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

Polymer Classification: Crystallinity01:21

Polymer Classification: Crystallinity

Unlike ionic or small covalent molecules, polymers do not form crystalline solids due to the diffusion limitations of their long-chain structures. However, polymers contain microscopic crystalline domains separated by amorphous domains.
Crystalline domains are the regions where polymer chains are aligned in an orderly manner and held together in proximity by intermolecular forces. For example, chains in the crystalline domains of polyethylene and nylon are bound together by van der Waals...
Polymer Classification: Stereospecificity01:26

Polymer Classification: Stereospecificity

Polymerization generates chiral centers along the entire backbone of a polymer chain. Accordingly, the stereochemistry of the substituent group has a significant effect on polymer properties. Polymers formed from monosubstituted alkene monomers feature chiral carbons at every alternate position in the polymer backbone. Relative to the predominant orientation of substituents at the adjacent chiral carbons, the polymer can exist in three different configurations: isotactic, syndiotactic, and...
Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

The cationic polymerization mechanism consists of three steps: initiation, propagation, and termination. In the initiation step of the polymerization process, the π bond of a monomer gets protonated by the Lewis acid catalyst, which is formed from boron trifluoride and water. The protonation of the π bond generates a carbocation stabilized by the electron‐donating group. In the propagation step, the π bond of the second monomer acts as a nucleophile and attacks the generated carbocation,...
Debye–Huckel–Onsager Conductance Equation01:28

Debye–Huckel–Onsager Conductance Equation

The Debye-Hückel-Onsager equation is a cornerstone of physical chemistry, providing a method to determine the molar conductance (Λm) and molar conductance at infinite dilution (Λ°m) for uni-univalent electrolytes.Uni-univalent electrolytes are electrolytes that dissociate in solution to produce one cation with a +1 charge and one anion with a –1 charge per formula unit.This equation addresses two crucial phenomena: the asymmetry effect and the electrophoretic effect. According to this equation,...

You might also read

Related Articles

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

Sort by
Same author

Comprehensive Insight into the Emerging World of Carbon Dots for Applications in Energy and Metal Ion Sensing.

Precision chemistry·2026
Same author

Functionalized spirogyra biowaste as a sustainable cathode material for high performance aqueous rechargeable Zn-I<sub>2</sub> battery with dual mechanism.

Journal of colloid and interface science·2025
Same author

Unconventional Photocapacitor Utilizing Metal-Organic Dye Capable of Operating in Low Intensity Light.

ACS applied materials & interfaces·2025
Same author

Decoding Plant-Based Green Synthesis of Zinc Oxide Nanoparticles.

Chemistry & biodiversity·2025
Same author

Self-assembly of cationic surfactant in choline chloride-based deep eutectic solvents: structural solvation and dynamics.

Physical chemistry chemical physics : PCCP·2024
Same author

Synergistic Enhancement of Water-Splitting Performance Using MOF-Derived Ceria-Modified g-C<sub>3</sub>N<sub>4</sub> Nanocomposites: Synthesis, Performance Evaluation, and Stability Prediction with Machine Learning.

Langmuir : the ACS journal of surfaces and colloids·2024

Related Experiment Video

Updated: May 27, 2026

Thermal Scanning Conductometry (TSC) as a General Method for Studying and Controlling the Phase Behavior of Conductive Physical Gels
10:01

Thermal Scanning Conductometry (TSC) as a General Method for Studying and Controlling the Phase Behavior of Conductive Physical Gels

Published on: January 23, 2018

Ionic conductivity through thermoresponsive polymer gel: ordering matters.

Saurabh S Soni1, Kishan B Fadadu, Alain Gibaud

  • 1Department of Chemistry, Sardar Patel University, Vallabh Vidyanagar-388 120, Gujarat, India. soni_b21@yahoo.co.in

Langmuir : the ACS Journal of Surfaces and Colloids
|November 11, 2011
PubMed
Summary

This study developed a polymer gel electrolyte using Pluronic F77, finding optimal ionic conductivity in the Im3m phase due to enhanced ion diffusion through its unique structure.

More Related Videos

Solid-state Graft Copolymer Electrolytes for Lithium Battery Applications
05:33

Solid-state Graft Copolymer Electrolytes for Lithium Battery Applications

Published on: August 12, 2013

Monitoring the Effects of Illumination on the Structure of Conjugated Polymer Gels Using Neutron Scattering
06:16

Monitoring the Effects of Illumination on the Structure of Conjugated Polymer Gels Using Neutron Scattering

Published on: December 21, 2017

Related Experiment Videos

Last Updated: May 27, 2026

Thermal Scanning Conductometry (TSC) as a General Method for Studying and Controlling the Phase Behavior of Conductive Physical Gels
10:01

Thermal Scanning Conductometry (TSC) as a General Method for Studying and Controlling the Phase Behavior of Conductive Physical Gels

Published on: January 23, 2018

Solid-state Graft Copolymer Electrolytes for Lithium Battery Applications
05:33

Solid-state Graft Copolymer Electrolytes for Lithium Battery Applications

Published on: August 12, 2013

Monitoring the Effects of Illumination on the Structure of Conjugated Polymer Gels Using Neutron Scattering
06:16

Monitoring the Effects of Illumination on the Structure of Conjugated Polymer Gels Using Neutron Scattering

Published on: December 21, 2017

Area of Science:

  • Materials Science
  • Polymer Chemistry
  • Electrochemistry

Background:

  • Thermoreversible polymer gels are formed by self-assembly of block copolymers like PEO-PPO-PEO (Pluronic F77).
  • These gels can transition into polymer gel electrolytes (PGEs) upon electrolyte addition, influencing ionic conductivity.
  • The microcrystalline phases formed by the block copolymer impact the material's properties.

Purpose of the Study:

  • To investigate the relationship between the microcrystalline phases of a Pluronic F77-based thermoreversible polymer gel and its ionic conductivity.
  • To identify the optimal phase for achieving high ionic conductivity in polymer gel electrolytes.
  • To understand the mechanism behind the enhanced ionic transport in specific phases.

Main Methods:

  • Preparation of thermoreversible polymer gels using PEO-PPO-PEO (Pluronic F77).
  • Conversion of gels to polymer gel electrolytes (PGEs) with LiI/I(2) electrolyte.
  • Small-angle X-ray scattering (SAXS) to identify crystalline phases based on polymer concentration.
  • Characterization of ionic conductivity, FTIR, ionic transference number, and diffusion coefficients.

Main Results:

  • Pluronic F77 self-assembles into cubic, 2D-hexagonal, and lamellar microcrystalline phases.
  • Ionic conductivity is dependent on the microphase structure of the PGE.
  • The Im3m phase exhibited the highest ionic conductivity (approximately 1 × 10(-3) S cm(-1)).
  • Enhanced ion diffusion in the 3D-interconnected micellar nanochannels of the Im3m phase was observed.

Conclusions:

  • The Im3m phase of the Pluronic F77-based polymer gel electrolyte provides optimal conditions for ionic transport.
  • The unique 3D-interconnected nanochannel structure facilitates faster ion diffusion, leading to higher conductivity.
  • This research highlights the importance of microphase control for developing efficient polymer gel electrolytes.