Selective growth of Al2O3 on size-selected platinum clusters by atomic layer deposition

被引:12
作者
Gorey, Timothy J. [1 ]
Dai, Yang [1 ]
Anderson, Scott L. [1 ]
Lee, Sungsik [2 ]
Lee, Sungwon [2 ]
Siefert, Soenke [2 ]
Winans, Randall E. [2 ]
机构
[1] Univ Utah, Dept Chem, 315 S 1400 E, Salt Lake City, UT 84112 USA
[2] Argonne Natl Lab, Xray Sci Div, 9700 South Cass Ave, Argonne, IL 60439 USA
关键词
QUARTZ-CRYSTAL MICROBALANCE; ELECTRON-IMPACT IONIZATION; THIN-FILM GROWTH; THERMAL-STABILITY; METAL-CLUSTERS; CROSS-SECTIONS; ALUMINUM-OXIDE; CATALYSTS; WATER; TRIMETHYLALUMINUM;
D O I
10.1016/j.susc.2019.121485
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In heterogeneous catalysis, atomic layer deposition (ALD) has been developed as a tool to stabilize and reduce carbon deposition on supported nanoparticles. Here, we discuss use of high vacuum ALD to deposit alumina films on size-selected, sub-nanometer Pt/SiO2 model catalysts. Mass-selected Pt-24 clusters were deposited on oxidized Si(100), to form model Pt-24/SiO2 catalysts with particles shown to be just under 1 nm, with multilayer three dimensional structure. Alternating exposures to trimethyl-aluminum and water vapor in an ultra-high vacuum chamber were used to grow alumina on the samples without exposing them to air. The samples were probed in situ using X-ray photoelectron spectroscopy (XPS), low-energy ion scattering spectroscopy (ISS), and CO temperature-programmed desorption (TPD). Additional samples were prepared for ex situ experiments using grazing incidence small angle x-ray scattering spectroscopy (GISAXS). Alumina growth is found to initiate at least 60 times more efficiently at the Pt-24 cluster sites, compared to bare SiO2/Si, with a single ALD cycle depositing a full alumina layer on top of the clusters, with substantial additional alumina growth initiating on SiO2 sites surrounding the clusters. As a result, the clusters were completely passivated, with no exposed Pt binding sites.
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页数:10
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