Document Type
Article
Publication Date
11-4-2025
Journal / Book Title
ACS Applied Materials & Interfaces
Abstract
Bactericidal activity of sulfur-doped carbon has been investigated against a common Gram-negative bacterium, Escherichia coli K-12 (E. coli), in aqueous solution. Under dark conditions, 1 h contact of carbon with bacteria resulted in a 3–4 log decrease from the initial concentration of 7 log. When exposed to visible light, a 6–7 log decrease in E. coli was observed. The bactericidal activity under dark conditions was linked to the effects of functional groups, particularly sulfonic groups, which released protons that contributed to bacterial death. Even though under visible light no reactive oxygen species (ROS) were detected in electron paramagnetic resonance (EPR) and scavenger experiments, the enhanced bactericidal activity was due to the generation of holes in the carbon matrix. The photoactivity of sulfur-doped carbon is attributed to hole generation in aqueous solution under visible light, further enhancing its bactericidal effect. Bacterial death was not affected by the surface area or the porous structure of carbons.
DOI
10.1021/acsami.5c14239
Montclair State University Digital Commons Citation
Sadikaj, Danela; Fekri, Abanob; Bautista, Isabelle; Davis, Nafisatu; Alkla, Tasnim Agha; Mirza, Muhammad Moueed Haider; Wang, Jiaying; Stallworth, Phillip; Hudson-Smith, Natalie; Bandosz, Teresa J.; Yu, Xiaojun; Greenbaum, Steven; and Li, Wanlu, "Importance of S-Doped Porous Carbon Acidity and Visible Light Photoactivity for Its Antibacterial Activity" (2025). Department of Chemistry and Biochemistry Faculty Scholarship and Creative Works. 609.
https://digitalcommons.montclair.edu/chem-biochem-facpubs/609
Rights
This publication is licensed under CC-BY 4.0.
Published Citation
Sadikaj, Danela, et al. “Importance of S-Doped Porous Carbon Acidity and Visible Light Photoactivity for Its Antibacterial Activity.” ACS Applied Materials & Interfaces, Nov. 2025, p. acsami.5c14239. DOI.org (Crossref), https://doi.org/10.1021/acsami.5c14239.