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Synthetic organic pigments like xanthene and azo dyes from the direct discharge of textile effluents are considered colossal global issues and attract the concern of scholars. Photocatalysis continues to be a very valuable pollution control method for industrial wastewater. Incorporations of metal oxide catalysts such as zinc oxide (ZnO) on mesoporous Santa Barbara Armophous-15 (SBA-15) support to improve catalyst thermo-mechanical stability have been comprehensively reported. However, charge separation efficiency and light absorption of ZnO/SBA-15 continue to be limiting its photocatalytic activity. Herein, we report a successful preparation of Ruthenium-induced ZnO/SBA-15 composite via conventional incipient wetness impregnation technique with the aim of boosting the photocatalytic activity of the incorporated ZnO. Physicochemical properties of the SBA-15 support, ZnO/SBA-15, and Ru-ZnO/SBA-15 composites were characterized by X-ray diffraction (XRD), N physisorption isotherms at 77 K, Fourier-transform infrared (FTIR), scanning electron microscopy (SEM), energy dispersive X-ray (EDS), and transmission electron microscopy (TEM). The characterization outcomes exhibited that ZnO and ruthenium species have been successfully embedded into SBA-15 support, andtheSBA-15 support maintains its structured hexagonal mesoscopic ordering in both ZnO/SBA-15 and Ru-ZnO/SBA-15 composites. The photocatalytic activity of the composite was assessed through photo-assisted mineralization of aqueous MB solution, and the process was optimized for initial dye concentration and catalyst dosage. 50 mg catalyst exhibited significant degradation efficiency of 97.96% after 120 min, surpassing the efficiencies of 77% and 81% displayed by 10 and 30 mg of the as-synthesized catalyst. The photodegradation rate was found to decrease with an increase in the initial dye concentration. The superior photocatalytic activity of Ru-ZnO/SBA-15 over the binary ZnO/SBA-15 may be attributed to the slower recombination rate of photogenerated charges on the ZnO surface with the addition of ruthenium.
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http://dx.doi.org/10.3390/polym15051210 | DOI Listing |
Chem Commun (Camb)
September 2025
State Key Laboratory of Advanced Technology for Materials Synthesis and Processing & State Key Laboratory of Silicate Materials for Architectures & School of Chemistry, Chemical Engineering and Life Sciences & School of Materials Science and Engineering, Wuhan University of Technology, Wuhan, 430070
Photocatalytic seawater splitting (PSWS), which utilizes abundant solar and ocean resources, is one of the most promising technologies for sustainable hydrogen production. However, the complex composition of seawater significantly limits the durability and activity of photocatalysts. In this review, we first identify the primary factors that contribute to photocatalyst deactivation during PSWS, including chloride induced corrosion and loss of active sites, and light shielding caused by precipitation of metal cation salts.
View Article and Find Full Text PDFJ Fluoresc
September 2025
Chemical Engineering Department, College of Engineering, University of Ha'il, P.O. Box 2440, 81441, Ha'il, Saudi Arabia.
This review delivers a focused and critical evaluation of recent progress in the green synthesis of carbon quantum dots (CQDs), with particular attention to state-of-the-art approaches utilizing renewable biomass as precursors. The main objective is to systematically examine innovative, environmentally friendly methods and clarify their direct influence on the core properties and photocatalytic performance of CQDs. The novelty of this review stems from its comprehensive comparison of green synthetic pathways, revealing how specific processes determine key structural, optical, and electronic attributes of the resulting CQDs.
View Article and Find Full Text PDFInorg Chem
September 2025
State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002, P. R. China.
The photocatalytic reduction of carbon dioxide (CO) to chemicals holds significant importance for mitigating the current energy crisis. Rational design of catalytic centers within well-defined structures can effectively enhance the reaction activity and selectivity. In this study, we constructed interrupted zeolitic boron imidazolate frameworks (BIFs) featuring unsaturated coordination at the central Co ion.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
Hefei National Research Center for Physical Sciences at the Microscale, School of Chemistry and Materials Science, State Key Laboratory of Precision and Intelligent Chemistry, National Synchrotron Radiation Laboratory, University of Science and Technology of China, Hefei, Anhui, 230026, China.
The construction of C─N bonds from simple precursors under ambient conditions is a fundamental challenge in green chemistry, especially when it comes to avoiding energy-intensive protocols. Here, we present a continuous flow photocatalytic platform that enables the efficient coupling of C─N bonds between methanol and ammonia at ambient temperature and pressure. By synergistically engineering a Pd clusters-decorated TiO photocatalyst (1Pd/TiO) and a mass transfer-enhanced gas-liquid-solid Taylor flow reactor, the system achieves a remarkable formamide productivity of 256.
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2025
Ministry-of-Education Key Laboratory for the Green Preparation and Application of Functional Materials, Hubei Key Laboratory of Polymer Materials, School of Materials Science & Engineering, Hubei University, Wuhan 430062, PR China. Electronic address:
Effective removal of ethylene (CH) during fruit and vegetables storage and transport remains a critical challenge for post-harvest preservation. Although S-scheme heterojunctions can improve charge separation and redox capacity for ethylene degradation, their efficiency is still restricted by limited carrier transfer and sluggish oxygen activation. Here, we rationally designed a novel 2D/2D SnNbO/BiMoO monolayer S-scheme heterojunction integrated with Pt co-catalyst to address these limitations.
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