Exceptional Alkaline Methanol Electrooxidation on Bi-modified Pt3M Intermetallics: Kinetic Origins and an OH Binding Energy Descriptor

Abstract

The exploration of advanced CO-free catalysts and clarifying the ambiguous kinetic origins and governing factors would undoubtedly open up opportunities to overcome the sluggish kinetics of methanol electrooxidation and promote the development of direct methanol fuel cells. Herein, we constructed a family of Bi-modified Pt3M intermetallic catalysts (Bi-Pt3M/C, M=Cr, Mn, Co, Zn, In, Ga, and Sn) that follow CO-free dominated pathway and exhibit exceptional catalytic activity. More significantly, leveraging this platform, we have identified the pivotal factor governing the reaction kinetics in CO-free pathway, namely OH binding energy (OHBE). This arises because the rate-determining step (RDS) encompasses both C-H bond activation and water dissociation, whose respective barriers can be reflected by the OHBE. Accordingly, OHBE can act as an activity descriptor. Specifically, Bi-Pt3In/C stands out from other Bi-Pt3M/C and delivers the unprecedented mass activity of 36.7 A mgPt-1 at peak potential, far exceeding state-of-the-art Pt-based catalysts reported to date. Taking Bi-Pt3In/C as a proof of concept, we clearly elucidate the origin of enhanced MOR activity by combining theoretical calculations, kinetic isotope effects, and formaldehyde electrooxidation. Moreover, there exhibits a volcano-type trend between OHBE and the activity of Bi-Pt3M/C. Beyond the discovery of ultrahigh-performance catalysts, these findings provide a detailed mechanistic picture of RDS and offer an innovative design principle for advanced catalysts.