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Formation of PdFe alloy clusters in zeolite Y

Journal Article · · Journal of Physical Chemistry; (United States)
DOI:https://doi.org/10.1021/j100146a028· OSTI ID:5526022
; ;  [1]; ;  [2]
  1. Northwestern Univ., Evanston, IL (United States)
  2. Univ. of Wisconsin, Madison, WI (United States)

Reduction of ion-exchanged PdFe/NaY with H[sub 2] at 773 K results in the formation of Fe[sup 2+] ions and PdFe alloy clusters; no Fe[sup 0] is formed by reducing Fe/NaY. The extent of Pd-enhanced reduction of Fe[sup 2+] to Fe[sup 0] decreases with increasing proton concentration in the zeolite. Data obtained by Moessbauer spectroscopy, ferromagnetic resonance, and FTIR of adsorbed CO indicate prevalent formation of PdFe alloy clusters. Temperature-programmed reduction (TPR) and desorption (TPD) show the extent of Fe reduction and the reoxidation by zeolite protons of Fe[sup 0] in bimetal particles. An average composition of Pd[sub 16]Fe and Pd[sub 10]Fe[sub 3] was found for the reduced clusters in PdFe/NaHY and neutralized PdFe/NaY, respectively. No [alpha]-Pd hydride is formed with PdFe[sub x] under conditions where this hydride is prevalent for unalloyed Pd clusters. The propensity to form Pd hydride is restored by oxidative leaching of the Fe atoms from the bimetallic clusters. A strong ferromagnetic resonance signal from PdFe[sub x] particles isolated in different zeolite cages and containing only one or two Fe atoms suggests that Pd atoms surrounding an Fe atom become polarized. 71 refs., 8 figs., 4 tabs.

OSTI ID:
5526022
Journal Information:
Journal of Physical Chemistry; (United States), Journal Name: Journal of Physical Chemistry; (United States) Vol. 97:44; ISSN JPCHAX; ISSN 0022-3654
Country of Publication:
United States
Language:
English