Enhancing photocatalytic reduction of Cr(VI) in water through morphological manipulation of g-C3N4 photocatalysts: A comparative study of 1D, 2D, and 3D structures.

In this research, the dimensional catalysts of pure g-C3N4 photocatalysts (1D, 2D, and 3D) were investigated for the reduction of the highly toxic/carcinogenic Cr(VI) under visible light irradiation. The catalysts underwent explanation through various surface analysis techniques. According to the BET data, the specific surface area of the 3D catalyst was 1.3 and 7 times higher than those of the 2D and 1D CN catalysts, respectively. The 3D catalyst demonstrated superior performance, achieving an efficiency greater than 99% within 60 min under visible light irradiation in the presence of EDTA due to the abundance of active sites. The study also delved into the influence of factors such as the amount of EDTA-hole scavenger, pH, catalyst dosage, and temperature on the photocatalytic reduction of Cr(VI). Moreover, the 3D catalyst showed excellent reusability, maintaining an efficiency of more than 80% even after 10 cycles, and performed effectively in real water samples. The 3D CN catalyst, with its facile synthesis process, excellent visible light harvesting properties, high reduction efficiency that sustains over multiple cycles, and outstanding performance in real water samples, presents a significant advancement for practical applications in environmental remediation. This research contributes to a new understanding of developing efficient degradation methods for heavy metals in polluted water, highlighting the potential of 3D g-C3N4 catalysts in environmental cleanup efforts.

Kumquat peel-derived biochar to support zeolitic imidazole framework-67 (ZIF-67) for enhancing peracetic acid activation to remove acetaminophen from aqueous solution.

This study presents the synthesis of a novel composite catalyst, ZIF-67, doped on sodium bicarbonate-modified biochar derived from kumquat peels (ZIF-67@KSB3), for the enhanced activation of peracetic acid (PAA) in the degradation of acetaminophen (APAP) in aqueous solutions. The composite demonstrated a high degradation efficiency, achieving 94.3% elimination of APAP at an optimal condition of 200 mg L-1 catalyst dosage and 0.4 mM PAA concentration at pH 7. The degradation mechanism was elucidated, revealing that superoxide anion (O2•-) played a dominant role, while singlet oxygen (1O2) and alkoxyl radicals (R-O•) also contributed significantly. The degradation pathways of APAP were proposed based on LC-MS analyses and molecular electrostatic potential calculations, identifying three primary routes of transformation. Stability tests confirmed that the ZIF-67@KSB3 catalyst retained an 86% efficiency in APAP removal after five successive cycles, underscoring its durability and potential for application in pharmaceutical wastewater treatment.

Enhanced photocatalytic activity of tin oxide-doped molybdenum disulfide nanohybrids under visible light irradiation: Antibiotics elimination, heavy metal reduction and antibacterial behavior.

Nano-heterojunction photocatalytic can operate removal of pollutants, which is basic for the sustainable development of a clean environment. Herein, we propose a novel MoS2/SnO2 (MS) S-scheme heterojunction by a facile hydrothermal process, which is cheap, easily available, highly visible-light response, and good stability. The MS nano-heterojunction suggested superior performance with the photocatalytic degradation of 97.6% within 100 min for ciprofloxacin (CIP) removal, which was 5.74 and 4.88 folds higher than that of pristine MoS2 and SnO2, respectively. The fabricated MS photocatalysts displayed outstanding photocatalytic efficiency toward Cr (VI) reduction. The removal capability of Cr (VI) reached up to 92.5% within 60 min. The photodegradation efficiency was 5.2 folds that of pristine MoS2. In addition, the antibacterial performance approximately approached 100% for E. coli within 10 min, which was more apparent than the others. A series of excellent results implied that MS nano-heterojunction had a high ultraviolet and visible light absorbance, larger specific surface area, outstanding electron-hole pairs migration and higher capability of photo-response electrons and holes separation rate. This system offers a novel window into the evolution of nano-heterojunction for wastewater treatment and solar energy harvesting applications.

A novel tungsten diselenide nanoparticles for enhanced photocatalytic performance of Cr (VI) reduction and ciprofloxacin (CIP).

