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Hierarchically Organized and Anisotropic Porous Carbon Monoliths
Author(s) -
Florian Putz,
Lukas Ludescher,
Michael S. Elsaesser,
Oskar Paris,
Nicola Hüsing
Publication year - 2020
Publication title -
chemistry of materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.741
H-Index - 375
eISSN - 1520-5002
pISSN - 0897-4756
DOI - 10.1021/acs.chemmater.0c00302
Subject(s) - materials science , anisotropy , carbonization , porosity , mesoporous material , carbon fibers , microstructure , nanotechnology , scanning electron microscope , chemical engineering , composite material , organic chemistry , chemistry , optics , physics , composite number , engineering , catalysis
Anisotropy is a key factor regarding mechanical or transport properties and thus the functionality of porous materials. However, the ability to deliberately design the pore structure of hierarchically organized porous networks toward anisotropic features is limited. Here, we report two straightforward routes toward hierarchically structured porous carbon monoliths with an anisotropic alignment of the microstructure on the level of macro- and mesopores. One approach is based on nanocasting (NC) of carbon precursors into hierarchical and anisotropic silica hard templates. The second route, a direct synthesis approach based on soft templating (ST), makes use of the flexibility of hierarchically structured resorcinol-formaldehyde gels, which are compressed and simultaneously carbonized in the deformed state. We present structural data of both types of carbon monoliths obtained by electron microscopy, nitrogen adsorption analysis, and SAXS measurements. In addition, we demonstrate how the degree of anisotropy can easily be controlled via the ST route.

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