Kinetic and Thermodynamic Factors Influencing Palladium Nanoparticle Redispersion into Mononuclear Pd(II) Cations in Zeolite Supports

• Published in: Journal of physical chemistry. C Vol. 126; no. 19; pp. 8337 - 8353
• Main Authors: Lardinois, Trevor M., Mandal, Keka, Yadav, Vamakshi, Wijerathne, Asanka, Bolton, Brandon K., Lippie, Harrison, Li, Christina W., Paolucci, Christopher, Gounder, Rajamani
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 19.05.2022
• Subjects: C: Chemical and Catalytic Reactivity at Interfaces; Chemistry; Materials Science; Science & Technology - Other Topics
• ISSN: 1932-7447; 1932-7455
• DOI: 10.1021/acs.jpcc.2c01613

Palladium cations and nanoparticles supported on oxides and zeolites are used as catalysts and adsorbents for a wide range of chemical reactions of practical importance, with various and distinct active site requirements. Consequently, sintering and redispersion processes that interconvert site-isolated Pd cations and agglomerated nanoparticles underpin catalyst activation and deactivation phenomena, yet the influence of Pd nanoparticle size distribution and gas conditions on the thermodynamic and kinetic factors influencing such interconversion is imprecisely understood. Here, we prepare Pd nanoparticles of different particle size and distribution (normal, log–normal) supported on high-symmetry crystalline zeolites to access well-defined materials whose Pd site distributions can be quantitatively characterized by experiments and modeled accurately by theory. Ab initio thermodynamic modeling and isothermal (593–973 K) wet and dry air treatments of Pd-zeolites reveal that the widely observed deactivation in low-temperature hydrous environments reflects site interconversion thermodynamics that favor the agglomeration of isolated Pd cations into nanoparticles. Under high-temperature anhydrous conditions, experimental kinetic measurements and kinetic Monte Carlo simulations evince the preeminence of kinetic factors on Pd nanoparticle redispersion into cations, which proceeds at rates that are strongly influenced by the initial Pd particle size distribution and via a substrate diffusion-mediated Ostwald ripening process whereby Pd monomers are captured in an atom trapping process at anionic exchange sites (framework Al) in the zeolite support. These findings resolve longstanding questions regarding the roles of H2O and support interactions in Pd redispersion processes and identify strategies to enhance or suppress Pd site interconversion by modifying oxide supports and gas conditions.