Solvothermal Template‐Induced Hierarchical Porosity in Covalent Organic Frameworks: A Pathway to Enhanced Diffusivity

F Fabian Heck (Nanochemistry Department Max Planck Institute for Solid State Research Stuttgart Germany) L Lars Grunenberg (Max Planck Institute for Solid State Research Heisenbergstr. 1 70569 Stuttgart Germany) N Nadine Schnabel (Collaborative Research Center 1333 Universität Stuttgart Pfaffenwaldring 55 70569 Stuttgart Germany) A Amelie Heilmaier (Max Planck Institute for Solid State Research Heisenbergstr. 1 70569 Stuttgart Germany) T Thomas Sottmann (Collaborative Research Center 1333 Universität Stuttgart Pfaffenwaldring 55 70569 Stuttgart Germany) L Liang Yao (State Key Laboratory of Luminescent Materials and Devices, Institute of Polymer Optoelectronic Materials and Devices, Guangdong Basic Research Center of Excellence for Energy and Information Polymer Materials) B Bettina V. Lotsch (Nanochemistry Department, Max Planck Institute for Solid State Research, Heisenbergstraße 1, 70569 Stuttgart, Germany)

Abstract

Abstract The rapid advancement of covalent organic frameworks (COFs) in recent years has firmly established them as a new class of molecularly precise and highly tuneable porous materials. However, compared to other porous materials, such as zeolites and metal‐organic frameworks, the successful integration of hierarchical porosity into COFs remains largely unexplored. The challenge lies in identifying appropriate synthetic methods to introduce secondary pores without compromising the intrinsic structural porosity of COFs. In this study, a template‐induced synthetic methodology is realized to facilitate the construction of hierarchically porous COFs (hCOFs). This novel approach utilizes commercially available zinc oxide nanoparticles as a hard template, enabling to increase the total pore volume of a series of β ‐ketoenamine‐linked COFs as well as an imine‐based COF while preserving their surface areas. In addition to transmission electron microscopy and gas adsorption analyses, small‐angle X‐ray scattering and pulsed field gradient nuclear magnetic resonance techniques are employed to investigate the hierarchical porosity and diffusivity of guest molecules within hCOFs. This study demonstrates that the hierarchically porous nature of hCOFs significantly reduces diffusion limitations, thus leading to simultaneous enhancements in adsorption capacity, diffusivity, and catalytic performance.

Article Details

Volume / Issue Vol. 37, Issue 52
Published December 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (7)

F

Fabian Heck

Nanochemistry Department Max Planck Institute for Solid State Research Stuttgart Germany

L

Lars Grunenberg

Max Planck Institute for Solid State Research Heisenbergstr. 1 70569 Stuttgart Germany

N

Nadine Schnabel

Collaborative Research Center 1333 Universität Stuttgart Pfaffenwaldring 55 70569 Stuttgart Germany

A

Amelie Heilmaier

Max Planck Institute for Solid State Research Heisenbergstr. 1 70569 Stuttgart Germany

T

Thomas Sottmann

Collaborative Research Center 1333 Universität Stuttgart Pfaffenwaldring 55 70569 Stuttgart Germany

L

Liang Yao

State Key Laboratory of Luminescent Materials and Devices, Institute of Polymer Optoelectronic Materials and Devices, Guangdong Basic Research Center of Excellence for Energy and Information Polymer Materials

B

Bettina V. Lotsch

Nanochemistry Department, Max Planck Institute for Solid State Research, Heisenbergstraße 1, 70569 Stuttgart, Germany