Stable Tetravalent Metal-Organic Frameworks for Electrocatalysis and Aqueous Electrochemical Energy Storage
Chou-Hung Hsueh1, Chung-Wei Kung1,2
1Department of Chemical Engineering, National Cheng Kung University, Tainan 70101, Taiwan.
Abstract:
Owing to their chemical stability in water, relatively high specific surface area, and high tunability in both pore structures and chemical functionality in their pores, metal-organic frameworks (MOFs) constructed from tetravalent metal-based nodes, including zirconium-based MOFs, titanium-based MOFs, hafnium-based MOFs, cerium(IV)-based MOFs and thorium-based MOFs, have been widely explored for various applications requiring humid or aqueous environments. In particular, over the past ten years, these MOFs have been widely employed in various aqueous electrochemical applications, including water splitting, oxygen reduction, carbon dioxide reduction, ammonia production, electrocatalytic sensing, aqueous supercapacitors, zinc-ion batteries, and vanadium flow batteries. Classified by the type of applications and the role that MOFs could play, progress in this research field is overviewed. Limitations and opportunities in this field for future studies are discussed.
More Related Videos
10:15Solar-Driven Electrochemical Green Fuel Production from CO2 and Water Using Ti3C2Tx MXene-Supported CuZn and NiCo Catalysts
Published on: November 7, 2025
10:57Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction
Published on: April 10, 2018
Related Concept Videos
Batteries and Fuel Cells
Crystal Field Theory - Tetrahedral and Square Planar Complexes
Crystal field theory (CFT) is applicable to molecules in geometries other than octahedral. In octahedral complexes, the lobes of the dx2−y2 and dz2 orbitals point directly at the ligands. For tetrahedral complexes, the d orbitals remain in place, but with only four ligands located between the axes. None of the orbitals points directly at the tetrahedral ligands. However, the dx2−y2 and dz2 orbitals (along the Cartesian axes) overlap with the ligands less than the dxy,...
