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Porous graphitic carbon nitride (g-C(3)N(4)) was prepared by a simple pyrolysis of urea, and then a g-C(3)N(4)-Pt-TiO(2) nanocomposite was fabricated via a facile chemical adsorption followed by a calcination process. The obtained products were characterized by X-ray diffraction, X-ray photoelectron spectroscopy, UV-vis diffuse reflectance absorption spectra, and electron microscopy. It is found that the visible-light-induced photocatalytic hydrogen evolution rate can be remarkably enhanced by coupling TiO(2) with the above g-C(3)N(4), and the g-C(3)N(4)-Pt-TiO(2) composite with a mass ratio of 70 : 30 has the maximum photoactivity and excellent photostability for hydrogen production under visible-light irradiation, and the stable photocurrent of g-C(3)N(4)-TiO(2) is about 1.5 times higher than that of the bare g-C(3)N(4). The above experimental results show that the photogenerated electrons of g-C(3)N(4) can directionally migrate to Pt-TiO(2) due to the close interfacial connections and the synergistic effect existing between Pt-TiO(2) and g-C(3)N(4) where photogenerated electrons and holes are efficiently separated in space, which is beneficial for retarding the charge recombination and improving the photoactivity.
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Chai et al. (2012) studied this question.
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