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Direct Visualization of 2-Butanol Adsorption and Dissociation on TiO2(110)

Journal Article · · Journal of Physical Chemistry C, 111(7):3021-3027
DOI:https://doi.org/10.1021/jp067461c· OSTI ID:909246

Atomically resolved scanning tunneling microscopy (STM) images of identical regions of a TiO2(110) surface were gathered before and after controlled doses of 2-butanol (CH3CH2CH(OH)CH3) at ambient temperature (~ 300 K). When dosing is initiated, 2-butanol preferentially adsorbs at bridge-bonded oxygen vacancy (BBOv) sites and dissociates via O—H, not C—O, bond scission to form paired 2-butoxy and hydroxyl species evidenced by two local maxima in STM line profiles. The measured separation is 0.4 nm, slightly larger than the measured separation (0.3 nm) between neighboring bridge-bonded oxygen anions in the surface unit cell of TiO2(110). As the dose increases, but before all the BBOv are occupied, there is direct STM evidence of hydroxyl proton hopping to an adjacent oxygen anion row. This process is facilitated by species bound to 5-coordinate Ti4+ rows, presumably undissociated 2-butanol, that hop slowly compared the STM imaging time scale. The backbones of these mobile species are centered over the Ti4+ rows with preference for lying parallel to these rows. On the other hand, the carbon backbones of the 2-butoxy species that fill BBOv's are centered over the O2- rows and prefer an orientation perpendicular to these rows. As the oxygen vacancy concentration increases from 0.4 to 11 % and 2-butanol is dosed the ratio of mobile species to 2-butoxy species decreases for doses that do not fill all the BBOv.

Research Organization:
Pacific Northwest National Laboratory (PNNL), Richland, WA (US), Environmental Molecular Sciences Laboratory (EMSL)
Sponsoring Organization:
USDOE
DOE Contract Number:
AC05-76RL01830
OSTI ID:
909246
Report Number(s):
PNNL-SA-51362; 14591; 22091; KC0302020
Journal Information:
Journal of Physical Chemistry C, 111(7):3021-3027, Journal Name: Journal of Physical Chemistry C, 111(7):3021-3027 Journal Issue: 7 Vol. 111
Country of Publication:
United States
Language:
English

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