Ultraviolet Light Irradiation Research Articles

Synthesis of Z-scheme amorphous WO3-loaded TiO2 photocatalyst for enhanced photocatalytic degradation of dichloromethane: Internal electric field and mechanism exploration

Photocatalytic technology is a highly efficient means for treatment of volatile organic compounds (VOCs) and mitigation of environmental issues. In this study, we successfully prepared the Z-scheme WO3/TiO2 heterojunction catalyst through the impregnation sintering process. The photocatalytic performance of dichloromethane (DCM) was examined by monitoring its concentration changes under ultraviolet light irradiation. The results demonstrated that 3 % WO3/TiO2 exhibited the most excellent performance, achieving a degradation performance of 98 % under a continuous airflow of 0.8 L/min and an initial DCM concentration of 200 ppm. Importantly, the catalyst maintained its performance without any significant decrease even after 100 h of continuous testing. The excellent performance was mainly thanks to built-in electric field and narrower bandgap, which effectively reduced electron and hole complexation, thereby increasing the production of more reactive oxygen species. Gas phase capture testing revealed that •O2- radicals played a crucial role in DCM degradation. Additionally, the improvement of surface acidity by WO3 and preferential breaking of C-Cl bond effectively prevented the production of phosgene (COCl2). This research finding addresses the gap in the understanding of photocatalytic degradation of DCM with TiO2 modified by metal oxides and lays a strong foundation for future industrial applications.

One-Step Physical and Chemical Dual-Reinforcement with Hydrophobic Drug Delivery in Gelatin Hydrogels for Antibacterial Wound Healing.

Gelatin-based bioadhesives, especially methacrylated gelatin (GelMA), have emerged as superior alternatives to sutureless wound closure. Nowadays, their mechanical improvement and therapeutic delivery, particularly for hydrophobic antibiotics, have received ever-increasing interest. Herein, a reinforced gelatin-based hydrogel with a hydrophobic drug delivery property for skin wound treatment was reported. First, photosensitive monomers of N'-(2-nitrobenzyl)-N-acryloyl glycinamide (NBNAGA) were grafted onto GelMA via Michael addition, namely, GelMA-NBNAGA. Second, gelation of the GelMA-NBNAGA solution was accomplished in a few seconds under one step of ultraviolet (UV) light irradiation. Multiple effects were realized simultaneously, including chemical cross-linking initiated by lithium phenyl-2,4,6-trimethylbenzoylphosphinate (LAP), physical cross-linking of uncaged dual hydrogen bonding, and hydrophobic drug release along with o-NB group disintegration. The mechanical properties of the dual-reinforcement hydrogels were verified to be superior to those only with a chemical or physical single-cross-linked network. The hydrophobic anticancer doxorubicin (DOX) and antibiotic rifampicin (Rif) were successfully charged into the hydrogels, separately. The in vitro antimicrobial tests confirmed the antibacterial activity of the hydrogels against Gram-negative (Escherichia coli) and Gram-positive (Staphylococcus aureus) bacteria. The in vivo wound-healing assessment in mice further assured their drug release and efficacy. Therefore, this NBNAGA-modified GelMA hydrogel has potential as a material in skin wound dressing with a hydrophobic antibiotic on-demand delivery.

Regulating band structure, charge transfer and separation, oxygen adsorption and activation by surface ion modification.

