Perfluorinated cobalt phthalocyanine effectively catalyzes water electrooxidation
Type
ArticleKAUST Department
Catalysis for Energy Conversion (CatEC)Chemical Science Program
KAUST Catalysis Center (KCC)
Physical Science and Engineering (PSE) Division
Date
2014-12-08Online Publication Date
2014-12-08Print Publication Date
2015-01Permanent link to this record
http://hdl.handle.net/10754/563914
Metadata
Show full item recordAbstract
Efficient electrocatalysis of water oxidation under mild conditions at neutral pH was achieved by a fluorinated cobalt phthalocyanine immobilized on fluorine-doped tin oxide (FTO) surfaces with an onset potential at 1.7 V vs. RHE. Spectroscopic, electrochemical, and inhibition studies indicate that phthalocyanine molecular species are the operational active sites. Neither free cobalt ions nor heterogeneous cobalt oxide particles or films were observed. During long-term controlled-potential electrolysis at 2 V vs. RHE (phosphate buffer, pH 7), electrocatalytic water oxidation was sustained for at least 8 h (TON ≈ 1.0 × 105), producing about 4 μmol O2 h-1 cm-2 with a turnover frequency (TOF) of about 3.6 s-1 and no measurable catalyst degradation.Citation
Morlanés, N., Joya, K. S., Takanabe, K., & Rodionov, V. (2014). Perfluorinated Cobalt Phthalocyanine Effectively Catalyzes Water Electrooxidation. European Journal of Inorganic Chemistry, 2015(1), 49–52. doi:10.1002/ejic.201403015Sponsors
Funding from King Abdullah University of Science and Technology Office of Competitive Research (KAUST OCRF) (award project "Design and Engineering of Photocatalytic Material Structures for Solar Hydrogen") is acknowledged with thanks.Publisher
Wileyae974a485f413a2113503eed53cd6c53
10.1002/ejic.201403015