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      Simple size-controlled synthesis of Au nanoparticles and their size-dependent catalytic activity

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          Abstract

          The controlled preparation of Au nanoparticles (NPs) in the size range of 6 to 22 nm is explored in this study. The Au NPs were prepared by the reduction of tetrachloroauric acid using maltose in the presence of nonionic surfactant Tween 80 at various concentrations to control the size of the resulting Au NPs. With increasing concentration of Tween 80 a decrease in the size of produced Au NPs was observed, along with a significant decrease in their size distribution. The size-dependent catalytic activity of the synthesized Au NPs was tested in the reduction of 4-nitrophenol with sodium borohydride, resulting in increasing catalytic activity with decreasing size of the prepared nanoparticles. Eley-Rideal catalytic mechanism emerges as the more probable, in contrary to the Langmuir-Hinshelwood mechanism reported for other noble metal nanocatalysts.

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          Most cited references54

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          Onset of Catalytic Activity of Gold Clusters on Titania with the Appearance of Nonmetallic Properties

          M. Valden (1998)
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            Identification of active gold nanoclusters on iron oxide supports for CO oxidation.

            Gold nanocrystals absorbed on metal oxides have exceptional properties in oxidation catalysis, including the oxidation of carbon monoxide at ambient temperatures, but the identification of the active catalytic gold species among the many present on real catalysts is challenging. We have used aberration-corrected scanning transmission electron microscopy to analyze several iron oxide-supported catalyst samples, ranging from those with little or no activity to others with high activities. High catalytic activity for carbon monoxide oxidation is correlated with the presence of bilayer clusters that are approximately 0.5 nanometer in diameter and contain only approximately 10 gold atoms. The activity of these bilayer clusters is consistent with that demonstrated previously with the use of model catalyst systems.
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              Catalysis by metallic nanoparticles in aqueous solution: model reactions.

              Catalysis by metallic nanoparticles is certainly among the most intensely studied problems in modern nanoscience. However, reliable tests for catalytic performance of such nanoparticles are often poorly defined, which makes comparison and benchmarking rather difficult. We tackle in this tutorial review a subset of well-studied reactions that take place in aqueous phase and for which a comprehensive kinetic analysis is available. Two of these catalytic model reactions are under consideration here, namely the reduction of (i) p-nitrophenol and (ii) hexacyanoferrate (iii), both by borohydride ions. Both reactions take place at the surface of noble metal nanoparticles at room temperature and can be accurately monitored by UV-vis spectroscopy. Moreover, the total surface area of the nanoparticles in solution can be known with high precision and thus can be directly used for the kinetic analysis. Hence, these model reactions represent cases of heterogeneous catalysis that can be modelled with the accuracy typically available for homogeneous catalysis. Both model reactions allow us to discuss a number of important concepts and questions, namely the dependence of catalytic activity on the size of the nanoparticles, electrochemistry of nanoparticles, surface restructuring, the use of carrier systems and the role of diffusion control.
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                Author and article information

                Contributors
                libor.kvitek@upol.cz
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                15 March 2018
                15 March 2018
                2018
                : 8
                : 4589
                Affiliations
                [1 ]ISNI 0000 0001 1245 3953, GRID grid.10979.36, Department of Physical Chemistry, , Regional Centre of Advanced Technologies and Materials, Faculty of Science, Palacky University Olomouc, ; Slechtitelu 27, 783 71 Olomouc, Czech Republic
                [2 ]ISNI 0000 0001 1939 4845, GRID grid.187073.a, Materials Science Division, , Argonne National Laboratory, ; 9600 South Cass Avenue, Lemont, Illinois 60439 USA
                [3 ]ISNI 0000 0004 1936 7822, GRID grid.170205.1, Institute for Molecular Engineering, , The University of Chicago, ; 5640 South Ellis Avenue, Chicago, Illinois 60637 USA
                Author information
                http://orcid.org/0000-0003-0578-6383
                http://orcid.org/0000-0002-3147-2196
                Article
                22976
                10.1038/s41598-018-22976-5
                5854582
                29545580
                bf4f1235-3f2e-40fb-8e71-10ecc647f3b7
                © The Author(s) 2018

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 3 January 2018
                : 28 February 2018
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