Post-synthetically modified metal-porphyrin framework for carbon dioxide adsorption and energy storage in Li-S batteries
Lithium-sulphur batteries attract increasing interest due to their high theoretical specific capacity, advantageous economy, and "eco-friendliness". In this study, a metal-organic framework (MOF) GaTCPP containing a porphyrinic base ligand was used as a conductive additive for sulphur. GaT...
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Published in | RSC advances Vol. 12; no. 37; pp. 23989 - 242 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
24.08.2022
|
Online Access | Get full text |
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Summary: | Lithium-sulphur batteries attract increasing interest due to their high theoretical specific capacity, advantageous economy, and "eco-friendliness". In this study, a metal-organic framework (MOF)
GaTCPP
containing a porphyrinic base ligand was used as a conductive additive for sulphur.
GaTCPP
was synthesized, characterized, and post-synthetically modified by the transition metal ions (Co
2+
/Ni
2+
). The doping of
GaTCPP
ensured an increase in the carbon dioxide adsorption capacities, which were measured under different conditions. Post-synthetic modification of
GaTCPP
with Co
2+
/Ni
2+
ions has been shown to increase carbon dioxide storage capacity from 22.8 wt% for unmodified material to 23.1 wt% and 26.5 wt% at 0 C and 1 bar for Co
2+
and Ni
2+
-doped analogues, respectively. As a conductive part of cathode material, MOFs displayed successful sulphur capture and encapsulation proven by stable charge/discharge cycle performances, high-capacity retention, and coulombic efficiency. The electrodes with pristine
GaTCPP
showed a discharge capacity of 699 mA h g
−1
at 0.2C in the fiftieth cycle. However, the doping of
GaTCPP
by Ni
2+
has a positive impact on the electrochemical properties, the capacity increased to 778 mA h g
−1
in the fiftieth cycle at 0.2C.
Metal-porphyrin framework
GaTCPP
was used for carbon dioxide adsorption and as a host for preparation of a Li-S battery cathode material. |
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Bibliography: | Electronic supplementary information (ESI) available. See https://doi.org/10.1039/d2ra03301a |
ISSN: | 2046-2069 |
DOI: | 10.1039/d2ra03301a |