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Journal article

Trends in Activity and Dissolution on RuO2 under Oxygen Evolution Conditions: Particles versus Well-Defined Extended Surfaces

From

Department of Physics, Technical University of Denmark1

Surface Physics and Catalysis, Department of Physics, Technical University of Denmark2

Massachusetts Institute of Technology3

University of Copenhagen4

Rutile RuO2 catalysts are the most active pure metal oxides for oxygen evolution; however, they are also unstable toward dissolution. Herein, we study the catalytic activity and stability of oriented thin films of RuO2 with (111), (101), and (001) orientations, in comparison to a (110) single crystal and commercial nanoparticles.

These surfaces were all tested in aqueous solutions of 0.05 M H2SO4. The initial catalyst activity ranked as follows: (001) > (101) > (111) ≈ (110). We complemented our activity data with inductively coupled plasma mass spectroscopy, to measure Ru dissolution products occurring in parallel to oxygen evolution.

In contrast to earlier reports, we find that, under our experimental conditions, there is no correlation between the activity and stability.

Language: English
Publisher: American Chemical Society
Year: 2018
Pages: 2045-2051
ISSN: 23808195
Types: Journal article
DOI: 10.1021/acsenergylett.8b01178
ORCIDs: Roy, Claudie , Chorkendorff, Ib , Stephens, Ifan E. L. , 0000-0002-6655-3105 , 0000-0002-3431-8290 , 0000-0001-8714-2121 and 0000-0001-7749-6567

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