Precise Control of Pt Particle Size for Surface Structure–Reaction Activity Relationship
Author(s) -
Reem Al-Shareef,
Moussab Harb,
Youssef Saih,
Samy OuldChikh,
Dalaver H. Anjum,
J.P. Candy,
JeanMarie Basset
Publication year - 2018
Publication title -
the journal of physical chemistry c
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.401
H-Index - 289
eISSN - 1932-7455
pISSN - 1932-7447
DOI - 10.1021/acs.jpcc.8b06346
Subject(s) - hydrogenolysis , catalysis , platinum , particle size , isomerization , chemisorption , particle (ecology) , heterogeneous catalysis , organometallic chemistry , metal , materials science , adsorption , hydrogen , transition metal , chemical engineering , chemical physics , inorganic chemistry , nanotechnology , chemistry , organic chemistry , metallurgy , oceanography , engineering , geology
The use of surface organometallic chemistry on metal (SOMC/M) allows the controlled and stepwise variation of the platinum particle size in Pt/SiO2 catalysts. This SOMC/M method is possible thanks to the better affinity of most organometallic compounds with the surface of zerovalent metal particles covered with hydrogen than their support. In this paper, Pt(acac)2 was used as the organometallic precursor, silica as a support, and then hydrogen to reduce the adsorbed organometallic layer on top of the starting Pt nanoparticle. We partially succeeded in adding one Pt layer with a stepwise particle size increase of around 0.6 nm when going from the first (1G) to the second (2G) refilling run, as obtained from TEM and H2 chemisorption analysis and then confirmed by DFT calculations. The metal loading could be kept at a very low level (<1–2 wt %), which is relevant for catalytic applications. The particle size distribution remained relatively narrow even after two refilling runs, allowing more precise relation...
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