S-scheme mesoporous Li2MnO3/g-C3N4 heterojunctions as efficient photocatalysts for the mineralization of trichloroethylene in aqueous media.

Novel mesoporous Li2MnO3/g-C3N4 heterostructures were prepared for the first time by utilizing the sol-gel route in the presence of a nonionic surfactant. TEM and XRD measurements showed that Li2MnO3 (5-10 nm) with monoclinic structures was uniformly distributed onto porous g-C3N4 for the construction of Li2MnO3/g-C3N4 heterojunctions. The obtained photocatalysts were assessed for mineralization and removal of trichloroethylene (TCE) in aqueous media under visible light exposure. Complete degradation of TCE over a 3 %Li2MnO3/g-C3N4 heterostructure within 120 min was achieved. The degradation rate over Li2MnO3/g-C3N4 heterostructures was significantly enhanced, and the 3% Li2MnO3/g-C3N4 heterostructure exhibited a large degradation rate of 7.04 µmolL-1 min-1, which was enhanced by 5 and 3.8 fold compared to those of pristine g-C3N4 (1.39 µmolL-1 min-1) and Li2MnO3 (1.85 µmolL-1 min-1), respectively. The photocatalytic efficiency of the Li2MnO3/g-C3N4 heterojunction was outstandingly promoted because integrating Li2MnO3 with g-C3N4 could create close interfaces with well-matched band potentials for easy mobility and low recombination of photoinduced carriers. The coexistence of Li2MnO3/g-C3N4 interfaces led to a synergic effect, which is considered the key factor in photoinduced electron-hole separation. The synthesis procedure that was employed here is a promising process for the preparation of effective g-C3N4-based photocatalyst systems for photocatalysis applications.

Selective and Fast Detection of Fluoride-Contaminated Water Based on a Novel Salen-Co-MOF Chemosensor.

The development of selective and fast optical sensitive chemosensors for the detection and recognition of different cations and anions in a domain is still a challenge in biological, industrial, and environmental fields. Herein, we report a novel approach for the detection and determination of fluoride ion (F-) sensing based on a salen-cobalt metal-organic framework (Co(II)-MOF). By a simple method, the Co(II)-MOF was synthesized and characterized using several tools to elucidate the structure and morphology. The photoluminescence (PL) spectrum of the Co(II)-MOF (100.0 nM/L) was examined versus different ionic species like F-, Br-, Cl-, I-, SO4 2-, and NO3 - and some cationic species like Mg2+, Ca2+, Na+, and K+. In the case of F- ions, the PL intensity of the Co(II)-MOF was scientifically enhanced with a remarkable red shift. With the increase of F- concentration, the Co(II)-MOF PL emission spectrum was also professionally enhanced. The limit of detection (LOD) for the Co(II)-MOF chemosensor was 0.24 µg/L, while the limit of quantification (LOQ) was 0.72 µg/L. Moreover, a comparison of the Co(II)-MOF optical approach with other published reports was studied, and the mechanism of interaction was also investigated. Additionally, the applicability of the current Co(II)-MOF approach in different real water samples, such as tap water, drinking water, Nile River water, and wastewater, was extended. This easy-to-use future sensor provides reliable detection of F- in everyday applications for nonexpert users, especially in remote rural areas.

Hydrogen Generation over RuO2 Nanoparticle-Decorated LaNaTaO3 Perovskite Photocatalysts under UV Exposure.

The efficacy of LaNaTaO3 perovskites decoration RuO2 at diverse contents for the photocatalytic H2 generation has been explored in this study. The photocatalytic performance of RuO2 co-catalyst onto mesoporous LaNaTaO3 was evaluated for H2 under UV illumination. 3%RuO2/LaNaTaO3 perovskite photocatalyst revealed the highest photocatalytic H2 generation performance, indicating that RuO2 nanoparticles could promote the photocatalytic efficiency of LaNaTaO3 perovskite significantly. The H2 evolution rate of 3%RuO2/LaNaTaO3 perovskite is 11.6 and 1.3 times greater than that of bare LaNaTaO3 perovskite employing either 10% CH3OH or pure H2O, respectively. Interestingly, the photonic efficiency of 3%RuO2/LaNaTaO3 perovskite was enhanced 10 times than LaNaTaO3 perovskite in the presence of aqueous CH3OH solutions as a hole sacrificial agent. The high separation of charge carriers is interpreted by the efficient hole capture using CH3OH, hence leading to greater H2 generation over RuO2/LaNaTaO3 perovskites. This is attributed to an adjustment position between recombination electron-hole pairs and also the reduction of potential conduction alignment as a result of RuO2 incorporation. The suggested mechanisms of RuO2/LaNaTaO3 perovskites for H2 generation employing either CH3OH or pure H2O were discussed. The photocatalytic performances of the perovskite photocatalyst were elucidated according to the PL intensity and the photocurrent response investigations.

