Abstract

Tetrathiafulvalene (TTF), one of the well-known organic photoelectric materials, was served as active sites to accelerate the activation of molecular oxygen to degrade organic pollutants. Herein, a kind of Z-scheme heterojunction photocatalysis was constructed based on g-C3N4 and TTF. According to the experimental results, the mechanism of Z-scheme heterojunction was supported, in which photogenerated electrons transferred from g-C3N4 to TTF. More importantly, TTF on the catalyst surface could serve not only as electron donor, but also as the terminal active site to transfer photoexcited electrons to adsorbed oxygen molecules, producing mass of ⋅O2–. Meanwhile, the activation rate constant of TCN-5 for RhB was 0.0624 min−1, which was 10 and 5 times of g-C3N4 and TTF, respectively. In addition, the results of EPR spectra, rotating disk electrode measurement and molecular oxygen activation measurement also demonstrated that this catalyst was energetically favorable to generate ⋅O2– through the single-electron reduction pathway of molecular oxygen. Finally, four possible photodegradation routes for RhB were proposed based on the results of HPLC-MS. This work provides a new insight on the application of organic photoelectric materials in the purification of wastewater by the molecular oxygen activation.

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