Layered double hydroxide-derived bimetallic-MOF as a promising platform: Urea-coupled water oxidation and
Nitika Bhutani1, Premkumar Murugesan2, Sushmita Baro1
1School of Chemical sciences, Indian Institute of Technology Mandi, Kamand, Himachal Pradesh 175005, India.
Abstract:
Developing a two-dimensional (2D) ultrathin metal-organic framework plays a significant role in energy conversion and storage systems. This work introduced a facile strategy for engineering ultrathin NiMn-MOF nanosheets on Ni foam (NF) via in situ conversion from NiMn-layered double hydroxide (LDH). The as-synthesized LDH-derived NiMn-MOF (LDH-D NiMn-MOF) nanosheet exhibited an overpotential of 350 mV to drive a current density of 100 mA cm-2 during oxygen evolution reaction (OER) owing to its better redox activity, hierarchical architecture, and intercalating ability. The similar effective catalytic trend was noticed during the urea-assisted water oxidation process. The developed catalyst required only a potential of 1.39 V vs. RHE at 100 mA cm-2 towards urea oxidation reaction (UOR). Moreover, the urea-assisted overall water-splitting voltage was found to be 1.5 V at the current density of 10 mA cm-2. Furthermore, the same catalyst was explored as an energy-storage material for supercapattery application with an aerial specific capacity value of 2613.9 mC cm-2 at 1 mA cm-2 which was found to be 1.5 times higher than NiMn-LDH (1724.3 mC cm-2). Additionally, an aqueous asymmetric supercapattery device was fabricated which demonstrated the best electrochemical performance and provided a maximum energy density of 64.1 Wh kg-1 at a power density of 493 W kg-1 with 77.8 percent capacity retention after a continuous run of 8000 cycles at 10 mA cm-2 current density. Hence, the multifaceted properties of energy conversion and storage of LDH-D NiMn-MOF outline its performance in real-world applications.
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