g-C3N4/UiO-66 nanohybrids with enhanced photocatalytic activities for the oxidation of dye under visible light irradiation

被引:323
作者
Zhang, Xiaodong [1 ]
Yang, Yang [1 ]
Huang, Wenyuan [1 ]
Yang, Yiqiong [1 ]
Wang, Yuxin [2 ]
He, Chi [3 ]
Liu, Ning [1 ]
Wu, Minghong [4 ]
Tang, Liang [4 ]
机构
[1] Univ Shanghai Sci & Technol, Sch Environm & Architecture, Dept Environm Sci & Engn, Shanghai 200093, Peoples R China
[2] Taizhou Vocat & Tech Coll, Inst Appl Biotechnol, Taizhou 318000, Zhejiang, Peoples R China
[3] Xi An Jiao Tong Univ, State Key Lab Multiphase Flow Power Engn, Sch Energy & Power Engn, Xian 710049, Shaanxi, Peoples R China
[4] Shanghai Univ, Sch Environm & Chem Engn, Shanghai 200444, Peoples R China
基金
中国国家自然科学基金;
关键词
g-C3N4; UiO-66; Photocatalysis; Visible light; Rhodamine B; METAL-ORGANIC-FRAMEWORK; FACILE SYNTHESIS; CATALYTIC-OXIDATION; DRIVEN PHOTOCATALYST; HYDROGEN-PRODUCTION; CO OXIDATION; EFFICIENT; ZNO; NANOCOMPOSITES; REDUCTION;
D O I
10.1016/j.materresbull.2017.11.028
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
In this study, g-C3N4 nanosheets coated UiO-66 nanohybrids were fabricated via a simple solvothermal method. The physicochemical parameters, structural and electrochemical properties of g-C3N4/UiO-66 nanohybrids (CNUO-x) were investigated. The nanohybrids were systematically characterized by XRD, FT-IR, TGA, TEM, SEM, EDS elemental mappings, XPS, NZ adsorption-desorption isotherms, PL and DRS. It was found that the addition of moderate g-C3N4 could enhance the separation and migration rate of photo-induced charges, consequently leading to the increase of photocatalytic efficiency. The CNUO-1 nanohybrid exhibited better photocatalytic activity for the oxidation of Rh B under visible light irradiation, and displayed about 6.0 and 3.3 times faster than that of g-C3N4 and UiO-66, respectively. Meanwhile, the nanohybrid showed excellent stability and reusability in four cyclic experiments. Finally, the increased photocatalytic reaction mechanism was also proposed. center dot O-2(-), h(+) and center dot OH were further found to be the main active contributors.
引用
收藏
页码:349 / 358
页数:10
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