Unveiling the formation mechanism of PbPd intermetallic phases in solvothermal synthesis using X-ray total scattering

• Published in: Nanoscale Vol. 15; no. 45; pp. 18481 - 18488
• Main Authors: Borup, Anders Bæk, Bertelsen, Andreas Dueholm, Kløve, Magnus, Christensen, Rasmus Stubkjær, Broge, Nils Lau Nyborg, Dippel, Ann-Christin, Jørgensen, Mads Ry Vogel, Iversen, Bo Brummerstedt
• Format: Journal Article
• Published: 23.11.2023
• ISSN: 2040-3364; 2040-3372
• DOI: 10.1039/d3nr03901c

Pd possesses attractive catalytic properties and nano-structuring is an obvious way to enhance catalytic activity. Alloying Pd with Pb has been shown to enhance the catalytic effect of alcohol oxidation. Further optimization of the catalytic effect can be accomplished by controlling the particle size and key to this is understanding the formation mechanism. By monitoring solvothermal syntheses using in situ X-ray total scattering, this study unveils the formation mechanism of Pb x Pd y intermetallic nanoparticles. The formation occurs through a multi-step mechanism. Initially, Pd nanoparticles are formed, followed by incorporation of Pb into the Pd-structure, thus forming Pb x Pd y intermetallic nanoparticles. By varying the reaction time and temperature, the incorporation of Pb can be controlled, thereby tailoring the phase outcome. Based on the in situ solvothermal syntheses, ex situ autoclave syntheses were performed, resulting in the synthesis of Pb 3 Pd 5 and Pb 9 Pd 13 with a purity above 93%. The catalytic effect of these intermetallic phases towards the hydrogen evolution reaction (HER) is assessed. It is found that Pd, Pb 3 Pd 5 , and Pb 9 Pd 13 have comparable stabilities, however, the overpotential increases with increasing amounts of Pb. The formation of Pb x Pd y intermetallic nanoparticles happens through a complex multistep mechanism as revealed by in situ PDF analysis.