2008 Joint Annual Meeting (5-9 Oct. 2008): Water Ordering and Redox Process at Hematite-Water Interfaces

295-1 Water Ordering and Redox Process at Hematite-Water Interfaces



Wednesday, 8 October 2008: 8:00 AM
George R. Brown Convention Center, 350DEF
Jeffrey G. Catalano, Earth and Planetary Sciences, Washington University in St. Louis, One Brookings Drive, Campus Box 1169, Saint Louis, MO 63130, Paul Fenter, Chemistry Division, Argonne National Laboratory, 9700 South Cass Avenue, Argonne, IL 60439, Changyong Park, Chemistry Division, Argonne National Laboratory, Argonne, IL 60439 and Kevin M. Rosso, Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, P.O. Box 999, MSIN K8-96, Richland, WA 99352
Reactions at hematite-water interfaces affect contaminant fate and transport, partially control biogeochemical iron cycling, and fractionate iron isotopes. The ability to predict and quantify these and other important processes in nature requires a fundamental understanding of the structure of hematite-water interfaces and the reactions that occur here. The ordering of water at hematite surfaces and the structural transformations these surfaces undergo as a result of reaction with aqueous Fe(II) have been characterized. Water takes on an ordered arrangement near the hematite (012) and (110) surfaces, with the degree of ordering declining away from the surface on the length scale of approximately 1-2 nanometers. Fe(II) induces orientation-dependent structural changes to hematite surfaces that suggest growth occurs on (001) and dissolution on (110) and (012). This behavior occurs under both neutral (pH 7) and acidic (pH 3) conditions. Fe(II) presumably serves a catalytic role, transporting Fe between different surfaces through solution with electrons conducting back through the hematite structure in the reverse direction. This dynamic interfacial redox process may be responsible for the recent observations of electron transfer and isotope fractionation in Fe(II)-iron oxide systems.