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Decoupling H-Release and OH – Management at Pd@TiO 2 Interfaces for Efficient Alkaline Hydrogen Oxidation Reaction

Year: 2026

Type: article

Abstract: High Resolution Image Download MS PowerPoint Slide Operando-level insight into catalyst degradation and reaction mechanisms is essential for progress in the alkaline hydrogen oxidation reaction (HOR). Herein, these aspects are investigated using a core–shell Pd@TiO 2 /C catalyst synthesized by thermal reduction followed by atomic layer deposition. The obtained catalyst exhibits high stability and delivers a mass exchange current density ( j 0,m ) of 97.5 mA mg Pd –1, more than three times that of uncoated Pd/C (27.5 mA mg Pd –1 ). Identical location transmission electron microscopy reveals a growth–detachment degradation pathway for Pd/C during accelerated durability testing, whereas the TiO 2 shell in Pd@TiO 2 /C effectively suppresses this degradation, resulting in enhanced structural stability. Operando X-ray absorption spectroscopy under device-relevant conditions demonstrates the complementary functions of the two components: hydrogen dissociates and forms PdH x on the Pd core, lowering its Fermi level and driving electron transfer from TiO 2 to Pd, while the TiO 2 shell facilitates hydrogen desorption and provides OH – adsorption sites, thereby accelerating the reaction kinetics. These findings elucidate the dual stabilizing and catalytic roles of TiO 2 and suggest a promising strategy for the design of durable and efficient alkaline HOR catalysts.

Source: ACS Catalysis

DOI: 10.1021/acscatal.5c08285