Difference in TiO sub(2) photocatalytic mechanism between rutile and anatase studied by the detection of active oxygen and surface species in water

• Published in: Physical chemistry chemical physics : PCCP 2015-07, Vol.17 (28), p.18691-18698
• Main Authors: Kakuma, Yusuke, Nosaka, Atsuko Y, Nosaka, Yoshio
• Format: Article
• Language: English
• Subjects: Anatase; Photocatalysis; Photocatalysts; Rutile; Surface chemistry; Surface properties; Titanium; Titanium dioxide
• ISSN: 1463-9076; 1463-9084
• DOI: 10.1039/c5cp02004b

Various kinds of TiO sub(2) photocatalysts have been practically applied in various fields. Knowing the exact surface properties is a prerequisite to develop further and efficient applications. However, the cause of the essential difference in the activities of the two polymorphs of TiO sub(2), rutile and anatase, has not been clearly elucidated yet. We tried to clarify the cause in terms of active oxygen species (&z.rad; OH, &z.rad; O sub(2) super(-), and H sub(2)O sub(2)) photogenerated on the surfaces, which are considered practically involved in the photocatalytic reactions. It was revealed that for anatase the rate of &z.rad; OH generation was high, but it decreased in the presence of H sub(2)O sub(2). On the other hand, for rutile, &z.rad; OH generation was very low but it increased in the presence of H sub(2)O sub(2). The formation rate of &z.rad; O sub(2) super(-) for rutile was higher than that for anatase, suggesting that the photoinduced reduction process should not be accountable for the higher photocatalytic activity of anatase. Since the Ti-Ti distance on a rutile surface is smaller than that for anatase, rutile is capable of forming a surface structure such as Ti-OO-Ti, leading to readily form O sub(2). The mechanism of fast coupling of two photoinduced conduction band holes to form Ti-OO-Ti was proposed, which is accountable for the lower reactivity of rutile. This mechanism was verified by the analysis of surface species with ATR-IR spectroscopy.