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Atomically dispersed Pd on nanostructured TiO 2 for NO removal by solar light
Author(s) -
Fujiwara Kakeru,
Pratsinis Sotiris E.
Publication year - 2017
Publication title -
aiche journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.958
H-Index - 167
eISSN - 1547-5905
pISSN - 0001-1541
DOI - 10.1002/aic.15495
Subject(s) - materials science , annealing (glass) , amorphous solid , noble metal , adsorption , single crystal , transmission electron microscopy , particle size , nanoparticle , chemical engineering , scanning electron microscope , photocatalysis , analytical chemistry (journal) , nanotechnology , metal , crystallography , catalysis , metallurgy , composite material , chemistry , biochemistry , engineering , chromatography
Reducing the particle size of noble metals on ceramic supports can maximize noble metal performance and minimize its use. Here Pd clusters onto nanostructured TiO 2 particles are prepared in one step by scalable flame aerosol technology while controlling the Pd cluster size from a few nanometers to that of single atoms. Annealing such materials at appropriate temperatures leads to solar photocatalytic NO x removal in a standard ISO reactor up to 10 times faster than that of commercial TiO 2 (P25, Evonik). Such superior performance can be attained by only 0.1 wt.% Pd loading on TiO 2 . Annealing these flame‐made powders in air up to 600 °C decreases the amorphous TiO 2 fraction and increases its crystal and particle sizes as observed by x‐ray diffraction (XRD) and N 2 adsorption. The growth of single Pd atoms to Pd clusters on TiO 2 prepared at different Pd loading and annealing conditions was investigated by scanning transmission electron microscopy and XRD. The single Pd atoms and clusters on TiO 2 are stable up to, at least, 600 °C for 2 h in air but at 800 °C they grow into PdO nanoparticles whose fraction is comparable with the nominal Pd loading. Hence, most of Pd atoms are on the TiO 2 surface where at 800 °C they diffuse and coalesce. Diffuse reflectance infrared Fourier transform spectroscopy reveals NO adsorption on single, double, three and fourfold coordinated Pd atoms depending on their synthesis and annealing conditions. The peak intensity of NO adsorption sites involving multiple Pd atoms is substantially lower in TiO 2 containing 0.1 wt.% than 1 wt.% Pd but that intensity from single Pd atoms is comparable. This indicates the dominance of isolated Pd atoms compared to clusters in Pd/TiO 2 containing 0.1 wt.% Pd that match or exceed the photocatalytic NO x removal of Pd/TiO 2 of higher Pd contents. © 2016 American Institute of Chemical Engineers AIChE J , 63: 139–146, 2017

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