C
Curtis P. Berlinguette
Researcher at University of British Columbia
Publications - 204
Citations - 13868
Curtis P. Berlinguette is an academic researcher from University of British Columbia. The author has contributed to research in topics: Catalysis & Electrolysis. The author has an hindex of 51, co-authored 173 publications receiving 10157 citations. Previous affiliations of Curtis P. Berlinguette include Foundation University, Islamabad & Canadian Institute for Advanced Research.
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Journal ArticleDOI
Photochemical Route for Accessing Amorphous Metal Oxide Materials for Water Oxidation Catalysis
Rodney D. L. Smith,Mathieu S. Prévot,Randal D. Fagan,Zhipan Zhang,Pavel A. Sedach,Man Kit Jack Siu,Simon Trudel,Curtis P. Berlinguette +7 more
TL;DR: It is demonstrated that a low-temperature process, photochemical metal-organic deposition, can produce amorphous (mixed) metal oxide films for OER catalysis, which contain a homogeneous distribution of metals with compositions that can be accurately controlled.
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Water Oxidation Catalysis: Electrocatalytic Response to Metal Stoichiometry in Amorphous Metal Oxide Films Containing Iron, Cobalt, and Nickel
TL;DR: This work represents the first mechanistic study of amorphous phases of binary and ternary metal oxides for use as water oxidation catalysts, and provides the foundation for the broad exploration of other mixed-metal oxide combinations.
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Electrolytic CO2 Reduction in a Flow Cell.
TL;DR: This Account examines some of the systems-level strategies that have been applied in an effort to tailor flow reactor components to improve electrocatalytic reduction and highlights the challenges associated with precise and controlled water management in gas phase CO2 electrolyzers.
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Molecular electrocatalysts can mediate fast, selective CO 2 reduction in a flow cell.
Shaoxuan Ren,Dorian Joulié,Dorian Joulié,Danielle A. Salvatore,Kristian Torbensen,Min Wang,Marc Robert,Curtis P. Berlinguette +7 more
TL;DR: It is shown that cobalt phthalocyanine, a widely available molecular catalyst, can mediate CO2 to CO formation in a zero-gap membrane flow reactor with selectivities > 95% at 150 mA/cm2, and that design of the surrounding electrochemical cell can substantially boost both features.
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Electrochemical evidence for catalytic water oxidation mediated by a high-valent cobalt complex.
TL;DR: The pH-dependent electrochemical behavior for a Co(II) complex, [Co(Py5)(OH(2))](ClO(4))(2) (1; Py5 = 2,6-(bis(bis-2-pyridyl)methoxymethane)pyridine), indicates consecutive (proton-coupled) oxidation steps furnish a Co (IV) species that catalyzes the oxidation of water in basic media.