Journal
JOURNAL OF COLLOID AND INTERFACE SCIENCE
Volume 598, Issue -, Pages 14-23Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2021.04.026
Keywords
Photocatalysis; Graphitic carbon nitride nanosheets; Hollow TiO2 nanosphere; Dielectric resonator; Water splitting
Categories
Funding
- National Natural Science Foundation of China [61775129]
- Fundamental Research Funds for Central Universities [GK201902001]
- Funded Projects for the Academic Leaders and Academic Backbones of Shaanxi Normal University [18QNGG008]
- Scientific and Technological Funds for Returned Overseas Students of Shaanxi Province [2018007]
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The study enhanced the light absorption of CN nanosheets by introducing hollow TiO2 dielectric resonators, leading to improved photocatalytic performance and potential applications in various reactions.
Graphitic carbon nitride (CN) generally needs to be exfoliated into ultrathin nanosheets to reduce photocarrier recombination. However, the exfoliation of CN into nanosheets also reduces the light absorption. How to simultaneously realize low photocarrier recombination and high light absorption remains a challenge in the practical application of CN in photocatalysis. Herein, the light absorption of CN nanosheets was enhanced by introducing hollow TiO2 (h-TiO2) dielectric resonators. The h-TiO2/CN heterostructures were prepared by thermally polymerizing dicyandiamide in the presence of h-TiO2. The electromagnetic resonances of the h-TiO2 resonator creates strong electric field enhancement within, inside, and near external surface of the introduced h-TiO2 nanoshells. The enhanced electric field greatly improves the light absorption of CN located in these regions. The largest hydrogen evolution rate for h-TiO2/CN can reach 6.3 mmol g(-1) h(-1), which is over 3-fold that of pure CN (2.0 mmol g(-1) h(-1)). It is also found that the small amount of CN within and inside h-TiO2 majorly contributes to the photocatalytic performance. These findings open a new avenue by which to enhance the performance of photocatalysts and will be helpful in the design of highly efficient photocatalysts for various reactions. (C) 2021 Elsevier Inc. All rights reserved.
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