4.8 Article

Influence of Surface Oxygen Vacancies and Ruthenium Valence State on the Catalysis of Pyrochlore Oxides

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 12, Issue 4, Pages 4520-4530

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.9b19352

Keywords

pyrochlore oxides; oxygen evolution reaction; oxygen vacancies; Ru valence state; A site doping

Funding

  1. National Key Research and Development Program of China [2017YFB0102701]
  2. Shenzhen Peacock Plan [KQTD2016022620054656]
  3. Development and Reform Commission of Shenzhen Municipality [1106]
  4. Guangdong Innovative and Entrepreneurial Research Team Program [2016ZT06N500]
  5. Guangdong Provincial Key Laboratory of Energy Materials for Electric Power [2018B030322001]
  6. Shenzhen Key Laboratory project [ZDSYS201603311013489]

Ask authors/readers for more resources

Proton exchange membrane (PEM) water electrolysis is a promising energy storage solution by electrochemically splitting water into hydrogen fuel and oxygen. However, the sluggish kinetics, high operating potential, and corrosive acidic environment during the oxygen evolution reaction (OER) require the use of scarce and costly Ir-based oxides, tremendously hampering its large-scale commercialization: Hence, developing active and stable anode catalysts with reduced precious-metal usage is desperately essential. For the first time, we report a group of Y2-xBaxRu2O7 pyrochlore oxides and employ them in acid OER and PEM electrolyzers. We reveal the mechanism for the promoted OER performance of Ba-doped Y2Ru2O7 in which partially replacing Y3+ by Ba2+ in Y2Ru2O7 greatly facilitates the hole-doping effect, which generates massive oxygen vacancy and multivalence of Ru5+/Ru4+, thus boosting the OER performance of Y2-xBaxRu2O7. This work provides an effective method and paradigm for improving the electrocatalytic property of pyrochlore oxides.

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