Carbon Chain Length Dependence of Graphene Formation via Thermal Decomposition of Alkenes on Pt(111)

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11320%2F19%3A10405805" target="_blank" >RIV/00216208:11320/19:10405805 - isvavai.cz</a>

Výsledek na webu

<a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=BEgmdlYKeb" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=BEgmdlYKeb</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1021/acs.jpcc.8b07165" target="_blank" >10.1021/acs.jpcc.8b07165</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Carbon Chain Length Dependence of Graphene Formation via Thermal Decomposition of Alkenes on Pt(111)

Popis výsledku v původním jazyce

Graphene layers were prepared by isothermal decomposition of different unsaturated hydrocarbons on Pt(111) single crystal surface and characterized by SRPES and LEED. Four different alkenes (ethene, propene, 1pentene, 1-hexene) were used in order to elucidate the eventual role of the carbon chain length in the graphene growth kinetics. The process of dehydrogenation was followed stepwise from sample temperatures of 160 K (molecular adsorption) to over 1000 K, at which the surface carbon remains almost exclusively in the form of graphene. Reaction intermediates were identified for each alkene and the corresponding reaction rates were determined. The attachment of carbon during the thermally activated growth of graphene islands on Pt(111) and similar metals is predicted to proceed via prior formation of small clusters or chains in order to overcome a large energetic and spatial barrier which exists between a single adsorbed C atom (monomer) and the graphene layer. In accordance with this assumption the growth process is shown to depend on the size of the initial reactant molecule, with a distinct preference for Cs species.

Název v anglickém jazyce

Carbon Chain Length Dependence of Graphene Formation via Thermal Decomposition of Alkenes on Pt(111)

Popis výsledku anglicky

Graphene layers were prepared by isothermal decomposition of different unsaturated hydrocarbons on Pt(111) single crystal surface and characterized by SRPES and LEED. Four different alkenes (ethene, propene, 1pentene, 1-hexene) were used in order to elucidate the eventual role of the carbon chain length in the graphene growth kinetics. The process of dehydrogenation was followed stepwise from sample temperatures of 160 K (molecular adsorption) to over 1000 K, at which the surface carbon remains almost exclusively in the form of graphene. Reaction intermediates were identified for each alkene and the corresponding reaction rates were determined. The attachment of carbon during the thermally activated growth of graphene islands on Pt(111) and similar metals is predicted to proceed via prior formation of small clusters or chains in order to overcome a large energetic and spatial barrier which exists between a single adsorbed C atom (monomer) and the graphene layer. In accordance with this assumption the growth process is shown to depend on the size of the initial reactant molecule, with a distinct preference for Cs species.

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

Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.

Návaznosti

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>S - Specificky vyzkum na vysokych skolach<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2019

Kód důvěrnosti údajů

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

Název periodika

Journal of Physical Chemistry C

ISSN

1932-7447

e-ISSN

—

Svazek periodika

123

Číslo periodika v rámci svazku

13

Stát vydavatele periodika

US - Spojené státy americké

Počet stran výsledku

11

Strana od-do

7911-7921

Kód UT WoS článku

000463844500040

EID výsledku v databázi Scopus

2-s2.0-85053889334