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二维共价有机框架:跨越不同长度尺度的结构洞察及其对光催化效率的影响

Two-Dimensional Covalent Organic Frameworks: Structural Insights across Different Length Scales and Their Impact on Photocatalytic Efficiency.

作者信息

Khalil Islam E, Das Prasenjit, Thomas Arne

机构信息

Department of Chemistry, Functional Materials Technische Universität Berlin, 10623 Berlin, Germany.

出版信息

Acc Chem Res. 2024 Nov 5;57(21):3138-3150. doi: 10.1021/acs.accounts.4c00491. Epub 2024 Oct 22.

DOI:10.1021/acs.accounts.4c00491
PMID:39435871
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11542146/
Abstract

ConspectusCovalent organic frameworks (COFs) are a rapidly emerging class of crystalline porous polymers, characterized by their highly defined, predictable, and tunable structure, porosity, and properties. COFs can form both two-dimensional (2D) and three-dimensional (3D) architectures, each with unique characteristics and potential applications. 2D COFs have attracted particular interest due to their favorable structural and optoelectronic properties. They can be equipped with a range of different functional moieties in their backbone, ranging from acidic to basic, from hydrophilic to hydrophobic, and from metal-coordinating to redox-active functions. In addition, their crystallinity, high specific surface area, and remarkable thermal and chemical stability make them attractive for a variety of applications, including gas separation, catalysis, energy storage, and optoelectronics.This Account provides a detailed overview of our recent efforts to synthesize and apply 2D COFs. First, various synthesis routes are discussed, focusing on methods that involve reversible and irreversible linkage reactions. Reversible reactions, such as imine or boronate ester formation, are advantageous for producing highly crystalline COFs because they allow for error correction during synthesis. In contrast, irreversible reactions, such as carbon-carbon or carbon-nitrogen bond formation, yield COFs with greater chemical stability, although controlling crystallinity can be more challenging. Our group has contributed significantly to refining these methods to balance crystallinity and stability, enhancing the performance of the resulting 2D COFs.In addition to different binding patterns, we have also developed strategies to control the micro- and macromorphologies of COFs, which is crucial for optimizing their properties for specific applications. For example, we have explored the synthesis of hierarchical porous COFs by using templating techniques or by forming composites with other functional materials. These strategies enable us to fine-tune the porosity and surface properties of COFs, thereby improving their performance in applications like catalysis. Hierarchical structures in particular enhance photocatalytic efficiency by providing a larger surface area for light absorption and facilitating the transport of photogenerated charge carriers.We further examine the practical applications of 2D COFs, with a primary focus on photocatalysis. Photocatalysis uses light to enable or accelerate chemical reactions, and 2D COFs are ideal for this purpose due to their tunable band gaps and large surface areas. Our research has shown that 2D COFs are highly versatile photocatalysts that can effectively catalyze reactions such as water splitting, carbon dioxide reduction, hydrogen peroxide formation, and cross-coupling reactions. By exploiting the unique properties of 2D COFs, we have achieved significant improvement in many photocatalytic reactions.With this comprehensive overview, we aim to contribute to the further development and understanding of 2D COFs and encourage further research and innovation in this promising field.

摘要

综述

共价有机框架(COF)是一类迅速兴起的结晶多孔聚合物,其特点是具有高度规整、可预测和可调谐的结构、孔隙率及性质。COF可以形成二维(2D)和三维(3D)结构,每种结构都有独特的特性和潜在应用。二维COF因其良好的结构和光电性质而备受关注。它们的主链可以配备一系列不同的功能基团,从酸性到碱性,从亲水性到疏水性,从金属配位到氧化还原活性功能。此外,它们的结晶性、高比表面积以及出色的热稳定性和化学稳定性使其在包括气体分离、催化、能量存储和光电子学等各种应用中具有吸引力。

本综述详细概述了我们最近在合成和应用二维COF方面所做的努力。首先,讨论了各种合成路线,重点是涉及可逆和不可逆连接反应的方法。可逆反应,如亚胺或硼酸酯的形成,有利于制备高度结晶的COF,因为它们在合成过程中允许纠错。相比之下,不可逆反应(如碳 - 碳或碳 - 氮键的形成)产生的COF具有更高的化学稳定性,尽管控制结晶性可能更具挑战性。我们团队在改进这些方法以平衡结晶度和稳定性方面做出了重大贡献,从而提高了所得二维COF的性能。

除了不同的键合模式外,我们还开发了控制COF微观和宏观形态的策略,这对于优化其在特定应用中的性能至关重要。例如,我们探索了通过使用模板技术或与其他功能材料形成复合材料来合成分级多孔COF。这些策略使我们能够微调COF的孔隙率和表面性质,从而提高它们在催化等应用中的性能。分级结构尤其通过提供更大的光吸收表面积和促进光生电荷载流子的传输来提高光催化效率。

我们进一步研究了二维COF的实际应用,主要集中在光催化方面。光催化利用光来引发或加速化学反应,二维COF由于其可调谐的带隙和大表面积,是实现这一目的的理想材料。我们的研究表明,二维COF是高度通用的光催化剂,可以有效催化诸如水分解、二氧化碳还原、过氧化氢形成和交叉偶联反应等反应。通过利用二维COF的独特性质,我们在许多光催化反应中取得了显著进展。

通过这一全面综述,我们旨在为二维COF的进一步发展和理解做出贡献,并鼓励在这个有前途的领域进行进一步的研究和创新。

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Ambient Aqueous Synthesis of Imine-Linked Covalent Organic Frameworks (COFs) and Fabrication of Freestanding Cellulose Nanofiber@COF Nanopapers.亚胺连接的共价有机框架(COF)的环境水相合成及独立式纤维素纳米纤维@COF纳米纸的制备
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Photocatalytic CO reduction to syngas using metallosalen covalent organic frameworks.使用金属-萨伦共价有机框架将光催化一氧化碳还原为合成气
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