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Chlorpyrifos, one of the organophosphorus pesticide commonly used in the environment, may bring about an irreversible harm such as lung cancer to human body. Photoelectrochemical (PEC) detection techniques based on g-CN for sensing chlorpyrifos have attracted increasing attentions, but impeded by several inherent constraints such as a limit of active sites and carriers transfer. To conquer these challenges, a photoelectrochemical sensor of BiOI@N/g-CN with a step scheme heterojunction was thereby proposed for the sensitive and selective detection of trace chlorpyrifos. Herein, the created N vacancies facilitated the migration of photo-electrons from BiOI to recombine with the holes of N/g-CN under light irradiation. A powerful oriented built-in electric field was established directing from N/g-CN to BiOI. The photocurrent intensity of the as-prepared sensor exhibited over 7.6 times higher than that of pure g-CN, showing a well PEC performance. High selectivity of the developed sensor was attributed to the specific interaction between Bi sites of the developed composites and the S, N atoms in chlorpyrifos. Such sensitive and steady PEC sensor exhibited a linear detection range from 0.01 to 20 ppb with a detection limit of 0.004 ppb. Further, the sensor displayed reliable performance when applied to real river water and soil samples, achieving nice recovery rates. Unlike traditional PEC sensor, this one was prepared into S-scheme heterojunction by creating a N defect-induced driving force based on the altered built-in electric field. The work not only provides experimental evidences but also advances the fundamental theories so as to offer a robust g-CN-based PEC platform for environmental analysis.
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http://dx.doi.org/10.1016/j.aca.2025.344102 | DOI Listing |
Int J Biol Macromol
September 2025
Department of Chemical Engineering, Faculty of Engineering, University of Isfahan, Isfahan, Iran.
The persistent presence of Metronidazole (MTZ), a commonly used antibiotic, in water bodies is a serious environmental and health concern because of its genotoxic and carcinogenic potential. Here, we report an effective visible-light photocatalyst system comprising an S-scheme glycine-modified TiO/FeO heterojunction immobilized on chitosan-polyacrylonitrile nanofibers. The photocatalyst nanocomposite was synthesized through a sol-gel and ultrasonication process coupled with electrospinning-assisted immobilization.
View Article and Find Full Text PDFChem Sci
August 2025
Key Laboratory of the Ministry of Education for Advanced Catalysis Materials, College of Chemistry and Materials Science, Zhejiang Normal University Jinhua Zhejiang 321004 P. R. China
Selective photoreduction of CO with HO to hydrocarbons is challenged by inadequate and uncontrollable electron and proton feeding. Herein, this limitation is overcome by integrating HO dissociation, CO reduction, and O evolution catalysts into a dual S-scheme heterojunction and regulating exposed facets of the heterojunction supports. In this design, H and OH species generated by HO dissociation on the NH-MIL-125 support transfer to the T-COF shell and FeO insert for CO reduction and O evolution, respectively.
View Article and Find Full Text PDFLangmuir
September 2025
School of Chemistry and Chemical Engineering, Ningxia Key Laboratory of Solar Chemical Conversion Technology, Key Laboratory for Chemical Engineering and Technology, State Ethnic Affairs Commission, North Minzu University, Yinchuan 750021, China.
A simple solvothermal method was used in this paper. ZnCoS (ZCS) nanoparticles were smoothly synthesized by this method and loaded on the external surface of MnCd0S (MCS) to form an S-scheme heterojunction. A comparative evaluation was performed with two other single catalysts, and the compound catalyst MCS/ZCS achieved great gain in the process of catalytic action of H generated under sunlight.
View Article and Find Full Text PDFAdv Mater
September 2025
Laboratory of Solar Fuel, Faculty of Materials Science and Chemistry, China University of Geosciences, 68 Jincheng St., Wuhan, 430078, P. R. China.
Photocatalysis enabled by step-scheme (S-scheme) heterojunction has emerged as a promising strategy for addressing the global energy crisis and achieving carbon neutrality. However, mechanisms regulating the interfacial charge transfer dynamics of S-scheme heterojunctions remain elusive. Herein, the electron transfer mechanisms are elucidated for a model S-scheme heterojunction composed of cadmium sulfide and a covalent organic framework material using synchrotron-based in situ soft X-ray absorption spectroscopy, substantiating the well-established in situ irradiated X-ray photoelectron spectroscopy.
View Article and Find Full Text PDFNanomicro Lett
September 2025
School of Microelectronics, Northwestern Polytechnical University, Xi'an, 710129, People's Republic of China.
Metal halide perovskites (MHPs) with striking electrical and optical properties have appeared at the forefront of semiconductor materials for photocatalytic redox reactions but still suffer from some intrinsic drawbacks such as inferior stability, severe charge-carrier recombination, and limited active sites. Heterojunctions have recently been widely constructed to improve light absorption, passivate surface for enhanced stability, and promote charge-carrier dynamics of MHPs. However, little attention has been paid to the review of MHPs-based heterojunctions for photocatalytic redox reactions.
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