Functionalization of Open Two-Dimensional Metal?Organic Templates through the Selective Incorporation of Metal Atoms

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216305%3A26620%2F13%3APU103573" target="_blank" >RIV/00216305:26620/13:PU103573 - isvavai.cz</a>

Výsledek na webu

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DOI - Digital Object Identifier

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Jazyk výsledku

angličtina

Název v původním jazyce

Functionalization of Open Two-Dimensional Metal?Organic Templates through the Selective Incorporation of Metal Atoms

Popis výsledku v původním jazyce

Surface-confined molecular networks can serve as templates to steer the adsorption and organization of secondary ligands, metal atoms, and clusters. Here, the incorporation of Ni atoms and clusters into open two-dimensional robust metal?organic templatesself-assembled from butadiyne dibenzoic acid molecules and Fe atoms on Au(111) and Ag(100) surfaces is investigated by scanning tunneling microscopy. The metal substrate plays a crucial role in the interaction of Ni atoms with the metal?organic host networks. On Ag(100) the metal?organic template steers the growth of Ni clusters underneath the network pattern near the central butadiyne moiety. In contrast, on Au(111) Ni interacts preferentially with the benzene rings forming size-limited clusters inside the network cavities. Thereby, on both surfaces Ni clusters consisting of a few atoms with both high areal density and thermal stability up to 450 K are realized. The Ni-functionalized networks enable the coordination of additional mole

Název v anglickém jazyce

Functionalization of Open Two-Dimensional Metal?Organic Templates through the Selective Incorporation of Metal Atoms

Popis výsledku anglicky

Surface-confined molecular networks can serve as templates to steer the adsorption and organization of secondary ligands, metal atoms, and clusters. Here, the incorporation of Ni atoms and clusters into open two-dimensional robust metal?organic templatesself-assembled from butadiyne dibenzoic acid molecules and Fe atoms on Au(111) and Ag(100) surfaces is investigated by scanning tunneling microscopy. The metal substrate plays a crucial role in the interaction of Ni atoms with the metal?organic host networks. On Ag(100) the metal?organic template steers the growth of Ni clusters underneath the network pattern near the central butadiyne moiety. In contrast, on Au(111) Ni interacts preferentially with the benzene rings forming size-limited clusters inside the network cavities. Thereby, on both surfaces Ni clusters consisting of a few atoms with both high areal density and thermal stability up to 450 K are realized. The Ni-functionalized networks enable the coordination of additional mole

Druh

J_x - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

CEP obor

BM - Fyzika pevných látek a magnetismus

OECD FORD obor

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Projekt

<a href="/cs/project/ED1.1.00%2F02.0068" target="_blank" >ED1.1.00/02.0068: CEITEC - central european institute of technology</a><br>

Návaznosti

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Rok uplatnění

2013

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Journal of Physical Chemistry C (print)

ISSN

1932-7447

e-ISSN

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Svazek periodika

117

Číslo periodika v rámci svazku

17

Stát vydavatele periodika

US - Spojené státy americké

Počet stran výsledku

7

Strana od-do

8871-8877

Kód UT WoS článku

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EID výsledku v databázi Scopus

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