4.3 Article

Enhanced visible-light photocatalytic activity of g-C3N4-ZnWO4 by fabricating a heterojunction: investigation based on experimental and theoretical studies

期刊

JOURNAL OF MATERIALS CHEMISTRY
卷 22, 期 44, 页码 23428-23438

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c2jm34965e

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资金

  1. National Natural Science Foundation of China [91022034, 51172127, 21173131]
  2. Excellent Youth Foundation of Shandong Scientific Committee [JQ201015]
  3. Youth Scientist (Doctoral) Foundation of Shandong Province of China [BS2009CL038]
  4. Independent Innovation Foundation of Shandong University [2012TS212]
  5. Graduate Independent Innovation Foundation of Shandong University [yzc12118]

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We present a systematic investigation of the microscopic mechanism of interface interaction, charge transfer and separation, as well as their influence on the photocatalytic activity of heterojunctions by a combination of theoretical calculations and experimental techniques for the g-C3N4-ZnWO4 composite. HRTEM results and DFT calculations mutually validate each other to indicate the reasonable existence of g-C3N4 (001)-ZnWO4 (010) and g-C3N4 (001)-ZnWO4 (011) interfaces. The g-C3N4-ZnWO4 heterojunctions show higher photocatalytic activity for degradation of MB than pure g-C3N4 and ZnWO4 under visible-light irradiation. Moreover, the heterojunctions significantly enhance the oxidation of phenol in contrast to pure g-C3N4, the phenol oxidation capacity of which is weak, clearly demonstrating a synergistic effect between g-C3N4 and ZnWO4. Interestingly, based on the theoretical calculations, we find that electrons in the upper valence band can be directly excited from g-C3N4 to the conduction band, that is, the W 5d orbital of ZnWO4, under visible-light irradiation, which should yield well-separated electron-hole pairs, with high photocatalytic performance in g-C3N4-ZnWO4 heterojunctions as shown by our experiment. The microcosmic mechanisms of interface interaction and charge transfer in this system can be helpful for fabricating other effective heterostructured photocatalysts.

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