Alkali-Metal-Intercalated Percolation Network Regulates Self-Assembled Electronic Aromatic Molecules.
aromatic molecule
charge-transfer
molecular self-assembly
percolation network
Journal
Advanced materials (Deerfield Beach, Fla.)
ISSN: 1521-4095
Titre abrégé: Adv Mater
Pays: Germany
ID NLM: 9885358
Informations de publication
Date de publication:
Mar 2019
Mar 2019
Historique:
received:
06
11
2018
revised:
13
12
2018
pubmed:
27
1
2019
medline:
27
1
2019
entrez:
26
1
2019
Statut:
ppublish
Résumé
In the continuously growing field of correlated electronic molecular crystals, there is significant interest in addressing alkali-metal-intercalated aromatic hydrocarbons, in which the possibility of high-temperature superconductivity emerges. However, searching for superconducting aromatic molecular crystals remains elusive due to their small shielding fraction volume. To exploit this potential, a design principle for percolation networks of technologically important film geometry is indispensable. Here the effect of potassium-intercalation is shown on the percolation network in self-assembled aromatic molecular crystals. It is demonstrated that one-dimensional (1D) dipole pairs, induced by dipole interaction, regulate the conductivity, as well as the electronic and optical transitions, in alkali-metal-intercalated molecular electronic crystals. A solid-solution growth methodology of aromatic molecular films with a broad range of stability is developed to uncover electronic and optical transitions of technological importance. The light-induced electron interactions enhance the charge-carrier itinerancy, leading to a switchable metal-to-insulator transition. This discovery opens a route for the development of aromatic molecular electronic solids and long-term modulation of electronic efficacy in nanotechnologically important thin films.
Identifiants
pubmed: 30680821
doi: 10.1002/adma.201807178
doi:
Types de publication
Journal Article
Langues
eng
Pagination
e1807178Subventions
Organisme : U.S. Department of Energy, Office of Basic Energy Sciences, Division of Materials Sciences and Engineering
ID : DE-SC0018631
Organisme : U.S. Army Research Office
ID : W911NF-18-2-0202
Organisme : U.S. Department of Energy, Office of Science
ID : DE-AC02-06CH11357
Organisme : National Science Foundation
ID : DMR-1455039
Informations de copyright
© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.