Issue 29, 2024

An anthraquinone-based conjugated donor–acceptor (D–A) polymer as a highly efficient photocatalyst for hydrogen peroxide production

Abstract

Photocatalytic hydrogen peroxide (H2O2) generation from oxygen and water using a polymeric photocatalyst is a promising method for solar to chemical energy transformation. Here, we report the hydrothermal synthesis of anthraquinone-based conjugated polymer (ACP) nanoparticles (NPs) for efficient H2O2 generation. This synthesis avoids the use of a metal-based catalyst. Anthraquinone (AQ) is crosslinked to resorcinol units of the polymeric chains via a methylene linker to obtain ACP NPs. In the polymeric framework, AQ acts as an acceptor (A), whereas resorcinol acts as a donor (D) through its benzenoid/quinoid forms. The arrangement of donor–acceptor units in the polymeric framework and π-stacked aromatic structure resulted in a broad range of visible light absorption with a low bandgap of 1.78 eV. Hydrothermal synthesis produced ACP as uniformly grown globular-shaped particles with an average size of ∼450 nm. The ACP photocatalyst demonstrated high activity of H2O2 generation with a solar-to-chemical energy conversion efficiency of 1.92% in pure water without a sacrificial proton donor. We could achieve a 28.09 millimolar concentration of H2O2 after 20 h irradiation in pure water under ambient conditions with an initial rate of H2O2 generation of 6097 μmol g−1 h−1. This concentration is almost sufficient for direct use in single-compartment H2O2 fuel cells.

Graphical abstract: An anthraquinone-based conjugated donor–acceptor (D–A) polymer as a highly efficient photocatalyst for hydrogen peroxide production

Supplementary files

Article information

Article type
Paper
Submitted
23 Feb 2024
Accepted
11 Jun 2024
First published
26 Jun 2024

J. Mater. Chem. A, 2024,12, 18433-18439

An anthraquinone-based conjugated donor–acceptor (D–A) polymer as a highly efficient photocatalyst for hydrogen peroxide production

A. V. Munde, D. M. Sanke, N. G. Ghosh, J. Bezboruah, S. Roy and S. S. Zade, J. Mater. Chem. A, 2024, 12, 18433 DOI: 10.1039/D4TA01248H

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