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      Printable logic circuits comprising self-assembled protein complexes

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          Abstract

          This paper describes the fabrication of digital logic circuits comprising resistors and diodes made from protein complexes and wired together using printed liquid metal electrodes. These resistors and diodes exhibit temperature-independent charge-transport over a distance of approximately 10 nm and require no encapsulation or special handling. The function of the protein complexes is determined entirely by self-assembly. When induced to self-assembly into anisotropic monolayers, the collective action of the aligned dipole moments increases the electrical conductivity of the ensemble in one direction and decreases it in the other. When induced to self-assemble into isotropic monolayers, the dipole moments are randomized and the electrical conductivity is approximately equal in both directions. We demonstrate the robustness and utility of these all-protein logic circuits by constructing pulse modulators based on AND and OR logic gates that function nearly identically to simulated circuits. These results show that digital circuits with useful functionality can be derived from readily obtainable biomolecules using simple, straightforward fabrication techniques that exploit molecular self-assembly, realizing one of the primary goals of molecular electronics.

          Abstract

          Proteins are promising molecular materials for next-generation electronic devices. Here, the authors fabricated printable digital logic circuits comprising resistors and diodes from self-assembled photosystem I complexes that enable pulse modulation.

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          Most cited references57

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          Preparation and Characterization of Fulleroid and Methanofullerene Derivatives

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            Eutectic Gallium–Indium (EGaIn): A Moldable Liquid Metal for Electrical Characterization of Self-Assembled Monolayers

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              Covalently bonded single-molecule junctions with stable and reversible photoswitched conductivity.

              Through molecular engineering, single diarylethenes were covalently sandwiched between graphene electrodes to form stable molecular conduction junctions. Our experimental and theoretical studies of these junctions consistently show and interpret reversible conductance photoswitching at room temperature and stochastic switching between different conductive states at low temperature at a single-molecule level. We demonstrate a fully reversible, two-mode, single-molecule electrical switch with unprecedented levels of accuracy (on/off ratio of ~100), stability (over a year), and reproducibility (46 devices with more than 100 cycles for photoswitching and ~10(5) to 10(6) cycles for stochastic switching).

                Author and article information

                Contributors
                xq237@cam.ac.uk
                ryan.chiechi@ncsu.edu
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                28 April 2022
                28 April 2022
                2022
                : 13
                : 2312
                Affiliations
                [1 ]GRID grid.4830.f, ISNI 0000 0004 0407 1981, Stratingh Institute for Chemistry, , University of Groningen, ; Nijenborgh 4, 9747 AG Groningen, The Netherlands
                [2 ]GRID grid.40803.3f, ISNI 0000 0001 2173 6074, Department of Chemistry, , North Carolina State University, ; Raleigh, NC 27695-8204 United States
                [3 ]GRID grid.5335.0, ISNI 0000000121885934, Present Address: Optoelectronics Group, Cavendish Laboratory, , University of Cambridge, JJ Thomson Avenue, ; Cambridge, CB3 0HE UK
                Author information
                http://orcid.org/0000-0001-5857-6414
                Article
                30038
                10.1038/s41467-022-30038-8
                9050843
                35484124
                fbda839a-0169-4fff-ad64-543cf7f86c20
                © The Author(s) 2022

                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
                : 7 July 2021
                : 8 April 2022
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                © The Author(s) 2022

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                electronic materials,molecular self-assembly,electron transfer,molecular electronics

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