MoS2-FETs by inserting self-assembling monolayers (SAMs) between MoS2 and a SiO2 dielectric layer. The interface properties of MoS2/SiO2 were studied after the inductions of three different SAM structures including (perfluorophenyl)methyl phosphonic acid (PFPA), (4-aminobutyl) phosphonic acid (ABPA), and octadecylphosphonic acid (ODPA). The SiO2/ABPA/MoS2-FET exhibited significantly improved performances with the highest mobility of 528.7 cm2 V-1 s-1, which is 7.5 times that of SiO2/MoS2-FET, and an on/off ratio of ~106. Additionally, we investigated the effects of SAM molecular dipole vectors on device performances using density functional theory (DFT). Moreover, the first-principle calculations showed that ABPA SAMs reduced the frequencies of acoustic and optical phonons in the SiO2 dielectric layer, thereby suppressing the phonon scattering to the MoS2 channel and further improving the device's performance. This work provided a strategy for high-performance MoS2-FET fabrication by improving interface properties.

Hybridization of Sulfur-Defective MoS2 and Holey Expanded Graphite for a Long Cycling Lithium Oxygen Battery Cathode.

The development of MoS2 as a cathode electrocatalyst for lithium-oxygen batteries (LOBs) has attracted considerable attention due to its natural abundance, excellent catalytic activity, and chemical stability. However, the sluggish and complicated kinetic of insulating and bulk discharge products on the electrode surface is one of major factors for MoS2 as a cathode for high performance LOBs. Defect engineering of an electrocatalyst and its hybridization with highly conductive frameworks are effective strategies to address this critical issue. Herein, we report a hybrid of rich sulfur-defective MoS2 (MoS2-x) nanosheets grown on highly conductive holey expanded graphite (hEG) with well-defined "worm-like" and holey structures (MoS2-x/hEG). Benefiting from rich sulfur defects of MoS2-x and the highly conductive nature and holey structures of hEG, the MoS2-x/hEG hybrid as a cathode for LOBs displays outstanding electrochemical performance with an extremely high discharge capacity of 19000.3 mAh g-1 at 500 mA g-1 and an ultralong cycling life of over 500 cycles at 1000 mA g-1 with a controlled specific capacity of 1000 mAh g-1.

Photo-Energized MoS2/CNT Cathode for High-Performance Li-CO2 Batteries in a Wide-Temperature Range.

Li-CO2 batteries are considered promising energy storage systems in extreme environments such as Mars; however, severe performance degradation will occur at a subzero temperature owning to the sluggish reaction kinetics. Herein, a photo-energized strategy adopting sustainable solar energy in wide working temperature range Li-CO2 battery was achieved with a binder-free MoS2/carbon nanotube (CNT) photo-electrode as cathode. The unique layered structure and excellent photoelectric properties of MoS2 facilitate the abundant generation and rapid transfer of photo-excited carriers, which accelerate the CO2 reduction and Li2CO3 decomposition upon illumination. The illuminated battery at room temperature exhibited high discharge voltage of 2.95 V and mitigated charge voltage of 3.27 V, attaining superior energy efficiency of 90.2% and excellent cycling stability of over 120 cycles. Even at an extremely low temperature of - 30 °C, the battery with same electrolyte can still deliver a small polarization of 0.45 V by the photoelectric and photothermal synergistic mechanism of MoS2/CNT cathode. This work demonstrates the promising potential of the photo-energized wide working temperature range Li-CO2 battery in addressing the obstacle of charge overpotential and energy efficiency.

Nitrogen plasma-induced phase engineering and titanium carbide/carbon nanotubes dual conductive skeletons endow molybdenum disulfide with significantly improved lithium storage performance.

MoS2/Ti3C2 MXene composite has emerged as a promising anode material for lithium storage due to the synergistic combination of high specific capacity offered by MoS2 and conductive skeleton provided by Ti3C2 MXene. However, its two-dimensional/two-dimensional (2D/2D) structure is susceptible to collapse after long cycles, while the inherent low conductivity of MoS2 limits its rate performance. In this study, we developed a novel approach combining plasma-induced phase engineering with dual skeleton structure design to fabricate a unique P-MoS2/Ti3C2/CNTs anode material featuring highly conductive 1T phase MoS2 and a stable one-dimensional/two-dimensional (1D/2D) architecture. Within this architecture, growth of MoS2 nanosheets on the surface of Ti3C2 cross-linked by carbon nanotubes (CNTs) was achieved. The resulting Ti3C2/CNTs dual skeleton not only provides robust mechanical support to prevent structural collapse during long cycles but also offers increased specific surface area and additional Li+ storage space, thereby enhancing the lithium storage capacity of the composite. Subsequent N2 plasma treatment induced a phase transition in MoS2 from 2H to 1T configuration. Density functional theory (DFT) calculations confirmed that the induced 1T-MoS2 exhibits higher conductivity and lower Li+ diffusion barrier compared to 2H-MoS2. Benefiting from these synergistic effects, our P-MoS2/Ti3C2/CNTs anode demonstrated remarkable electrochemical performance including a high reversible specific capacity of 1120 mAh g-1 at 0.1 A g-1, excellent cycling stability with a specific capacity retention of 670 mAh g-1 after 600 cycles at 1 A/g, and superior rate performance with a specific capacity of 614 mAh g-1 at 2 A g-1. This combined modification strategy will serve as guidance for designing other energy storage materials.

Multistep Array-Based Sensing of Bioanalytes Using Modified MoS2, Fluorescence Proteins, and Cucurbituril.

