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      Stabilizing atomically precise metal nanoclusters as simultaneous charge relay mediators and photosensitizers

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          Abstract

          Atomically precise metal nanoclusters (NCs) are judiciously stabilized as simultaneous charge relay mediators and photosensitizers for photocatalytic organic transformation.

          Abstract

          Atomically precise metal nanoclusters (NCs) have been deemed to be emerging photosensitizers but suffer from a rapid charge recombination rate and poor photostability, which ruins the advantageous photosensitization efficacy of metal NCs and retards the construction of metal NC-based photosystems. Herein, we conceptually demonstrate the design of a transition metal chalcogenide quantum dot (TMCs QD)–metal NC–graphene (GR) ternary heterostructured photosystem via elaborate interface modulation, wherein atomically precise metal NCs are intercalated at the interface of TMC QDs and GR. The branched polyethylenimine (BPEI) molecule grafted on the GR framework functions as an efficient self-assembly-directing mediator, and simultaneously, stabilizes metal NCs to retain the generic photosensitization effect. The cooperative photosensitization effect of metal NCs and TMC QDs, interim charge relay mediator role of metal NCs, and electron-withdrawing capability of GR synergistically contribute to the cascade electron transport pathway for markedly boosting charge separation, resulting in considerably enhanced photoactivity towards selective organic transformation under visible light irradiation.

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          The impact of nanoscience on heterogeneous catalysis.

          Most catalysts consist of nanometer-sized particles dispersed on a high-surface-area support. Advances in characterization methods have led to a molecular-level understanding of the relationships between nanoparticle properties and catalytic performance. Together with novel approaches to nanoparticle synthesis, this knowledge is contributing to the design and development of new catalysts.
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            Core–Shell Palladium Nanoparticle@Metal–Organic Frameworks as Multifunctional Catalysts for Cascade Reactions

            Uniform core-shell Pd@IRMOF-3 nanostructures, where single Pd nanoparticle core is surrounded by amino-functionalized IRMOF-3 shell, are prepared by a facile mixed solvothermal method. When used as multifunctional catalysts, the Pd@IRMOF-3 nanocomposites exhibit high activity, enhanced selectivity, and excellent stability in the cascade reaction. Both experimental evidence and theoretical calculations reveal that the high catalytic performance of Pd@IRMOF-3 nanocomposites originates from their unique core-shell structures.
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              Size Focusing: A Methodology for Synthesizing Atomically Precise Gold Nanoclusters

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                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                JMCAET
                Journal of Materials Chemistry A
                J. Mater. Chem. A
                Royal Society of Chemistry (RSC)
                2050-7488
                2050-7496
                March 30 2022
                2022
                : 10
                : 13
                : 7006-7012
                Affiliations
                [1 ]College of Materials Science and Engineering, Fuzhou University, New Campus, Minhou, Fujian Province 350108, China
                [2 ]Fujian Science & Technology Innovation Laboratory for Optoelectronic Information of China, Fuzhou, Fujian 350108, P. R. China
                Article
                10.1039/D2TA00572G
                e90a87d3-6536-4edd-a851-c652d5a4d159
                © 2022

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

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