Search Results (65)

A strong interaction between Bi³⁺ and ZnO was used to successfully sensitize ZnO nanorods with quantum dots (QDs) of Bi₂O₃ through three different strategies. Although the Bi₂O₃ QDs had similar particle size distributions, their photocatalytic performance varied significantly, prompting the investigation of factors beyond particle size. The study revealed that the photochemical method selectively deposited Bi₂O₃ QDs onto electron-rich ZnO sites, providing a favorable pathway for efficient electron–hole separation and transfer. Consequently, abundant h⁺ and ·OH radicals were generated, which effectively degraded Rhodamine B (RhB). As demonstrated in the RhB degradation experiments, the Bi₂O₃/ZnO nanorod catalyst achieved an 89.3% degradation rate within 120 min, significantly outperforming catalysts with other morphologies. The photoluminescence (PL) and time-resolved photoluminescence (TRPL) results indicated that the Bi₂O₃/ZnO heterostructure constructed an effective interface to facilitate the spatial separation of photogenerated charge carriers, which effectively prolonged their lifetime. The electron paramagnetic resonance (EPR) results confirmed that the ·OH radicals played a key role in the degradation process. Full article

Volatile organic compound (VOC) emissions have become a critical environmental concern due to their contributions to photochemical smog formation, secondary organic aerosol generation, and adverse human health impacts in the context of accelerated industrialization and urbanization. Catalytic oxidation over perovskite-type catalysts is an attractive technological approach for efficient VOC abatement. This review systematically evaluates the advancements in perovskite-based catalysts for VOC oxidation, focusing on their crystal structure–activity relationships, electronic properties, synthetic methodologies, and nanostructure engineering. Emphasis is placed on metal ion doping strategies and supported catalyst configurations, which have been demonstrated to optimize catalytic performance through synergistic effects. The applications of perovskite catalysts in diverse oxidation systems, including photocatalysis, thermal catalysis, electrocatalysis, and plasma-assisted catalysis, are comprehensively discussed with critical analysis of their respective advantages and limitations. It summarizes the existing challenges, such as catalyst deactivation caused by carbon deposition, sulfur/chlorine poisoning, and thermal sintering, as well as issues like low energy utilization efficiency and the generation of secondary pollutants. By consolidating current knowledge and highlighting future research directions, this review provides a solid foundation for the rational design of next-generation perovskite catalysts for sustainable VOC management. Full article

With unique photochemical properties, graphitic carbon nitride (g-C₃N₄) has gained significant attention for application in photocatalytic degradation of a wide range of organic pollutants. However, its performance is limited by the rapid electron–hole recombination and the relatively weak redox capability. Substantial progress has been made in the preparation of g-C₃N₄-based photocatalysts with enhanced photocatalytic activity. This review summarizes the recent advances in strategies to improve the photocatalytic activity of g-C₃N₄-based photocatalysts and their application in the photocatalytic degradation of organic pollutants. Morphology control, doping, functionalization, metal deposition, dye sensitization, defect engineering, and construction of heterojunctions can be used to improve the photocatalytic activity of g-C₃N₄ through promoting charge carrier separation, reducing the bandgap, and suppressing charge recombination. Furthermore, a range of oxidants, such as hydrogen peroxide and persulfate, can be coupled with g-C₃N₄-based photocatalysts to enhance the generation of reactive oxygen species and boost the photocatalytic degradation of organic pollutants. Precise control over the g-C₃N₄ structure during the synthesis process remains a challenge, and further improvements are required in photocatalyst stability and the mineralization rates of organic pollutants. More research and development effort is needed to address the existing challenges, refine the design of g-C₃N₄-based photocatalysts to improve their activity, and promote their practical application in pollutant degradation. Full article

