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![Protein Film Infrared Electrochemistry Demonstrated for Study of H2 Oxidation by a [NiFe] Hydrogenase](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F55858.jpg&w=3840&q=50)
Protein Film Infrared Electrochemistry Demonstrated for Study of H2 Oxidation by a [NiFe] Hydrogenase
Published on: December 4, 2017
Identification of hydroxyl on Ni(111)
Junjun Shan1, Aart W Kleyn, Ludo B F Juurlink
1Leiden Institute of Chemistry, Universiteit Leiden, Gorlaeus Laboratories, PO Box 9502, 2300 RA Leiden, The Netherlands.
Abstract:
Hydroxyl (OH) is identified and characterized on the Ni(111) surface by high-resolution electron energy loss spectroscopy. We find clear evidence of stretching, bending, and translational modes that differ significantly from modes observed for H(2)O and O on Ni(111). Hydroxyl may be produced from water by two different methods. Annealing of water co-adsorbed with atomic oxygen at 85 K to above 170 K leads to the formation of OH with simultaneous desorption of excess water. Pure water layers treated in the same fashion show no dissociation. However, the exposure of pure water to 20 eV electrons at temperatures below 120 K produces OH in the presence of adsorbed H(2)O. In combination with temperature-programmed desorption studies, we show that the OH groups recombine between 180 and 240 K to form O and immediately desorbing H(2)O. The lack of influence of co-adsorbed H(2)O at 85 K on the O-H stretching mode indicates that OH does not participate in a hydrogen-bonding network.
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