4.8 Article

Carbon nitride nanotubes with in situ grafted hydroxyl groups for highly efficient spontaneous H2O2 production

Journal

APPLIED CATALYSIS B-ENVIRONMENTAL
Volume 288, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.apcatb.2021.119993

Keywords

g-C3N4; Hydroxyl groups; Photocatalysis; Spontaneous; H2O2 production

Funding

  1. National Key Research and Development Program [2016YFA0204200]
  2. National Natural Science Foundation of China [22006038, 21777044, 22076046]
  3. China Postdoctoral Science Foundation [2020M681209]
  4. Science and Technology Commission of Shanghai Municipality [19ZR1472400, 19230711300]
  5. Korean National Research Foundation [2017R1E1A1A01074890]
  6. National Research Foundation of Korea [5199991614244, 2017R1E1A1A01074890] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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A novel alkalinization process was used to successfully synthesize g-C3N4 (CN) nanotubes functionalized with surface > OH groups, which provide a large surface area and improved mass transfer properties for efficient H2O2 production. The in situ grafted > OH groups capture photogenerated holes, promoting charge separation and enabling the production of H2O2 without sacrificial agents. This work presents a new strategy for spontaneous H2O2 production using a metal-free CN photocatalyst.
An active and inexpensive photocatalyst for H2O2 production is desirable for industrial applications. However, obtaining high photocatalytic activity from metal-free catalysts without the use of sacrificial electron donors is difficult. Herein, g-C3N4 (CN) nanotubes functionalized with surface > OH groups that are grafted in situ were successfully synthesized via a novel alkalinization process. The nanotube structures provide a large surface area and improved mass transfer properties. In situ grafted > OH groups can capture photogenerated holes to promote separation of photogenerated charge, enabling the ready availability of electrons and hydrogen ions for H2O2 production. Further, the surface > OH groups help to suppress H2O2 self-decomposition. Consequently, a high rate of 240.36 mu mol h(-1) g(-1) of H2O2 production can be achieved without sacrificial agents, which is the highest H2O2 production in a spontaneous system for metal-free photocatalysts. This work provides a new strategy for an efficient and spontaneous H2O2 production method using a metal-free CN photocatalyst.

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