Three new lanthanide-MOFs, [(TATMB) 2 Ce 2 ⋅3DMSO-H 2 O]⋅7H 2 O (MOFÀ Ce), [(TATMB) 2 Pr 2 ⋅4DMSO]⋅7H 2 O⋅DMF (MOFÀ Pr) and [(TATMB) 2 Nd 2 ⋅3DMSO⋅H 2 O]⋅6H 2 O (MOFÀ Nd) were synthesized by the reaction of hydrated lanthanide salts and 3,3',3''-((1,3,5triazine-2,4,6-triyl)tris(azanediyl))tribenzoic acid (H 3 TATMB) under solvothermal reaction condition. All MOFs were characterized by standard instrumentation techniques, for example, FT-IR spectroscopy, elemental analysis, etc. The solid-state structures were determined by single-crystal X-ray diffraction analyses. It revealed that all MOFs formed two-dimensional frameworks by the coordination assisted pathway of ligand molecules and lanthanide(III) ions. All MOFs were investigated as supercapacitor electrode material by using the conventional three-electrode method by using TEABF 4 in acetonitrile as electrolyte. It was observed that MOFÀ Ce exhibited a maximum specific capacitance of 572 Fg À 1 at a current density of 1 A g À 1 among all three MOFs. The specific capacitance retention of the material was found to be 81% after successful completion of 5000 charging-discharging cycles. To the best of our knowledge, the specific capacitance of MOFÀ Ce is highest reported for lanthanide MOFs without any redox-active additive until now. Moreover, for the first time, MOFÀ Ce has been used to fabricate a device, which exhibited significant responses for various LED lights and showed a maximum specific capacitance of 88 Fg À 1 at a current density of 2 A g À 1 .