4.8 Article

Nanocavity-assisted single-crystalline Ti3+ self-doped blue TiO2(B) as efficient cocatalyst for high selective CO2 photoreduction of g-C3N4

Journal

MATERIALS TODAY CHEMISTRY
Volume 24, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.mtchem.2022.100827

Keywords

Blue TiO2; 2D porous g-C3N4; Photocatalyst; CO2 conversion; Heterogenious catalysis

Funding

  1. National Research Foundation of Korea - Korean government (MEST) [2020H1D3A1A02081461, 2020R1A4A1017737, 2021R1A2C1003767]
  2. National Research Foundation of Korea - Korean government (MSIP) [2020H1D3A1A02081461, 2020R1A4A1017737, 2021R1A2C1003767]
  3. National Research Foundation of Korea [2020H1D3A1A02081461, 2020R1A4A1017737, 2021R1A2C1003767] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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This study successfully enhanced the activity and selectivity of CO2 photocatalytic conversion by introducing porosity in graphitic carbon nitride and integrating it with other materials. The heterostructure material BT/PCN demonstrated superior photocatalytic performance due to effective separation and transportation of charge carriers.
Two-dimensional (2D) graphitic carbon nitride (g-C3N4) has invoked significant interest for photocatalytic applications for its excellent features such as high surface area, visible light absorption, and easy transportation of photogenerated charge carriers, but the most reported g-C3N4 show relatively low photoactivity due to inferior conductivity and rapid recombination of carriers. These can be overcome by inducing porosity in g-C3N4, followed by exfoliation and combining with other materials. Herein, we synthesize nanocavity-assisted oxygen-deficient Ti3+ self-doped blue TiO2(B) nanorods (BT) and integrate them on exfoliated porous g-C3N4 (PCN). The synthesized materials are tested for photocatalytic conversion of CO2 into solar fuels (H-2, CO, and CH4). The fabricated BT/PCN heterostructures exhibit higher photocatalytic CO2 conversion activity and 92% CO-evolving selectivity than BT and PCN. The enhancement in activity of BT/PCN can be attributed to the efficient separation and transportation of charge carriers, facilitated by the unique properties of BT, PCN, and their synergistic interactions. We believe that these results can contribute to the improvement of cost-effectiveness, feasibility, and overall performance for real photocatalytic systems. (C) 2022 Elsevier Ltd. All rights reserved.

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