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      Photocatalytic generation of H 2O 2 over a Z-scheme Fe 2O 3@C@1T/2H-MoS 2 heterostructured catalyst for high-performance Fenton reaction

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          Abstract

          A Z-scheme Fe 2O 3@C@1T/2H-MoS 2 heterostructured catalyst is constructed using carbon and 1T-MoS 2 as bridging layers, realizing high-performance H 2O 2 generation and a self-sufficient heterogeneous photo-Fenton reaction.

          Abstract

          The wide application of the Fenton reaction has been severely restricted by the requirement of continuous feeding of H 2O 2, the iron-slurry production, and the slow recycle rate of Fe 3+/Fe 2+. This work reports transforming type-II Fe 2O 3@2H-MoS 2 heterostructures to a Z-scheme Fe 2O 3@C@1T/2H-MoS 2 catalyst capable of photocatalytic in situ generation of H 2O 2 as an oxidant for the subsequent Fenton reaction. With MoS 2 as a co-catalyst to improve the reduction from Fe 3+ to Fe 2+, the cascade process demonstrates high performance in oxidative degradation of organics ( e.g., 100 mg L −1 tetracycline within 100 min). The in situ generated H 2O 2, with a yield as high as 1575 μmol g −1 h −1 in air-saturated methanol solution (75 vol%), accounts for 43.5% of the total degradation efficiency. The current system represents an effective solution to the challenges in the traditional Fenton reaction, holding great potential for organic pollutant degradation in wastewater.

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          Heterojunction Photocatalysts.

          Semiconductor-based photocatalysis attracts wide attention because of its ability to directly utilize solar energy for production of solar fuels, such as hydrogen and hydrocarbon fuels and for degradation of various pollutants. However, the efficiency of photocatalytic reactions remains low due to the fast electron-hole recombination and low light utilization. Therefore, enormous efforts have been undertaken to solve these problems. Particularly, properly engineered heterojunction photocatalysts are shown to be able to possess higher photocatalytic activity because of spatial separation of photogenerated electron-hole pairs. Here, the basic principles of various heterojunction photocatalysts are systematically discussed. Recent efforts toward the development of heterojunction photocatalysts for various photocatalytic applications are also presented and appraised. Finally, a brief summary and perspectives on the challenges and future directions in the area of heterojunction photocatalysts are also provided.
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            Generation and Detection of Reactive Oxygen Species in Photocatalysis.

            The detection methods and generation mechanisms of the intrinsic reactive oxygen species (ROS), i.e., superoxide anion radical (•O2-), hydrogen peroxide (H2O2), singlet oxygen (1O2), and hydroxyl radical (•OH) in photocatalysis, were surveyed comprehensively. Consequently, the major photocatalyst used in heterogeneous photocatalytic systems was found to be TiO2. However, besides TiO2 some representative photocatalysts were also involved in the discussion. Among the various issues we focused on the detection methods and generation reactions of ROS in the aqueous suspensions of photocatalysts. On the careful account of the experimental results presented so far, we proposed the following apprehension: adsorbed •OH could be regarded as trapped holes, which are involved in a rapid adsorption-desorption equilibrium at the TiO2-solution interface. Because the equilibrium shifts to the adsorption side, trapped holes must be actually the dominant oxidation species whereas •OH in solution would exert the reactivity mainly for nonadsorbed reactants. The most probable routes of generating intrinsic ROS at the surfaces of two polymorphs of TiO2, anatase and rutile, were discussed along with some plausible rational reaction processes. In addition to the four major ROS, three ROS, that is organic peroxides, ozone, and nitric oxide, which are less common in photocatalysis are also briefly reviewed.
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              Advanced Oxidation Processes for Organic Contaminant Destruction Based on the Fenton Reaction and Related Chemistry

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                Author and article information

                Contributors
                Journal
                JMCAET
                Journal of Materials Chemistry A
                J. Mater. Chem. A
                Royal Society of Chemistry (RSC)
                2050-7488
                2050-7496
                January 24 2023
                2023
                : 11
                : 4
                : 1991-2001
                Affiliations
                [1 ]State Key Lab Urban Water Resource and Environment, School of Chemistry and Chemical Engineering, Harbin Institute of Technology, Harbin, China
                [2 ]Department of Chemistry, University of California, Riverside, CA 92521 USA
                [3 ]Key Laboratory of Functional Inorganic Material Chemistry, Ministry of Education, School of Chemistry and Materials Science, Heilongjiang University, Harbin, China
                Article
                10.1039/D2TA08145H
                9d1b9e23-f011-4ff2-bf53-c7b2f6a21327
                © 2023

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

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