Ni phytotoxicity has been attributed to its multidirectional detrimental effects on plant cell structure and function. However, relatively little is known about Ni’s impact on phenolic metabolism in plants. The objective of our study was to obtain insight into the effect of Ni treatment on phenolic compound composition, phenol-related enzyme activities, and lignin accumulation in cucumber plants. Besides growth reduction, the chlorophyll a and carotenoid contents as well as the chlorophyll a fluorescence parameters, namely, the maximum photochemical efficiency of PS II and non-photochemical quenching, were significantly decreased in the Ni-treated cucumber plants. Application of Ni resulted in changes in the phenolic acid and flavonoid profiles; however, the total content of the detected phenolic compounds remained unchanged in the leaf and slightly decreased in the root. The Ni-induced release of free phenolic acids from their conjugates was found in the leaf. Ni treatment led to a marked increase in leaf peroxidase activities assayed with various phenolic substrates, while it did not influence phenyl ammonia lyase and polyphenol oxidase activities. Increased lignin deposition was observed in the leaf blade of Ni-exposed plants. Neither lignin accumulation nor induction of peroxidase activities were found in the root. Our results indicate that the Ni effect on phenolic compound composition and related enzyme activities is organ-specific. The observed changes in the content of individual compounds might result rather from the metal-triggered conversions of the compounds constitutively present in the cucumber tissues than from de novo synthesis. Full article

Given the increasingly severe environmental problems caused by water pollution, the degradation of organic dyes can be effectively achieved through the utilization of photocatalysis. In this work, metal alkoxides and a combination of alcohol/hydrophobic solvents are employed to prepare BaTiO₃ aerogels via a liquid-phase and template-free synthetic route. The preparation process of the aerogels solely entails facile agitation and supercritical drying, eliminating the need for additional heat treatment. The binary solvent of ethanol and toluene is identified as the optimal choice, resulting in a significantly enhanced surface area (up to 223 m²/g) and an abundant pore structure of BaTiO₃ aerogels compared to that of the BaTiO₃ nanoparticles. Thus, the removal efficiency of the BaTiO₃ aerogel sample for MO is nearly twice as high as that of the BaTiO₃ nanoparticles sample. Noble metal Ag nanoparticles’ deposition onto the BaTiO₃ aerogel surface is further achieved via the photochemical deposition method, which enhances the capture of photogenerated electrons, thereby ensuring an elevated level of photocatalytic efficiency. As a result, Ag nanoparticles deposited on BaTiO₃ aerogel can degrade MO completely after 40 min of illumination, while the corresponding aerogel before modification can only remove 80% of MO after 60 min. The present work not only complements the preparatory investigation of intricate aerogels but also offers a fresh perspective for the development of diverse perovskite aerogels with broad applications. Full article

To revolutionize the photochemical efficiency of quantum dots sensitized solar cells (QDSSCs) devices, herein, a passivation of the cells with multilayer material has been developed for heterojunctions TiO₂/NiS/MnS/HI-30/Pt devices. In this study, NiS and MnS were deposited on a photoanode for the first time as passivated photon absorbers at room temperature. The adoption of NiS as a passisvative layer could tailor the active surface area and improve the photochemical properties of the newly modified cells. The vibrational shifts obtained from the Raman spectra imply that the energy change is influenced by the surface effect, giving rise to better electronic conductivity. The electrochemical stability and durability test for the N/M-3 device slows down and remains at 8.88% of its initial current after 3500 s, as compared to the N/M-1 device at 7.20%. The disparity in charge recombination implies that both the outer and inner parts of the nanoporous material are involved in the photogeneration reaction. The hybridized N/M-3 cell device reveals the highest current density with a low potential onset, indicating that power conversion occurs more easily because photons tend to be adsorbed easily on the surface of the MnS. The Nyquist plot for N/M-1 and N/M-3 promotes the faster transport of electrolytic ions across the TiO₂/NiS/MnS, providing a good interaction for the electrolyte. The I-J Value of 9.94% shows that the passivation with the NiS layer promotes electron transport and enhances the performance of the modified cells. The passivation of the TiO₂ layer with NiS attains a better power conversion efficiency among the scant studies so far on the surface passivation of QDSCs. Full article

