Lanthanides
have been proved to be unprecedented when it comes
to organized nanoporous materials with high coordination environment.
In the quest to enhance the applications for energy-storage materials,
three lanthanide-based metal–organic frameworks (MOFs) have
been synthesized by facile hydrothermal conditions using 5-nitroisophthalic
acid (H2L) as a ligand, namely, Ce–H2L, Sm–H2L, and Eu–H2L. These
nanoporous MOFs consist of nine coordination sites around the lanthanide
metal ion giving rise to distorted monocapped square antiprism geometry
and 3D crystal structures. The electrochemical measurements demonstrate
that charge storage in these MOFs occurs through faradaic redox reactions.
The charge–discharge studies show that these nanoporous MOF
materials deliver high specific capacity. Ce–H2L,
Sm–H2L, and Eu–H2L deliver specific
capacities of 625, 356, and 252 C g–1 (1389, 791,
and 560 F g–1), respectively, at a current density
of 1 A g–1. A symmetric supercapacitor Swagelok
device has been fabricated using Ce–H2L as an electrode
to further demonstrate the advantage of as-synthesized MOF. The developed
symmetric supercapacitor gives a maximum specific energy of 13.6 Wh
kg–1 and a maximum specific power of 7110 W kg–1 in the voltage window of 1.425 V. The energy storage
trend in these nanoporous materials is Ce–H2L >
Sm–H2L > Eu–H2L, which is further
supported by the DFT calculations.