1 D tungsten oxide nanostructures on a Cu(110) surface

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11320%2F18%3A10389466" target="_blank" >RIV/00216208:11320/18:10389466 - isvavai.cz</a>

Výsledek na webu

<a href="https://doi.org/10.1088/1361-648X/aae3bb" target="_blank" >https://doi.org/10.1088/1361-648X/aae3bb</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1088/1361-648X/aae3bb" target="_blank" >10.1088/1361-648X/aae3bb</a>

Jazyk výsledku

angličtina

Název v původním jazyce

1 D tungsten oxide nanostructures on a Cu(110) surface

Popis výsledku v původním jazyce

Thin epitaxial layers of tungsten oxide on metal substrates are suitable as model systems for investigation of chemical reactivity and catalytic properties. However, the ability to prepare epitaxial tungsten oxide model system in situ is quite rare. Here we present a method to prepare highly ordered tungsten oxide thin film on a Cu(1 1 0) single crystal substrate using physical vapor deposition in a reactive atmosphere of atomic oxygen. The oxygen induced reconstruction of the copper substrate gives rise to unique self-organized 1D structures of tungsten oxide parallel with the Cu[1 -10] crystallographic direction. Utilizing a combination of photoemission spectroscopy and density functional theory calculations we reveal emergent physicochemical properties related to the low-dimensionality of the system. Specifically, we observe a support mediated charge redistribution at the interface and a momentum dependent modulation of the valence-band electronic structure. The unusual character of the 1D oxide nanostructures on Cu(1 1 0) surface opens up a unique avenue for preparation of tungsten oxide-based functionalized nanostructures and provides options for further investigation of the fundamental properties of tungsten oxide.

Název v anglickém jazyce

1 D tungsten oxide nanostructures on a Cu(110) surface

Popis výsledku anglicky

Thin epitaxial layers of tungsten oxide on metal substrates are suitable as model systems for investigation of chemical reactivity and catalytic properties. However, the ability to prepare epitaxial tungsten oxide model system in situ is quite rare. Here we present a method to prepare highly ordered tungsten oxide thin film on a Cu(1 1 0) single crystal substrate using physical vapor deposition in a reactive atmosphere of atomic oxygen. The oxygen induced reconstruction of the copper substrate gives rise to unique self-organized 1D structures of tungsten oxide parallel with the Cu[1 -10] crystallographic direction. Utilizing a combination of photoemission spectroscopy and density functional theory calculations we reveal emergent physicochemical properties related to the low-dimensionality of the system. Specifically, we observe a support mediated charge redistribution at the interface and a momentum dependent modulation of the valence-band electronic structure. The unusual character of the 1D oxide nanostructures on Cu(1 1 0) surface opens up a unique avenue for preparation of tungsten oxide-based functionalized nanostructures and provides options for further investigation of the fundamental properties of tungsten oxide.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

10305 - Fluids and plasma physics (including surface physics)

Projekt

<a href="/cs/project/GA15-06759S" target="_blank" >GA15-06759S: Modelové systémy pro katalýzu na jednotlivých atomech</a><br>

Návaznosti

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

Rok uplatnění

2018

Kód důvěrnosti údajů

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

Název periodika

Journal of Physics Condensed Matter

ISSN

0953-8984

e-ISSN

—

Svazek periodika

30

Číslo periodika v rámci svazku

46

Stát vydavatele periodika

GB - Spojené království Velké Británie a Severního Irska

Počet stran výsledku

8

Strana od-do

—

Kód UT WoS článku

000448151700001

EID výsledku v databázi Scopus

2-s2.0-85055667460