Issue 20, 2024

Bi-directional charge transfer channels in highly crystalline carbon nitride enabling superior photocatalytic hydrogen evolution

Abstract

Introducing a donor–acceptor (D–A) unit is an effective approach to facilitate charge transfer in polymeric carbon nitride (PCN) and enhance photocatalytic performance. However, the introduction of hetero-molecules can lead to a decrease in crystallinity, limiting interlayer charge transfer and inhibiting further improvement. In this study, we constructed a novel D–A type carbon nitride with significantly higher crystallinity and a bi-directional charge transfer channel, which was achieved through 2,5-thiophenedicarboxylic acid (2,5-TDCA)-assisted self-assembly followed by KCl-templated calcination. The thiophene and cyano groups introduced serve as the electron donor and acceptor, respectively, enhancing in-plane electron delocalization. Additionally, introduced potassium ions are intercalated among the adjacent layers of carbon nitride, creating an interlayer charge transfer channel. Moreover, the highly ordered structure and improved crystallinity further facilitate charge transfer. As a result, the as-prepared photocatalyst exhibits superior photocatalytic hydrogen evolution (PHE) activity of 7.449 mmol h−1 g−1, which is 6.03 times higher than that of pure carbon nitride. The strategy of developing crystalline D–A-structured carbon nitride with controlled in-plane and interlayer charge transfer opens new avenues for the design of carbon nitride with enhanced properties for PHE.

Graphical abstract: Bi-directional charge transfer channels in highly crystalline carbon nitride enabling superior photocatalytic hydrogen evolution

Supplementary files

Article information

Article type
Paper
Submitted
25 2月 2024
Accepted
21 4月 2024
First published
07 5月 2024

Nanoscale, 2024,16, 9802-9810

Bi-directional charge transfer channels in highly crystalline carbon nitride enabling superior photocatalytic hydrogen evolution

R. Liu, S. Liu, J. Lin, X. Zhang, Y. Li, H. Pan, L. Kong, S. Zhu and J. Wang, Nanoscale, 2024, 16, 9802 DOI: 10.1039/D4NR00796D

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