As a most promising environmental technology, the substantial enhancement of photocatalytic efficiency is still a big challenge for practical applications. In this work, the surface of Bi2O2CO3 (BOC) nanotubes are modified by Cl and I. The as-obtained samples at different hydrothermal temperatures (T) are designated as T-X-BOC (X = Cl, I). X-ray diffraction (XRD), energy dispersive X-ray (EDX) spectroscopy and X-ray photoelectron spectroscopy (XPS) prove that Cl and I merely chemically adsorb on the BOC surface, rather than dope into the crystal lattice. The surface modification of Cl and I slightly increases light absorption range, while significantly promotes the photoelectron migration from bulk to the surface that greatly enhances the carrier separation efficiency. Density functional theory (DFT) calculations further prove that surface Cl and I have adjusted band structure and surface charge distribution. Besides, the surface Cl and I favor the O2 adsorption and trap the surface photoelectrons, thus promoting the formation of •O2-; while the surface Cl and I impede the surface adsorption of H2O, thus refraining the generation of •OH. In the degradation of rhodamine B (RhB), holes and •O2- radicals play the crucial role. Under ultraviolet light irradiation (λ < 420nm) for 45min, the RhB degradation ratios over 150-Cl-BOC (94%) and 150-I-BOC (85%) are 4.2 and 3.7 times higher than that of original BOC (18%), respectively. This work demonstrates that the simple surface halogenation modification greatly improves the photocatalytic activity.

The effects of side-chain flexibility on the photosensitivity of polyimide alignment film

ABSTRACT To examine the impact of side-chain flexibility on the photosensitivity of polyimide liquid crystal (LC) alignment films, two polyimides (OD-HAB-CA and OD-HAB6-CA) were synthesised. OD-HAB6-CA contains flexible hexamethylene side chains. This study demonstrates that the OD-HAB-CA alignment film can induce LC molecular alignment after 80 min of non-polarised ultraviolet light (NPUVL) irradiation. In contrast, the OD-HAB6-CA alignment film can achieve the same result after only 35 min of irradiation. This suggests that the flexibility of the side-chain can significantly improve the photosensitivity of the alignment film and shorten the required irradiation time. In addition, OD-HAB-CA and OD-HAB6-CA exhibit good thermal stability and light transmittance properties. The resulting LC cell have pretilt angles of 0.2° and 0.5°, respectively, which are suitable for in-plane switching mode LCDs.

Investigation of the preparation and performance of Ag-modified ZnO nanowall ultraviolet detector

In this paper, silver (Ag) nanoparticle-modified zinc oxide (ZnO) nanowall photoconductive ultraviolet photodetector was prepared by using magnetron sputtering technology, electron beam evaporation method and hydrothermal method. The results showed that ZnO nanowalls exhibited a hexagonal wurtzite structure. ZnO nanowalls grew uniformly perpendicular to the substrate, and metallic Ag nanoparticles were uniformly attached to the surface of ZnO nanowalls, effectively improving the ZnO nanowall absorption capability in the ultraviolet light region. The dark current of the Ag-modified ZnO nanowall UV detector deposited by sputtering for 40[Formula: see text]s was 0.042[Formula: see text]mA, revealing a decrease of 44%. Under the irradiation of ultraviolet light with a wavelength of 325[Formula: see text]nm, the photocurrent reached 3.088[Formula: see text]mA, which increased by four times. The responsivity increased from 27.29 to 101.07[Formula: see text]mA/W, and the sensitivity increased from 8.07 to 73.52. In addition to the good repeatability and stability, the response time was reduced by 64%, and the recovery time was decreased by 50%.

Photodegradation of Methylene Blue Using ZnO/Perlite under Ultraviolet Light

The disposal of waste in the continuously growing industries leads to pollution caused by pollutants. One of them is liquid waste originating from the textile industry, which contains toxic coloring agents such as methylene blue that are difficult to decompose in the environment. Therefore, an effort is needed to tackle this issue using photocatalysis. A frequently used photocatalyst material is a semiconductor metal oxide like ZnO. However, ZnO semiconductors still have limitations in their applications. To overcome these limitations, ZnO catalysts will be modified with a supporting material like perlite, which is a lightweight and porous material. This study aims to examine the effectiveness of ZnO/Perlite in degrading methylene blue. The ZnO/Perlite composite with a 20% composition shows the highest photocatalytic activity compared to the ZnO/Perlite composites with 10% and 30% compositions. The optimum condition for ZnO/Perlite 20% in degrading methylene blue is achieved with a mass of 0.3 grams, at pH 11, with 2 hours of stirring under ultraviolet light irradiation, resulting in a photocatalytic activity of 47.59% and a combined adsorption and photocatalytic activity of 78.1%.

