Structural evolution of an intermetallic Pd–Zn catalyst selective for propane dehydrogenation. Issue 42 (20th March 2015)

• Record Type: Journal Article
• Authors: Gallagher, James R.; Childers, David J.; Zhao, Haiyan; Winans, Randall E.; Meyer, Randall J.; Miller, Jeffrey T.
• Is Part Of: Physical chemistry chemical physics. Volume 17:Issue 42(2015)
• Page Start: 28144
• Page End: 28153
• Publication Date: 2015-03-20
• Subjects: Chemistry, Physical and theoretical -- Periodicals; 541.3
• DOI: 10.1039/c5cp00222b
• Languages: English
• ISSNs: 1463-9076

Abstract

Abstract : Formation of PdZn intermetallic nanoalloys selective for propane dehydrogenation tracked using in situ synchrotron XRD. Abstract : We report the structural evolution of Pd–Zn alloys in a 3.6% Pd–12% Zn/Al2 O3 catalyst which is selective for propane dehydrogenation. High signal-to-noise, in situ synchrotron X-ray diffraction (XRD) was used quantitatively, in addition to in situ diffuse-reflectance infrared Fourier transform spectroscopy (DRIFTS) and extended X-ray absorption fine structure (EXAFS) to follow the structural changes in the catalyst as a function of reduction temperature. XRD in conjunction with DRIFTS of adsorbed CO indicated that the β1 -PdZn intermetallic alloy structure formed at reduction temperatures as low as 230 °C, likely first at the surface, but did not form extensively throughout the bulk until 500 °C which was supported by in situ EXAFS. DRIFTS results suggested there was little change in the surfaces of the nanoparticles above 325 °C. The intermetallic alloy which formed was Pd-rich at all temperatures but became less Pd-rich with increasing reduction temperature as more Zn incorporated into the structure. In addition to the β1 -PdZn alloy, a solid solution phase with face-center cubic structure (α-PdZn) was present in the catalyst, also becoming more Zn-rich with increasing reduction temperature.