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      Supramolecular Semiconductivity through Emerging Ionic Gates in Ion–Nanoparticle Superlattices

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          Abstract

          The self-assembly of nanoparticles driven by small molecules or ions may produce colloidal superlattices with features and properties reminiscent of those of metals or semiconductors. However, to what extent the properties of such supramolecular crystals actually resemble those of atomic materials often remains unclear. Here, we present coarse-grained molecular simulations explicitly demonstrating how a behavior evocative of that of semiconductors may emerge in a colloidal superlattice. As a case study, we focus on gold nanoparticles bearing positively charged groups that self-assemble into FCC crystals via mediation by citrate counterions. In silico ohmic experiments show how the dynamically diverse behavior of the ions in different superlattice domains allows the opening of conductive ionic gates above certain levels of applied electric fields. The observed binary conductive/nonconductive behavior is reminiscent of that of conventional semiconductors, while, at a supramolecular level, crossing the “band gap” requires a sufficient electrostatic stimulus to break the intermolecular interactions and make ions diffuse throughout the superlattice’s cavities.

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          GROMACS: High performance molecular simulations through multi-level parallelism from laptops to supercomputers

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            Molecular dynamics with coupling to an external bath

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              A DNA-based method for rationally assembling nanoparticles into macroscopic materials.

              Colloidal particles of metals and semiconductors have potentially useful optical, optoelectronic and material properties that derive from their small (nanoscopic) size. These properties might lead to applications including chemical sensors, spectroscopic enhancers, quantum dot and nanostructure fabrication, and microimaging methods. A great deal of control can now be exercised over the chemical composition, size and polydispersity of colloidal particles, and many methods have been developed for assembling them into useful aggregates and materials. Here we describe a method for assembling colloidal gold nanoparticles rationally and reversibly into macroscopic aggregates. The method involves attaching to the surfaces of two batches of 13-nm gold particles non-complementary DNA oligonucleotides capped with thiol groups, which bind to gold. When we add to the solution an oligonucleotide duplex with 'sticky ends' that are complementary to the two grafted sequences, the nanoparticles self-assemble into aggregates. This assembly process can be reversed by thermal denaturation. This strategy should now make it possible to tailor the optical, electronic and structural properties of the colloidal aggregates by using the specificity of DNA interactions to direct the interactions between particles of different size and composition.
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                Author and article information

                Journal
                ACS Nano
                ACS Nano
                nn
                ancac3
                ACS Nano
                American Chemical Society
                1936-0851
                1936-086X
                22 December 2022
                10 January 2023
                : 17
                : 1
                : 275-287
                Affiliations
                []Department of Applied Science and Technology, Politecnico di Torino , Corso Duca degli Abruzzi 24, 10129 Torino, Italy
                []Department of Innovative Technologies, University of Applied Sciences and Arts of Southern Switzerland, Polo Universitario Lugano , Campus Est, Via la Santa 1, 6962 Lugano-Viganello, Switzerland
                [§ ]Department of Organic Chemistry, Weizmann Institute of Science , Rehovot 76100, Israel
                Author notes
                Author information
                https://orcid.org/0000-0002-7491-8952
                https://orcid.org/0000-0001-8885-3080
                https://orcid.org/0000-0002-6320-8875
                https://orcid.org/0000-0002-3473-8471
                Article
                10.1021/acsnano.2c07558
                9835987
                36548051
                f494d98f-a8f3-438a-8e9b-5d2482763c84
                © 2022 The Authors. Published by American Chemical Society

                Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 29 July 2022
                : 09 December 2022
                Funding
                Funded by: H2020 European Research Council, doi 10.13039/100010663;
                Award ID: 818776
                Funded by: Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung, doi 10.13039/501100001711;
                Award ID: IZLIZ2_183336
                Categories
                Article
                Custom metadata
                nn2c07558
                nn2c07558

                Nanotechnology
                colloidal superlattices,ion dynamics,supramolecular semiconductivity,ionic conductivity,molecular dynamics,coarse-graining,machine learning

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