One pot sensor by multiplexing in the array is an attractive system for rapid discrimination of multiple analytes. Multiplexing can be achieved in two ways, i.e., using multiple signal transducers or adding sequential agents to the sensor media. Herein, we have used a combination of both multichannel and sequential ON-OFF strategies for the discrimination of different bioanalytes. The sensor array was constructed by implementing positively charged MoS2 as a receptor and different fluorescent proteins possessing distinguishable emission profiles as signal transducers. The sensing setup was constructed with the interaction between oppositely charged MoS2 and the host-guest combination between a cationic headgroup of MoS2 and Cucurbit [7] uril (CB7) to alter the fluorescence of signal transducers in situ noncovalently. Electrodynamic analysis and optical assays suggest that the electrostatic interaction played a major role in the modulation of the fluorescence outcomes in the array. Both cationic and anionic proteins were discriminated at a 50 nM concentration. The detection limit of the sensor array by using ß-gal protein was found to be 1 nM. The sensor array was further implemented for the discrimination of normal and diseased cell lines and lysates, which indicates the versatile detection ability of this reported sensor array.

MoS2/NiO heterocatalyst featuring stacking Structures, oxygen Vacancies, and hydrophilic Interfaces for hydrogen production via urea electrolysis.

Two-dimensional nano-MoS2 holds remarkable potential for widespread use in hydrogen evolution reaction (HER) applications owing to its high catalytic activity, abundant availability, and low cost. However, its electrocatalytic performance is significantly lower than that of Pt-based catalysts necessitating strategies to improve its catalytic activity. We developed an effective strategy for enhancing the HER performance of MoS2 based on the synergistic effect of oxygen vacancies (Ov), heterostructures, and interfacial wettability. In particular, highly graphitized wood-based carbon (GWC) was used as a platform to prepare a hydrophilic/aerophobic MoS2@Ov-NiO-GWC heterocatalyst featuring nanosheet stacking and containing abundant Ov. Consequently, a current density of 10 mA cm-2 and an overpotential of only 77 mV were achieved in a 1 M KOH electrolyte using the prepared catalyst; notably, the overpotential increase was only 1.2 % after continuous operation for 90 h. Density functional theory calculations showed that coupling MoS2 with the Ov-NiO heterointerface increased the exposure of the MoS2 active sites on the heterointerface and accelerated the electron transfer between NiO and the MoS2 interface, considerably enhancing the HER performance. Moreover, an overall urea electrolysis cell assembled using this heterocatalyst demonstrated excellent hydrogen production activity and durability, with current densities of 10 and 100 mA cm-2 at cell voltages of only 1.33 and 1.46 V, respectively. Even after continuous operation for 75 h at a current density of 100 mA cm-2, the cell exhibited a voltage retention rate of 92.8 %. These results demonstrate the potential of this nano-heterocatalyst to efficiently produce hydrogen via overall urea electrolysis.

MoS2_CNTs_aerogel-based PEDOT nanocomposite electrochemical sensor for simultaneous detection of chloramphenicol and furazolidone in food samples.

Toxic intermediates in food caused by chloramphenicol (CP) and furazolidone (FZ) have gained interest in research toward their detection. Hence, fast, reliable, and accurate detection of CP and FZ in food products is of utmost importance. Here, a novel molybdenum disulfide-connected carbon nanotube aerogel/poly (3,4-ethylenedioxythiophene) [MoS2/CNTs aerogel/PEDOT] nanocomposite materials are constructed and deposited on the pretreated carbon paste electrode (PCPE) by a facile eletropolymerization method. The characterization of MoS2/CNTs aerogel/PEDOT nanocomposite was analyzed by scanning electron microscopy (SEM), cyclic voltammetry, and differential pulse voltammetry. The modified MoS2/CNTs aerogel/PEDOT nanocomposite has improved sensing characteristics for detecting CP and FZ in PBS solution. For this work, we have studied various parameters like electrocatalytic activity, the effect of scan rates, pH variation studies, and concentration variation studies. Under optimum conditions, the modified electrode exhibited superior sensing ability compared to the bare and pretreated CPE. This improvement in electrocatalytic activity can be the higher conductivity, larger surface area, increased heterogeneous rate constant, and presence of more active sites in the MoS2/CNTs aerogel/PEDOT nanocomposite. The modified electrode demonstrated distinct electrochemical sensing toward the individual and simultaneous analysis of CP and FZ with a high sensitivity of 0.701 µA. µM-1 .cm-2 for CP and 0.787 µA. µM-1 .cm-2 for FZ and a low detection limit of 3.74 nM for CP and 3.83 nM for FZ with good reproducibility, repeatability, and interferences. Additionally, the prepared sensor effectively detects CP and FZ in food samples (honey and milk) with an acceptable recovery range and a relative standard deviation below 4%.

Meeting the Industrial Challenges of CO2 Photocatalytic Reduction: Moving From Molybdenum Disulfides to Oxysulfides Based Materials?

Reducing CO2 emissions is one of the greatest challenges of the century. Among the means employed to tackle CO2 emissions, the photocatalytic conversion of CO2 is an appealing way to valorize CO2 since it uses the sun energy, which is abundant. However, nowadays, the best photocatalytic systems still report too low efficiencies, and use expensive materials, so they cannot be readily industrialized for use at large scale. In this report, we first highlight general industrial and process challenges (including operating conditions). Then, focusing on MoS2/TiO2 heterojunction systems, we analyze advantages and limitations of such systems and open perspectives on Mo oxysulfides supported on TiO2 discussing their potential to reach higher efficiency for CO2 photoconversion.