Nitrogen-Doped Carbon Quantum Dots with Photoactivation Properties for Ultraviolet Ray Detection.

Photoactivation is a phenomenon that could enhance the photoluminescence (PL) and photostability upon UV/vis light exposure, which is usually observed in CdSe/ZnS quantum dots (QDs). However, the photoactivation phenomenon has been scarcely reported in fluorescent carbon quantum dots (CQDs). Herein, the nitrogen-doped carbon quantum dots (N-CQDs) were prepared through a facile solvothermal approach with naphthalenetracarboxylic dianhydride and serine as precursors. Upon simple UV light irradiation for 10 min, the fluorescence quantum yield (QY) of N-CQDs could increase up to 10-fold. Based on this phenomenon, the N-CQDs were explored as an ultraviolet (UV) light sensor to assess the intensity of ultraviolet radiation in sunlight and indirectly evaluate the UV-blocking efficiency of various sunscreen products. Thus, this contribution not only provided an insight into developing a low-cost UV detector but also opened a door for the development of carbon quantum dots with converse-photobleaching properties.

On-Site Inactivation for Disinfection of Antibiotic-Resistant Bacteria in Hospital Effluent by UV and UV-LED.

The problem of antimicrobial resistance (AMR) is not limited to the medical field but is also becoming prevalent on a global scale in the environmental field. Environmental water pollution caused by the discharge of wastewater into aquatic environments has caused concern in the context of the sustainable development of modern society. However, there have been few studies focused on the treatment of hospital wastewater, and the potential consequences of this remain unknown. This study evaluated the efficacy of the inactivation of antimicrobial-resistant bacteria (AMRB) and antimicrobial resistance genes (AMRGs) in model wastewater treatment plant (WWTP) wastewater and hospital effluent based on direct ultraviolet (UV) light irradiation provided by a conventional mercury lamp with a peak wavelength of 254 nm and an ultraviolet light-emitting diode (UV-LED) with a peak emission of 280 nm under test conditions in which the irradiance of both was adjusted to the same intensity. The overall results indicated that both UV- and UV-LED-mediated disinfection effectively inactivated the AMRB in both wastewater types (>99.9% after 1-3 min of UV and 3 min of UV-LED treatment). Additionally, AMRGs were also removed (0.2-1.4 log10 for UV 254 nm and 0.1-1.3 log10 for UV 280 nm), and notably, there was no statistically significant decrease (p < 0.05) in the AMRGs between the UV and UV-LED treatments. The results of this study highlight the importance of utilizing a local inactivation treatment directly for wastewater generated by a hospital prior to its flow into a WWTP as sewage. Although additional disinfection treatment at the WWTP is likely necessary to remove the entire quantity of AMRB and AMRGs, the present study contributes to a significant reduction in the loads of WWTP and urgent prevention of the spread of infectious diseases, thus alleviating the potential threat to the environment and human health risks associated with AMR problems.

A molecule with aggregation-induced emission for the pH sensing and anti-counterfeiting applications

In this paper, a meaningful pH sensor (E)-4-(4-(1,2,2-triphenylvinyl) styryl)quinoline (TPQ) with aggregation-induced emission (AIE) effect was synthesized based on the conjugated 4-(1,2,2-triphenylvinyl)benzaldehyde and 4-methylquinoline connected by a CC bond. The conjugated quinoline moiety acts as a proton acceptor, and the small variations of pH value in the linear range of 4.01–7.03 and 7.96–9.45 can cause obvious fluorescence fluctuations. The TPQ has good selectivity and reversibility in pH detection, and importantly, it can detect pH fluctuations in real-time in practical applications by fluorescent means. Moreover, TPQ can also be used as a potential viscosity fluorescence sensor for organic solvents. In addition, by combining various color changes of TPQ caused by acid, alkali, water and ammonia stimulation under sunlight and 365 nm ultraviolet light irradiation, it provides a novel concealed optical anti-counterfeiting technique with high security. Therefore, TPQ is a multifunctional molecule with great potential for applications in pH, viscosity sensing and anti-counterfeiting.

