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Related Concept Videos

Ionic Bonding and Electron Transfer02:48

Ionic Bonding and Electron Transfer

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Ions are atoms or molecules bearing an electrical charge. A cation (a positive ion) forms when a neutral atom loses one or more electrons from its valence shell, and an anion (a negative ion) forms when a neutral atom gains one or more electrons in its valence shell. Compounds composed of ions are called ionic compounds (or salts), and their constituent ions are held together by ionic bonds: electrostatic forces of attraction between oppositely charged cations and anions. 
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An ionic compound is stable because of the electrostatic attraction between its positive and negative ions. The lattice energy of a compound is a measure of the strength of this attraction. The lattice energy (ΔHlattice) of an ionic compound is defined as the energy required to separate one mole of the solid into its component gaseous ions. For the ionic solid sodium chloride, the lattice energy is the enthalpy change of the process:
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Crystal Field Theory
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.
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Coordination compounds and complexes exhibit different colors, geometries, and magnetic behavior, depending on the metal atom/ion and ligands from which they are composed. In an attempt to explain the bonding and structure of coordination complexes, Linus Pauling proposed the valence bond theory, or VBT, using the concepts of hybridization and the overlapping of the atomic orbitals. According to VBT, the central metal atom or ion (Lewis acid) hybridizes to provide empty orbitals of suitable...
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Tetrahedral Complexes
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Updated: Jan 12, 2026

Quantitative Atomic-Site Analysis of Functional Dopants/Point Defects in Crystalline Materials by Electron-Channeling-Enhanced Microanalysis
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Tri-Sites Element Doping with Eu─Al─F Toward Stable High-Voltage LiCoO2.

Yutong Yao1, Guo Wang1, Xiaokun Zhang1

  • 1School of Materials and Energy, University of Electronic Science and Technology of China, Chengdu, Sichuan, 611731, China.

Small (Weinheim an Der Bergstrasse, Germany)
|November 7, 2025
PubMed
Summary
This summary is machine-generated.

Researchers developed a novel doping strategy for lithium cobalt oxide (LCO) cathodes to enhance lithium-ion battery performance. This approach improves capacity retention at high voltages, crucial for advanced electronics.

Keywords:
high‐voltagelithium batterylithium cobalt oxidemultiple doping

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Area of Science:

  • Materials Science
  • Electrochemistry
  • Energy Storage

Background:

  • Lithium cobalt oxide (LCO) is a primary cathode material for lithium-ion batteries.
  • Current LCO performance limitations hinder the development of high-energy-density batteries for advanced electronics.
  • Increasing charging voltage improves LCO capacity but leads to degradation and capacity fade.

Purpose of the Study:

  • To enhance the high-voltage performance and cyclic stability of LCO cathodes.
  • To investigate a tri-sites multi-element doping strategy using Europium (Eu), Aluminum (Al), and Fluorine (F).

Main Methods:

  • Developed a tri-sites co-doping strategy with Eu, Al, and F elements for LCO.
  • Tested the modified LCO cathode at a high cut-off voltage of 4.55 V.
  • Analyzed structural and electrochemical properties to evaluate performance and stability.

Main Results:

  • The Eu-Al-F co-doped LCO cathode achieved an initial discharge capacity of 205 mAh g⁻¹ at 4.55 V.
  • The modified cathode maintained over 80% capacity retention after 250 cycles.
  • The doping strategy effectively suppressed irreversible phase transitions, oxygen loss, and internal stress.

Conclusions:

  • The tri-sites co-doping strategy significantly improves the cyclic stability of high-voltage LCO.
  • This method offers a promising pathway for developing advanced lithium-ion batteries with higher energy density and durability.
  • The study provides insights into mitigating degradation mechanisms in high-voltage cathode materials.