4.8 Article

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

期刊

ADVANCED FUNCTIONAL MATERIALS
卷 23, 期 29, 页码 3661-3667

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.201203732

关键词

hydrogen-bonded networks; cooperative assembly; carbon nitride; photocatalysis

资金

  1. Project Light2Hydrogen of the BMBF [03IS2071D]
  2. KBSI [T31605]
  3. Brain Korea 21 (BK21)
  4. Advanced Biomass R&D Center of Global Frontier Project [ABC-2011-0031354]
  5. Ministry of Education, Science, and Tech-nology of Korea
  6. University of California Lab Fees Research Program

向作者/读者索取更多资源

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.

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