Direct Excitation Strategy for Deacylative Couplings of Ketones.

The homolysis of chemical bonds represents one of the most fundamental reactivities of excited molecules. Historically, it has been exploited to generate radicals under ultraviolet (UV) light irradiation. However, unlike most contemporary radical-generating mechanisms, the direct excitation to homolyze chemical bonds and produce aliphatic carbon-centered radicals under visible light remains rare, especially in metallaphotoredox cross couplings. Herein, we present our design of the dihydropyrimidoquinolinone (DHPQ) reagents derived from ketones, which can undergo formal deacylation and homolytic C-C bond cleavage to release alkyl radicals without external photocatalysts. Spectroscopic and computational analysis reveal unique optical and structural features of DHPQs, rationalizing their faster kinetics in alkyl radical generation than a structurally similar but visible-light transparent radical precursor. Such a capability allows DHPQ to facilitate a wide range of Ni-metallaphotoredox cross couplings with aryl, alkynyl and acyl halides. Other catalytic and non-catalyzed alkylative transformations of DHPQs are also feasible with various radical acceptors. We believe this work would be of broad interest, aiding the synthetic planning with simplified operation and expanding the synthetic reach of photocatalyst-free approaches in cutting-edge research.

Direct excitation strategy for deacylative couplings of ketones

The homolysis of chemical bonds represents one of the most fundamental reactivities of excited molecules. Historically, it has been exploited to generate radicals under ultraviolet (UV) light irradiation. However, unlike most contemporary radical‐generating mechanisms, the direct excitation to homolyze chemical bonds and produce aliphatic carbon‐centered radicals under visible light remains rare, especially in metallaphotoredox cross couplings. Herein, we present our design of the dihydropyrimidoquinolinone (DHPQ) reagents derived from ketones, which can undergo formal deacylation and homolytic C–C bond cleavage to release alkyl radicals without external photocatalysts. Spectroscopic and computational analysis reveal unique optical and structural features of DHPQs, rationalizing their faster kinetics in alkyl radical generation than a structurally similar but visible‐light transparent radical precursor. Such a capability allows DHPQ to facilitate a wide range of Ni‐metallaphotoredox cross couplings with aryl, alkynyl and acyl halides. Other catalytic and non‐catalyzed alkylative transformations of DHPQs are also feasible with various radical acceptors. We believe this work would be of broad interest, aiding the synthetic planning with simplified operation and expanding the synthetic reach of photocatalyst‐free approaches in cutting‐edge research.

Effect of crosslinking density on the self-healing and self-reporting properties of epoxy anti-corrosion coatings

This work developed a novel coating with self-healing and self-reporting performance by embedding polyurethane/poly-(urea-formaldehyde) (PU/UF) microcapsules in a shape memory epoxy polymer. 2’7’-Dichlorofluorescein (DCF) and linseed oil were applied as the coloring agent and healing agent, respectively, which are encapsulated into the PU/UF microcapsules (DL@PU/UF microcapsules) via a facile one-step method. To adjust the shape memory effect and the self-reporting performance of epoxy system, two kinds of curing agents (D230 and D400) were reacted with bisphenol A diglycidyl ether epoxy monomer to design a series of coating samples, finally the optimal coating system was selected by three indexes including barrier performance, residual amino content and coating hardness. When the composite coating was damaged, DCF can flow out of the broken microcapsules and react with the residual amino groups in the epoxy coating matrix, which can be recognized red signals in natural light and yellow fluorescent signals under ultraviolet light irradiation. More importantly, the excellent self-reporting property of the coating can be achieved on various metal substrates that broaden the application range of the coating. As for self-healing performance, the damaged coating can be healed quickly due to the shape memory effect of the coating as well as the filling of linseed oil in the scratched region. The Rct value of the healed coating containing 6 % DL@PU/UF microcapsules after immersing in 3.5 wt% NaCl solution for 5 days was more than 3 times that of the scratched coating, and the Rc value was about 16 times that of the scratched coating, indicating its corrosion protection performance. The novel coting not only achieve timely self-reporting ability of color and fluorescence, but also rapidly repair the coating damage, which is essential to practical applications.

