Chemicals such as N-acetylcysteine (NAC) were purchased from Sigma-Aldrich (St. Louis, MO, USA). UV light-responsive pure TiO2 NPs (Degussa P25; Evonik, Germany) were used as previously described12 (link),19 (link),32 (link). The crystal structure of P25 TiO2 was a mixture of 75% anatase and 25% rutile TiO2. The purity was at least 99.5% TiO2 and primary particle size was 21 nm ± 10 nm, with a specific surface area of 50 ± 15 m2/g. Carbon-containing TiO2 NPs [TiO2(C)] were prepared using a sol–gel method19 (link),33 (link). The powders were subjected to calcination at 200 °C, and named C200; the detailed preparation of C200 has been reported elsewhere19 (link),33 (link). By photoreduction process using H2PtCl6 and TiO2 NPs as a platinum precursor and a pristine photocatalyst, respectively, platinum-containing TiO2 NPs [TiO2(Pt)] were prepared and characterized following previously described methods13 (link),15 (link). The NPs of zinc oxide (ZnO; < 40 nm)9 (link) single-walled carbon nanotubes (CNTs), and silicon dioxide (SiO2; 10–20 nm) were purchased from Sigma–Aldrich. Nanodiamond (ND) NPs, with average sizes of 5 and 100 nm9 (link),34 (link),35 (link), were purchased from Kay Diamond Products (Boca Raton, FL, USA).
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