Excellent self-assembly properties of Iron Phthalocyanines on alumina for locally ordered single-atom catalysts
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11320%2F25%3A10510158" target="_blank" >RIV/00216208:11320/25:10510158 - isvavai.cz</a>
Výsledek na webu
<a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=aldvgXDW~J" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=aldvgXDW~J</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.physo.2025.100259" target="_blank" >10.1016/j.physo.2025.100259</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Excellent self-assembly properties of Iron Phthalocyanines on alumina for locally ordered single-atom catalysts
Popis výsledku v původním jazyce
In a biomimetic approach, metal Phthalocyanines (Pcs) can be considered to efficiently model single atom catalysts (SACs), hosting catalytically active single metal atoms in their macrocyclic cages. An ordered 2D array of SACs can thus be obtained when metal Pcs are assembled in a regular framework. In this work we consider in particular Iron Pcs (FePcs) on an ultra-thin alumina film grown on the Ni3Al(111) surface. Intrinsic modulations in the potential energy surface related with the oxide film structure drive the self-assembly of FePc molecules into a regular array, with molecular vacancies forming a hexagonal Bravais lattice with the same periodicity of the substrate, i.e. with a lattice parameter of about 4 nm. The symmetry of the supramolecular structure is dictated by the template rather than by the C4v symmetry of the individual molecules, thus indicating prevalence of molecule-substrate interactions with respect to intermolecular forces. The same hexagonal periodicity extends also to the multilayer, which starts forming already before completion of the first, interfacial monolayer. The latter exhibits a local definite chirality, also propagating to the multilayer in a determined stacking sequence.
Název v anglickém jazyce
Excellent self-assembly properties of Iron Phthalocyanines on alumina for locally ordered single-atom catalysts
Popis výsledku anglicky
In a biomimetic approach, metal Phthalocyanines (Pcs) can be considered to efficiently model single atom catalysts (SACs), hosting catalytically active single metal atoms in their macrocyclic cages. An ordered 2D array of SACs can thus be obtained when metal Pcs are assembled in a regular framework. In this work we consider in particular Iron Pcs (FePcs) on an ultra-thin alumina film grown on the Ni3Al(111) surface. Intrinsic modulations in the potential energy surface related with the oxide film structure drive the self-assembly of FePc molecules into a regular array, with molecular vacancies forming a hexagonal Bravais lattice with the same periodicity of the substrate, i.e. with a lattice parameter of about 4 nm. The symmetry of the supramolecular structure is dictated by the template rather than by the C4v symmetry of the individual molecules, thus indicating prevalence of molecule-substrate interactions with respect to intermolecular forces. The same hexagonal periodicity extends also to the multilayer, which starts forming already before completion of the first, interfacial monolayer. The latter exhibits a local definite chirality, also propagating to the multilayer in a determined stacking sequence.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10305 - Fluids and plasma physics (including surface physics)
Návaznosti výsledku
Projekt
—
Návaznosti
—
Ostatní
Rok uplatnění
2025
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Physics Open
ISSN
2666-0326
e-ISSN
2666-0326
Svazek periodika
23
Číslo periodika v rámci svazku
May
Stát vydavatele periodika
NL - Nizozemsko
Počet stran výsledku
8
Strana od-do
100259
Kód UT WoS článku
001435235500001
EID výsledku v databázi Scopus
2-s2.0-85218872942