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      Recent advances in ordered meso/macroporous metal oxides for heterogeneous catalysis: a review

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          Abstract

          The present review article highlights the preparation, characterization, properties, and recent developments in porous metal oxide catalysts for heterogeneous catalysis.

          Abstract

          Ordered meso/macroporous metal oxides have gained increasing attention in heterogeneous catalysis arising from their large surface areas and pore volumes, elevated catalytic activity and good thermal stability. Compared to nonporous metal oxides, their most prominent feature is the ability to interact with molecules not only at their exterior surface but also within the large interior surface of the material. The past decade has witnessed substantial advances in the synthesis of new porous metal oxides with ordered structures for use in a wide range of applications. By recalling some of the classical fundamentals of porous materials, this review examines the recent developments in ordered meso- and macro-porous metal oxide catalysts for heterogeneous catalysis. Additionally, we outline the current challenges in the field of nanoparticle-based catalysis, including the role played by the morphology (size, shape, and porosity) of ordered meso/macroporous metal oxides, and provide a perspective on the need for further advances in porous materials so that their contribution to heterogeneous catalysis can continue to expand.

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          A new family of mesoporous molecular sieves prepared with liquid crystal templates

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            Triblock Copolymer Syntheses of Mesoporous Silica with Periodic 50 to 300 Angstrom Pores

            D. Zhao (1998)
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              Pd-Pt bimetallic nanodendrites with high activity for oxygen reduction.

              Controlling the morphology of Pt nanostructures can provide a great opportunity to improve their catalytic properties and increase their activity on a mass basis. We synthesized Pd-Pt bimetallic nanodendrites consisting of a dense array of Pt branches on a Pd core by reducing K2PtCl4 with L-ascorbic acid in the presence of uniform Pd nanocrystal seeds in an aqueous solution. The Pt branches supported on faceted Pd nanocrystals exhibited relatively large surface areas and particularly active facets toward the oxygen reduction reaction (ORR), the rate-determining step in a proton-exchange membrane fuel cell. The Pd-Pt nanodendrites were two and a half times more active on the basis of equivalent Pt mass for the ORR than the state-of-the-art Pt/C catalyst and five times more active than the first-generation supportless Pt-black catalyst.
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                Author and article information

                Journal
                JMCAET
                Journal of Materials Chemistry A
                J. Mater. Chem. A
                Royal Society of Chemistry (RSC)
                2050-7488
                2050-7496
                2017
                2017
                : 5
                : 19
                : 8825-8846
                Affiliations
                [1 ]Particles and Catalysis Research Group
                [2 ]School of Chemical Engineering
                [3 ]The University of New South Wales
                [4 ]Sydney
                [5 ]Australia
                [6 ]Beijing Key Laboratory for Green Catalysis and Separation
                [7 ]Laboratory of Catalysis Chemistry and Nanoscience
                [8 ]Beijing University of Technology
                [9 ]Beijing 100124
                [10 ]China
                Article
                10.1039/C6TA10896B
                d6b2c215-5bcd-4f9b-8589-7741249ae2a7
                © 2017
                History

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