Metal organic frameworks (MOFs) with diverse structural chemistry are being projected as futuristic
electrode materials for Li-ion batteries. In this work, we report synthesis of Mn-1,3,5-benzenetricarboxylate MOF by a simple solvothermal method and its application as an
anode material for the first time. Scanning electron microscopy of the synthesized MOF shows a bar shaped morphology where these bars, about 1 μm wide and of varied lengths between 2 and 20 μm, are made of porous sheets containing mesoporous walls and macroporous channels. The MOF
anode, when examined in the potential window of 0.01-2.0 V versus Li/Li(+), shows high specific capacities of 694 and 400 mAh g(-1) at current densities of 0.1 and 1.0 A g(-1) along with good cyclability, retention of capacity, and sustenance of the MOF network. Ex situ X-ray diffraction, Fourier transform infrared, and X-ray photoelectron spectroscopy studies on the
electrode material at different states of charge suggest that the usual
conversion reaction for Li storage might not be applicable in this case. Conjugated carboxylates being weakly electron withdrawing
ligands with a stronger π-π interaction, a probable alternative Li storage mechanism has been proposed that involves the organic moiety. The present results show promise for applying Mn-1,3,5-benzenetricarboxylate MOF as high performance <2 V
anode.