Probing Water and CO₂ Interactions at the Surface of Collapsed Titania Nanotubes Using IR Spectroscopy

• Published in: Molecules (Basel, Switzerland) Vol. 20; no. 9; pp. 15469 - 15487
• Main Authors: Bhattacharyya, Kaustava, Wu, Weiqiang, Weitz, Eric, Vijayan, Baiju K, Gray, Kimberly A
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 26.08.2015; MDPI
• Subjects: Adsorption; Annealing; Biochemistry & Molecular Biology; Carbon Dioxide - chemistry; Catalysis; Chemistry; CO2 adsorption; collapsed titania nanotubes; defect sites; FTIR; Hydrogen Bonding; Morphology; Nanotubes - chemistry; OH stretches; Oxidation; Photocatalysis; Photochemistry; Spectrophotometry, Infrared - methods; Temperature; Thermodynamics; Titanium - chemistry; Water - chemistry; United States > US; OH stretches; CO2 adsorption; FTIR; collapsed titania nanotubes; defect sites
• ISSN: 1420-3049; 1420-3049
• DOI: 10.3390/molecules200915469

Collapsed titania nanotubes (cTiNT) were synthesized by the calcination of titania nanotubes (TiNT) at 650 °C, which leads to a collapse of their tubular morphology, a substantial reduction in surface area, and a partial transformation of anatase to the rutile phase. There are no significant changes in the position of the XPS responses for Ti and O on oxidation or reduction of the cTiNTs, but the responses are more symmetric than those observed for TiNTs, indicating fewer surface defects and no change in the oxidation state of titanium on oxidative and/or reductive pretreatment. The interaction of H₂O and CO₂ with the cTiNT surface was studied. The region corresponding to OH stretching absorptions extends below 3000 cm(-1), and thus is broader than is typically observed for absorptions of the OH stretches of water. The exchange of protons for deuterons on exposure to D₂O leads to a depletion of this extended absorption and the appearance of new absorptions, which are compatible with deuterium exchange. We discuss the source of this extended low frequency OH stretching region and conclude that it is likely due to the hydrogen-bonded OH stretches. Interaction of the reduced cTiNTs with CO₂ leads to a similar but smaller set of adsorbed carbonates and bicarbonates as reported for reduced TiNTs before collapse. Implications of these observations and the presence of proton sources leading to hydrogen bonding are discussed relative to potential chemical and photochemical activity of the TiNTs. These results point to the critical influence of defect structure on CO₂ photoconversion.