Biomimetic D–A1–A2 Organic Cages with Recombination-Suppressed Sequential Charge Transfer for Hydrogen Peroxide Photosynthesis

View at publisher
Authors: Zhao Gao, Zihao Wang, Xupeng Ji, Qi Wen, Yuncong Xue, Wei Jun Tian
Cited by: 1
References: 77

Abstract

Photocatalytic synthesis of hydrogen peroxide (H 2 O 2 ) offers a sustainable route toward green oxidation and environmental remediation, yet its efficiency is fundamentally constrained by rapid backward charge recombination, underscoring the synthetic challenge of creating molecular architectures capable of enforcing directional and recombination-suppressed charge transfer. Inspired by the stepwise electron transfer within the compartmentalized reaction centers of thylakoid membranes in natural photosynthesis, we design here biomimetic donor–acceptor 1–acceptor 2 (D–A1–A2) organic cages, where donors and acceptors are orderly positioned along an energy gradient to achieve a recombination-suppressed sequential charge transfer (RS-SCT) process, thereby promoting photocatalytic H 2 O 2 production. Two single crystals of D–A1–A2 organic cages, BNC-O and BNC-S, are successfully constructed from in situ generated ditopic boronated monomers and C 3 -symmetric monomers via B–N dative bonds. Both cages show the RS-SCT process from electron-rich triphenylamines as the D through coordinated pyridines as A1 to more electron-deficient benzoxadiazoles or benzothiadiazoles as A2, which enable sequential charge migration and suppress backward charge recombination with prolonged excited-state lifetimes. As a result, the self-assembled two-dimensional crystalline cages featuring well-organized active sites exhibit significantly enhanced photocatalytic H 2 O 2 production performance, achieving a rate of 4.15 mmol g –1 h –1 for crystalline BNC-O, which is markedly higher than those of the corresponding components lacking RS-SCT, including the individual D, A1, A2, and D–A systems. Furthermore, these D–A1–A2 organic cages are implemented in a photocatalytic microflow reactor for controllable in situ H 2 O 2 generation under sunlight, which is further integrated into a cascade phenol-containing wastewater treatment system.

Fields of Study & Subjects

Supramolecular Chemistry and Complexes Covalent Organic Framework Applications Luminescence and Fluorescent Materials

Publication details

Journal / source
Journal of the American Chemical Society
Publisher
American Chemical Society (ACS)
Volume
148
Issue
28
Pages
30265–30277
Publication date
11 July 2026
Language
EN