An anionic two dimensional covalent organic framework from tetratopic borate centres pillared by lithium ions

Non-covalent interactions play an important role for the framework formation of two-dimensional covalent organic frameworks. Until now, π-π interactions and hydrogen bonding are the main reported forces facilitating the stacking of framework layers. Here, we present a two-dimensional anionic covalent organic framework based on tetratopic borate linkages, where layers are connected by ionic interactions between the linkage site and counter cations. The crystalline covalent organic framework is accessed through the formation of an amorphous borate-based polymer and subsequent solvothermal treatment. The progress of crystallization is investigated, revealing the crystallite growth and morphological change from agglomerated dense particles to hollow crystallite spheres. Due to the pillared nature, the crystallites can be exfoliated into nanosheets by sonication of the material in the presence of methanol. The crystallization and ordered arrangement of the lithium ions in the interlayer space is shown to benefit the conductivity tenfold compared to the amorphous material.

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Publication Details

Journal
Nature Communications
Published
2024-08-15
DOI
https://doi.org/10.1038/s41467-024-50953-2
Citations
16
Primary Topic
Covalent Organic Framework Applications
Type
article
Field-Weighted Citation Impact
1.87

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article

An anionic two dimensional covalent organic framework from tetratopic borate centres pillared by lithium ions

Veniamin Chevelkov, Julia Grüneberg, Jérôme Roeser, Hüseyin Küçükkeçeci et al.
16 citations
Nature Communications
Covalent Organic Framework Applications
1.87
article

An anionic two dimensional covalent organic framework from tetratopic borate centres pillared by lithium ions

Veniamin Chevelkov, Julia Grüneberg, Jérôme Roeser, Hüseyin Küçükkeçeci, Adam Lange, Samrat Ghosh, Bruce Dunn, Yunkai Luo, Arne Thomas, Michael Gradzielski, Darosch Asgari, Sabrina Fischer-Lang
article en
16 citations

Abstract

Non-covalent interactions play an important role for the framework formation of two-dimensional covalent organic frameworks. Until now, π-π interactions and hydrogen bonding are the main reported forces facilitating the stacking of framework layers. Here, we present a two-dimensional anionic covalent organic framework based on tetratopic borate linkages, where layers are connected by ionic interactions between the linkage site and counter cations. The crystalline covalent organic framework is accessed through the formation of an amorphous borate-based polymer and subsequent solvothermal treatment. The progress of crystallization is investigated, revealing the crystallite growth and morphological change from agglomerated dense particles to hollow crystallite spheres. Due to the pillared nature, the crystallites can be exfoliated into nanosheets by sonication of the material in the presence of methanol. The crystallization and ordered arrangement of the lithium ions in the interlayer space is shown to benefit the conductivity tenfold compared to the amorphous material.

Nature CommunicationsVol. 15(1)
Central Leather Research Institute (IN), University of California, Los Angeles (US), Osnabrück University (DE), Leibniz-Forschungsinstitut für Molekulare Pharmakologie (DE), Technische Universität Berlin (DE)
Deutsche Forschungsgemeinschaft, Bundesministerium für Bildung und Forschung, International Max Planck Research School for Advanced Methods in Process and Systems Engineering
Openalex Percentile: Top 10%
Covalent Organic Framework Applications
1.87
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