Tuning Catalytic Performance through a Single or Sequential Post Synthesis Reaction(s) in a Gas Phase

Catalytic performance of a bimetallic catalyst is determined by geometric structure and electronic state of the surface or even the near-surface region of the catalyst. Here we report that single and sequential postsynthesis reactions of an as-synthesized bimetallic nanoparticle catalyst in one or more gas phases can tailor surface chemistry and structure of the catalyst in a gas phase, by which catalytic performance of this bimetallic catalyst can be tuned. Pt Cu regular nanocube (Pt-Cu ANC) and concave nanocube (Pt-Cu CNC) are chosen as models of bimetallic catalysts. Surface chemistry and catalyst structure under different reaction conditions and during catalysis were explored in gas phase of one or two reactants with ambient-pressure X-ray photoelectron spectroscopy (AP-XPS) and extended X-ray absorption fine structure (EXAFS) spectroscopy. The newly formed surface structures of Pt Cu ANC and Pt Cu CNC catalysts strongly depend on the reactive gas(es) used in the postsynthesis reaction(s). A reaction of Pt-Cu RNC-as synthesized with H-2 at 200 degrees C generates a near-surface alloy consisting of a Pt skin layer, a Cu-rich subsurface, and a Pt-rich deep layer. This near-surface alloy of Pt Cu RNC-as synthesized-H-2 exhibits a much higher catalytic activity in CO oxidation in terms of a low activation barrier of 39 +/- 4 kJ/mol in contrast to 128 +/- 7 kJ/mol of Pt-Cu ANC-as synthesized. Here the significant decrease of activation barrier demonstrates a method to tune catalytic performances of as-synthesized bimetallic catalysts. A further reaction of Pt Cu ANC-as synthesized-H-2 with CO forms a Pt-Cu alloy surface, which exhibits quite different catalytic performance in CO oxidation. It suggests the capability of generating a different surface by using another gas. The capability of tuning surface chemistry and structure of bimetallic catalysts was also demonstrated in restructuring of Pt-Cu CNC-as synthesized.