Abstract
In the context of recent progress in designing metal-organic framework (MOF)-based supercapacitor electrodes, we report herein the successful growth of two different crystal morphologies of a cerium-based MOF, octahedral crystals named IRH-2-O and elongated square-bipyramidal crystals named IRH-2-ESBP (IRH = Institute de Recherche sur l'Hydrogène). The identical crystal structure of both materials was confirmed by powder X-ray diffraction (PXRD). Furthermore, scanning electron microscopy and energy-dispersive X-ray mapping analysis corroborated this fact and showed the crystal shape variation versus the surface composition of synthesized materials. Fourier transform infrared spectroscopy, UV-vis spectroscopy, and PXRD were used to confirm the purity of pristine MOFs as well as desired MOF//PANI composites. Cyclic voltammetry and electrochemical impedance spectroscopy highlighted the effect of crystal shape on the electrochemical performance of IRH-2 MOFs; the specific capacitance tripled from 43.1 F·g(-1) for IRH-2-O to 125.57 F·g(-1) for IRH-2-ESBP at 5 mV·s(-1). The cycling stability was notably ameliorated from 7 K for IRH-2-O to 20 K for IRH-2-ESBP. Regarding the composites, the cell voltage was notably ameliorated from 1.8 to 1.95 V. However, the electrochemical performance of IRH-2/PANI composites was drastically decreased due to instability in the acidic media. To the best of our knowledge, our work is the first work that related the MOF crystal shape and the electrochemical performance.