High Throughput Study of Catalytic Surface Chemistry Over CuxAuyPd1-X-Y Alloys

Thursday, October 20, 2011: 3:55 PM
200 H (Minneapolis Convention Center)
A.J. Gellman1, James B. Miller1, Petro Kondratyuk2 and Deepika Priyadarshini1, (1)Chemical Engineering, Carnegie Mellon University, Pittsburgh, PA, (2)Dept. of Chemical Engineering, Carnegie Mellon University, Pittsburgh, PA

A suite of tools has been developed and is now being applied for the high throughput study of catalytic surface chemistry on composition spread alloy films (CSAFs) and on surface structure spread single crystals (S4Cs).  

A fairly simple offset filament tools is being used for deposition of PdxCuyAu1-x-y CSAFs.  These alloys have been chosen for study because of their use as dense metal membranes for hydrogen separation and purification from coal gas.  The PdxCuyAu1-x-y CSAFs are being used as libraries for the study of surface segregation in both binary and ternary alloys.  Segregation impacts the ability of these PdxCuyAu1-x-y alloys to dissociatively adsorb hydrogen, the first step in hydrogen transport through their bulk.  X-ray photoemission spectroscopy (XPS) and low energy ion scattering (LEIS) are being used to determine the near surface and the topmost surface compositions as functions of the bulk film composition.  Surface energetics favors the segregation of Cu and Au to the alloy surfaces.  In parallel with these efforts, a multichannel microreactor has been developed for high throughput measurements of catalytic surface chemistry.  It is being used to study to composition dependence of the kinetics of H2-D2 exchange on the PdxCuyAu1-x-y alloys.


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See more of this Session: Fundamentals of Surface Reactivity I
See more of this Group/Topical: Catalysis and Reaction Engineering Division