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      The Mott–Schottky heterojunction MoC@NG@ZIS with enhanced kinetic response for promoting photocatalytic hydrogen production

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          Abstract

          The Mott–Schottky heterojunction MoC@NG@ZIS exhibits an excellent photocatalytic hydrogen evolution performance of 32.96 mmol g −1 h −1 with great stability. The enhanced charge and reaction kinetics explain the remarkable photocatalytic activity.

          Abstract

          Mott–Schottky heterojunctions have been widely used to enhance photocatalytic activity by improving the separation and transfer of photogenerated charges. However, an in-depth exploration of design concepts and photocatalytic mechanisms of Mott–Schottky heterojunctions is still lacking. In this work, we have constructed the two-dimensional (2D) ultrathin Mott–Schottky heterojunction MoC@NG@ZIS by combining the photon capturer ZnIn 2S 4 (ZIS) with electrocatalyst MoC@NG (nitrogen-doped graphene loaded with MoC quantum dots). The addition of MoC@NG not only boosts the reaction kinetics but also provides abundant and high-activity reactive sites for hydrogen production. Meanwhile, the 2D ultrathin structure and plentiful interfaces of Mott–Schottky heterojunction MoC@NG@ZIS facilitate mass transfer and provide numerous channels for charge transport. Spectroscopic and electrochemical analyses reveal that MoC@NG@ZIS has extended light absorption and enhanced photoelectric response. Furthermore, due to the presence of a Schottky barrier, efficient charge separation is realized through the unidirectional pathway of charge transfer. Therefore, the optimized photocatalyst MoC@NG-15@ZIS exhibits a great hydrogen evolution performance of 32.96 mmol g −1 h −1 with excellent photochemical stability, which is higher than those of most reported ZIS-based photocatalysts. This study provides constructive insights into the design of efficient Mott–Schottky heterojunctions and reveals the mechanism of performance enhancement.

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          Ultrathin 2D/2D WO3/g-C3N4 step-scheme H2-production photocatalyst

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            2D Transition-Metal-Dichalcogenide-Nanosheet-Based Composites for Photocatalytic and Electrocatalytic Hydrogen Evolution Reactions.

            Hydrogen (H2) is one of the most important clean and renewable energy sources for future energy sustainability. Nowadays, photocatalytic and electrocatalytic hydrogen evolution reactions (HERs) from water splitting are considered as two of the most efficient methods to convert sustainable energy to the clean energy carrier, H2. Catalysts based on transition metal dichalcogenides (TMDs) are recognized as greatly promising substitutes for noble-metal-based catalysts for HER. The photocatalytic and electrocatalytic activities of TMD nanosheets for the HER can be further improved after hybridization with many kinds of nanomaterials, such as metals, oxides, sulfides, and carbon materials, through different methods including the in situ reduction method, the hot-injection method, the heating-up method, the hydro(solvo)thermal method, chemical vapor deposition (CVD), and thermal annealing. Here, recent progress in photocatalytic and electrocatalytic HERs using 2D TMD-based composites as catalysts is discussed.
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              Boron-doped nitrogen-deficient carbon nitride-based Z-scheme heterostructures for photocatalytic overall water splitting

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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
                October 18 2022
                2022
                : 10
                : 40
                : 21465-21473
                Affiliations
                [1 ]Beijing Advanced Innovation Center for Materials Genome Engineering, University of Science and Technology Beijing, Beijing 100083, China
                [2 ]Institute for Advanced Material and Technology, University of Science and Technology Beijing, Beijing 100083, China
                [3 ]School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing 100083, China
                Article
                10.1039/D2TA05932K
                8fad97e1-fe2c-4438-927f-4e6a44fbc5e0
                © 2022

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

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