Fixed nitrogen species generated by the early Earth’s atmosphere are thought to be critical to the emergence of life and the sustenance of early metabolisms. A previous study estimated nitrogen fixation in the Hadean Earth’s N₂/CO₂-dominated atmosphere; however, that previous study only considered a limited chemical network that produces NO_x species (i.e., no HCN formation) via the thermochemical dissociation of N₂ and CO₂ in lightning flashes, followed by photochemistry. Here, we present an updated model of nitrogen fixation on Hadean Earth. We use the Chemical Equilibrium with Applications (CEA) thermochemical model to estimate lightning-induced NO and HCN formation and an updated version of KINETICS, the 1-D Caltech/JPL photochemical model, to assess the photochemical production of fixed nitrogen species that rain out into the Earth’s early ocean. Our updated photochemical model contains hydrocarbon and nitrile chemistry, and we use a Geant4 simulation platform to consider nitrogen fixation stimulated by solar energetic particle deposition throughout the atmosphere. We study the impact of a novel reaction pathway for generating HCN via HCN₂, inspired by the experimental results which suggest that reactions with CH radicals (from CH₄ photolysis) may facilitate the incorporation of N into the molecular structure of aerosols. When the HCN₂ reactions are added, we find that the HCN rainout rate rises by a factor of five in our 1-bar case and is about the same in our 2- and 12-bar cases. Finally, we estimate the equilibrium concentration of fixed nitrogen species under a kinetic steady state in the Hadean ocean, considering loss by hydrothermal vent circulation, photoreduction, and hydrolysis. These results inform our understanding of environments that may have been relevant to the formation of life on Earth, as well as processes that could lead to the emergence of life elsewhere in the universe. Full article

Nowadays, metal oxide semiconductor gas sensors have diverse applications ranging from human health to smart agriculture with the development of Internet of Things (IoT) technologies. However, high operating temperatures and an unsatisfactory detection capability (high sensitivity, fast response/recovery speed, etc.) hinder their integration into the IoT. Herein, a ternary heterostructure was prepared by decorating WO₃ nanoplates with Au and SnO₂ nanoparticles through a facial photochemical deposition method. This was employed as a sensing material for 3-hydroxy-2-butanone (3H-2B), a biomarker of Listeria monocytogenes. These Au/SnO₂–WO₃ nanoplate-based sensors exhibited an excellent response (R_a/R_g = 662) to 25 ppm 3H-2B, which was 24 times higher than that of pure WO₃ nanoplates at 140 °C. Moreover, the 3H-2B sensor showed an ultrafast response and recovery speed to 25 ppm 3H-2B as well as high selectivity. These excellent sensing performances could be attributed to the rich Au/SnO₂–WO₃ active interfaces and the excellent transport of carriers in nanoplates. Furthermore, a wireless portable gas sensor equipped with the Au/SnO₂–WO₃ nanoplates was assembled, which was tested using 3H-2B with known concentrations to study the possibilities of real-time gas monitoring in food quality and safety. Full article

The preparation of electrocatalysts with high performance for the ethanol oxidation reaction is vital for the large-scale commercialization of direct ethanol fuel cells. Here, we successfully synthesized a high-performance electrocatalyst of a AuPd alloy with a decreased alloying degree via pulsed laser irradiation in liquids. As indicated by the experimental results, the photochemical effect-induced surficial deposition of Pd atoms, combined with the photothermal effect-induced interdiffusion of Au and Pd atoms, resulted in the formation of AuPd alloys with a decreased alloying degree. Structural characterization reveals that L-AuPd exhibits a lower degree of alloying compared to C-AuPd prepared via the conventional co-reduction method. This distinct structure endows L-AuPd with outstanding catalytic activity and stability in EOR, achieving mass and specific activities as high as 16.01 A mg_Pd⁻¹ and 20.69 mA cm⁻², 9.1 and 5.2 times than that of the commercial Pd/C respectively. Furthermore, L-AuPd retains 90.1% of its initial mass activity after 300 cycles. This work offers guidance for laser-assisted fabrication of efficient Pd-based catalysts in EOR. Full article

