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      Shaping Silica Rods by Tuning Hydrolysis and Condensation of Silica Precursors

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          Abstract

          We present the synthesis of colloidal silica particles with new shapes by manipulating the growth conditions of rods that are growing from polyvinylpyrrolidone-loaded water-rich droplets containing ammonia and ethanol. The silica rods grow by ammonia-catalyzed hydrolysis and condensation of tetraethoxysilane (TEOS). The lengthwise growth of these silica rods gives us the opportunity to change the conditions at any time during the reaction. In this work, we vary the availability of hydrolyzed monomers as a function of time and study how the change in balance between the hydrolysis and condensation reactions affects a typical synthesis (as described in more detail by our group earlier1). First, we show that in a “standard” synthesis, there are two silica growth processes occurring; one in the oil phase and one in the droplet. The growth process in the water droplet causes the lengthwise growth of the rods. The growth process in the oil phase produces a thin silica layer around the rods, but also causes the nucleation of 70 nm silica spheres. During a typical rod growth, silica formation mainly takes place in the droplet. The addition of partially hydrolyzed TEOS or tetramethoxysilane (TMOS) to the growth mixture results in a change in balance between the hydrolysis and condensation reaction. As a result, the growth also starts to take place on the surface of the water droplet and thus from the oil phase, not only from inside the droplet onto a silica rod sticking out of the droplet. Carefully tuning the growth from the droplet and the growth from the oil phase allowed us to create nanospheres, hollow silica rods, hollow sphere rod systems (colloidal matchsticks), and bent silica rods.

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          Colloidal nanocrystal synthesis and the organic-inorganic interface.

          Colloidal nanocrystals are solution-grown, nanometre-sized, inorganic particles that are stabilized by a layer of surfactants attached to their surface. The inorganic cores possess useful properties that are controlled by their composition, size and shape, and the surfactant coating ensures that these structures are easy to fabricate and process further into more complex structures. This combination of features makes colloidal nanocrystals attractive and promising building blocks for advanced materials and devices. Chemists are achieving ever more exquisite control over the composition, size, shape, crystal structure and surface properties of nanocrystals, thus setting the stage for fully exploiting the potential of these remarkable materials.
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            Shape control in gold nanoparticle synthesis.

            In this tutorial review, we summarise recent research into the controlled growth of gold nanoparticles of different morphologies and discuss the various chemical mechanisms that have been proposed to explain anisotropic growth. With the overview and discussion, we intended to select those published procedures that we consider more reliable and promising for synthesis of morphologies of interest. We expect this to be interesting to researchers in the wide variety of fields that can make use of metal nanoparticles.
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              Dense packing and symmetry in small clusters of microspheres.

              When small numbers of colloidal microspheres are attached to the surfaces of liquid emulsion droplets, removing fluid from the droplets leads to packings of spheres that minimize the second moment of the mass distribution. The structures of the packings range from sphere doublets, triangles, and tetrahedra to exotic polyhedra not found in infinite lattice packings, molecules, or minimum-potential energy clusters. The emulsion system presents a route to produce new colloidal structures and a means to study how different physical constraints affect symmetry in small parcels of matter.
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                Author and article information

                Journal
                Chem Mater
                Chem Mater
                cm
                cmatex
                Chemistry of Materials
                American Chemical Society
                0897-4756
                1520-5002
                15 December 2018
                22 January 2019
                : 31
                : 2
                : 521-531
                Affiliations
                Debye Institute for Nanomaterials Science, Utrecht University , Princetonplein 1, 3584 CC Utrecht, The Netherlands
                Author notes
                [* ]E-mail: f.hagemans@ 123456uu.nl (F.H.).
                [* ]E-mail: a.vanblaaderen@ 123456uu.nl (A.v.B.).
                [* ]E-mail: a.imhof@ 123456uu.nl (A.I.).
                Article
                10.1021/acs.chemmater.8b04607
                6345103
                30686858
                fb38104f-efb6-4957-ad03-a3029d95e9a8
                Copyright © 2018 American Chemical Society

                This is an open access article published under a Creative Commons Attribution (CC-BY) License, which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.

                History
                : 02 November 2018
                : 14 December 2018
                Categories
                Article
                Custom metadata
                cm8b04607
                cm-2018-046072

                Materials science
                Materials science

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