Nanoparticles (NPs) fabrication is a significant approach to enhance the visible light response of photocatalysts, to realize inexpensive and more harmful compound removal, at larger scale. The poor electrons and holes separation capability and low light activity of bulk materials can be notably enhanced through developing NPs. From photocatalytic investigation, better performance was received in the tungsten diselenide (WSe2) NPs than that in bare WSe2, exhibiting the action of restrained recombination of charge carriers in the NPs. The photocatalytic Cr(VI) reduction efficiency of WSe2 NPs is 2.7 folds greater than that by bare WSe2. On the other hand, the photocatalytic efficiency follows the order of nano WSe2-3 > nano WSe2-2 > nano WSe2-1 > bare WSe2, nano WSe2-3 is nearly 2.7 folds greater than that of bare WSe2. The results imply the fabrication of WSe2 NPs and it possesses improved visible light utilization. The proposed WSe2 NPs have merged with the three aspects of photocatalytic capability including the visible light activity, the valid separation of photo-response charge carriers and enough surface active sites owing to the nanoscale formed. This research endows conduct on the potential style of NPs for photo-response water environmental remediation.

Phosphoric acid-activated biochar derived from sunflower seed husk: Selective antibiotic adsorption behavior and mechanism.

In recent years, the unnecessary overuse of antibiotics has increased globally, resulting in antibiotic contamination of water, which has become a significant environmental concern. This study aims to examine the adsorption behavior of antibiotics (Tetracycline TC, Ciprofloxacin CIP, Ibuprofen IBP, and Sulfamethoxazole SMX) onto H3PO4-activated sunflower seed husk biochar (PSF). The results demonstrated that H3PO4 could enhance the specific surface area (378.8 m2/g) and create a mesoporous structure of biochar. The adsorption mechanism was investigated using kinetic models, isotherms, and thermodynamics. The maximum adsorption capacities (qmax) of TC, CIP, SMX, and IBP are 429.3, 361.6, 251.3, and 251.1 mg g-1, respectively. The adsorption mechanism of antibiotics on PSF was governed by complex mechanisms, including chemisorption, external diffusion, and intraparticle diffusion. This research provides an environmentally friendly method for utilizing one of the agricultural wastes for the removal of a variety of antibiotics from the aquatic environment.

A visible-light sensitive MoSSe nanohybrid for the photocatalyticdegradationof tetracycline, oxytetracycline, and chlortetracycline.

A MoSSe nanohybrids (NHs) was synthesized, characterized, and tested for the degradation of tetracycline, oxytetracycline, and chlortetracycline under visible light irradiation. The Z-scheme MoSSe NHs exhibited higher specific surface area (∼10 times), faster charge separation, and greater photo-absorption than MoS2 nanoparticles (NPs) or MoSe2 NPs catalyst. The photocatalysts were characterized by ultraviolet-visible spectroscopy, X-ray diffraction, scanning electron microscopy, elemental mapping, transmission electron microscope, thermo-gravimetric analysis, X-ray photoelectron spectroscopy, photoluminescence, and electrochemical measurements. The MoSSe NHs exhibited significantly marked photocatalytic activity, achieving 95% of tetracycline (TC) degradation in 60 min with a rate constant of 0.1 min-1, which was about 5- and âˆ¼ 6- fold that of MoS2 NPs and MoSe2 NPs, respectively. Superoxide radical (̇O2-) played the major role in catalytic reactivity. The mechanism and pathway of TC degradation on the Z-scheme nanohybrid photocatalyst was established. Moreover, the nanohybrid photocatalyst exhibited high structural stability, visible light absorption, and reusability in the removal of recalcitrant contaminants, namely, tetracycline, oxytetracycline, and chlortetracycline.

Novel MoS2 quantum dots as a highly efficient visible-light driven photocatalyst in water remediation.

A direct and efficient hydrothermal system has been established for the synthesis of MoS2 quantum dots (QDs). Novel MoS2 QDs are an excellent potential photocatalysts to enhance photocatalytic response by charge separation under visible light irradiation. The optimum capability of QDs demonstrated the excellent photocatalytic ability for the degradation of organic pollutants. The microstructural, morphological, and optical properties of the MoS2 QDs are defined via X-ray diffraction (XRD), SEM, HRTEM, XPS, and UV-Vis absorption spectroscopy techniques. Under visible light irradiation, MoS2 QDs have great photocatalytic response for the degradation of Rh B that is 20 times higher than those of bulk MoS2 materials. The QDs possess practically the same catalytic response after 5 recycle runs, which is an evident proof of its stability. This course might pave the route toward creating current visible-light caused QD photocatalyst strategies for the highly valuable degradation of organic pollutants or antibiotics.

Correction: Synthesis and optical properties of lead-free cesium germanium halide perovskite quantum rods.

[This corrects the article DOI: 10.1039/C8RA01150H.].

Wavelength-Tunable and Highly Stable Perovskite-Quantum-Dot-Doped Lasers with Liquid Crystal Lasing Cavities.

