摘要
Graphitic carbon nitride (g-C 3 N 4 ), as an organic polymer semiconductor, has been the focus of photocatalysts due to its physical and chemical stability, low cost and non-toxicity. However, pristine g-C 3 N 4 also has many drawbacks, such as small specific surface area and easy recombination of photoexcited carriers, which hampered its practical application. In this work, we first propose a design idea of embedding stereo molecular scaffold into g-C 3 N 4 framework with a facile copolymerization method for better exfoliating g-C 3 N 4 to reach a better photocatalytic hydrogen evolution under ordinary pressure. The stereo molecular scaffold looses the interlayer stacking of bulk g-C 3 N 4 , benefitting the exfoliation of g-C 3 N 4 . The hydrogen evolution activity of stereo molecular scaffold doped g-C 3 N 4 (AMCN-3-E) is about 7.54 times higher than that of the pristine MCN, which may due to the activated π → π * and n → π * electron transitions, creating more electron transition paths and accelerating the separation of photoexcited electrons and holes.
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