From Melamine-Cyanuric Acid Supramolecular Aggregates to Carbon Nitride Hollow Spheres

被引:812
|
作者
Jun, Young-Si [1 ]
Lee, Eun Zoo [2 ]
Wang, Xinchen [3 ]
Hong, Won Hi [2 ]
Stucky, Galen D. [1 ]
Thomas, Arne [4 ]
机构
[1] Univ Calif Santa Barbara, Dept Chem & Biochem, Santa Barbara, CA 93106 USA
[2] Korea Adv Inst Sci & Technol, Dept Chem & Biomol Engn, Taejon 305701, South Korea
[3] Fuzhou Univ, Res Inst Photocatalysis, State Key Lab Breeding Base Photocatalysis, Fuzhou 350002, Peoples R China
[4] Tech Univ Berlin, Dept Chem Funct Mat, D-10623 Berlin, Germany
关键词
hydrogen-bonded networks; cooperative assembly; carbon nitride; photocatalysis; SOLID-STATE NMR; METAL NITRIDE; G-C3N4; PHOTODEGRADATION; SEMICONDUCTORS; NANOPARTICLES; CONDENSATION; OXIDATION; POWDER; WATER;
D O I
10.1002/adfm.201203732
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Graphitic carbon nitride (g-CN) is a promising heterogeneous metal-free catalyst for organic photosynthesis, solar energy conversion, and photodegradation of pollutants. Its catalytic performance is easily adjustable by modifying texture, optical, and electronic properties via nanocasting, doping, and copolymerization. However, simultaneous optimization has yet to be achieved. Here, a facile synthesis of mesoporous g-CN using molecular cooperative assembly between triazine molecules is reported. Flower-like, layered spherical aggregates of melamine cyanuric acid complex (MCA) are formed by precipitation from equimolecular mixtures in dimethyl sulfoxide (DMSO). Thermal polycondensation of MCA under nitrogen at 550 degrees C produces mesoporous hollow spheres comprised of tri-s -triazine based g-CN nanosheets (MCA-CN) with the composition of C3N4.14H1.98. The layered structure succeeded from MCA induces stronger optical absorption, widens the bandgap by 0.16 eV, and increases the lifetime of photoexcited charge carriers by twice compared to that of the bulk g-CN, while the chemical structure remains similar to that of the bulk g-CN. As a result of these simultaneous modifi cations, the photodegradation kinetics of rhodamine B on the catalyst surface can be improved by 10 times.
引用
收藏
页码:3661 / 3667
页数:7
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