Nitrogen oxides (NO_X) in the atmosphere cause oxidation reactions with photochemical radicals and volatile organic compounds, leading to the accumulation of ozone (O₃). NO_X constitutes a significant portion of the NO_y composition, with nitrous acid (HONO) and nitric acid (HNO₃) following. HONO plays a crucial role in the reaction cycle of NO_X and hydrogen oxides. The majority of HNO₃ reduction mechanisms result from aerosolization through heterogeneous reactions, having adverse effects on humans and plants by increasing secondary aerosol concentrations in the atmosphere. The investigation of the formation and conversion mechanisms of HONO and HNO₃ is important; however, research in this area is currently lacking. In this study, we observed HONO, HNO₃, and their precursor gases were observed in the atmosphere using parallel-plate diffusion scrubber-ion chromatography. A 0-D box model simulated the compositional distribution of NO_y in the atmosphere. The formation reactions and conversion mechanisms of HONO and HNO₃ were quantified using reaction equations and reaction coefficients. Among the various mechanisms, dominant mechanisms were identified, suggesting their importance. According to the calculation results, the produce of HONO was predominantly attributed to heterogeneous reactions, excluding an unknown source. The sink processes were mainly governed by photolysis during daytime and reactions with OH radicals during nighttime. HNO₃ showed dominance in its production from N₂O₅, and in its conversion mechanisms primarily involving aerosolization and deposition. Full article

This study evaluated the environmental impact of landfill, incineration, and lightweight aggregate production for sewage sludge management techniques and compared the utilization of sewage-produced lightweight aggregates with natural aggregates in terms of building material production. Two scenarios were established for the life cycle assessment (LCA) of the sludge and associated product that was carried out after sludge generation. Sludge incineration and landfill deposition includes emissions from the drying, transportation, incineration of sludge, and landfill, and the production of lightweight aggregates and natural aggregates includes transportation to manufacturing facilities, the manufacturing processes themselves, and transportation of the produced aggregates to construction sites. We calculated the amount of pollutant emissions for each process in each scenario and analyzed the environmental impact index considering the environmental impact of each pollutant using the Open LCA program. The parameters used for the environmental impact index analysis for sludge management are potential acidification, climate change, eutrophication potential, human toxicity, photochemical oxidation, and stratospheric ozone depletion. The environmental impact values of lightweight aggregates (LWA) are GWP 100 441 kg CO₂_Eq, AP 2.73 × 10⁻² kg SO_{2_}Eq, EP 4.46 × 10⁻³ kg PO₄⁻_Eq, HTP 4.15 × 10⁻² kg, 1,4-DCB_Eq, POCP 1.64 × 10⁻³ kg CH₄_Eq, and ODP 3.41 × 10⁻⁷ kg CFC-11_Eq. We found that these values were low compared to landfill and incineration as a sewage sludge disposal method and compared to natural aggregate as a construction material production method. The environmental impact index analysis during LCA of lightweight aggregates produced from the sludge verified its positive environmental impact compared to the other potential methods of sludge management. Full article

The streamlines of the energy flux (Poynting vectors) and chirality flux as well as the intensity of the electric field around various plasmonic nanostructures (nanocube, nanocuboid, nanotriangle, hexagonal nanoplate and bowtie nanoantenna) induced by a circularly polarized (CP) or linearly polarized (LP) light were studied theoretically. The boundary element method combined with the method of moment was used to solve a set of surface integral equations, based on the Stratton–Chu formulation, for analyzing the highly distorted electromagnetic (EM) field in the proximity of these nanostructures. We discovered that the winding behavior of these streamlines exhibits versatility for various modes of the surface plasmon resonance of different nanostructures. Recently, using plasmonic nanostructures to facilitate a photochemical reaction has gained significant attention, where the hot carriers (electrons) play important roles. Our findings reveal a connection between the flow pattern of energy flux and the morphology of the photochemical deposition around various plasmonic nanostructures irradiated by a CP light. For example, numerical results exhibit vertically helical streamlines of the Poynting vector around an Au nanocube and transversely twisted-roll streamlines around a nanocuboid. Additionally, the behaviors of the winding energy and chirality fluxes at the gap and corners of a plasmonic bowtie nanoantenna, implying a highly twisted EM field, depend on the polarization of the incident LP light. Our analysis of the streamlines of the Poynting vector and chirality flux offers an insight into the formation of plasmon-enhanced photocatalysis. Full article

