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      Emerging heterostructured C 3N 4photocatalysts for photocatalytic environmental pollutant elimination and sterilization

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          Abstract

          Photocatalysis is deemed a highly prominent technology to solve environmental problems such as pollution, CO 2emission and bacterial contamination.

          Abstract

          Photocatalysis is deemed a highly prominent technology to solve environmental problems such as pollution, CO 2emission and bacterial contamination. As an important photocatalyst, g-C3N4 has attracted a great amount of attention in environmental remediation owing to its good stability, excellent light response, low cost and environmentally friendly properties. However, the pristine g-C3N4 photocatalyst generally suffers from serious photoinduced charge carrier recombination, poor surface active sites, and insufficient visible light harvesting, thereby leading to unsatisfactory photocatalytic performance. Heterostructured C 3N 4photocatalysts have recently become a research focus in environmental fields thanks to their fast photoexcited electron–hole pair dissociation, broadened visible light response range, and sufficient photoredox capability. Herein, we critically review the up-to-date developments of heterostructured C 3N 4photocatalysts in organic pollutant elimination, heavy metal ion reduction, CO 2conversion and bacterial inactivation. Meanwhile, the strategies for constructing efficient C 3N 4based heterostructures with enhanced environmental photocatalytic capability are thoroughly described, which should help readers to quickly acquire in-depth knowledge and to inspire new concepts in heterostructure engineering. Finally, the challenges and opportunities in fabricating heterostructured C 3N 4photocatalysts for large-scale and commercial applications are discussed to give a clear study direction in this field.

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          Electrochemical Photolysis of Water at a Semiconductor Electrode

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            A metal-free polymeric photocatalyst for hydrogen production from water under visible light.

            The production of hydrogen from water using a catalyst and solar energy is an ideal future energy source, independent of fossil reserves. For an economical use of water and solar energy, catalysts that are sufficiently efficient, stable, inexpensive and capable of harvesting light are required. Here, we show that an abundant material, polymeric carbon nitride, can produce hydrogen from water under visible-light irradiation in the presence of a sacrificial donor. Contrary to other conducting polymer semiconductors, carbon nitride is chemically and thermally stable and does not rely on complicated device manufacturing. The results represent an important first step towards photosynthesis in general where artificial conjugated polymer semiconductors can be used as energy transducers.
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              Is Open Access

              In situ click chemistry generation of cyclooxygenase-2 inhibitors

              Cyclooxygenase-2 isozyme is a promising anti-inflammatory drug target, and overexpression of this enzyme is also associated with several cancers and neurodegenerative diseases. The amino-acid sequence and structural similarity between inducible cyclooxygenase-2 and housekeeping cyclooxygenase-1 isoforms present a significant challenge to design selective cyclooxygenase-2 inhibitors. Herein, we describe the use of the cyclooxygenase-2 active site as a reaction vessel for the in situ generation of its own highly specific inhibitors. Multi-component competitive-binding studies confirmed that the cyclooxygenase-2 isozyme can judiciously select most appropriate chemical building blocks from a pool of chemicals to build its own highly potent inhibitor. Herein, with the use of kinetic target-guided synthesis, also termed as in situ click chemistry, we describe the discovery of two highly potent and selective cyclooxygenase-2 isozyme inhibitors. The in vivo anti-inflammatory activity of these two novel small molecules is significantly higher than that of widely used selective cyclooxygenase-2 inhibitors.
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                Author and article information

                Contributors
                Journal
                ICFNAW
                Inorganic Chemistry Frontiers
                Inorg. Chem. Front.
                Royal Society of Chemistry (RSC)
                2052-1553
                June 27 2023
                2023
                : 10
                : 13
                : 3756-3780
                Affiliations
                [1 ]Center of Advanced Optoelectronic Materials, College of Materials and Environmental Engineering, Hangzhou Dianzi University, Hangzhou 310018, China
                [2 ]School of Energy and Environment, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong, China
                [3 ]Department of Materials, University of Oxford, Oxford, OX1 3PH, UK
                [4 ]Laboratory of Inorganic Materials Chemistry (CMI), University of Namur, 61 rue de Bruxelles, B-5000, Namur, Belgium
                [5 ]Department of Chemistry, Zhejiang Sci-Tech University, Hangzhou 310018, China
                [6 ]State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, 122, Luoshi Road, 430070 Wuhan, Hubei, China
                Article
                10.1039/D3QI00657C
                f8bfc270-d4b7-44dc-b4ef-e1d921d5c01e
                © 2023

                http://rsc.li/journals-terms-of-use

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