Spectroscopic and computational study demonstrates enhanced catalytic carbon monoxide oxidation on two-dimensional platinum diselenide, highlighting the utility of dense atomic transition metal sites.
A key challenge in heterogeneous catalysis is to design atomically dispersed catalysts with high surface density, while simultaneously preventing agglomeration and promoting electronic metal-support interaction. Transition metal dichalcogenides (TMDs), such as platinum diselenide (PtSe2), offer a promising solution due to their unique structural and electronic properties. This study proposes a catalyst design that utilizes atomically dispersed transition metal species within the topmost layer of TMD as catalytic reaction sites. The substantial presence of surface-exposed Pt species on PtSe2 and their role as catalytic reaction sites are elucidated using operando ambient-pressure X-ray photoelectron spectroscopy. Moreover, significantly high O2 coverage on PtSe2, achieved by mitigating the exclusive adsorption of carbon monoxide (CO), leads to enhanced CO oxidation performance. The characteristic d-band structure and resulting high O2 coverage of PtSe2 are further confirmed with density functional theory calculations. Overall, this study highlights the potential of densely distributed atomic transition metal on TMDs, which allows electronic metal-chalcogen interactions and diverse reaction mechanisms. A major challenge in heterogeneous catalysis is creating atomically dispersed catalysts with high surface density that resist agglomeration and enhance metal-support interactions. Here, the authors propose a design using atomically dispersed transition metal species in the top layer of transition metal dichalcogenides as active sites.
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Han et al. (2025) studied this question.
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