TY - JOUR
T1 - Efficient visible-light-driven removal of persistent antibiotics and synthetic dyes from wastewater using an engineered 2D/2D Bi2MoO6/NiAl–LDH S-scheme heterocatalyst with enhanced interfacial contact
AU - Lee, Dong Eun
AU - Moru, Satyanarayana
AU - Jo, Wan Kuen
AU - Tonda, Surendar
N1 - Publisher Copyright:
© 2024 Elsevier Inc.
PY - 2025/2/15
Y1 - 2025/2/15
N2 - Highly efficient photocatalysts for degrading persistent antibiotics and synthetic dye pollutants under visible light are crucial for sustainable environmental remediation. In this study, we engineered a novel Bi2MoO6 (BMO)/NiAl–LDH (layered double hydroxide) hybrid catalyst with a unique 2D/2D heterostructure, optimized for the visible-light-driven elimination of ciprofloxacin (CPF) and hazardous synthetic dyes such as rhodamine B and methylene blue. The optimized BMO-30/LDH hybrid demonstrated exceptional photocatalytic performance, achieving nearly complete degradation of CPF and synthetic dyes with high mineralization efficiency, surpassing many previously reported state-of-the-art photocatalysts. This superior activity is primarily attributed to the formation of an S-scheme heterojunction, which enhances charge separation while maintaining strong redox potentials in both components. This mechanism enables the simultaneous generation of reactive O2•− and •OH radicals. The hybrid's enhanced efficiency is further driven by synergistic effects, including strong visible light absorption, a large surface area, and a well-integrated 2D/2D configuration with face-to-face interfacial contact. These structural features maximize charge carrier separation, reduce recombination, and ensure robust photocatalytic activity. Additionally, the hybrid exhibited excellent reusability, retaining over 93% of its initial activity after five cycles. This study introduces a novel approach to engineering advanced 2D/2D heterojunction photocatalysts, highlighting their potential for practical water treatment and environmental remediation applications.
AB - Highly efficient photocatalysts for degrading persistent antibiotics and synthetic dye pollutants under visible light are crucial for sustainable environmental remediation. In this study, we engineered a novel Bi2MoO6 (BMO)/NiAl–LDH (layered double hydroxide) hybrid catalyst with a unique 2D/2D heterostructure, optimized for the visible-light-driven elimination of ciprofloxacin (CPF) and hazardous synthetic dyes such as rhodamine B and methylene blue. The optimized BMO-30/LDH hybrid demonstrated exceptional photocatalytic performance, achieving nearly complete degradation of CPF and synthetic dyes with high mineralization efficiency, surpassing many previously reported state-of-the-art photocatalysts. This superior activity is primarily attributed to the formation of an S-scheme heterojunction, which enhances charge separation while maintaining strong redox potentials in both components. This mechanism enables the simultaneous generation of reactive O2•− and •OH radicals. The hybrid's enhanced efficiency is further driven by synergistic effects, including strong visible light absorption, a large surface area, and a well-integrated 2D/2D configuration with face-to-face interfacial contact. These structural features maximize charge carrier separation, reduce recombination, and ensure robust photocatalytic activity. Additionally, the hybrid exhibited excellent reusability, retaining over 93% of its initial activity after five cycles. This study introduces a novel approach to engineering advanced 2D/2D heterojunction photocatalysts, highlighting their potential for practical water treatment and environmental remediation applications.
KW - 2D/2D hybrid configuration
KW - BiMoO
KW - Environmental remediation
KW - NiAl-LDH
KW - Pollutants degradation
KW - S-Scheme heterostructure
UR - https://www.scopus.com/pages/publications/85213570434
U2 - 10.1016/j.envres.2024.120699
DO - 10.1016/j.envres.2024.120699
M3 - Article
C2 - 39725142
AN - SCOPUS:85213570434
SN - 0013-9351
VL - 267
JO - Environmental Research
JF - Environmental Research
M1 - 120699
ER -