Cooperative effects in the oxidation of CO by palladium oxide cations

Abstract

Cooperative reactivity plays an important role in the oxidation of CO to CO2 by palladium oxide cations and offers insight into factors which influence catalysis. Comprehensive studies including guided-ion-beam mass spectrometry and theoretical investigations reveal the reaction products and profiles of PdO2+ and PdO3+ with CO through oxygen radical centers and dioxygen complexes bound to the Pd atom. O radical centers are more reactive than the dioxygen complexes, and experimental evidence of both direct and cooperative CO oxidation with the adsorption of two CO molecules are observed. The binding of multiple electron withdrawing CO molecules is found to increase the barrier heights for reactivity due to decreased binding of the secondary CO molecule, however, reactivity is enhanced by the increase in kinetic energy available to hurdle the barrier. We examine the effect of oxygen sites, cooperative ligands, and spin including two-state reactivity.

Document Details

Document Type
Pub Defense Publication
Publication Date
Dec 19, 2011
Source ID
10.1063/1.3669428

Entities

People

  • A. W. Castleman Jr.
  • Arthur C Reber
  • Christopher L. Harmon
  • Eric C. Tyo
  • Shiv N Khanna

Organizations

  • Air Force Office of Scientific Research
  • Pennsylvania State University
  • Virginia Commonwealth University

Tags

Fields of Study

  • Chemistry

Readers

  • Analytical Chemistry
  • Polymer Science and Technology
  • Quantum spin resonance or Electron Paramagnetic Resonance spectroscopy.

Technology Areas

  • Microelectronics