This technology precisely controls the 0–3D network structure and shell count of metal-organic frameworks (MOFs) by aminating transition metal nitride precursors before combining them with organic ligands, while adjusting the ratio of organic solvent to deionized water and the type of surfactant used.
Conventional MOFs suffer from low stability against heat, moisture, acids, and bases, as well as poor electrical conductivity, making long-term use difficult. In particular, they exhibit a sharp decline in performance under high current density conditions.
This technology implements an N-dimensional polymer network structure by aminating metal precursor sources, mixing them with organic ligands, and performing reduction treatment. It forms stable shell structures through dimension control based on solvent composition and step-by-step heat treatment temperature control. This allows for application in air-cathode catalysts for metal-air batteries and OER electrodes for water electrolysis, reducing reliance on precious metal catalysts while maintaining long-term bidirectional activity for oxygen reactions.
This invention was developed with support from the Ministry of Science and ICT for the development of a high-energy-density soft materials platform through the design of new organic superionic plastic crystal materials.
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