2008
DOI: 10.1021/jp801480t
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Pt−Ba/Al2O3 NSR Catalysts at Different Ba Loading: Characterization of Morphological, Structural, and Surface Properties

Abstract: Morphological, textural, and surface properties of several Pt-Ba/Al 2 O 3 NO x storage reduction (NSR) catalysts at different Ba loading in the range 0-30 wt % were characterized by means of X-ray diffraction, highresolution transmission electron microscopy, and Fourier-tranform infrared (FT-IR) spectroscopy using CO, CO 2 , and CH 3 CN as probe molecules. Upon increasing the Ba loading, the Pt exposure progressively decreased, accounting for sintering and masking of the Pt particles by Ba, whereas the interac… Show more

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Cited by 57 publications
(75 citation statements)
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“…With all g-Al 2 O 3 -supported catalysts, the promoter oxide was highly dispersed over the support, as was indicated by the absence of any X-ray diffraction (XRD) lines besides those related to g-Al 2 O 3 . [18] Only in the case of AuSrO/ Al 2 O 3 could a crystalline SrCO 3 phase be observed. The Au particle size distribution was determined by (scanning) transmission electron microscopy (STEM; Figure 1; see also Supporting Information).…”
Section: Resultsmentioning
confidence: 99%
“…With all g-Al 2 O 3 -supported catalysts, the promoter oxide was highly dispersed over the support, as was indicated by the absence of any X-ray diffraction (XRD) lines besides those related to g-Al 2 O 3 . [18] Only in the case of AuSrO/ Al 2 O 3 could a crystalline SrCO 3 phase be observed. The Au particle size distribution was determined by (scanning) transmission electron microscopy (STEM; Figure 1; see also Supporting Information).…”
Section: Resultsmentioning
confidence: 99%
“…[17]. Experiments recently performed on freshly PtK/Al 2 O 3 catalyst [18] showed the characteristic peaks of ␥-Al 2 O 3 ; monoclinic K 2 CO 3 (JCPDS 16-820) and cubic K 2 O (JCPDS 23-493) phases were also hardly recognized.…”
Section: Catalyst Characterizationmentioning
confidence: 98%
“…Consequently, the surface species comprised a mixture of newly formed carbonates and unreleased nitrates. As the DRIFT spectra of carbonates partially overlapped with nitrates, the gradually growing bands around 1592 cm −1 and 1320 cm −1 were tentatively ascribed to newly formed carbonates [41]. The location of these carbonate species deviated somewhat from those replaced by NO x during the storage process (negative peaks at 1535 and 1322 cm −1 ).…”
mentioning
confidence: 94%