This study applies a low-cost solvothermal method to synthesize all-inorganic (lead-free cesium tin halide) perovskite quantum dots (AIPQDs) and to fabricate AIPQD-doped lasers with cholesteric liquid crystal (CLC) lasing cavities. The lasers present highly qualified lasing features of low threshold (150 nJ/pulse) and narrow line width (0.20 nm) that are attributed to the conjunction of the suppression of photoluminescence (PL) loss caused by the quantum confinement of AIPQDs and the amplification of PL caused by the band-edge effect of the CLC-distributed feedback resonator. In addition, the lasers possess highly flexible lasing-wavelength tuning features and a long-term stability under storage at room temperature and under high humidity given the protective role of CLC. These advantages are difficult to confer to typical light-emitting perovskite devices. Given these merits, the AIPQD-doped CLC laser device has considerable potential applications in optoelectronic and photonic devices, including lighting, displays, and lasers.

Synthesis and optical properties of lead-free cesium germanium halide perovskite quantum rods.

Herein, the fabrication of a lead-free cesium germanium halide perovskite produced via a simple solvothermal process is reported for the first time. By tuning the composition of the CsGeX3 quantum rods, a power conversion efficiency of 4.92% under AM 1.5 G was achieved.

Synthesis and Optical Properties of Lead-Free Cesium Tin Halide Perovskite Quantum Rods with High-Performance Solar Cell Application.

Herein, the fabrication of a lead-free cesium tin halide perovskite produced via a simple solvothermal process is reported for the first time. The resulting CsSnX3 (X = Cl, Br, and I) quantum rods show composition-tunable photoluminescence (PL) emissions over the entire visible spectral window (from 625 to 709 nm), as well as significant tunability of the optical properties. In this study, we demonstrate that through hybrid materials (CsSnX3) with different halides, the system can be tunable in terms of PL. By replacing the halide of the CsSnX3 quantum rods, a power conversion efficiency of 12.96% under AM 1.5 G has been achieved. This lead-free quantum rod replacement has demonstrated to be an effective method to create an absorber layer that increases light harvesting and charge collection for photovoltaic applications in its perovskite phase.

Morphological appearances and photo-controllable coloration of dye-doped cholesteric liquid crystal/polymer coaxial microfibers fabricated by coaxial electrospinning technique.

This study systematically investigates the morphological appearance of azo-chiral dye-doped cholesteric liquid crystal (DDCLC)/polymer coaxial microfibers obtained through the coaxial electrospinning technique and examines, for the first time, their photocontrollable reflection characteristics. Experimental results show that the quasi-continuous electrospun microfibers can be successfully fabricated at a high polymer concentration of 17.5 wt% and an optimum ratio of 2 for the feeding rates of sheath to core materials at 25 °C and a high humidity of 50% ± 2% in the spinning chamber. Furthermore, the optical controllability of the reflective features for the electrospun fibers is studied in detail by changing the concentration of the azo-chiral dopant in the core material, the UV irradiation intensity, and the core diameter of the fibers. Relevant mechanisms are addressed to explain the optical-control behaviors of the DDCLC coaxial fibers. Considering the results, optically controllable DDCLC coaxial microfibers present potential applications in UV microsensors and wearable smart textiles or swabs.

Spatially tunable photonic bandgap of wide spectral range and lasing emission based on a blue phase wedge cell.

This study demonstrates for the first time a continuously tunable photonic bandgap (PBG) of wide spectral range based on a blue phase (BP) wedge cell. A continuously shifting PBG of the BP wedge cell occurs due to the thickness gradient of the wedge cell at a fixed temperature. The wedge cell provides a gradient of boundary force on the LCs and thus forms a distribution of BP crystal structure with a gradient lattice. Additionally, a spatially tunable lasing emission based on a dye-doped BP (DDBP) wedge cell is also demonstrated. The tunable band of the PBG and lasing emission is about 130 nm and 70 nm, respectively, which tuning spectral ranges are significantly wider than those of CLC and DDCLC wedge cells, respectively. Such a BP device has a significant potential in applications of tunable photonic devices and displays.

Synthesis and characterization of Cu(In(x)B(1-x))Se2 nanocrystals for low-cost thin film photovoltaics.

Chalcopyrite quaternary semiconductor Cu(In(x)B(1-x))Se(2) nanocrystals have been successfully prepared via a relatively simple and convenient solvothermal route. The effect of different solvents on the formation of the product also indicates that diethylenetriamine is the optimal solvent for this reaction. The device parameters for a single junction Cu(In(x)B(1-x))Se(2) solar cell under AM1.5G are as follows: an open circuit voltage of 265 mV, a short-circuit current of 25.90 mA/cm(2), a fill factor of 34%, and a power conversion efficiency of 2.34%. Based on a series of comparative experiments under different reaction conditions, the probable formation mechanism of crystal Cu(In(x)B(1-x))Se(2) nanorods is proposed.