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Transformation of Bulk Pd to Pd Cations in Small-Pore CHA Zeolites Facilitated by NO
Author(s) -
Shunsaku Yasumura,
Hajime Ide,
Taihei Ueda,
Yuan Jing,
Chong Liu,
Kenichi Kon,
Takashi Toyao,
Zen Maeno,
Kenichi Shimizu
Publication year - 2021
Publication title -
jacs au
Language(s) - English
Resource type - Journals
ISSN - 2691-3704
DOI - 10.1021/jacsau.0c00112
Subject(s) - x ray absorption spectroscopy , dispersion (optics) , diffuse reflectance infrared fourier transform , density functional theory , metal , zeolite , spectroscopy , chemistry , palladium , adsorption , catalysis , atom (system on chip) , fourier transform infrared spectroscopy , absorption (acoustics) , absorption spectroscopy , inorganic chemistry , materials science , chemical engineering , computational chemistry , organic chemistry , physics , photocatalysis , quantum mechanics , computer science , optics , composite material , embedded system , engineering
Atomic dispersion of metal species has attracted attention as a unique phenomenon that affects adsorption properties and catalytic activities and that can be used to design so-called single atom materials. In this work, we describe atomic dispersion of bulk Pd into small pores of CHA zeolites. Under 4% NO flow at 600 °C, bulk Pd metal on the outside of CHA zeolites effectively disperses, affording Pd 2+ cations on Al sites with concomitant formation of N 2 O, as revealed by microscopic and spectroscopic characterizations combined with mass spectroscopy. In the present method, even commercially available submicrosized Pd black can be used as a Pd source, and importantly, 4.1 wt % of atomic Pd 2+ cations, which is the highest loading amount reported so far, can be introduced into CHA zeolites. The structural evolution of bulk Pd metal is also investigated by in situ X-ray absorption spectroscopy (XAS) and diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS), as well as ab initio thermodynamic analysis using density functional theory (DFT) calculations.

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