Promoting Visible Light Generation of Hydrogen Using a Sol-Gel-Prepared MnCo2O4@g-C3N4 p-n Heterojunction Photocatalyst.

The production of hydrogen using a new type of heterogeneous photocatalyst under visible light is considered a remarkable essential pathway for sustainable, pure energy not only on the laboratory scale but also on a bigger scale. Hence, a new nanocomposite of mesoporous MnCo2O4, g-C3N4, and MnCo2O4@g-C3N4 was produced utilizing a sol-gel method with variable MnCo2O4 contents. The crystal structure of MnCo2O4 was effectively confirmed by the X-ray diffraction pattern and integrated onto the g-C3N4 structure. The MnCo2O4 nanoparticles were displayed as spherical particles by TEM images and dispersed in a uniform way inside the g-C3N4 nanosheet. The synthesized nanocomposites in the form of MnCo2O4@g-C3N4 were examined as a new effective photocatalyst against glycerol as a source for H2 production with visible light. The MnCo2O4 contents indicated a corroborative impact for the photocatalytic action related to the H2 production process. A maximum H2 production molecular value was observed (21,870 µmol·g-1·h-1) for a 1.5 wt % MnCo2O4@g-C3N4 nanocomposite as a considerable increase in its photocatalytic activity. The yields of H2 are ∼55 and 23 times higher than those of g-C3N4 and MnCo2O4, respectively. Up to five times cycles of visible lighting were the maximum number of repeated cycles by which the 1.5 wt % MnCo2O4@g-C3N4 product showed higher stability and durability.

Dual Naked-Eye and Optical Chemosensor for Morphine Detection in Biological Real Samples Based on Cr(III) Metal-Organic Framework Nanoparticles.

The analytical detection and quantification of abuse drugs such as morphine (MOR) in biological samples are vital missions and remains to attract challenges for forensic toxicology, law enforcement, world antidoping organization, and social health fields. MOR, a benchmark analgesic drug known as "pain killer", is one of the powerful opioid medications for relieving pain, and overdose of MOR is toxic. In this article, novel promising chromium metal-organic framework nanoparticles [Cr(III)-MOF-NPs] were produced via facile synthesis and characterized using high-resolution transmission electron microscopy, field-emission scanning electron microscopy/energy-dispersive X-ray spectroscopy, mass spectrometry, X-ray photoelectron spectroscopy, elemental analysis, UV-vis, Fourier transform infrared, and thermogravimetry/differential scanning calorimetry, as well as photoluminescence (PL) investigation and magnetic properties. The PL study results revealed that the Cr(III)-MOF-NPs exhibited an emission band at 593 nm. The Cr(III)-MOF-NPs could be used in fast, selective, and sensitive MOR detection and quantification. Under the optimum experimental conditions, with the addition of MOR, a blueshift from 593 to 566 nm occurred with a remarkable PL intensity enhancement, and the color changed from brown to yellow (visually/naked-eye detection). The Cr(III)-MOF-NPs optical chemosensor exhibited a stable response for MOR in a concentration range between 0.1 and 350 nM. The detection and quantification limits were 0.167 and 0.443 nM, respectively, with a correlation coefficient (r 2) of 0.96. The developed PL chemosensor showed high selectivity for MOR over other competing interfering matrices. Moreover, the ultrasensitive chemosensor was extensively used for the determination of MOR spiked in different real samples (serum and urine samples) with acceptable recoveries and satisfactory results.