6
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      A fivefold UO22+ node is a path to dodecagonal quasicrystal approximants in coordination polymers

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Pentacoordinated uranyl centers and triazolate bridges establish new boundaries for the quasicrystal hunt.

          Abstract

          Aperiodic formations continue to focus interest in areas ranging from advanced scientific theories to practical everyday applications. Starting from diverse and tightly bonded intermetallic compounds, this world showed an important breakthrough toward the so-called soft systems of meso/macroscale: liquid crystals, thin films, polymers, proteins, etc. This work opens a route for making bulk quasicrystals (QC) in an unprecedented but very common area, with molecular ligands. Since these systems are, to a large extent, transparent, they extend the possible areas of QC application to previously unreachable corners, e.g., photonics. We combined efficient bridging ligands with uranyl pentagonal bonding centers and, unexpectedly, brought the unique attributes of f-element coordination chemistry to an interdisciplinary area of aperiodic formations. Taking advantage of the planar coordination of uranyl ions, we were able to direct the structure expansion solely in two directions with a characteristic snub square tiling, a predicted but previously unobtainable dodecagonal approximant.

          Related collections

          Most cited references29

          • Record: found
          • Abstract: found
          • Article: not found

          Quasicrystalline order in self-assembled binary nanoparticle superlattices.

          The discovery of quasicrystals in 1984 changed our view of ordered solids as periodic structures and introduced new long-range-ordered phases lacking any translational symmetry. Quasicrystals permit symmetry operations forbidden in classical crystallography, for example five-, eight-, ten- and 12-fold rotations, yet have sharp diffraction peaks. Intermetallic compounds have been observed to form both metastable and energetically stabilized quasicrystals; quasicrystalline order has also been reported for the tantalum telluride phase with an approximate Ta(1.6)Te composition. Later, quasicrystals were discovered in soft matter, namely supramolecular structures of organic dendrimers and tri-block copolymers, and micrometre-sized colloidal spheres have been arranged into quasicrystalline arrays by using intense laser beams that create quasi-periodic optical standing-wave patterns. Here we show that colloidal inorganic nanoparticles can self-assemble into binary aperiodic superlattices. We observe formation of assemblies with dodecagonal quasicrystalline order in different binary nanoparticle systems: 13.4-nm Fe(2)O(3) and 5-nm Au nanocrystals, 12.6-nm Fe(3)O(4) and 4.7-nm Au nanocrystals, and 9-nm PbS and 3-nm Pd nanocrystals. Such compositional flexibility indicates that the formation of quasicrystalline nanoparticle assemblies does not require a unique combination of interparticle interactions, but is a general sphere-packing phenomenon governed by the entropy and simple interparticle potentials. We also find that dodecagonal quasicrystalline superlattices can form low-defect interfaces with ordinary crystalline binary superlattices, using fragments of (3(3).4(2)) Archimedean tiling as the 'wetting layer' between the periodic and aperiodic phases.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Supramolecular dendritic liquid quasicrystals.

            A large number of synthetic and natural compounds self-organize into bulk phases exhibiting periodicities on the 10(-8)-10(-6) metre scale as a consequence of their molecular shape, degree of amphiphilic character and, often, the presence of additional non-covalent interactions. Such phases are found in lyotropic systems (for example, lipid-water, soap-water), in a range of block copolymers and in thermotropic (solvent-free) liquid crystals. The resulting periodicity can be one-dimensional (lamellar phases), two-dimensional (columnar phases) or three dimensional ('micellar' or 'bicontinuous' phases). All such two- and three-dimensional structures identified to date obey the rules of crystallography and their symmetry can be described, respectively, by one of the 17 plane groups or 230 space groups. The 'micellar' phases have crystallographic counterparts in transition-metal alloys, where just one metal atom is equivalent to a 10(3)-10(4)-atom micelle. However, some metal alloys are known to defy the rules of crystallography and form so-called quasicrystals, which have rotational symmetry other than the allowed two-, three-, four- or six-fold symmetry. Here we show that such quasiperiodic structures can also exist in the scaled-up micellar phases, representing a new mode of organization in soft matter.
              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              New ordered state between crystalline and amorphous in Ni-Cr particles

                Bookmark

                Author and article information

                Journal
                Sci Adv
                Sci Adv
                SciAdv
                advances
                Science Advances
                American Association for the Advancement of Science
                2375-2548
                January 2020
                31 January 2020
                : 6
                : 5
                : eaay7685
                Affiliations
                [1 ]Department of Materials and Environmental Chemistry, Stockholm University, Svante Arrhenius väg 16C, Stockholm 10691, Sweden.
                [2 ]Department of Chemistry, University of Missouri, 601 S. College Avenue, Columbia, MO 65211, USA.
                [3 ]College of Arts and Sciences, The University of Alabama, Tuscaloosa, AL 35487, USA.
                Author notes
                [†]

                These authors contributed equally to this work.

                Author information
                http://orcid.org/0000-0003-0763-1457
                http://orcid.org/0000-0001-6755-4495
                http://orcid.org/0000-0002-2800-1684
                http://orcid.org/0000-0001-9843-7494
                Article
                aay7685
                10.1126/sciadv.aay7685
                6994202
                32064353
                12975047-99a9-430d-ada2-563e712b0d0e
                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
                : 16 July 2019
                : 22 November 2019
                Funding
                Funded by: Swedish Research Council (Vetenskapsrådet, VR);
                Award ID: VR-grant 2016-05405
                Funded by: Göran Gustafsson prize by the Royal Swedish Academy of Science;
                Funded by: Tage Erlander professorship;
                Award ID: VR grant 2018-00233
                Funded by: U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, Heavy Elements program;
                Award ID: DE-SC0019220
                Categories
                Research Article
                Research Articles
                SciAdv r-articles
                Materials Science
                Custom metadata
                Fritzie Benzon

                Comments

                Comment on this article