Flexible Organic Radical Cocrystal With 94% Photothermal Conversion Efficiency

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Authors: Bingrui Chen, Huixu Yang, Siqi Zhang, Zening Li, Fusang Jiang, Asif Equbal, Dongqian Xu, Xuan Zhang, Liang Li, Pancě Naumov, Yujian Zhang
Cited by: 1
References: 72

Abstract

ABSTRACT Flexible photothermal materials made of particulate carbon, metal, polymer, or semiconductors often suffer from interfacial incompatibility, leading to cracking and delamination over prolonged use. These limitations make it difficult for flexible composite materials to simultaneously meet the requirements of long‐term interfacial stability and high photothermal performance. Here we circumvented these persistent challenges by using flexible organic crystals, where the absorber is a structurally homogeneous radical cocrystal and strong light absorption is accomplished by charge transfer (CT) between two molecular components. We cocrystallized electron donor perylene (PE) and acceptor naphthalene diimide (NDI) to prepare mechanically flexible, centimeter‐size cocrystals (PE‐NDI), which demonstrate persistent radical characteristics with a spin coherence time of 2.1 µs. Prominent donor–acceptor interaction (−87.7 kJ mol −1 ) facilitates strong light absorption from 200 to 780 nm, while hydrogen bonds are thought to account for the reversible elastic bending. Excitation at 685 nm yields an extraordinarily high photothermal conversion efficiency of 94%. Integration of PE‐NDI in a thermoelectric generator enabled direct solar energy harvesting via a photo‐thermo‐electric conversion sequence, demonstrating the potential of flexible cocrystals for renewable energy harvesting. This work highlights the untapped potential of mechanically compliant organic crystals as flexible, single‐component, lightweight photothermal materials.

Fields of Study & Subjects

Synthesis and Properties of Aromatic Compounds Organic and Molecular Conductors Research Magnetism in coordination complexes

Publication details

Journal / source
Angewandte Chemie International Edition
Publisher
Wiley
Volume
65
Issue
23
Pages
e1702104–e1702104
Publication date
22 April 2026
Language
EN