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Molybdenum Doping Augments Platinum–Copper Oxygen Reduction Electrocatalyst

Yun LuoIC2MP, UMR-CNRS 7285 University of Poitiers 14 rue Michel Brunet 86022 Poitiers FranceBjörn KirchhoffInstitute of Electrochemistry Ulm University Albert Einstein-Allee 47 89081 Ulm GermanyDonato FantauzziHelmholtz-Institute Ulm (HIU) Electrochemical Energy Storage Helmholtz-Straße 16 89081 Ulm GermanyLaura CalvilloDepartment of Chemical Sciences University of Padova Via Marzolo 1 35131 Padova ItalyLuis Alberto Estudillo‐WongIC2MP, UMR-CNRS 7285 University of Poitiers 14 rue Michel Brunet 86022 Poitiers FranceGaetano GranozziDepartment of Chemical Sciences University of Padova Via Marzolo 1 35131 Padova ItalyTimo JacobHelmholtz-Institute Ulm (HIU) Electrochemical Energy Storage Helmholtz-Straße 16 89081 Ulm GermanyNicolás Alonso‐VanteIC2MP, UMR-CNRS 7285 University of Poitiers 14 rue Michel Brunet 86022 Poitiers France
2017en
ABI

Annotatsiya

Abstract Improving the efficiency of Pt‐based oxygen reduction reaction (ORR) catalysts while also reducing costs remains an important challenge in energy research. To this end, we synthesized highly stable and active carbon‐supported Mo‐doped PtCu (Mo‐PtCu/C) nanoparticles (NPs) from readily available precursors in a facile one‐pot reaction. Mo‐PtCu/C displays two‐to‐fourfold‐higher ORR half‐cell kinetics than reference PtCu/C and Pt/C materials, a trend that was confirmed in proof‐of‐concept experiments by using a H 2 /O 2 microlaminar fuel cell. This Mo‐induced activity increase mirrors observations for Mo‐PtNi/C NPs and possibly suggests an emerging trend. Electrochemical‐accelerated stability tests revealed that dealloying was greatly reduced in Mo‐PtCu/C in contrast to the binary alloys PtCu/C and PtMo/C. Supporting DFT studies suggested that the exceptional stability of Mo‐PtCu could be attributed to oxidative resistance of the Mo‐doped atoms. Furthermore, our calculations revealed that oxygen could induce segregation of Mo to the catalytic surface, at which it effected beneficial changes to the surface oxygen adsorption energetics in the context of the Sabatier principle.

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