4.6 Article

Microwave awakening the n-π* electronic transition in highly crystalline polymeric carbon nitride nanosheets for photocatalytic hydrogen generation

Journal

JOURNAL OF ENERGY CHEMISTRY
Volume 65, Issue -, Pages 541-547

Publisher

ELSEVIER
DOI: 10.1016/j.jechem.2021.07.002

Keywords

Polymeric carbon nitride; Microwave; n-pi* electronic transition; Hydrogen

Funding

  1. National Natural Science Foundation of China [52072001, 51872003, U1832148, U1932218]
  2. Anhui Provincial Natural Science Foundation [1908085J21, 1908085QB83]

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Activating the n-pi* electronic transition in polymeric carbon nitride (PCN) through microwave thermolysis of urea pellets significantly enhances photocatalytic hydrogen generation, leading to a substantial increase in H-2 production rate.
The n-pi* electronic transition in polymeric carbon nitride (PCN) can remarkably harvest visible light, which thus potentially promotes the photocatalytic hydrogen H-2 generation. However, awaking the n-pi* electronic transition has proven to be a grand challenge. Herein, we reported on the awakening of n-pi* electronic transition by microwave thermolysis of urea pellet, which yielded the PCN with absorption edge of 600 nm, near 140 nm red-shift from 460 nm of pristine PCN. The n-pi* electronic transition endows PCN with an increased photocatalytic H-2 generation, with a highest H-2 rate of 61.7 lmol h(-1) under visible light exposure, which is near 6 times higher than that by using the PCN from the thermolysis of urea pellets in an electric furnace (10.6 lmol h(-1)). Furthermore, the n-pi* transition in PCN leads to the longest wavelength of 535 nm that can initiate H-2 generation, remarkably longer than the absorption edge of pristine PCN (460 nm). This work manifests the advantages of microwave sintering route to awaken the n-pi* electronic transition in PCN for an increased photocatalytic performance. (C) 2021 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by ELSEVIER B.V. and Science Press. All rights reserved.

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