Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Molecular and Ionic Solids02:54

Molecular and Ionic Solids

19.7K
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...
19.7K
Ionic Crystal Structures02:42

Ionic Crystal Structures

16.6K
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...
16.6K
Metallic Solids02:37

Metallic Solids

20.3K
Metallic solids such as crystals of copper, aluminum, and iron are formed by metal atoms. The structure of metallic crystals is often described as a uniform distribution of atomic nuclei within a “sea” of delocalized electrons. The atoms within such a metallic solid are held together by a unique force known as metallic bonding that gives rise to many useful and varied bulk properties.
All metallic solids exhibit high thermal and electrical conductivity, metallic luster, and malleability....
20.3K
Phase Transitions: Melting and Freezing02:39

Phase Transitions: Melting and Freezing

14.4K
Heating a crystalline solid increases the average energy of its atoms, molecules, or ions, and the solid gets hotter. At some point, the added energy becomes large enough to partially overcome the forces holding the molecules or ions of the solid in their fixed positions, and the solid begins the process of transitioning to the liquid state or melting. At this point, the temperature of the solid stops rising, despite the continual input of heat, and it remains constant until all of the solid is...
14.4K
Colloidal precipitates01:09

Colloidal precipitates

4.5K
The high insolubility of some precipitates can result in an unfavorable relative supersaturation. This can lead to colloidal particles with a large surface-to-mass ratio, where adsorption is promoted. For instance, in the precipitation of silver chloride, silver ions are adsorbed on the surface of the colloidal particles, forming a primary layer. This layer attracts ions of opposite charge (such as nitrate ions), forming a diffuse secondary layer of adsorbed ions. This electric double layer...
4.5K
Recrystallization: Solid–Solution Equilibria01:10

Recrystallization: Solid–Solution Equilibria

2.0K
Recrystallization is a purification technique used to separate impurities from solid compounds. In this technique, no chemical reactions occur. Instead, it exploits physical properties only, specifically, the solubility differences between the desired compound and impurities, either at a single temperature or at different temperatures, and under other selected conditions. The solid-solution equilibrium (solubility equilibrium) of each component in the solution represents a binary phase...
2.0K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Engineering the Self-Assembly of Bacterial Microcompartment Shell Proteins via Charged Mutations.

ACS nano·2026
Same author

Solvent-Dependent Mechanical Response of De Novo Helix Repeat Proteins.

The journal of physical chemistry. B·2026
Same author

Mechanophore cross-linking enhances ballistic energy dissipation of polymers.

Nature·2026
Same author

Role of Polymer-Protein Interactions in the Dynamics of Polymer-Integrated Protein Crystals.

Journal of the American Chemical Society·2026
Same author

Electrostatically driven pattern formation in mixed charged-neutral multicomponent elastic membranes.

Proceedings of the National Academy of Sciences of the United States of America·2026
Same author

Rheological Isotope Effects for Molecular Insight in Covalent Adaptable Networks.

Macromolecules·2026

Related Experiment Video

Updated: Dec 24, 2025

Methods of Ex Situ and In Situ Investigations of Structural Transformations: The Case of Crystallization of Metallic Glasses
08:55

Methods of Ex Situ and In Situ Investigations of Structural Transformations: The Case of Crystallization of Metallic Glasses

Published on: June 7, 2018

8.8K

Sublattice melting in binary superionic colloidal crystals.

Yange Lin1, Monica Olvera de la Cruz2

  • 1Department of Chemistry, Northwestern University, Evanston, Illinois 60208, USA.

Physical Review. E
|April 16, 2020
PubMed
Summary
This summary is machine-generated.

Colloidal crystals with asymmetric particles exhibit sublattice melting, forming a novel superionic phase. This discovery offers new pathways for designing advanced solid-state electrolytes with tunable properties.

More Related Videos

From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding
06:44

From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding

Published on: March 24, 2018

69.5K
Orientational Transition in a Liquid Crystal Triggered by the Thermodynamic Growth of Interfacial Wetting Sheets
06:26

Orientational Transition in a Liquid Crystal Triggered by the Thermodynamic Growth of Interfacial Wetting Sheets

Published on: May 15, 2017

7.5K

Related Experiment Videos

Last Updated: Dec 24, 2025

Methods of Ex Situ and In Situ Investigations of Structural Transformations: The Case of Crystallization of Metallic Glasses
08:55

Methods of Ex Situ and In Situ Investigations of Structural Transformations: The Case of Crystallization of Metallic Glasses

Published on: June 7, 2018

8.8K
From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding
06:44

From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding

Published on: March 24, 2018

69.5K
Orientational Transition in a Liquid Crystal Triggered by the Thermodynamic Growth of Interfacial Wetting Sheets
06:26

Orientational Transition in a Liquid Crystal Triggered by the Thermodynamic Growth of Interfacial Wetting Sheets

Published on: May 15, 2017

7.5K

Area of Science:

  • Materials Science
  • Condensed Matter Physics
  • Colloid Science

Background:

  • Superionic compounds exhibit high ionic conductivity due to one component premelting.
  • Solid-state electrolytes are crucial for advanced energy storage applications.

Purpose of the Study:

  • To investigate sublattice melting in colloidal crystals with asymmetric particle sizes and charges.
  • To explore the formation of superionic phases in these colloidal systems.

Main Methods:

  • Creation of colloidal crystals from oppositely charged, highly asymmetric particles in salt solutions.
  • Temperature-dependent analysis to induce and observe sublattice melting.

Main Results:

  • Observed sublattice melting in colloidal crystals, leading to a superionic phase.
  • Formation of nonelectroneutral stoichiometric ratios in the superionic colloidal crystals.
  • Generation of structures with multiple ionic crystal domains within percolated superionic phases.

Conclusions:

  • Sublattice melting in colloidal systems provides a new route to superionic phases.
  • These findings enable the design of solid-state electrolytes with adjustable stoichiometries and enhanced ionic conductivity.