TY - JOUR
T1 - SnS2 integrated P-doped g-C3N4 with advanced photocatalytic efficiency towards organic pollutants decontamination
AU - Kumari, Monika
AU - Kumar, Naveen
AU - Sharma, Raj Kishore
AU - Tahir, Muhammad
AU - Selvaraj, Manickam
AU - Singh, Pardeep
AU - Jindal, Jitender
AU - Mittal, Anuj
N1 - Publisher Copyright:
© 2025 Elsevier Inc.
PY - 2025/6/1
Y1 - 2025/6/1
N2 - In this study, the P doping and SnS2 deposition was controlled to get SnS2 integrated P-doped g-C3N4 photocatalysts. The prepared photocatalysts were analyzed by XRD, FESEM, HRTEM, PL, UV-DRS, XPS, and Zeta potential emphasizing their crystalline structures, morphological characteristics, charge carrier recombination, band gap energies, chemical compositions, and surface charge. These results confirmed successful P doping by substituting C and formation of heterojunction with SnS2. Synthesized materials exhibited good photodegradation efficiency towards organic pollutants: the antibiotic ciprofloxacin (CP) and the cationic dye Rhodamine B (RhB). Among the optimized composites, PCSn-5 (containing 5 wt% of SnS2 on PCN-2, 1 mmol P doped g-C3N4) achieved the highest degradation rates, achieving 99.45% degradation of RhB within 100 min and 89.44% degradation of CP within 120 min. P doping introduced new energy levels that significantly enhanced charge separation and heterojunctions formed improved light absorption, thereby enhancing photocatalytic efficiency. Scavenger analysis acknowledge that holes were primarily responsible for RhB degradation, while in CP degradation both superoxide radicals and holes were dominant species. The photocatalytic efficiency of PCSn-5 was assessed at various pH levels exhibited the peak performance at pH 3 for RhB and at neutral pH for CP. The photocatalyst exhibited strong stability with ≈ 2% reduction in efficiency after five cycles for both pollutants. Electrochemical analysis, conducted through Mott-Schottky plots and electrochemical impedance spectroscopy (EIS), revealed increased donor density and reduced charge resistance following the formation of the composites.
AB - In this study, the P doping and SnS2 deposition was controlled to get SnS2 integrated P-doped g-C3N4 photocatalysts. The prepared photocatalysts were analyzed by XRD, FESEM, HRTEM, PL, UV-DRS, XPS, and Zeta potential emphasizing their crystalline structures, morphological characteristics, charge carrier recombination, band gap energies, chemical compositions, and surface charge. These results confirmed successful P doping by substituting C and formation of heterojunction with SnS2. Synthesized materials exhibited good photodegradation efficiency towards organic pollutants: the antibiotic ciprofloxacin (CP) and the cationic dye Rhodamine B (RhB). Among the optimized composites, PCSn-5 (containing 5 wt% of SnS2 on PCN-2, 1 mmol P doped g-C3N4) achieved the highest degradation rates, achieving 99.45% degradation of RhB within 100 min and 89.44% degradation of CP within 120 min. P doping introduced new energy levels that significantly enhanced charge separation and heterojunctions formed improved light absorption, thereby enhancing photocatalytic efficiency. Scavenger analysis acknowledge that holes were primarily responsible for RhB degradation, while in CP degradation both superoxide radicals and holes were dominant species. The photocatalytic efficiency of PCSn-5 was assessed at various pH levels exhibited the peak performance at pH 3 for RhB and at neutral pH for CP. The photocatalyst exhibited strong stability with ≈ 2% reduction in efficiency after five cycles for both pollutants. Electrochemical analysis, conducted through Mott-Schottky plots and electrochemical impedance spectroscopy (EIS), revealed increased donor density and reduced charge resistance following the formation of the composites.
KW - CN
KW - Degradation
KW - Organic pollutants
KW - Photocatalyst
KW - SnS
UR - https://www.scopus.com/pages/publications/86000135031
UR - https://www.scopus.com/pages/publications/86000135031#tab=citedBy
U2 - 10.1016/j.envres.2025.121210
DO - 10.1016/j.envres.2025.121210
M3 - Article
C2 - 40015434
AN - SCOPUS:86000135031
SN - 0013-9351
VL - 274
JO - Environmental Research
JF - Environmental Research
M1 - 121210
ER -