From AuPd Nanoparticle Alloys towards Core-Shell Motifs with Enhanced Alcohol Oxidation Activity

Author(s)

Silva, Tiago A. G. ; Teixeira-Neto, Erico ; Borges, Lais R. ; Neves-Garcia, Tomaz ; Braga, Adriano H. H. ; Rossi, Liane M. M.

• Document type: Journal article
• Source: CHEMCATCHEM; v. 15, n. 11, p. 9-pg., 2023-05-15.

Abstract

The best activity of bimetallic AuPd nanoparticles for alcohol oxidation reaction is usually achieved by adjusting the Au/Pd molar ratio. Herein, alloy AuPd nanoparticles of similar to 2.5-3.5 nm, ranging from Au-rich to Pd-rich compositions, were synthesized through a sol-immobilization method. A calcination step under air conditions caused an increase in size up to 5.5 nm, but also driven the segregation of Pd to the surface, which generated an Au rich core with Pd on the shell. At high Pd content, the shell structure is formed by PdO. The catalytic activity of Pd-rich samples (1 : 1, 1 : 2 and 1 : 4 Au : Pd) for benzyl alcohol oxidation increased similar to 4-fold after calcination. Upon reduction with H-2, surface PdO motifs are reduced to Pd that did not dissolve back into the AuPd alloy core, maintaining the metallic Pd shell. The catalytic activity decreased. Therefore, restructuring alloyed AuPd nanoparticles into core-shell like structures with PdO in the shell is beneficial to the catalytic activity, but reduction of PdO layer was detrimental. These results provide new insights on the optimization of AuPd catalysts, considering not only the Au/Pd molar ratio, but also the importance of PdO, which was not anticipated in the previous literature. (AU)

• FAPESP's process: 18/26253-6 - COOPERATIVE CATALYSIS: AN ALTERNATIVE FOR THE DEVELOPMENT OF GOLD AND EARTH-ABUNDANT TRANSITION METAL CATALYSTS
• Grantee: Liane Marcia Rossi
• Support Opportunities: Regular Research Grants
• FAPESP's process: 17/24347-0 - Catalytic activation of CO2 via frustrated Lewis pairs for carbonylation of olefins
• Grantee: Tomaz Neves Garcia
• Support Opportunities: Scholarships in Brazil - Doctorate