Eu doped g-C3N4 nanosheet coated on flower-like BiVO4 powders with enhanced visible light photocatalytic for tetracycline degradation

被引:54
|
作者
Wang, Min [1 ]
Guo, Pengyao [2 ]
Zhang, Yu [1 ]
Liu, Tingyu [3 ]
Li, Songlin [1 ]
Xie, Yuanhua [1 ]
Wang, Youzhao [1 ]
Zhu, Tong [1 ]
机构
[1] Northeastern Univ, Sch Mech Engn & Automat, Shenyang 110189, Liaoning, Peoples R China
[2] Northeastern Univ, Sch Resources & Civil Engn, Shenyang 110189, Liaoning, Peoples R China
[3] Shenyang Second Senior High Sch, Shenyang 110126, Liaoning, Peoples R China
基金
中国国家自然科学基金;
关键词
BiVO4; g-C3N4; Eu doped; Core-shell structure; Herterjunction; Photocatalysis; CHARGE-SEPARATION; GRAPHITIC C3N4; H-2; EVOLUTION; HETEROJUNCTION; PERFORMANCE; WATER; PHOTODEGRADATION; NANOCOMPOSITES; INSIGHTS; NITROGEN;
D O I
10.1016/j.apsusc.2018.05.084
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In present work, Eu-CN@BiVO4 core-hell heterojunction photocatalyst was successfully synthesized via exfoliating the bulk Eu doped g-C3N4 to nanosheet and then coating on the surface of flower-like BiVO4 via sonication impregnation and heating process. The samples were characterized by serials measurements including XRD, FT-IR, SEM, EDS, TEM, HRTEM, XPS, UV-vis DRS, BET, and PL. The results showed that this synthesis method can easily and tightly make g-C3N4 or Eu doped g-C3N4 nanosheet being combined with flower-like BiVO4 to form a core-hell heterojunction structure, which benefited in the charge transfer across the interface of CN (or Eu-CN) and BiVO4. And from the photocatalytic activity test, there are only about 65% of tetracycline (TC) being photodegraded in 50 min over BiVO4, but 90.79% of TC in 50 min over CN@BiVO4, and 92.1% of TC in 30 min over Eu-CN@BiVO4. The Eu-CN@BiVO4 photocatalyst has much higher photocatalytic than CN@BiVO4 due to the presence of Eu(III) in Eu-CN@BiVO4 capture photoinduced electrons and achieve the elevated photoinduced electron-hole transferring and separation rate, further to lead to superior photocatalytic efficiency.
引用
收藏
页码:11 / 22
页数:12
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