Related Experiment Video
Updated: Aug 28, 2025

Author Spotlight: Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks
Published on: June 9, 2023
Effect of Static Jahn-Teller Distortion on the Li+ Transport in a Copper Hexacyanoferrate Framework
Dan Ito1, Yoshihide Nakao2, Manabu Ishizaki1
1Faculty of Science, Yamagata University, 1-4-12 Kojirakawa-machi, Yamagata 990-8560, Japan.
Abstract:
Prussian blue (PB) and its analogues (PBAs) are potential cathode-active materials for rechargeable lithium-ion batteries. Although a body of research has assessed the performances of various PB/PBA cathodes with an eye to practical use, the underlying Li+-transport mechanism is still unclear. Focusing on copper hexacyanoferrate (CuHCF), a PBA that exhibits static Jahn-Teller (JT) distortion, we theoretically investigate how the framework's distortion affects the pathways and energetics of the Li+ transport. Density functional theory calculations of a local structure model of CuHCF reveal that the static JT distortion makes the favorable Li+-transport pathways quasi-two-dimensional, contrary to an intuitive picture of isotropic Li+ diffusion within the regular jungle-gym framework. The pathways are mutually interconnected, thereby creating an almost barrierless transport network. To better understand the distortion-induced transport anisotropy, we visually analyze the framework's electronic structure and noncovalent Li+-framework interactions. This study helps deepen the fundamental understanding of intrinsic Li+-transport properties of a distorted porous framework.
More Related Videos
09:06Visualizing Uniaxial-strain Manipulation of Antiferromagnetic Domains in Fe1+YTe Using a Spin-polarized Scanning Tunneling Microscope
Published on: March 24, 2019
06:561,3,5-Triphenylbenzene and Corannulene as Electron Receptors for Lithium Solvated Electron Solutions
Published on: October 10, 2016
Related Concept Videos
Crystal Field Theory - Octahedral Complexes
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
Colors and Magnetism
When atoms or molecules absorb light at the proper frequency, their electrons are excited to higher-energy orbitals. For many main group atoms and molecules, the absorbed photons are in the ultraviolet range of the electromagnetic spectrum, which cannot be detected by the human eye. For coordination compounds, the energy difference between the d orbitals often allows photons in the visible range to be absorbed and emitted, which is seen as colors by the human...
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,...
Bonding in Metals
Trends in Lattice Energy: Ion Size and Charge
Biasing of Metal-Semiconductor Junctions
In Schottky junctions, where the semiconductor is n-type, applying a positive voltage to the metal relative to the semiconductor reduces its Fermi...