4.8 Article

Construction of TiO2-x Confined by Layered Iron Silicate toward Efficient Visible-Light-Driven Photocatalysis-Fenton Synergistic Removal of Organic Pollutants

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 15, Issue 19, Pages 23124-23135

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.3c01981

Keywords

TiO2-x; heterojunction; layered iron silicate; photocatalysis-Fenton synergy; organic pollutants

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In this study, a novel heterojunction of oxygen vacancy-rich TiO2-x confined in the layer space of a synthetic montmorillonite-like iron silicate (TiO2-x/FeMMT) was developed to address the issue of unsatisfactory electron transfer in photocatalysis-Fenton synergistic reaction. The two-dimensional layered montmorillonite-like silicates in the heterojunction provided more active sites for the reaction and induced oxygen vacancies in TiO2-x through interfacial effects, enhancing the visible-light harvesting ability. The TiO2-x/FeMMT composites exhibited superior photocatalysis-Fenton performance for the degradation removal of phenol, dinotefuran (DIN), and sulfamethoxazole (SMX) under visible-light irradiation.
The photocatalysis-Fenton synergistic reaction has great potential for water purification but generally suffers from unsatisfactory electron transfer due to an undesirable interface structure. Herein, we developed a novel heterojunction of oxygen vacancy-rich TiO2-x confined in the layer space of a synthetic montmorillonite-like iron silicate (denoted as TiO2-x/FeMMT) that addresses the issue mentioned above. Two-dimensional layered montmorillonite-like silicates in heterojunctions as a support not only provided more active sites for the reaction but also induced oxygen vacancies in TiO2-x through interfacial effects to enhance the visible-light harvesting ability. Notably, such loading TiO2-x as an electron donor accelerated the Fe(III)/Fe(II) redox cycling and facilitated the effective activation of H2O2, while Fe(III) in the montmorillonite-like silicate as electron trap sites greatly improved the separation of photogenerated electron-hole pairs. More interestingly, the internal electric field and oxygen vacancies (Vo) existing at the interface realized the directional migration of photogenerated electrons and improved the energy band structure of the heterojunction, respectively. Eventually, the TiO2-x/FeMMT composites exhibited superior photocatalysis-Fenton performance toward degradation removal of phenol, dinotefuran (DIN), and sulfamethoxazole (SMX) under visible-light irradiation. This paves the way for the rational design of high-efficiency heterojunction catalysts based on layered silicates for environment-related applications.

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