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Photocatalytic technology is currently the most promising technology for environmental pollution control. The preparation of photocatalysts with excellent properties is the core of the development of photocatalytic technology. TiO2 can form a heterojunction with g-C3N4, which can effectively inhibit the recombination of photogenerated electron–hole pairs, improve the mobility of photogenerated carriers, and thus improve the photocatalytic performance. In this study, NaCl was used as a template, and the loose and porous g-C3N4/TiO2 heterojunction composite photocatalysts were prepared by the template method. Compared to the pure g-C3N4 prepared by the conventional thermal polycondensation method and TiO2, the g-C3N4/TiO2 heterojunction composite photocatalysts prepared in this study exhibited a greatly increased specific surface area, an improved light absorption performance, a significantly suppressed recombination of photogenerated electrons and holes. Furthermore, the g-C3N4/TiO2 heterojunction composite photocatalysts exhibited excellent photocatalytic performance. In this study, NaCl was used as a template, and the loose and porous g-C3N4/TiO2 heterojunction composite photocatalysts were prepared by the template method. Compared to the pure g-C3N4 prepared by the conventional thermal polycondensation method and TiO2, the g-C3N4/TiO2 heterojunction composite photocatalysts prepared in this study exhibited a greatly increased specific surface area, an improved light absorption performance, a significantly suppressed recombination of photogenerated electrons and holes. Furthermore, the g-C3N4/TiO2 heterojunction composite photocatalysts exhibited excellent photocatalytic performance. [ABSTRACT FROM AUTHOR]

Research has demonstrated that the formation of composites of titanium dioxide (TiO2) with silver phosphate (Ag3PO4) through the construction of heterojunctions can expand its light absorption range and suppress the recombination of photogenerated electron–hole pairs, thereby improving the photocatalytic performance. However, this method offers only limited performance improvements, and the composite photocatalysts are costly due to the expensive Ag3PO4. In this study, Ti3C2 MXene, which has good hydrophilicity and excellent electrical conductivity, is first used to form Schottky junction composites with bronze TiO2 (TiO2(B)) via electrostatic self-assembly. Then, Ag3PO4 quantum dots were further formed on the surface of the TiO2(B)/Ti3C2 MXene by in situ self-growth, and Ag3PO4 formed heterojunctions and Schottky junctions with TiO2(B) and Ti3C2 MXene, respectively. Finally, a ternary composite photocatalyst TiO2(B)/Ti3C2 MXene/Ag3PO4 was jointly constructed by these functional junctions. Under the synergistic effect of these functional junctions, the mobility and fast separation performance of photogenerated electron–hole pairs of the composite photocatalyst were significantly improved, the recombination of photogenerated electron–hole pairs was effectively suppressed, and the light absorption performance was enhanced. As a result, the composite photocatalyst exhibited excellent photocatalytic performances. [ABSTRACT FROM AUTHOR]

Photocatalytic degradation, as an emerging method to control environmental pollution, is considered one of the most promising environmental purification technologies. As Tibet is a region with some of the strongest solar radiation in China and even in the world, it is extremely rich in solar energy resources, which is ideal for applying photocatalytic technology to its ecological environment protection and governance. In this study, Na2Ti3O7 nanobelts were prepared via a hydrothermal method and converted to TiO2∙xH2O ion exchange, which was followed by high-temperature calcination to prepare TiO2(B) nanobelts ("B" in TiO2(B) means "Bronze phase"). A simple in situ method was used to generate Ag3PO4 particles on the surface of the TiO2 nanobelts to construct a Ag3PO4/TiO2(B) heterojunction composite photocatalyst. By generating Ag3PO4 nanoparticles on the surface of the TiO2(B) nanobelts to construct heterojunctions, the light absorption range of the photocatalyst was successfully extended from UV (ultraviolet) to the visible region. Furthermore, the recombination of photogenerated electron–hole pairs in the catalyst was inhibited by the construction of the heterojunctions, thus greatly enhancing its light quantum efficiency. Therefore, the prepared Ag3PO4/TiO2(B) heterojunction composite photocatalyst greatly outperformed the TiO2(B) nanobelt in terms of photocatalytic degradation. [ABSTRACT FROM AUTHOR]