TY - JOUR
T1 - Efficiently enhanced visible-light photocatalytic activity by in situ deposition of Ag@AgBr on g-C3N4/Fe3O4 magnetic heterogeneous materials
AU - Zhang, Xiao
AU - Ren, Bin
AU - Li, Xi
AU - Xu, Yanhua
AU - Liu, Biming
AU - Yu, Peng
AU - Sun, Yongjun
AU - Mei, Danhua
N1 - Publisher Copyright:
© 2020 Elsevier B.V.
PY - 2021/1/1
Y1 - 2021/1/1
N2 - In this study, graphitic carbon nitride (g-C3N4) (CN) was conveniently and environmentally modified into a stable and easily recyclable photocatalyst for the high removal efficiency of dye contaminants in water. Magnetic carrier (CN/Fe3O4) and heterojunction photocatalysts (Ag@AgBr/CN/Fe3O4) were prepared by ultrasonic and in situ deposition of Fe3O4 and Ag@AgBr nanoparticles on the CN, respectively, and characterized by the surface structure, optical, and electrochemical properties. The effects of different catalysts, silver loading, catalyst dosage, and different aeration conditions on the photocatalytic degradation of RhB were investigated. Results exhibited that the removal rate of RhB by Ag@AgBr/CN/Fe3O4 reached 96% within 150 min when the Ag loading was 5%, the catalyst dosage was 0.4 g/L, and the aeration was air. Furthermore, the degradation rate constant was 17.3 × 10−3 min−1, which was 4.3 and 3.4 times higher than that of CN and CN/Fe3O4, respectively. The stability study demonstrated that Ag@AgBr/CN/Fe3O4 had almost no risk of Ag and Fe leakage and showed high stability. Mechanism study indicated that the construction of Z-scheme heterojunction between Ag@AgBr and CN and trapping electron by Fe3+ promoted charge transfer and electron–hole pair separation, thus enhancing photocatalytic activity.
AB - In this study, graphitic carbon nitride (g-C3N4) (CN) was conveniently and environmentally modified into a stable and easily recyclable photocatalyst for the high removal efficiency of dye contaminants in water. Magnetic carrier (CN/Fe3O4) and heterojunction photocatalysts (Ag@AgBr/CN/Fe3O4) were prepared by ultrasonic and in situ deposition of Fe3O4 and Ag@AgBr nanoparticles on the CN, respectively, and characterized by the surface structure, optical, and electrochemical properties. The effects of different catalysts, silver loading, catalyst dosage, and different aeration conditions on the photocatalytic degradation of RhB were investigated. Results exhibited that the removal rate of RhB by Ag@AgBr/CN/Fe3O4 reached 96% within 150 min when the Ag loading was 5%, the catalyst dosage was 0.4 g/L, and the aeration was air. Furthermore, the degradation rate constant was 17.3 × 10−3 min−1, which was 4.3 and 3.4 times higher than that of CN and CN/Fe3O4, respectively. The stability study demonstrated that Ag@AgBr/CN/Fe3O4 had almost no risk of Ag and Fe leakage and showed high stability. Mechanism study indicated that the construction of Z-scheme heterojunction between Ag@AgBr and CN and trapping electron by Fe3+ promoted charge transfer and electron–hole pair separation, thus enhancing photocatalytic activity.
KW - Ag@AgBr
KW - Charge transfer
KW - FeO
KW - Graphitic carbon nitride
KW - Heterojunction
UR - http://www.scopus.com/inward/record.url?scp=85089520980&partnerID=8YFLogxK
U2 - 10.1016/j.seppur.2020.117596
DO - 10.1016/j.seppur.2020.117596
M3 - 文章
AN - SCOPUS:85089520980
SN - 1383-5866
VL - 254
JO - Separation and Purification Technology
JF - Separation and Purification Technology
M1 - 117596
ER -