Atmospheric nitrogen (N) deposition is coupled with organic nitrogen (ON) and inorganic nitrogen (IN); however, little is known about plant growth and the balance of elements in Torreya grandis growing under different ON/IN ratios. Here, we investigated the effects of ON/IN ratios (1/9, 3/7, 7/3, and 9/1) on leaf stoichiometry (LF), chlorophyll content, and chlorophyll fluorescence of T. grandis. We used ammonium nitrate as the IN source and an equal proportion of urea and glycine as the ON source. The different ON/IN ratios altered the stoichiometry and photochemical efficiency in T. grandis. Although the leaf P content increased significantly after treatment, leaf N and N:P maintained a certain homeostasis. Torreya grandis plants performed best at an ON/IN ratio of 3/7, with the highest values of chlorophyll-a, total chlorophyll, maximum photochemical efficiency, and photosynthetic performance index. Thus, both ON and IN types should be considered when assessing the responses of plant growth to increasing N deposition in the future. Our results also indicated that the leaf P concentration was positively correlated with Chl, Fv/Fm, and PIabs. This result further indicates the importance of the P element for plant growth against the background of nitrogen deposition. Overall, these results indicate that T. grandis might cope with changes in the environment by maintaining the homeostasis of element stoichiometry and the plasticity of PSII activity. Full article

In this work, photocatalytic materials constituted by Cr-doped TiO₂ (Cr-TiO₂) decorated with noble metals show high effectiveness in the mineralization of Acid Orange 7 (AO7) and in the disinfection of real river water. The materials were firstly obtained by sol-gel method to get Cr-TiO₂ that was subsequently modified by photochemical deposition of Ag or Pd nanoparticles (Ag/Cr-TiO₂, Pd/Cr-TiO₂). Chemical-physical characterization results evidenced that the noble metals were homogeneously distributed on the Cr-TiO₂ surface. By using Pd(0.25%)/Cr-TiO₂, the AO7 discoloration efficiency was about 91.4% after only 60 min of visible irradiation, which can be due to the lowest band gap of this material. Moreover, nitrates, chlorides, total hardness, and coliform bacteria content significantly decreased after the treatment of real river water samples (that is contaminated by industrial and domestic effluents) under UV and visible light irradiation in the presence of TiCrOx decorated with noble metals. One hundred percent of elimination rate for E. coli, total coliforms, and other enterobacteriaceae (without regrowth) was achieved by using Ag/Cr-TiO₂ as photocatalyst. Full article

Urban forests play a crucial role in both emitting and absorbing atmospheric pollutants. Understanding the ecological processes of biogenic volatile organic compounds (BVOCs) and secondary organic aerosols (SOAs) and their interactions in urban forests can help to assess how they influence air quality. Additionally, exploring the adaptation and feedback mechanisms between urban forests and their surrounding environments can identify new pollutants and potential risks in urban forests. However, the relationship between BVOC emissions and SOA formation is complex due to the influence of meteorological conditions, photochemical reactions, and other factors. This complexity makes it challenging to accurately describe this relationship. In this study, we used time-of-flight mass spectrometry and aerosol particle size spectrometry to monitor concentrations of BVOCs and particulate matter with a diameter less than 1 µm (PM₁; representing SOAs) at a frequency of 10–12 times per min in an urban forest near Shanghai. We then analyzed the temporal changes in concentrations of BVOCs, SOAs, and other chemical pollutants in different periods of the day by using subsequence clustering and causal inference methods. The results showed that after using this method for diurnal segmentation, PM₁ prediction accuracy was improved by 26.77%–47.51%, and the interaction rules of BVOCs and SOAs had sequential interaction characteristics. During the day, BVOCs are an important source of SOAs and have a negative feedback relationship with O₃. From night to early morning, BVOCs have a positive, balanced relationship with O₃, SOAs are affected by wind speed or deposition, BVOCs have no obvious relationship with O₃, and SOAs are affected by temperature or humidity. This study is the first to apply Toeplitz inverse covariance-based clustering and causal inference methods for the high-frequency monitoring of BVOCs and SOAs, revealing the temporal effects and characteristics of BVOCs and SOAs and providing a scientific basis and new methods for understanding the dynamic effects of urban forest communities on the environment. Full article