Heterojunctions for Photocatalytic Wastewater Treatment: Positive Holes, Hydroxyl Radicals and Activation Mechanism under UV and Visible Light Article uri icon

abstract

  • Forming heterojunctions by coupling two or more semiconductors is an important strategy to develop stable and efficient photocatalysts able to operate both under near-UV and visible light. Five novel heterojunction systems were synthesized in the present study, using a modified sol-gel method: Bi2Mo3O12/TiO2, ZnFe2O4/TiO2, FeTiO3/TiO2, WO3(US)/TiO2 and WO3/TiO2. These heterojunction semiconductors were characterized by using XRD, SEM and EDX, UV-Vis diffuse reflectance spectroscopy and BET. Their photocatalytic activities were evaluated using methyl orange (MO) degradation under both near-UV and visible light. From the various heterojunctions developed, the WO3(US)/TiO2 photocatalyst was the one that showed the highest photocatalytic efficiency with this being assigned to the formation of a double heterojunction involving anatase, rutile and monoclinic WO3 phases. On this basis, a photocatalyst activation mechanism applicable to near-UV and visible light irradiation was proposed. This mechanism explains how the photogenerated electrons (e-) and positive holes (h%2b) can be transferred to the various phases. As a result, and given the reduced holes and electron recombination surface, hydroxyl radicals found were more abundant. To confirm this assumption, hole formation in the valence band was studied, using hole-scavenging reactions involving ion iodine (I-), while hydroxyl radical production used fluorescence spectroscopy. © 2020 Walter de Gruyter GmbH, Berlin/Boston 2020.

publication date

  • 2020-01-01