TY - JOUR
T1 - Fast electron transfer and enhanced visible light photocatalytic activity by using poly-o-phenylenediamine modified AgCl/g-C3N4 nanosheets
AU - Sun, Linlin
AU - Liu, Chongyang
AU - Li, Jinze
AU - Zhou, Yaju
AU - Wang, Huiqin
AU - Huo, Pengwei
AU - Ma, Changchang
AU - Yan, Yongsheng
N1 - Publisher Copyright:
"© 2019, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved. "
PY - 2019/1/1
Y1 - 2019/1/1
N2 - Exfoliation of bulk graphitic carbon nitride (g-C3N4) into two-dimensional (2D) nanosheets is one of the effective strategies to improve its photocatalytic properties so that the 2D g-C3N4 nanosheets (CN) have larger specific surface areas and more reaction sites. In addition, poly-o-phenylenediamine (PoPD) can improve the electrical conductivity and photocatalytic activity of semiconductor materials. Here, the novel efficient composite PoPD/AgCl/g-C3N4 nanosheets was first synthesized by a precipitation reaction and the photoinitiated polymerization approach. The obtained photocatalysts have larger specific surface areas and could achieve better visible-light response. However, silver chloride (AgCl) is susceptible to agglomeration and photocorrosion. The PoPD/AgCl/CN composite exhibits an extremely high photocurrent density, which is three times that of CN. Obviously enhanced photocatalytic activities of PoPD/AgCl/g-C3N4 are revealed through the photodegradation of tetracycline. The stability of PoPD/AgCl/CN is demonstrated based on four cycles of experiments that reveal that the degradation rate only decreases slightly. Furthermore, •O2- and h+ are the main active species, which are confirmed through a trapping experiment and ESR spin-trap technique. Therefore, the prepared PoPD/AgCl/CN can be considered as a stable photocatalyst, in which PoPD is added as a charge carrier and acts a photosensitive protective layer on the surface of the AgCl particles. This provides a new technology for preparing highly stable composite photocatalysts that can effectively deal with environmental issues.
AB - Exfoliation of bulk graphitic carbon nitride (g-C3N4) into two-dimensional (2D) nanosheets is one of the effective strategies to improve its photocatalytic properties so that the 2D g-C3N4 nanosheets (CN) have larger specific surface areas and more reaction sites. In addition, poly-o-phenylenediamine (PoPD) can improve the electrical conductivity and photocatalytic activity of semiconductor materials. Here, the novel efficient composite PoPD/AgCl/g-C3N4 nanosheets was first synthesized by a precipitation reaction and the photoinitiated polymerization approach. The obtained photocatalysts have larger specific surface areas and could achieve better visible-light response. However, silver chloride (AgCl) is susceptible to agglomeration and photocorrosion. The PoPD/AgCl/CN composite exhibits an extremely high photocurrent density, which is three times that of CN. Obviously enhanced photocatalytic activities of PoPD/AgCl/g-C3N4 are revealed through the photodegradation of tetracycline. The stability of PoPD/AgCl/CN is demonstrated based on four cycles of experiments that reveal that the degradation rate only decreases slightly. Furthermore, •O2- and h+ are the main active species, which are confirmed through a trapping experiment and ESR spin-trap technique. Therefore, the prepared PoPD/AgCl/CN can be considered as a stable photocatalyst, in which PoPD is added as a charge carrier and acts a photosensitive protective layer on the surface of the AgCl particles. This provides a new technology for preparing highly stable composite photocatalysts that can effectively deal with environmental issues.
KW - AgCl
KW - G-CN nanosheets
KW - Photocatalytic
KW - Poly-o-phenylenediamine
KW - Visible light irradiation
UR - http://www.scopus.com/inward/record.url?scp=85066029367&partnerID=8YFLogxK
U2 - 10.1016/S1872-2067(18)63172-9
DO - 10.1016/S1872-2067(18)63172-9
M3 - 文章
AN - SCOPUS:85066029367
SN - 1872-2067
VL - 40
SP - 80
EP - 94
JO - Chinese Journal of Catalysis
JF - Chinese Journal of Catalysis
IS - 1
ER -