Boosting Hydrogen Peroxide Photosynthetic Efficiency via Enhanced Adsorption of Small Water Clusters

Abstract

Abstract The bottleneck of overall photosynthesis of hydrogen peroxide (H2O2) lies in the slow kinetic water oxidation half-reaction. This inefficiency arises from the principal species of the stable quadrilateral configuration in liquid water, which obstructs the effective extraction of hydrogen from water molecules necessary for the reduction of O2 to H2O2. In this study, the incorporation of sulfonic acid groups onto the organic polymer photocatalysts induced the adsorption of smaller water clusters with weak hydrogen bond, leading to the enhanced the kinetics of the photocatalytic water oxidation reaction. Notably, the introduction of various sulfonic acid groups significantly improved the photocatalytic H2O2 production of in alkaline conditions (1M NaOH) without the use of sacrificial reagents. The optimal sulfonated photocatalyst achieved a H2O2 production rate of 45.54 μmol h-1, representing a 14-fold increase compared to the pristine one. Furthermore, the solar-to-chemical conversion (SCC) efficiency in real outdoor environment reached 0.04%, surpassing all previously reported values. Thorough investigations into the underlying mechanisms demonstrated that the incorporation of sulfonate groups enhances the separation efficiency of photogenerated charge carriers. More importantly, this modification led to the enhanced adsorption of small water clusters, which mitigated the competition posed by water oxidation process and ultimately facilitated the extraction of hydrogen from water molecules for the photosynthetic production of H2O2.

Supplementary files

Article information

Article type
Paper
Submitted
25 Sep 2025
Accepted
02 Dec 2025
First published
04 Dec 2025

Energy Environ. Sci., 2025, Accepted Manuscript

Boosting Hydrogen Peroxide Photosynthetic Efficiency via Enhanced Adsorption of Small Water Clusters

R. Gao, M. Xia, Y. Deng, B. Yang, N. Huang, Y. Huang, H. Li, L. Bao, W. Liu, T. Ma and L. Ye, Energy Environ. Sci., 2025, Accepted Manuscript , DOI: 10.1039/D5EE05698E

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