Enhancing O2 adsorption and activation over porous S-doped g-C3N4 rod toward efficient photocatalytic rhodamine-B degradation
- Authors
- Xie, Zhuohong; Lin, Jianbin; Zhang, Weibin; Zhang, Chi; Yang, Woochul
- Issue Date
- Jan-2024
- Publisher
- Elsevier BV
- Keywords
- Oxygen adsorption; Superoxide radical evolution; Photocatalytic degradation
- Citation
- Diamond and Related Materials, v.141, pp 1 - 10
- Pages
- 10
- Indexed
- SCIE
SCOPUS
- Journal Title
- Diamond and Related Materials
- Volume
- 141
- Start Page
- 1
- End Page
- 10
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/26255
- DOI
- 10.1016/j.diamond.2023.110658
- ISSN
- 0925-9635
1879-0062
- Abstract
- Photocatalytic oxygen molecular (O2) activation to generate reactive oxygen species (ROS) is a promising strategy for the oxidative degradation of organic pollutants. Herein, a porous S-doped g-C3N4 rod (S-g-CN-rod) was synthesized and applied to photocatalytic superoxide radicals (.O2- ) evolution and rhodamine-B (RhB) degradation. The morphological, structural, and optical properties of all samples were investigated. DFT calculation demonstrated that the carbon site adjacent to S was energetically favorable for O2 adsorption, which was conducive to .O2- evolution. The porous S-g-CN-rod exhibited an excellent photocatalytic .O2- evolution rate of 268.2 mu mol L-1 h-1, which was the main active species to degrade RhB. Conceivably, the porous S-g-CN-rod demonstrated exceptionally high efficiency of photocatalytic RhB degradation and achieved almost complete disposal of RhB (99.7 %) in only 30 min, which was higher than most reported photocatalysts. The experimental results and theoretical calculations demonstrated that the preeminent photocatalytic activities were ascribed to enhanced light-harvesting, improved migration and separation of photo-induced electrons, and the superior O2 adsorption and activation induced by S doping.
- Files in This Item
- There are no files associated with this item.
- Appears in
Collections - College of Natural Science > Department of Physics > 1. Journal Articles

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.