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      Peroxymonosulfate Activation by Fe–Co–O-Codoped Graphite Carbon Nitride for Degradation of Sulfamethoxazole

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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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            Critical Review of rate constants for reactions of hydrated electronsChemical Kinetic Data Base for Combustion Chemistry. Part 3: Propane

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              Activation of persulfate (PS) and peroxymonosulfate (PMS) and application for the degradation of emerging contaminants

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                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                Environmental Science & Technology
                Environ. Sci. Technol.
                American Chemical Society (ACS)
                0013-936X
                1520-5851
                August 18 2020
                July 16 2020
                August 18 2020
                : 54
                : 16
                : 10361-10369
                Affiliations
                [1 ]Collaborative Innovation Center for Advanced Nuclear Energy Technology, INET, Tsinghua University, Beijing 100084, P. R. China
                [2 ]College of Chemistry and Materials Science, Sichuan Normal University, Chengdu, Sichuan 610068, P. R. China
                [3 ]Beijing Key Laboratory of Radioactive Wastes Treatment, Tsinghua University, Beijing 100084, P. R. China
                Article
                10.1021/acs.est.0c03256
                32672945
                da19e818-c1b4-457a-8264-b2a3b9422929
                © 2020

                https://doi.org/10.15223/policy-029

                https://doi.org/10.15223/policy-037

                https://doi.org/10.15223/policy-045

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