4.6 Article

Boosting visible light photocatalysis of Ag6Si2O7/dandelion shaped Bi2S3 heterojunctions

Publisher

ELSEVIER
DOI: 10.1016/j.colsurfa.2022.128732

Keywords

Heterojunction; Ag6Si2O7; Bi2S3; Charge carrier separation; Photocatalytic

Funding

  1. Innovation and Entrepreneurship Project of Shandong Province [S202110445206]

Ask authors/readers for more resources

This study successfully synthesized a novel dandelion-like Ag6Si2O7/Bi2S3 heterojunction material, which showed enhanced visible light absorption, efficient charge separation, and excellent photocatalytic performance.
Charge carrier separation is a very important factor in photocatalysis and can be accelerated by heterojunctions. Here, a novel and potential dandelion like Ag6Si2O7/Bi2S3 heterojunctions were successfully prepared through two steps: hydrothermal preparation of Bi2S3 matrix in advance and in-situ deposition of Ag6Si2O7 on the surface of Bi2S3. A series of characterization results show that Ag6Si2O7/Bi2S3 nanohybrids have better visible light absorption and more efficient charge separation than individual Bi2S3. The constructed Ag6Si2O7/Bi2S3-3 demonstrates excellent photocatalytic removal performance for RhB within 30 min. The K value for RhB degradation was nearly to 0.13 min-1 (within in 30 min) by Ag6Si2O7/Bi2S3-3 which was more than 350 times greater than Bi2S3 (0.00037 min-1 within in 40 min) and 2.2 times of Ag6Si2O7 (0.059 min-1 within in 40 min). The synergistic effect between the increased visible light harvest after the introduction of Ag6Si2O7 and the accelerated charge transfer in Ag6Si2O7/Bi2S3 heterojunction formed by Ag6Si2O7 and Bi2S3 are the reasons for the significant improvement of the catalytic activity of Ag6Si2O7/Bi2S3-3 materials.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available