Impact of ternary nanocomposite In2O3/SnO2/F-CDs composition on low ppm NO2 sensing performance

Nitrogen dioxide (NO2) is a significant air pollutant with a notable environmental impact, necessitating precise monitoring. However, most existing NO2 sensing materials exhibit low sensitivity and require high-temperature operation. In this study, we employed a hydrothermal and co-precipitation method to synthesize a novel ternary nanocomposite, In2O3/SnO2 nanoparticles (NPs)/fluorine-doped carbon quantum dots (F-CDs). By varying the mass ratio of In2O3 to SnO2 NPs, we investigated the gas-sensing performance of the composite towards NO2. The results demonstrate that when the ratio of SnO2 and In2O3 reaches to 1 : 2, the 2-In2O3/SnO2/F-CDs gas sensor exhibited the highest response, excellent selectivity, and remarkable stability under ultraviolet (UV) light irradiation at room temperature (∼25 °C). Furthermore, the response of the 2-In2O3/SnO2/F-CDs gas sensor displayed a strong linear relationship with the concentration of NO2 gas. At a NO2 gas concentration of 3 ppm, the sensitivity was 238, which is significantly higher than that of In2O3/SnO2 NPs and In2O3 sensors. The response time and recovery time were measured at 62 s and 33 s, respectively. Finally, based on experimental characterization results and band structure analysis, we confirmed the promising effects of ternary nanocomposite in enhancing gas sensing.

Conformal TiO2 Aerogel-Like Films by Plasma Deposition: from Omniphobic Antireflective Coatings to Perovskite Solar Cell Photoelectrodes.

The ability to control the porosity of thin oxide films is a key factor determining their properties. Despite the abundance of dry processes for synthesizing oxide porous layers, a high porosity range is typically achieved by spin-coating-based wet chemical methods. Besides, special techniques such as supercritical drying are required to replace the pore liquid with air while maintaining the porous network. In this study, we propose a new method for the fabrication of ultraporous titanium dioxide thin films at room or mild temperatures (T ≤ 120 °C) by a sequential process involving plasma deposition and etching. These films are conformal to the substrate topography even for high-aspect-ratio substrates and show percolated porosity values above 85% that are comparable to those of advanced aerogels. The films deposited at room temperature are amorphous. However, they become partly crystalline at slightly higher temperatures, presenting a distribution of anatase clusters embedded in the sponge-like open porous structure. Surprisingly, the porous structure remains after annealing the films at 450 °C in air, which increases the fraction of embedded anatase nanocrystals. The films are antireflective, omniphobic, and photoactive, becoming superhydrophilic when subjected to ultraviolet light irradiation. The supported, percolated, and nanoporous structure can be used as an electron-conducting electrode in perovskite solar cells. The properties of the cells depend on the aerogel-like film thickness, which reaches efficiencies close to those of commercial mesoporous anatase electrodes. This generic solvent-free synthesis is scalable and applicable to ultrahigh porous conformal oxides of different compositions, with potential applications in photonics, optoelectronics, energy storage, and controlled wetting.

Detection of Ultraviolet Light by Graphene Oxide Derived from Epitaxial Graphene on SiC and Graphite.

