TY - JOUR
T1 - Enhanced visible light photocatalysis and mechanism insight for novel Z-scheme MoS2/Ag2S/AgVOx ternary heterostructure with fast interfacial charges transfer
AU - Zeng, Yimei
AU - Lu, Dingze
AU - Kondamareddy, Kiran Kumar
AU - Wang, Hongmei
AU - Wu, Qiong
AU - Fan, Huiqing
AU - Wang, Qiuping
AU - Zhang, Boyu
AU - Xie, Lihao
AU - Zhang, Yuhao
AU - Wang, Zhennan
AU - Zhao, Bang
AU - Ho, Wingkei
N1 - Publisher Copyright:
© 2022 Elsevier B.V.
PY - 2022/7/5
Y1 - 2022/7/5
N2 - A Z-scheme MoS2/Ag2S/AgVOx ternary heterostructure was successfully synthesized by a facile hydrothermal method. The as-prepared MoS2/Ag2S/AgVOx ternary composite has been characterized by electron microscopy, XRD, XPS, UV-Vis DRS, PL, electrochemistry and ESR. TEM characterization revealed that Ag2S, Ag nanoparticles and AgVOx nanorods were dispersed homogeneously over the surface of MoS2 nanosheets The prepared heterojunction showed enhanced photocatalytic performance compared with single MoS2 and AgVOx. And 6%-MoS2/Ag2S/AgVOx heterojunction exhibits highest photocatalytic degradation efficiency, which can degrade fuchsine around 75% under visible light within 180 min. The enhanced photocatalytic activity can be attributed to the efficient separation of photogenerated charge carriers, the strong redox ability and enhancement of visible-light absorption derived from the construction of Z-scheme heterostructure. In-situ formed metallic Ag2S act as the electron mediator and Ag nanoparticles possess the surface plasmon resonance (SPR) effect. The prepared heterojunction showed decreased photoluminescence and increased photoelectrochemical performance, indicating high separation rate of photoinduced charge carriers. Furthermore, a possible degradation mechanism of fuchsine solution was proposed. And the results of radical trapping experiments indicated that superoxide radicals (∙O2-) and holes (h+) play major role during the photocatalytic degradation process. This work demonstrates an interesting Z-scheme photocatalytic system for photocatalysis applications.
AB - A Z-scheme MoS2/Ag2S/AgVOx ternary heterostructure was successfully synthesized by a facile hydrothermal method. The as-prepared MoS2/Ag2S/AgVOx ternary composite has been characterized by electron microscopy, XRD, XPS, UV-Vis DRS, PL, electrochemistry and ESR. TEM characterization revealed that Ag2S, Ag nanoparticles and AgVOx nanorods were dispersed homogeneously over the surface of MoS2 nanosheets The prepared heterojunction showed enhanced photocatalytic performance compared with single MoS2 and AgVOx. And 6%-MoS2/Ag2S/AgVOx heterojunction exhibits highest photocatalytic degradation efficiency, which can degrade fuchsine around 75% under visible light within 180 min. The enhanced photocatalytic activity can be attributed to the efficient separation of photogenerated charge carriers, the strong redox ability and enhancement of visible-light absorption derived from the construction of Z-scheme heterostructure. In-situ formed metallic Ag2S act as the electron mediator and Ag nanoparticles possess the surface plasmon resonance (SPR) effect. The prepared heterojunction showed decreased photoluminescence and increased photoelectrochemical performance, indicating high separation rate of photoinduced charge carriers. Furthermore, a possible degradation mechanism of fuchsine solution was proposed. And the results of radical trapping experiments indicated that superoxide radicals (∙O2-) and holes (h+) play major role during the photocatalytic degradation process. This work demonstrates an interesting Z-scheme photocatalytic system for photocatalysis applications.
KW - Mechanism insight
KW - MoS/AgS/AgVO
KW - Photogenerated carriers
KW - Visible-light-driven photocatalysis
KW - Z-scheme heterojunction
UR - http://www.scopus.com/inward/record.url?scp=85126872183&partnerID=8YFLogxK
U2 - 10.1016/j.jallcom.2022.164642
DO - 10.1016/j.jallcom.2022.164642
M3 - 文章
AN - SCOPUS:85126872183
SN - 0925-8388
VL - 908
JO - Journal of Alloys and Compounds
JF - Journal of Alloys and Compounds
M1 - 164642
ER -