4.3 Article

Preparation and hydrogen storage capacity of templated and activated carbons nanocast from commercially available zeolitic imidazolate framework

Journal

JOURNAL OF MATERIALS CHEMISTRY
Volume 22, Issue 1, Pages 146-152

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c1jm13314d

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Funding

  1. University of Nottingham
  2. King Abdulaziz University, Saudi Arabia

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A commercially available zeolitic imidazolate framework (ZIF), namely Basolite Z1200 (BASF), has been used as template for nanocasting of highly microporous ZIF-templated carbon. The hard template carbonization technique consists of liquid impregnation of furfuryl alcohol into the pores of the ZIF followed by polymerization and then carbonization during which the ZIF template is removed to generate the microporous carbon (90-95% microporosity) with a surface area of 900-1100 m(2) g(-1) and a pore volume of ca. 0.7 cm(3) g(-1). Chemical activation (with KOH at a relatively low temperature of 700 degrees C for 1 h and a carbon/KOH weight ratio of 1 : 4) of the ZIF-templated carbons increases their porosity by between 30 and 240% depending on their carbonization temperature, to achieve a surface area of up to 3200 m(2) g(-1) and a pore volume of 1.94 cm(3) g(-1). Despite the drastic increase in porosity, the activated ZIF-templated carbons retain significant microporosity with micropores contributing 80-90% of surface area and 60-70% of pore volume. This occurs because the activation process mainly enhances existing porosity rather than creating new larger pores. The activation enhances the hydrogen uptake capacity of the ZIF-templated carbons by between 25 and 140% from 2.6-3.1 wt% to the range 3.9-6.2 wt% (at -196 degrees C and 20 bar). The increase in hydrogen uptake after activation is closely related to rises in the micropore surface area and micropore volume rather than overall increase in porosity. Due to their microporous nature, the carbons exhibit high hydrogen storage density in the range 13.0-15.5 mu mol H(2) m(-2), which is much higher than that of most high surface area activated carbons.

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