Photothermal Conversion Porous Organic Polymers: Design, Synthesis, and Applications

Author:

Shi Yu1ORCID,Wang Yuzhu1,Meng Nan1ORCID,Liao Yaozu1ORCID

Affiliation:

1. State Key Laboratory for Modification of Chemical Fibers and Polymer Materials College of Materials Science and Engineering Donghua University Shanghai 201620 China

Abstract

AbstractSolar energy is a primary form of renewable energy, and photothermal conversion is a direct conversion process with tunable conversion efficiency. Among various kinds of photothermal conversion materials, porous organic polymers (POP) are widely investigated owing to their controllable molecular design, tailored porous structures, good absorption of solar light, and low thermal conductivity. A variety of POP, such as conjugated microporous polymers (CMP), covalent organic frameworks (COF), hyper‐crosslinked porous polymers (HCP), polymers of intrinsic microporosity (PIM), porous ionic polymers (PIP), are developed and applied in photothermal conversion applications of seawater desalination, latent energy storage, and biomedical fields. In this review, a comprehensive overview of the recent advances in POP for photothermal conversion is provided. The micro molecular structure characteristics and macro morphology of POP are designed for applications such as seawater desalination, latent heat energy storage, phototherapy and photodynamic therapy, and drug delivery. Besides, a probe into the underlying mechanism of structural design for constructing POP with excellent photothermal conversion performance is methodicalized. Finally, the remaining challenges and prospective opportunities for the future development of POP for solar energy‐driven photothermal conversion applications are elucidated.

Funder

National Natural Science Foundation of China

National Key Research and Development Program of China

Natural Science Foundation of Shanghai Municipality

Fundamental Research Funds for the Central Universities

Program of Shanghai Academic Research Leader

Publisher

Wiley

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