TY - JOUR
T1 - Perfluorinated cobalt phthalocyanine effectively catalyzes water electrooxidation
AU - Morlanes, Natalia Sanchez
AU - Joya, Khurram Saleem
AU - Takanabe, Kazuhiro
AU - Rodionov, Valentin
N1 - KAUST Repository Item: Exported on 2020-10-01
Acknowledgements: 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.
PY - 2014/12/8
Y1 - 2014/12/8
N2 - 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.
AB - 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.
UR - http://hdl.handle.net/10754/563914
UR - http://doi.wiley.com/10.1002/ejic.201403015
UR - http://www.scopus.com/inward/record.url?scp=84920719166&partnerID=8YFLogxK
U2 - 10.1002/ejic.201403015
DO - 10.1002/ejic.201403015
M3 - Article
SN - 1434-1948
VL - 2015
SP - 49
EP - 52
JO - European Journal of Inorganic Chemistry
JF - European Journal of Inorganic Chemistry
IS - 1
ER -