Because of their tunable band gap, flexibility, and high surface-to-volume ratio, two-dimensional materials have appeared as the most promising materials for ultraviolet (UV) light sensors. Here, we report the detection of UV light by oxidized epitaxial graphene (EG) formed on the Si-face of the SiC substrate and graphene oxide (GO) produced by Hummer oxidation of graphite. Both epitaxial graphene oxide (EGO) and GO were characterized by Raman and X-ray photoelectron spectroscopy, and the devices were made simply by placing two parallel copper electrodes onto the graphene oxide layers. Irradiation of UV light onto the graphene oxides was realized by the real-time current measurements between two electrodes at a fixed bias of 1 V. The sudden upward jump of the current (Ids) upon UV light irradiation was observed in both EGO- and GO-based devices, which were returned to the original value, while the UV source was turned OFF. The photocurrent (I ph), the magnitude of the current jump by the UV irradiation, for EGO, was estimated at 8 mA with a channel distance of 2 mm and UV power of 80 mW/cm2. The I phlinearly increases with UV power. In the case of GO, I phwas estimated at 0.2 nA with a similar setup. The photoresponse time and responsivity for EGO are ∼11 s and 5.6 A/W, respectively, which are higher than those of GO. The quantum efficiencies (η) for EGO and GO are calculated as 1907 and 2.3 × 10-6 %, respectively, with an incident power of UV light at 9 mW/cm-2. Because of the advantages of the EG on SiC concerning the stability and wafer scale growth, the present study is expected to lead the development of lab-on-chip-based ultrasensitive UV sensors.

Biomass-derived multiatom-doped carbon dots for water sensing based on excited state intraparticle proton transfer in organic solvents

The presence of trace water impurities in organic solvents can significantly influence chemical reactions and product quality; thus, the accurate detection of water content in these solvents is a critical requirement for industrial applications. Accordingly, an eco-friendly, effective, and economical sensor for detecting trace quantities of miscible water in organic solvents is required for industrial applications. In this study, we synthesized biomass-derived multi-atom-doped carbon dots (MACDs) as fluorescent probes and employed them for the detection of trace amounts of water impurities in several water-miscible organic solvents. The MACDs exhibited stable dual-color fluorescence emission under ultraviolet light irradiation and red and blue emissions in organic solvents and water. The fluorescence quantum yield was approximately 11 %, which indicates an excited intraparticle proton transfer response due to an increase in the water content within a wide response range from 0 % to 100 % (v/v) in organic solvents. The intensity of the red emission signal at 670 nm gradually decreased with an increase in the water content in the organic solvent. The MACDs could detect water with an instant response time of 55 s, a high sensitivity, and low limits of detection of 0.08 %, 1.36 %, 0.03 %, 0.04 %, 0.12 %, and 0.05 % (v/v) in ethanol, acetonitrile, dimethylformamide, methanol, isopropanol, and tetrahydrofuran, respectively. Hence, biomass-derived MACDs can serve as efficient and eco-friendly water sensors in organic solvents.

Forensic stability evaluation of selected miRNA and circRNA markers in human bloodstained samples exposed to different environmental conditions

Recently, RNA markers have been used to identify tissue origins of different kinds of body fluids. Herein, circRNA and miRNA markers were carried out to examine the presence or absence of peripheral blood (PB) in bloodstained samples exposed to different external environmental conditions, which mimicked PB samples left at the crime scenes. PB samples were placed on sterile swabs and then exposed to different high temperatures (37°C, 55°C and 95°C) and ultraviolet light irradiation for 0 d, 0.5 d, 1 d, 3 d, and 7 d, ultra-low and low temperatures (-80°C, −20°C, and 4°C) for 30 d, 180 d and 365 d and different kinds of disinfectants. Total RNA was extracted from bloodstained samples under the above different conditions, and the expressions of target RNAs (including miR16–5p, miR451a, circ0000095, and two reference genes RNU6b and 18 S rRNA) were detected by the reverse transcription-quantitative polymerase chain reaction (RT-qPCR) method. Results showed that these selected RNA markers could be successfully measured at all observation points with their unique degradation rates, which exhibited relative stability in degraded bloodstained samples exposed to different environmental conditions. This study provides insights into the applications of these studied miRNA and circRNA markers in forensic science.

