Effects of pH on the Photocatalytic Activity and Degradation Mechanism of Rhodamine B over Fusiform Bi Photocatalysts under Visible Light

27Citations
Citations of this article
46Readers
Mendeley users who have this article in their library.

Abstract

In this study, fusiform bismuth (Bi) was synthesized, and its photocatalytic performance, degradation mechanism, and pathways for removing rhodamine B (RhB) at different pH levels were investigated. Additionally, the morphologies, structural characteristics, surface electronic states, optical properties, active species, and potential degradation pathways of RhB over the fusiform Bi were analyzed. The comparison of the results before and after RhB degradation using the fusiform Bi revealed the formation of a Bi/BiOCl heterojunction photocatalyst. At pH 2.0, 3.0, 5.0, 7.0, and 9.0, the heterojunction exhibited excellent photocatalytic activity, with RhB removal efficiencies of ~97%, 96.7%, 72.6%, 53.5%, and 27.6%, respectively. Moreover, total organic carbon and chemical oxygen demand analyses were performed to evaluate the mineralization rates of RhB with the fusiform Bi at pH 3.0 and 7.0. Furthermore, the effects of catalyst content, initial RhB concentration, light source distance, inorganic anions, and reactant temperature on the photocatalytic performance of the fusiform Bi were investigated. Additionally, the types of active species and potential photocatalytic mechanisms for RhB degradation over the fusiform Bi at different pH levels (3.0 and 7.0) were elucidated. The appropriate degradation pathways were identified via liquid chromatography–mass spectrometry at pH 3.0 and 7.0.

Cite

CITATION STYLE

APA

Chen, Y., Ma, D., He, G., & Pan, S. (2024). Effects of pH on the Photocatalytic Activity and Degradation Mechanism of Rhodamine B over Fusiform Bi Photocatalysts under Visible Light. Water (Switzerland), 16(17). https://doi.org/10.3390/w16172389

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free