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Journal ArticleDOI

Covalent Organic Frameworks: Design, Synthesis, and Functions.

TLDR
A comprehensive review of the COF field is targeted, providing a historic overview of the chemistry, the advances in the topology design and synthetic reactions, illustrate the structural features and diversities, and scrutinize the development and potential of various functions through elucidating structure-function correlations.
Abstract
Covalent organic frameworks (COFs) are a class of crystalline porous organic polymers with permanent porosity and highly ordered structures. Unlike other polymers, a significant feature of COFs is that they are structurally predesignable, synthetically controllable, and functionally manageable. In principle, the topological design diagram offers geometric guidance for the structural tiling of extended porous polygons, and the polycondensation reactions provide synthetic ways to construct the predesigned primary and high-order structures. Progress over the past decade in the chemistry of these two aspects undoubtedly established the base of the COF field. By virtue of the availability of organic units and the diversity of topologies and linkages, COFs have emerged as a new field of organic materials that offer a powerful molecular platform for complex structural design and tailor-made functional development. Here we target a comprehensive review of the COF field, provide a historic overview of the chemistry of the COF field, survey the advances in the topology design and synthetic reactions, illustrate the structural features and diversities, scrutinize the development and potential of various functions through elucidating structure-function correlations based on interactions with photons, electrons, holes, spins, ions, and molecules, discuss the key fundamental and challenging issues that need to be addressed, and predict the future directions from chemistry, physics, and materials perspectives.

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Journal ArticleDOI

Bulk COFs and COF nanosheets for electrochemical energy storage and conversion

TL;DR: The preparation strategies of COF NSs via bottom-up and top-down approaches are described, and the applications of bulk COFs and COFNSs in EES and EEC are summarized, such as in batteries, supercapacitors, and fuel cells.
Journal ArticleDOI

Covalent organic frameworks: an ideal platform for designing ordered materials and advanced applications

TL;DR: This review focuses on analysing the historic developments of COFs to uncover a full materials and application picture by providing comprehensive yet clear guidance for molecular design, synthetic control and functional exploration.

Hydroxylated Graphene-Sulfur Nanocomposites for High-Rate Lithium-Sulfur Batteries

TL;DR: In this article, the authors used hydroxylated graphene nanosheets as a substrate to produce graphene-amorphous sulfur nanocomposites, exhibiting superior cyclability at high rates, by a facile in situ deposition method.
Journal ArticleDOI

New synthetic strategies toward covalent organic frameworks.

TL;DR: This review scrutinised the recently developed "two-in-one" molecular design strategy to showcase advantages in optimising synthetic conditions such as catalyst, monomer feeding rate and tolerance to functional groups and proposed key underlying challenges to be solved and predicted future frontiers from the perspectives of synthesising high quality crystallites and films.
References
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Journal ArticleDOI

Aggregation-Induced Emission: Together We Shine, United We Soar!

TL;DR: This paper presents a meta-analysis of the chiral stationary phase transition of Na6(CO3)(SO4)2, a major component of the response of the immune system to Na2CO3.
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Carbon Dioxide Capture in Metal–Organic Frameworks

TL;DR: Kenji Sumida, David L. Rogow, Jarad A. Mason, Thomas M. McDonald, Eric D. Bloch, Zoey R. Herm, Tae-Hyun Bae, Jeffrey R. Long
Journal ArticleDOI

Porous, Crystalline, Covalent Organic Frameworks

TL;DR: Covalent organic frameworks (COFs) have been designed and successfully synthesized by condensation reactions of phenyl diboronic acid and hexahydroxytriphenylene to form rigid porous architectures with pore sizes ranging from 7 to 27 angstroms.
Journal ArticleDOI

Benchmarking Heterogeneous Electrocatalysts for the Oxygen Evolution Reaction

TL;DR: In this paper, the authors report a protocol for evaluating the activity, stability, and Faradaic efficiency of electrodeposited oxygen-evolving electrocatalysts for water oxidation.
Journal ArticleDOI

Hydrogen Storage in Microporous Metal-Organic Frameworks

TL;DR: Inelastic neutron scattering spectroscopy of the rotational transitions of the adsorbed hydrogen molecules indicates the presence of two well-defined binding sites (termed I and II), which are associated with hydrogen binding to zinc and the BDC linker, respectively.
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