Polyacid-Protonated Covalent Organic Frameworks Enable Stable and Efficient Photothermal Textiles

Protonation is an effective strategy to enhance light trapping and photothermal conversion in covalent organic frameworks (COFs), yet conventional protonation sites are prone to environmental deactivation, leading to diminished stability and photothermal performance. Inspired by the stability of protein matrices, we developed polyacid-protonated COFs (PaCOFs) through in situ polymerization of dimercaptobutanesioic acid via dynamic disulfide bonds within COF pore channels. The resulting PaCOFs exhibit exceptional protonation stability and deliver a superior photothermal conversion efficiency of 77.8%, surpassing those of most conventional photothermal nanomaterials. Notably, PaCOFs can be readily processed by electrospinning into dual-mode thermal management textiles that achieve radiative cooling (∼7.2 °C) and solar heating (∼10.1 °C) under sunlight. These textiles outperform their commercial counterparts in wearable applications, establishing polyacid protonation as a robust strategy for stabilizing COFs and advancing their integration into photothermal energy conversion and personal thermal management.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-12-19
DOI
https://doi.org/10.1021/jacs.5c16049
Citations
2
Primary Topic
Covalent Organic Framework Applications
Type
article
Field-Weighted Citation Impact
1.04
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article

Polyacid-Protonated Covalent Organic Frameworks Enable Stable and Efficient Photothermal Textiles

Da‐Wei Gu, Yongwu Peng, Guinan Chen, Yaojun Liu et al.
2 citations
Journal of the American Chemical Society
Covalent Organic Framework Applications
1.04
article

Polyacid-Protonated Covalent Organic Frameworks Enable Stable and Efficient Photothermal Textiles

Da‐Wei Gu, Yongwu Peng, Guinan Chen, Yaojun Liu, Jianhan Hong, Chuyi Wang, Zhipeng Chang, Jing Li, Xiaohui Li, Xiaohu Wang, Xingyun Liu, Liangjun Chen, Luyao Xu, Luoting Zhou, Guang Zhang
article en
2 citations

Abstract

Protonation is an effective strategy to enhance light trapping and photothermal conversion in covalent organic frameworks (COFs), yet conventional protonation sites are prone to environmental deactivation, leading to diminished stability and photothermal performance. Inspired by the stability of protein matrices, we developed polyacid-protonated COFs (PaCOFs) through in situ polymerization of dimercaptobutanesioic acid via dynamic disulfide bonds within COF pore channels. The resulting PaCOFs exhibit exceptional protonation stability and deliver a superior photothermal conversion efficiency of 77.8%, surpassing those of most conventional photothermal nanomaterials. Notably, PaCOFs can be readily processed by electrospinning into dual-mode thermal management textiles that achieve radiative cooling (∼7.2 °C) and solar heating (∼10.1 °C) under sunlight. These textiles outperform their commercial counterparts in wearable applications, establishing polyacid protonation as a robust strategy for stabilizing COFs and advancing their integration into photothermal energy conversion and personal thermal management.

Journal of the American Chemical SocietyVol. 148(3)
Zhejiang International Studies University (CN), Shaoxing University (CN), Department of Physics, Mathematics and Informatics (BY), Ministry of Education (TW), Careers Europe (GB), Zhejiang University of Technology (CN), Beihang University (CN)
Openalex Percentile: Top 21%
Covalent Organic Framework Applications
1.04
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