Rational Design of MOF/COF Hybrid Materials for Photocatalytic H2 Evolution in the Presence of Sacrificial Electron Donors

被引:584
|
作者
Zhang, Feng-Ming [1 ]
Sheng, Jing-Li [1 ]
Yang, Zhao-Di [1 ]
Sun, Xiao-Jun [1 ]
Tang, Hong-Liang [1 ]
Lu, Meng [2 ]
Dong, Hong [1 ]
Shen, Feng-Cui [2 ]
Liu, Jiang [2 ]
Lan, Ya-Qian [2 ]
机构
[1] Harbin Univ Sci & Technol, Key Lab Green Chem Engn & Technol, Coll Heilongjiang Prov, Coll Chem & Environm Engn, 4 Linyuan Rd, Harbin 150040, Heilongjiang, Peoples R China
[2] Nanjing Normal Univ, Jiangsu Collaborat Innovat Ctr Biomed Funct Mat, Jiangsu Key Lab New Power Batteries, Sch Chem & Mat Sci, 1 Wenyuan Rd, Nanjing 210023, Jiangsu, Peoples R China
关键词
covalent organic frameworks; hybrid materials; metal-organic frameworks; photocatalytic hydrogen evolution; COVALENT ORGANIC FRAMEWORKS; HYDROGEN-PRODUCTION; HIGHLY CRYSTALLINE; CARBON NITRIDE; H-2; EVOLUTION; WATER; SEMICONDUCTOR; PHOTOCATHODES; ENHANCEMENT; GENERATION;
D O I
10.1002/anie.201806862
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Crystalline and porous covalent organic frameworks (COFs) and metal-organic frameworks (MOFs) materials have attracted enormous attention in the field of photocatalytic II2 evolution due to their long-range order structures, large surface areas, outstanding visible light absorbance, and tunable band gaps. In this work, we successfully integrated two-dimensional (2D) COF with stable MOF. By covalently anchoring NH2-UiO-66 onto the surface of TpPa-1-COF, a new type of MOF/COF hybrid materials with high surface area, porous framework, and high crystallinity was synthesized. The resulting hierarchical porous hybrid materials show efficient photocatalytic H-2 evolution under visible light irradiation. Especially, NH2-UiO-66/TpPa-1-COF (4:6) exhibits the maximum photocatalytic H-2 evolution rate of 23.41mmolg(-1)h(-1) (with the TOF of 402.36 h(-1)), which is approximately 20 times higher than that of the parent TpPa-1-COF and the best performance photocatalyst for H-2 evolution among various MOF- and COF-based photocatalysts.
引用
收藏
页码:12106 / 12110
页数:5
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