Poly(heptazine imide) with enlarged interlayers spacing for efficient photocatalytic NO decomposition

Min ZHOU, Libin ZENG, Rong LI, Can YANG, Xing QIN, Wing Kei HO, Xinchen WANG

Research output: Contribution to journalArticlespeer-review

Abstract

Sluggish charge kinetics and NO diffusion largely restrict the photocatalytic efficiency of low-dose NO removal by layered carbon nitride (CN). Herein, a novel poly(heptazine imide)-based CN (CN-NaLi) with enlarged interlayer spacing was fabricated by an easy, efficient and unique molten-salt approach. The charge flows induced by the poly(heptazine imide) structure can be delocalized/separated/transferred, resulting in a significantly boosted efficiency of charge kinetics. The enlarged interlayers distance of CN-NaLi reduced the charge-recombination probability and promoted NO diffusion/adsorption/activation. Accordingly, abundant separated light-induced electrons can be supplied to react and activate the O₂ molecules. Meanwhile, large amounts of adsorbed NO were fixed and converted into the intermediate product during the same time compared with unmodified CN. The reduced energy barrier endowed CN-NaLi with superior visible-light-driven performance, high stability, and decreased generation of toxic products in NO purification. This research highlighted the vital concerns in affecting the interlayer NO diffusion/adsorption/activation and charge delocalization/separation/transportation. Copyright © 2022 Elsevier B.V. All rights reserved.
Original languageEnglish
Article number121719
JournalApplied Catalysis B: Environmental
Volume317
Early online date19 Jul 2022
DOIs
Publication statusE-pub ahead of print - 19 Jul 2022

Citation

Zhou, M., Zeng, L., Li, R., Yang, C., Qin, X., Ho, W., & Wang, X. (2022). Poly(heptazine imide) with enlarged interlayers spacing for efficient photocatalytic NO decomposition. Applied Catalysis B: Environmental, 317. Retrieved from https://doi.org/10.1016/j.apcatb.2022.121719

Keywords

  • Poly(heptazine imide)
  • Enlarged interlayer spacing
  • NO diffusion
  • Charge kinetics
  • Photocatalysis

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