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Ultrahigh Mass Activity for the Hydrogen Evolution Reaction by Anchoring Platinum Single Atoms on Active {100} Facets of TiC via Cation Defect Engineering

机译:Ultrahigh Mass Activity for the Hydrogen Evolution Reaction by Anchoring Platinum Single Atoms on Active {100} Facets of TiC via Cation Defect Engineering

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摘要

Improving the platinum (Pt) mass activity for low-cost electrochemicalhydrogen evolution is an important and arduous task. Here, a selectiveetching-reducing fluidized bed reactor technique is reported to create Tivacancies and firmly anchor single Pt atoms on the active {100} facets oftitanium carbide (TiC) to increase the Pt utilization efficiency and improvecatalytic activity significantly by a synergistic effect between Ti vacancies andPt atoms. The generated Ti vacancies are negatively charged and stabilizePt atoms by forming covalent PtC bonds, showing excellent long-termdurability. Pt single atoms (ultralow load of 1.2 μg cm~(?2)) on the defective TiC{100} show remarkable activity (24.9 mV at 10 mA cm~(?2)) and a mass activity(49.69 A mg~(?1)) ≈190 times that of the state-of-the-art Pt-C catalyst and nearlydouble the previously reported best values. The developed cation defect engineeringexhibits excellent potential for fabricating next-generation advancedsingle-atom catalysts for large-scale hydrogen evolution at a low cost.

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