Development of room-temperature operable TiO2-x-based hydrogen gas sensor with light irradiation

In this research work, TiO2-x-thin films are deposited through a radio-frequency magnetron sputtering technique by varying the oxygen partial pressure (pO2) of 6.0 %, 6.4 %, and 6.8 %. The X-ray diffraction analysis depicts the formation of the anatase phase of the annealed thin film with a high crystalline nature. The existence of higher oxygen vacancies and surface roughness are confirmed by the X-ray photoelectron spectroscopy and the atomic force microscopy analyses, respectively, in the 6.0 % pO2 grown thin film. At room temperature (30 °C) and dark conditions, the optimized TiO2-x-based hydrogen gas sensor device depicts a notable response of 22.9 % on exposure to 100 ppm of H2 gas. The irradiation of the ultra-violet (UV) light (λ = 365 nm) on the sensing material promotes desorption of the oxygen species and hence improves the responsivity of the sample. The highest responsivity of 87.7 %, along with faster response and recovery time of 9.4 s and 7.8 s, respectively, is achieved under the UV light irradiation and 100 ppm of H2 gas for the sample grown at 6.0 % pO2, which signifies its potential for the development of room temperature operable hydrogen gas sensor.

Photocatalytic performance of (Zn,Me)–SnO2 nanoparticles (Me= Nb5+ or W6+) under UV light for efficiently degradation of organic dye pollutants

In this study (Zn,Nb)-doped SnO2 and (Zn,W)-doped SnO2 were synthetized using chemical route by calcination at 600 °C/2 h and milling at 500 rpm/1 h to verify its behavior as a photocatalyst. The powders showed high surface area: 57.1 m2/g for (Zn,Nb)-doped SnO2 and 74.3 m2/g for (Zn,W)-doped SnO2, both showed 10–25 nm of average diameter and rutile crystalline phase after morphological and structural characterizations. UV–vis spectroscopy indicated a band gap of 3.53 eV for (Zn,Nb)–SnO2 and 3.35 for (Zn,W)–SnO2. The photocatalytic activity was verified through the decomposition of Rodhamine B (RhB) aqueous solution under ultraviolet light radiation of 9W. After 120 min the efficiency of (Zn,Nb)–SnO2 was 68.5 % and for (Zn,W)–SnO2 was 71.1 %. Using a UV-lamp of 11W the efficiency in photodiscoloration of RhB aqueous solution increased to 83.2 % with (Zn,W)-doped SnO2 powder in a shorter irradiation time (90 min), indicating its potential use as nanostructured photocatalyst ceramic powder.

Detection of sulphur(II) of carbon dots synthesized from Gardenia residue.

The detection of anions using carbon dots (CDs) has received less attention compared to cations. Therefore, the present study aimed to develop a fluorescence sensor based on carbon dots (CDs) capable of detecting S2- in real water samples. The CDs were successfully prepared from the residues of a traditional Chinese herb, Gardenia, which emitted green photoluminescence (PL) under ultraviolet light irradiation. The as-prepared CDs were quasi-spherical in shape and ranged in size from 10 to 30 nm. Different detailed analyses proved that the CDs had good morphology, various functional groups, high water solubility, great optical features, and excellent stability under diverse environmental conditions. The ion detection showed that only Ag+ had the strongest fluorescence quenching effect on the CDs, however, the addition of S2- could recover their fluorescence. Based on these results, an "off-on" fluorescence sensor was achieved to selectively detect the concentration of S2- in real water samples with a limit of detection (LOD) of 39 μM, which further expanded the application of residues from traditional Chinese herbal medicine.