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Related Concept Videos

Ionic Crystal Structures02:42

Ionic Crystal Structures

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Ionic crystals consist of two or more different kinds of ions that usually have different sizes. The packing of these ions into a crystal structure is more complex than the packing of metal atoms that are the same size.
Most monatomic ions behave as charged spheres, and their attraction for ions of opposite charge is the same in every direction. Consequently, stable structures for ionic compounds result (1) when ions of one charge are surrounded by as many ions as possible of the opposite...
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Imperfections in Crystal Structure: Stoichiometric Point Defects01:26

Imperfections in Crystal Structure: Stoichiometric Point Defects

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Schottky defects arise when some lattice points in a crystal, such as those in NaCl, remain unoccupied, creating lattice vacancies without disturbing the overall electrical neutrality of the crystal. This defect is common in ionic crystals where the positive and negative ions are similar in size, as seen in sodium chloride and cesium chloride. The presence of Schottky defects enables the crystal to conduct electricity to a small extent through an ionic mechanism. Electric fields cause nearby...
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Ionic Association01:28

Ionic Association

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The ionic association is the association of oppositely charged ions in an electrolyte solution to form ion pairs. Bjerrum defined ion pairs as two oppositely charged ions whose electrostatic attraction exceeds the thermal energy of the system, typically expressed as 2kT. Electrostatic attraction depends on ionic charge, separation distance, and the dielectric constant of the medium. Thermal energy, represented by kT, reflects the tendency of ions to move independently due to molecular motion.
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Ion Exchange01:17

Ion Exchange

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Ion exchange chromatography separates charged molecules from a solution by reversibly exchanging them with mobile, or 'active', ions associated with the oppositely charged stationary phase. This method can be used to separate ions, soften and deionize water, and purify solutions. The polymers comprising the ion-exchange column are high-molecular-weight and chemically stable polymers, crosslinked to be porous and essentially insoluble. They are also functionalized with either acidic or...
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Molecular and Ionic Solids02:54

Molecular and Ionic Solids

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Crystalline solids are divided into four types: molecular, ionic, metallic, and covalent network based on the type of constituent units and their interparticle interactions.
Molecular Solids
Molecular crystalline solids, such as ice, sucrose (table sugar), and iodine, are solids that are composed of neutral molecules as their constituent units. These molecules are held together by weak intermolecular forces such as London dispersion forces, dipole-dipole interactions, or hydrogen bonds, which...
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The Electrical Double Layer01:30

The Electrical Double Layer

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In the region where two bulk phases meet, an intricate electric charge distribution arises due to charge transfer, ion adsorption, molecular orientation, and charge distortion. This complex distribution is commonly referred to as the electrical double layer.When a solid electrode interfaces with ions in an electrolyte solution, the speed of electron transfer dictates the rates of oxidation and reduction. The electrode acquires a charge through the escape of atoms into the solution as cations or...
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Characterization of Electrode Materials for Lithium Ion and Sodium Ion Batteries Using Synchrotron Radiation Techniques
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Characterization of Electrode Materials for Lithium Ion and Sodium Ion Batteries Using Synchrotron Radiation Techniques

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Crystalline/Amorphous Interface Engineering for Superior Sodium-Ion Storage.

Jie Sheng1, Yang Li2, Shaoyu Chai1

  • 1School of Materials Science and Engineering, Lanzhou University of Technology, Lanzhou 730050, China.

ACS Applied Materials & Interfaces
|March 12, 2026
PubMed
Summary
This summary is machine-generated.

This study introduces a novel crystalline/amorphous heterojunction for sodium-ion batteries (SIBs) that reduces interfacial stress. This approach significantly enhances battery capacity and cycling stability, paving the way for advanced SIBs.

Keywords:
amorphous cobaltous sulfidecrystalline vanadium tetrasulfidecrystalline/amorphous heterojunctionsinterface interactionsodium-ion batteries

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Area of Science:

  • Materials Science
  • Electrochemistry
  • Energy Storage

Background:

  • Crystalline/crystalline heterojunctions in sodium-ion batteries (SIBs) show promise but suffer from interfacial stress due to mismatched expansion coefficients.
  • This stress leads to cracking and degradation, limiting capacity and cycling durability.

Purpose of the Study:

  • To develop a crystalline/amorphous (C/A) heterojunction strategy to alleviate interfacial stress in SIBs.
  • To enhance the electrochemical performance of SIBs by improving Na+ diffusion and stability.

Main Methods:

  • Fabrication of a C/A heterojunction using crystalline VS4 and amorphous CoS.
  • Utilizing theoretical calculations to understand Na+ diffusion kinetics and interfacial stress modulation.
  • Electrochemical testing of the material in SIBs, including rate capability and long-term cycling stability tests.
  • Assembly and testing of a full cell with Na3V2(PO4)3 cathode.

Main Results:

  • The C/A heterojunction effectively reduces interfacial stress, improving Na+ diffusion kinetics.
  • The synthesized material achieved a high reversible specific capacity of 700.25 mAh g-1 after 100 cycles at 1.0 A g-1 with minimal capacity decay.
  • Excellent rate capability (481.4 mAh g-1 at 20 A g-1 after 1200 cycles) and long-term cycling stability were demonstrated.
  • The full cell retained 90.8% capacity after 11000 cycles at 5.0 A g-1.

Conclusions:

  • The C/A heterojunction is a viable strategy for overcoming interfacial stress limitations in SIBs.
  • This approach significantly enhances Na+ storage capacity, rate capability, and cycling durability.
  • The study presents a novel pathway for designing next-generation heterojunction materials for high-performance SIBs.