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Title: | Room-temperature synthesis of bimetallic Co-Zn based zeolitic imidazolate frameworks in water for enhanced CO2 and H2 uptakes |
Authors: | Rai, R.K. Tyagi, Deepika Singh, Sanjay Kumar |
Keywords: | Atomic emission spectroscopy;Binary alloys;Carbon dioxide;Pore size;X ray diffraction;Electron micrograph;H2-uptake;Pore volume;Powder X-ray diffraction (pXRD);Room temperature synthesis;Surface area;Zeolitic imidazolate frameworks;Zn precursors;Cobalt |
Issue Date: | 2016 |
Publisher: | Royal Society of Chemistry |
Citation: | Kaur, G., Rai, R. K., Tyagi, D., Yao, X., Li, P. -., Yang, X. -., . . . Singh, S. K. (2016). Room-temperature synthesis of bimetallic co-zn based zeolitic imidazolate frameworks in water for enhanced CO2 and H2 uptakes. Journal of Materials Chemistry A, 4(39), 14932-14938. doi:10.1039/c6ta04342a |
Abstract: | A simple methodology was explored to access highly robust bimetallic Co-Zn based zeolitic imidazolate frameworks at room temperature. By tuning the content of Co and Zn precursors, CoZn-ZIF-8 frameworks with varying Co:Zn (25-90% of Co2+ as confirmed by ICP-AES results) were synthesized. Electron micrographs and powder X-ray diffraction (PXRD) patterns confirmed the formation of bimetallic CoZn-ZIF-8 frameworks of 150-300 nm size, where Zn atoms were partially replaced by Co atoms. The as-synthesized CoZn-ZIF-8 frameworks displayed a tuned pore size, pore volume and surface area, with the highest surface area (enhanced by ∼40% compared to Zn-ZIF-8) and pore volume (enhanced by ∼33% compared to Zn-ZIF-8) for Co75Zn25-ZIF-8. The as-synthesized CoZn-ZIF-8 frameworks also displayed enhanced CO2 and H2 uptakes at 298 K and 77 K, respectively, at 1 bar. Noteworthy enhancement of ∼30% in the CO2 and ∼23% in the H2 uptake was displayed by Co75Zn25-ZIF-8 frameworks as compared to Zn-ZIF-8 under analogous conditions. © 2016 The Royal Society of Chemistry. |
URI: | https://doi.org/10.1039/c6ta04342a https://dspace.iiti.ac.in/handle/123456789/9236 |
ISSN: | 2050-7488 |
Type of Material: | Journal Article |
Appears in Collections: | Department of Chemistry |
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