Effects of aqueous buffers on electrocatalytic water oxidation with an iridium oxide material electrodeposited in thin layers from an organometallic precursor
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作者:
Kushner-Lenhoff, Maxwell N.
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Yale Univ, Dept Chem, New Haven, CT 06520 USAYale Univ, Dept Chem, New Haven, CT 06520 USA
Kushner-Lenhoff, Maxwell N.
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Blakemore, James D.
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Yale Univ, Dept Chem, New Haven, CT 06520 USAYale Univ, Dept Chem, New Haven, CT 06520 USA
Blakemore, James D.
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Schley, Nathan D.
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Yale Univ, Dept Chem, New Haven, CT 06520 USAYale Univ, Dept Chem, New Haven, CT 06520 USA
Schley, Nathan D.
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]
Crabtree, Robert H.
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Yale Univ, Dept Chem, New Haven, CT 06520 USAYale Univ, Dept Chem, New Haven, CT 06520 USA
Crabtree, Robert H.
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Brudvig, Gary W.
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Yale Univ, Dept Chem, New Haven, CT 06520 USAYale Univ, Dept Chem, New Haven, CT 06520 USA
A thin layer of an amorphous, mixed-valence iridium oxide (electrodeposited from an organometallic precursor, [Cp*Ir(H2O)(3)](2+)) is a heterogeneous catalyst among the most active and stable currently available for electrochemical water oxidation. We show that buffers can improve the oxygen-evolution activity of such thin-layer catalysts near neutral pH, but that buffer identity and concentration, as well as the solution pH, remain key determinants of long-term electrocatalyst activity and stability; for example, phosphate buffer can reduce the overpotential by up to 173 mV.