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Probing the Structure and Dynamics of Interfacial Water with Scanning Tunneling Microscopy and Spectroscopy
Published on: May 27, 2018
Imaging water dissociation on TiO2(110): Evidence for inequivalent geminate OH groups
Z Zhang1, O Bondarchuk, Bruce D Kay
1Department of Chemistry and Biochemistry, Center for Materials Chemistry, University of Texas at Austin, Texas 78712, USA.
Abstract:
Identical regions of partially reduced TiO2(110) surfaces with bridge-bonded oxygen vacancy (BBO(V)) concentrations of approximately 10% ML (1 ML = 5.2 x 10(14) cm(-2)) were imaged using scanning tunneling microscopy (STM) before and after dosing H2O at ambient temperature (approximately 300 K). Atomically resolved images confirm that H2O adsorbs dissociatively on the BBO(V) sites, producing two hydroxyl species, one positioned at BBO(V) and denoted OH(V) and the other, denoted OH(B), formed by protonation at either of the two nearest-neighbor bridge-bonded oxygen atoms. Hydrogen hopping along the [001] direction is observed at ambient temperature, with a strong preference for OH(B) (approximately 10x) hydrogen motion. This powerful imbalance demonstrates the inequality of OH(V) and OH(B) and suggests differences in their charge and/or binding configuration.
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