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      Electron microscopy of nanoparticle superlattice formation at a solid-liquid interface in nonpolar liquids

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          Abstract

          Liquid-phase electron microscopy reveals how self-assembly of nanoparticle superlattices depends on the type of nonpolar solvent.

          Abstract

          Nanoparticle superlattice films form at the solid-liquid interface and are important for mesoscale materials, but are notoriously difficult to analyze before they are fully dried. Here, the early stages of nanoparticle assembly were studied at solid-liquid interfaces using liquid-phase electron microscopy. Oleylamine-stabilized gold nanoparticles spontaneously formed thin layers on a silicon nitride (SiN) membrane window of the liquid enclosure. Dense packings of hexagonal symmetry were obtained for the first monolayer independent of the nonpolar solvent type. The second layer, however, exhibited geometries ranging from dense packing in a hexagonal honeycomb structure to quasi-crystalline particle arrangements depending on the dielectric constant of the liquid. The complex structures formed by the weaker interactions in the second particle layer were preserved, while the surface remained immersed in liquid. Fine-tuning the properties of the involved materials can thus be used to control the three-dimensional geometry of a superlattice including quasi-crystals.

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          Self-Assembly of Colloidal Nanocrystals: From Intricate Structures to Functional Materials.

          Chemical methods developed over the past two decades enable preparation of colloidal nanocrystals with uniform size and shape. These Brownian objects readily order into superlattices. Recently, the range of accessible inorganic cores and tunable surface chemistries dramatically increased, expanding the set of nanocrystal arrangements experimentally attainable. In this review, we discuss efforts to create next-generation materials via bottom-up organization of nanocrystals with preprogrammed functionality and self-assembly instructions. This process is often driven by both interparticle interactions and the influence of the assembly environment. The introduction provides the reader with a practical overview of nanocrystal synthesis, self-assembly, and superlattice characterization. We then summarize the theory of nanocrystal interactions and examine fundamental principles governing nanocrystal self-assembly from hard and soft particle perspectives borrowed from the comparatively established fields of micrometer colloids and block copolymer assembly. We outline the extensive catalog of superlattices prepared to date using hydrocarbon-capped nanocrystals with spherical, polyhedral, rod, plate, and branched inorganic core shapes, as well as those obtained by mixing combinations thereof. We also provide an overview of structural defects in nanocrystal superlattices. We then explore the unique possibilities offered by leveraging nontraditional surface chemistries and assembly environments to control superlattice structure and produce nonbulk assemblies. We end with a discussion of the unique optical, magnetic, electronic, and catalytic properties of ordered nanocrystal superlattices, and the coming advances required to make use of this new class of solids.
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            Real-space imaging of nucleation and growth in colloidal crystallization.

            Crystallization of concentrated colloidal suspensions was studied in real space with laser scanning confocal microscopy. Direct imaging in three dimensions allowed identification and observation of both nucleation and growth of crystalline regions, providing an experimental measure of properties of the nucleating crystallites. By following their evolution, we identified critical nuclei, determined nucleation rates, and measured the average surface tension of the crystal-liquid interface. The structure of the nuclei was the same as the bulk solid phase, random hexagonal close-packed, and their average shape was rather nonspherical, with rough rather than faceted surfaces.
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              PbSe nanocrystal solids for n- and p-channel thin film field-effect transistors.

              Initially poorly conducting PbSe nanocrystal solids (quantum dot arrays or superlattices) can be chemically "activated" to fabricate n- and p-channel field effect transistors with electron and hole mobilities of 0.9 and 0.2 square centimeters per volt-second, respectively; with current modulations of about 10(3) to 10(4); and with current density approaching 3 x 10(4) amperes per square centimeter. Chemical treatments engineer the interparticle spacing, electronic coupling, and doping while passivating electronic traps. These nanocrystal field-effect transistors allow reversible switching between n- and p-transport, providing options for complementary metal oxide semiconductor circuits and enabling a range of low-cost, large-area electronic, optoelectronic, thermoelectric, and sensing applications.
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                Author and article information

                Journal
                Sci Adv
                Sci Adv
                SciAdv
                advances
                Science Advances
                American Association for the Advancement of Science
                2375-2548
                May 2020
                13 May 2020
                : 6
                : 20
                : eaba1404
                Affiliations
                [1 ]INM—Leibniz Institute for New Materials, Saarbrücken, Germany.
                [2 ]Colloid and Interface Chemistry, Saarland University, Saarbrücken, Germany.
                [3 ]Department of Physics, Saarland University, Saarbrücken, Germany.
                Author notes
                [*]

                These authors contributed equally to this work.

                [†]

                Present address: SPECS Surface Nano Analysis, Berlin, Germany.

                [‡]

                Present address: European XFEL, Schenefeld, Germany.

                [§ ]Corresponding author. Email: tobias.kraus@ 123456leibniz-inm.de (T.K.); niels.dejonge@ 123456leibniz-inm.de (N.d.J.)
                Author information
                http://orcid.org/0000-0002-5571-5789
                http://orcid.org/0000-0003-1837-2593
                http://orcid.org/0000-0003-2951-1704
                http://orcid.org/0000-0002-3969-6821
                Article
                aba1404
                10.1126/sciadv.aba1404
                7220325
                4c8651a1-1f6a-4104-b1ed-784f7f97c681
                Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC).

                This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license, which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.

                History
                : 08 November 2019
                : 28 February 2020
                Categories
                Research Article
                Research Articles
                SciAdv r-articles
                Materials Science
                Materials Science
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                Jeanelle Ebreo

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