4.7 Article

Tailoring of Pt Island RuO2/C Catalysts by Galvanic Replacement to Achieve Superior Hydrogen Oxidation Reaction and CO Poisoning Resistance

期刊

ACS APPLIED ENERGY MATERIALS
卷 4, 期 8, 页码 8098-8107

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsaem.1c01397

关键词

hydrogen oxidation reaction; CO tolerance; electronic effect; bifunctional effect; platinum nanoparticle; ruthenium oxide

资金

  1. National Research Foundation of Korea (NRF) - Korea government [2018M1A2A2061975, 2021M3H4A1A02042948]
  2. New & Renewable Energy Core Technology Program of KETEP [20203020030010]
  3. KIST Institutional Program [2E31002]
  4. National Research Foundation of Korea [2021M3H4A1A02042948] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

Pure hydrogen is necessary for the commercialization of fuel cells, as carbon monoxide (CO) present in hydrogen can directly affect fuel cell performance. The Pt island RuO2/C (PiR/C) catalyst shows excellent CO management capabilities and high hydrogen oxidation reaction activity, confirmed through various electrochemical analyses.
For the commercialization of fuel cells, it is necessary to use pure hydrogen. This is because carbon monoxide (CO) present in hydrogen generated by the reformation of hydrocarbon-based fuels directly affects the fuel cell performance when Pt is used. To improve CO oxidation reactions on the Pt surface, various methods have been reported such as tuning the electronic structure of Pt to weaken the Pt-CO bond (electronic effect) and increasing the amount of the supplied oxygen species (bifunctional effect). Herein, we synthesized a Pt island RuO2/C (PiR/C) catalyst, in which Pt nanoparticles were placed like islands on RuO2 using the galvanic replacement method. PiR/C showed excellent hydrogen oxidation reaction activity despite its low Pt content. The analysis of the electronic structure of Pt confirmed that PiR/C prevents CO poisoning. Additionally, electrochemical analyses including CO stripping and CO bulk oxidation were performed. By these analyses, it is confirmed that CO was first removed at the high CO coverage on the PiR/C surface by the Eley-Rideal mechanism and further CO oxidation reactions were promoted by the Langmuir-Hinshelwood mechanism. Finally, superior CO management under the actual operating conditions of PiR/C was verified by single-cell analysis.

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