A multicomponent Bi-based Z-scheme photocatalyst, BISB, was developed through a hydrothermal method. In this sample, two semiconducting nanostructures, BiOI and Bi2S3, were linked together with the metal Bi nanoparticle. As compared with BiOI (BI) and heterojunction BiOI/Bi2S3 (BIS) samples, the BISB had optimal Rhodamine B (RhB) photodecomposition performance. High efficiency separation of photoexcited electrons and holes, decreased band gap energy, extended specific surface area, and promotional redox potential were key factors for enhancing the photocatalytic activity of the prepared sample. The photoexcited holes were the key active radicals during the RhB photodecomposition process over the BISB catalyst, while ·O2 ¯ was also involved to a smaller extent. Additionally, the photocatalyst demonstrated excellent reusability and stability during the photoreaction process, suggesting that the BISB sample could be a candidate for water purification applications.

The S-scheme photocatalyst system has become increasingly popular in recent years for its ability to efficiently degrade various pollutants, including organic dyes, pesticides, and other harmful substances. This system uses two semiconductor photocatalysts with different bandgap energies, working together in a redox reaction to produce a highly reactive species capable of pollutant breakdown. Here, an S-scheme Ag2WO4/Ag6Si2O7 p-n heterojunction nanocomposite was successfully developed by a coprecipitation method. By decomposing Rhodamine B (RhB) under visible-light irradiation, the photocatalytic activities of Ag6Si2O7/Ag2WO4 showed enhanced photocatalytic degradation performance of organic dyes, especially at a 4% molar ratio of the Ag2WO4-modified Ag6Si2O7 sample, whose degradation rate was 23.7 and 4.65 times those of Ag2WO4 and Ag6Si2O7, respectively. The physical and chemical properties of the samples were determined by identifying the physical structure, chemical element composition, and optical responsiveness. The optimum composite amongst the prepared materials was AgSW-4, achieving the maximum RhB degradation efficiency of 97.5%, which was higher by 60% and 20% than its counterparts Ag6Si2O7 and Ag2WO4, respectively. These results showed that in the nanocomposite structure, Ag6Si2O7 was a p-type semiconductor and Ag2WO4 was an n-type semiconductor. Based on the analysis data, a comprehensive p-n heterojunction S-scheme process was proposed to demonstrate the enhanced photocatalytic performance of the Ag6Si2O7/Ag2WO4 nanocomposite.

Sonodynamic therapy (SDT) is an emerging non-invasive cancer treatment method in the field of nanomedicine, which has the advantages of deep penetration, good therapeutic efficacy, and minimal damage to normal tissues. Sonosensitizers play a crucial role in the process of SDT, as their structure and properties directly determine the treatment outcome. Inorganic sonosensitizers, with their high stability and longer circulation time in the human body, have great potential in SDT. In this review, the possible mechanisms of SDT including the ultrasonic cavitation, reactive oxygen species generation, and activation of immunity are briefly discussed. Then, the latest research progress on inorganic sonosensitizers is systematically summarized. Subsequently, strategies for optimizing treatment efficacy are introduced, including combination therapy and image-guided therapy. The challenges and future prospects of sonodynamic therapy are discussed. It is hoped that this review will provide some guidance for the screening of inorganic sonosensitizers.

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