The degradation mechanism of methyl orange under photo-catalysis of TiO2

文献情報

出版日 2012-01-05

DOI 10.1039/C2CP23226J

インパクトファクター 3.676

著者

Lihong Yu, Jingyu Xi, Ming-De Li, Hung Tat Chan, Tao Su, David Lee Phillips, Wai Kin Chan

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要旨

The properties of photo-generated reactive species, holes and electrons in bulk TiO2 (anatase) film and nano-sized TiO2 were studied and their effects towards decomposing pollutant dye methyl orange (MO) were compared by transient absorption spectroscopies. The recombination of holes and electrons in nano-sized TiO2 was found to be on the microsecond time scale consistent with previous reports in the literature. However, in bulk TiO2 film, the holes and electrons were found to be on the order of picoseconds due to ultra fast free electrons. The time-correlated single-photon counting (TCSPC) technique combined with confocal fluorescence microscopy revealed that the fluorescence intensity of MO is at first enhanced noticeably by TiO2 under UV excitation and soon afterwards weakened dramatically, with the lifetime prolonged. Photo-generated holes in nano-sized TiO2 can directly oxidize MO on the time scale of nanoseconds, while free electrons photo-generated in bulk TiO2 film can directly inject into MO on the order of picoseconds. Through cyclic voltammetry measurements, it was found that MO can be reduced at −0.28 V and oxidized at 1.4 V (vs.SCE) and this provides thermodynamic evidence for MO to be degraded by electrons and holes in TiO2. Through comparison of the hole-scavenging effect of MO and water, it was found that in polluted water when MO is above 1.6 × 10−4 M, the degradation is mainly due to a direct hole oxidation process, while below 1.6 × 10−4 M, hydroxyl oxidation competes strongly and might exceed the hole oxidation.

掲載誌

Physical Chemistry Chemical Physics

CiteScore: 5.5

自己引用率: 10.3%

年間論文数: 3036

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.