Fabrication of BiOI@UIO-66(NH2)@g-C3N4 ternary Z-scheme heterojunction with enhanced visible-light photocatalytic activity

被引:115
作者
Liang, Qian [1 ]
Cui, Sainan [1 ]
Jin, Jie [1 ]
Liu, Changhai [3 ]
Xu, Song [1 ]
Yao, Chao [1 ]
Li, Zhongyu [1 ,2 ]
机构
[1] Changzhou Univ, Adv Catalysis & Green Mfg Collaborat Innovat Ctr, Sch Petrochem Engn, Changzhou 213164, Peoples R China
[2] Changzhou Univ, Sch Environm & Safety Engn, Changzhou 213164, Peoples R China
[3] Changzhou Univ, Sch Mat Sci & Engn, Jiangsu Collaborat Innovat Ctr Photovolat Sci & E, Changzhou 213164, Peoples R China
基金
中国国家自然科学基金;
关键词
BiOI; UIO-66(NH2); Photodegradation; Z-scheme heterojunction; METAL-ORGANIC FRAMEWORK; GRAPHENE OXIDE; H-2; EVOLUTION; CO2; REDUCTION; DEGRADATION; NANOCOMPOSITE; REMOVAL; WATER; NANOPARTICLES; SELECTIVITY;
D O I
10.1016/j.apsusc.2018.06.173
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
A novel ternary heterojunction BiOI@UIO-66(NH2)@g-C3N4 (BiOI@UNCN) was synthesized by in-situ solvothermal-hydrothermal approach, showing superior photocatalytic degradation of RhB and TC under visible-light irradiation. The optimal BiOI@UNCN-40 composite exhibits the highest degradation efficiency of RhB (95%) in 80 min and TC (80%) in 180 min in comparison with pristine BiOI, UIO-66(NH2) and UIO-66(NH2)@g-C3N4. The improved photocatalytic activity of BiOI@UNCN can be ascribed to its improved visible-light absorption range, the large specific surface area based on UIO-66(NH2) as well as the formation of an effective n-pn type heterojunction driven by Z-scheme mechanism. The formed Z-scheme mechanism at the interface of ternary composite facilitates the separation and transfer of photoexcited charge carrier, which is confirmed from the results of PL and EIS spectra. The photocatalytic mechanism is further proposed based on the trapping experiment, and the transfer process of photoinduced electron-hole pairs is discussed. This work provides an effective strategy for designing a new ternary photocatalytic system toward degradation of organic pollutants.
引用
收藏
页码:899 / 907
页数:9
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