TY - JOUR
T1 - Synthesis and stabilization of small Pt nanoparticles on TiO2 partially masked by SiO2
AU - Bo, Zhenyu
AU - Ahn, Sol
AU - Ardagh, M. Alexander
AU - Schweitzer, Neil M.
AU - Canlas, Christian P.
AU - Farha, Omar K.
AU - Notestein, Justin M.
N1 - Funding Information:
This material is based upon work supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences under Award Number DOE DE-FG02-03-ER154757. S. A. and O. K. F. acknowledge support from the Inorganometallic Catalyst Design Center, an Energy Frontier Research Center , funded by the U.S. Department of Energy, Office of Science, Basic Energy Sciences , under Award DESC0012702. This work made use of the Keck-II facility of the NUANCE Center at Northwestern University, which has received support from the Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource ( NSF NNCI-1542205 ); the MRSEC program ( NSF DMR-1121262 ) at the Materials Research Center; the International Institute for Nanotechnology (IIN); the Keck Foundation; and the State of Illinois, through the IIN.
Publisher Copyright:
© 2017 Elsevier B.V.
PY - 2018/2/5
Y1 - 2018/2/5
N2 - Controlling metal nanoparticle size and preserving metal dispersion at elevated temperature remain key challenges in designing new supported metal catalysts. Many methods have been proposed to stabilize metal nanoparticles for catalysis, but the use of specialized equipment or metal precursors can limit the application of these methods for scalable production. Here, we demonstrate a synthesis strategy to improve the dispersion and thermal stability of Pt nanoparticles on an oxide support. A thin SiO2 coat (<2 nm) was deposited on TiO2 through repeated condensation cycles of tetraethyl orthosilicate (TEOS) with or without an organic template on the surface. H2PtCl6 was deposited using wetness impregnation, and the samples were dried, calcined, and reduced. The as-synthesized Pt nanoparticles are 1–2 nm by TEM and maintain dispersion >45% by CO chemisorption even after prolonged heating at 500 °C, whereas Pt nanoparticles on unmodified TiO2 are less dispersed (∼33%) and their dispersion falls further upon prolonged heating. Ethylene hydrogenation demonstrates that the Pt nanoparticles on modified TiO2 preserve the catalytic activities of Pt on unmodified TiO2. The use of wet chemistry-based oxide modification and wetness impregnation makes this strategy a scalable and generalizable synthesis method to prepare other supported metal nanoparticles for catalysis applications.
AB - Controlling metal nanoparticle size and preserving metal dispersion at elevated temperature remain key challenges in designing new supported metal catalysts. Many methods have been proposed to stabilize metal nanoparticles for catalysis, but the use of specialized equipment or metal precursors can limit the application of these methods for scalable production. Here, we demonstrate a synthesis strategy to improve the dispersion and thermal stability of Pt nanoparticles on an oxide support. A thin SiO2 coat (<2 nm) was deposited on TiO2 through repeated condensation cycles of tetraethyl orthosilicate (TEOS) with or without an organic template on the surface. H2PtCl6 was deposited using wetness impregnation, and the samples were dried, calcined, and reduced. The as-synthesized Pt nanoparticles are 1–2 nm by TEM and maintain dispersion >45% by CO chemisorption even after prolonged heating at 500 °C, whereas Pt nanoparticles on unmodified TiO2 are less dispersed (∼33%) and their dispersion falls further upon prolonged heating. Ethylene hydrogenation demonstrates that the Pt nanoparticles on modified TiO2 preserve the catalytic activities of Pt on unmodified TiO2. The use of wet chemistry-based oxide modification and wetness impregnation makes this strategy a scalable and generalizable synthesis method to prepare other supported metal nanoparticles for catalysis applications.
KW - Dispersion
KW - Hydrogenation
KW - Sintering
KW - Sol-gel
KW - Supported Pt
KW - Wetness impregnation
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U2 - 10.1016/j.apcata.2017.11.017
DO - 10.1016/j.apcata.2017.11.017
M3 - Article
AN - SCOPUS:85039413343
SN - 0926-860X
VL - 551
SP - 122
EP - 128
JO - Applied Catalysis A: General
JF - Applied Catalysis A: General
ER -