Issue 34, 2022

Effective modification of photocatalytic and piezocatalytic performances for poly(heptazine imide) by carbon dots decoration

Abstract

As the high-crystalline phase of carbon nitride, poly(heptazine imide) (PHI) has attracted much attention in recent years, considering the more effective light absorption, better charge carrier behavior, and higher surface area of PHI compared with its counterpart with a melon structure that is commonly synthesized through thermal polymerization. Nevertheless, exploring effective strategies to further improve the performance of PHI is still highly desirable. In this work, it is revealed that the photocatalytic as well as piezocatalytic performances of PHI are greatly promoted by coupling with carbon dots (CDots) through a facile ultrasonication process. Detailed structure characterizations indicate that a very low content of CDots (0.05%) decoration can double the light absorbance and achieve the efficient separation and transfer of photogenerated charge carriers. The optimal photocatalytic hydrogen evolution rate of PHI/CDots is about 2.49 and 2.81 times that of PHI, under UV-Visible and visible light irradiation, respectively. Moreover, the piezocatalytic H2O2 generation and KMnO4 degradation activities of PHI/CDots are around 2 times that of PHI. The results obtained in this work provide references for the modification of PHI and may inspire new strategies for the design of highly efficient carbonaceous photocatalysts.

Graphical abstract: Effective modification of photocatalytic and piezocatalytic performances for poly(heptazine imide) by carbon dots decoration

Supplementary files

Article information

Article type
Paper
Submitted
09 Jun 2022
Accepted
19 Jul 2022
First published
03 Aug 2022

Dalton Trans., 2022,51, 13015-13021

Effective modification of photocatalytic and piezocatalytic performances for poly(heptazine imide) by carbon dots decoration

S. Wang, H. Zhang, R. Nie, Y. Ning, C. Zhao, Z. Xia, P. Niu, L. Li and S. Wang, Dalton Trans., 2022, 51, 13015 DOI: 10.1039/D2DT01819E

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