2D/2D p-n Heterojunctions of CaSb2O6/g-C3N4for Visible Light-Driven Photocatalytic Degradation of Tetracycline

被引:12
作者
Li, Yuanyuan [1 ]
Shen, Jinfeng [1 ]
Quan, Wenxuan [1 ]
Diao, Yue [1 ]
Wu, Meijun [1 ]
Zhang, Bin [3 ]
Wang, Yaoqiong [2 ]
Yang, Dingfeng [2 ]
机构
[1] Chongqing Univ Educ, Cooperat Innovat Ctr Lipid Resources & Childrens, Dept Biol & Chem Engn, Chongqing 400067, Peoples R China
[2] Chongqing Univ Technol, Coll Chem & Chem Engn, 69 Hongguang Rd, Chongqing 400054, Peoples R China
[3] Chongqing Univ, Analyt & Testing Ctr, Chongqing 401331, Peoples R China
基金
美国国家科学基金会;
关键词
P-n heterojunction; CaSb2O6; g-C3N4; Photoelectrochemistry; Tetracycline; CARBON NITRIDE NANOSHEETS; IN-SITU SYNTHESIS; G-C3N4; PERFORMANCE; NANOCOMPOSITE; ENHANCEMENT; FABRICATION; EFFICIENCY; STABILITY; EVOLUTION;
D O I
10.1002/ejic.202000635
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Despite many attempts to build g-C(3)N(4)based heterojunctions there are currently no systematic guidelines for designing such composites. Herein, we rationally designed and synthesized a novel CaSb2O6/g-C(3)N(4)2D/2D heterojunction with ideal lattice matching. The as-synthesized heterojunctions had superior visible light-driven photodegradation toward tetracycline solution compared with those of pristine g-C(3)N(4)and CaSb2O6. The corresponding maximum apparent kinetic rate constant was 0.01388 min(-1), which was approximately 2.4 and 53 times greater than those of g-C(3)N(4)and CaSb2O6, respectively. Additionally, photoelectrochemical measurements indicated that the enhanced photocatalytic performance was attributed to generation of an internal electric field by the intimate contact p-n heterojunction. The main reactive species were(center dot)OH,(center dot)O(2)(-)and h(-)are the dominate reactive species in the photocatalytic process. This study will inspire efforts to build 2D/2D heterojunction photocatalysts with efficient carrier separation and higher photocatalytic performance through structural chemistry or solid state chemistry analysis.
引用
收藏
页码:3852 / 3858
页数:7
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