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Out‐Of‐Plane Metal Coordination for a True Solvent‐Free Building with Molecular Bricks: Dodging the Surface Ligand Effect for On‐Surface Vacuum Self‐Assembly
Author(s) -
Orbelli Biroli Alessio,
Calloni Alberto,
Bossi Alberto,
Jagadeesh Madan S.,
Albani Guglielmo,
Duò Lamberto,
Ciccacci Franco,
Goldoni Andrea,
Verdini Alberto,
Schio Luca,
Floreano Luca,
Bussetti Gianlorenzo
Publication year - 2021
Publication title -
advanced functional materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.069
H-Index - 322
eISSN - 1616-3028
pISSN - 1616-301X
DOI - 10.1002/adfm.202011008
Subject(s) - materials science , molecule , electrode , ligand (biochemistry) , decoupling (probability) , heterojunction , metal , stoichiometry , nanotechnology , chemical physics , optoelectronics , chemistry , organic chemistry , metallurgy , biochemistry , receptor , control engineering , engineering
The desirable self‐assembly (SA) of repeated 2D stacked layers requires a “holistic analysis” of three interconnected components: the electrode, the interface, and the molecular component; among them, the contact interface bears the largest burden responsibilities. Epitaxial growth (EG) of coherent 2D+ n stacked heterojunction by solvent‐free deposition holds great promise, although the feasibility has never been demonstrated given multiple drawbacks (e.g., surface‐ligand effect, SLE). Here, it is demonstrated how a coherent 2D+ n ( n = 3) layered heterorganic film is grown on an archetypal Fe metal electrode. The groundbreaking achievement is the result of the in‐vacuum integration of: i) chemical decoupling of the basal organic layer (a Zn II ‐tetraphenylporphyrine, ZnTPP) from the metal electrode, ii) 2D‐ordering of the ZnTPP commensurate to the substrate, iii) rigid, stoichiometric, and orthogonally arranged, the molecule‐to‐molecule coupling between ZnTPP and a ditopic linear bridging ligand (i.e., DPNDI) guided by SA coordination chemistry, and iv) sharp (chemical) termination of the layered film.