journal article·2024-08

Novel A–D–A Type Naphthalenediimide Supramolecule for H2O2 Photosynthesis with Solar‐to‐Chemical Conversion 1.03%

Rong Ji, Yuming Dong, Xinyu Sun, Pengken Li, Renbao Zhang, Chengsi Pan, Hui Zhao, Yongfa Zhu

Advanced Energy Materials· Volume 14· Issue 30
Publisher page

Abstract

Abstract Organic supermolecules have shown great promise for photocatalytic hydrogen peroxide (H2O2) production. However, the limitation of intramolecular charge separation efficiency is still a crucial scientific problem. In this study, a novel acceptor–donor–acceptor (A–D–A) type naphthalenediimide supramolecule (SA‐NDI) is successfully designed for overcoming fundamental issues in organic supermolecule. Composed of one electron‐rich core (naphthalenediimide) and two electron‐poor units (aminopyridine), the supramolecule possesses strong intramolecular charge transfer ability. Meanwhile, the SA‐NDI has an obviously stronger internal electric field, which is 2.83 times higher than that of D–A type supramolecule. The A–D–A type SA‐NDI efficiently accelerates charge separation, so that the intramolecular electron quickly migrates to the acceptor for a two‐electron oxygen reduction reaction. The SA‐NDI supramolecule shows excellent H2O2 accumulation ability (13.7 mm) and stable cyclic time above 120 h. Meanwhile, the catalyst exhibits a superior solar‐to‐chemical conversion efficiency of 1.03% under simulated solar irradiation. This work provides an entirely new idea to design an organic supramolecule with an efficient intramolecular charge transfer monomer.
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Research context

OpenAlex topics: Advanced Photocatalysis Techniques · Perovskite Materials and Applications · TiO2 Photocatalysis and Solar Cells

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

International Joint Research Center for Photo‐responsive Molecules and Materials School of Chemical and Material Engineering Jiangnan University Wuxi 214122 China

Department of Chemistry Tsinghua University Beijing 100084 China

Funding

National Natural Science Foundation of China

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