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Chapter 1 Surface Structure and Reactivity of Iron Oxide-Water Interfaces.

Book ·
OSTI ID:1008425

The surface structure and composition of the three distinct iron-(hydr)oxide systems, goethite (1 0 0), hematite (1{bar 1}02), and magnetite (1 1 1) were determined under hydrated conditions at room temperature using crystal truncation rod (CTR) analysis. The prediction of surface protonation states and the overall chemical plausibility of the experimental surface models are performed using a bond-valence (BV) analysis. Further analysis of the surface energetics is carried out using density functional theory (DFT). The analysis of three common iron-(hydr)oxide surface systems reveals the differences in interface structure and distribution of hydroxyl groups at substrate-water interfaces. The goethite (1 0 0) interface structure is determined to have a relaxed double hydroxyl termination with the presence of two semi-ordered water layers that expose a surface with A-type (Fe-OH{sub 2}) and B-type (Fe{sub 2}-OH) hydroxyl groups. The hydrated hematite (1{bar 1}02) interface structure has vacancies in the near surface metal sites, resulting in three types of surface functional groups: A type, B type, and C type (Fe{sub 3}-O). The interface structure of magnetite (1 1 1) shows two chemically nonequivalent oxygen surface terminations in the surface ratio of 70 O{sub 4}-Fe{sub oh}-O{sub 4}-Fe{sub td1-oh-td2}:30 O{sub 4}-Fe{sub td1-oh-td2}-O{sub 4}-Fe{sub oh} suggesting that the octahedral irons are the principal irons involved at the environmental interfaces. In the above three systems, there also is evidence for multiple domains with fractional ordered unit cell steps determined by atomic force microscopy (AFM). Results obtained for the structure of the iron-(hydr)oxide-water interfaces from the CTR and DFT analyses are different from stoichiometric termination of the bulk structure or hydroxylation of the ultra high vacuum (UHV) determined surface structures.

Research Organization:
Advanced Photon Source (APS), Argonne National Laboratory (ANL), Argonne, IL (US)
Sponsoring Organization:
USDOE
OSTI ID:
1008425
Country of Publication:
United States
Language:
ENGLISH

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