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Related Concept Videos

Electrolyte and Nonelectrolyte Solutions02:21

Electrolyte and Nonelectrolyte Solutions

Substances that undergo either a physical or a chemical change in solution to yield ions that can conduct electricity are called electrolytes. If a substance yields ions in solution, that is, if the compound undergoes 100% dissociation, then the substance is a strong electrolyte. Complete dissociation is indicated by a single forward arrow. For example, water-soluble ionic compounds like sodium chloride dissociate into sodium cations and chloride anions in aqueous solution.
Batteries and Fuel Cells03:12

Batteries and Fuel Cells

A battery is a galvanic cell that is used as a source of electrical power for specific applications. Modern batteries exist in a multitude of forms to accommodate various applications, from tiny button batteries such as those that power wristwatches to the very large batteries used to supply backup energy to municipal power grids. Some batteries are designed for single-use applications and cannot be recharged (primary cells), while others are based on conveniently reversible cell reactions that...
Ion Exchange01:17

Ion Exchange

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 basic...
The Debye–Hückel Theory of Electrolyte Solutions01:27

The Debye–Hückel Theory of Electrolyte Solutions

The Debye–Hückel theory, established by Peter Debye and Erich Hückel in 1923, is a fundamental concept in physical chemistry. It provides an understanding of the behavior of strong electrolytes in solution, particularly explaining their deviations from ideal behavior.The theory is based on Coulombic interactions (the attraction or repulsion between charged particles) between ions in solution. In an ionic solution, oppositely charged ions tend to attract each other. This means that cations...
Ionic Association01:28

Ionic Association

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.
Theory of Strong Electrolytes01:23

Theory of Strong Electrolytes

The interionic forces of the strong electrolytes depend on the solvent's dielectric constant, which is the ability of a solvent to store electrical energy, based on its polarizability. and the solution's concentration. In high-dielectric solvents and in dilute solutions, weak electrostatic forces keep ions apart. However, in low-dielectric solvents or concentrated solutions, stronger interionic forces may cause ions to pair up as ionic doublets despite being fully ionized. The theory of strong...

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Updated: Jun 25, 2026

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

Functionality Selection Principle for High Voltage Lithium-ion Battery Electrolyte Additives.

Chi-Cheung Su, Meinan He1, Cameron Peebles

  • 1Department of Mechanical Engineering, Worcester Polytechnic Institute , 100 Institute Road, Worcester, Massachusetts 01609, United States.

ACS Applied Materials & Interfaces
|August 19, 2017
PubMed
Summary
This summary is machine-generated.

New cyclic fluorinated phosphate ester additives stabilize high-voltage lithium-ion battery cathodes. These additives form a protective surface layer, significantly improving capacity retention in LiNi0.5Mn0.3Co0.2O2 (NMC532) batteries.

Keywords:
LiNi0.5Mn0.3Co0.2O2 cathodeelectrolyte additivefluorinated cyclic phosphatefunctionality selection principlehigh voltage electrolytepost-test analysis

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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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Synthesis of Ionic Liquid Based Electrolytes, Assembly of Li-ion Batteries, and Measurements of Performance at High Temperature
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Synthesis of Ionic Liquid Based Electrolytes, Assembly of Li-ion Batteries, and Measurements of Performance at High Temperature

Published on: December 20, 2016

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Last Updated: Jun 25, 2026

Solid-state Graft Copolymer Electrolytes for Lithium Battery Applications
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Characterization of Electrode Materials for Lithium Ion and Sodium Ion Batteries Using Synchrotron Radiation Techniques
10:03

Characterization of Electrode Materials for Lithium Ion and Sodium Ion Batteries Using Synchrotron Radiation Techniques

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Synthesis of Ionic Liquid Based Electrolytes, Assembly of Li-ion Batteries, and Measurements of Performance at High Temperature
11:04

Synthesis of Ionic Liquid Based Electrolytes, Assembly of Li-ion Batteries, and Measurements of Performance at High Temperature

Published on: December 20, 2016

Area of Science:

  • Materials Science
  • Electrochemistry
  • Battery Technology

Background:

  • High-voltage operation of lithium-ion batteries requires stable cathode-electrolyte interfaces.
  • Existing electrolyte additives have limitations in stabilizing advanced cathode materials like LiNi0.5Mn0.3Co0.2O2 (NMC532) at high potentials (>4.6 V).

Purpose of the Study:

  • To rationally design and synthesize a new class of electrolyte additives based on cyclic fluorinated phosphate esters.
  • To investigate the electrochemical performance and stabilization mechanism of these additives in NMC532/graphite cells.

Main Methods:

  • Synthesis and characterization of novel cyclic fluorinated phosphate ester additives.
  • Electrochemical cycling of NMC532/graphite cells with and without additives in a voltage range of 3.0-4.6 V.
  • Surface analysis using X-ray photoelectron spectroscopy (XPS) and nuclear magnetic resonance (NMR) to elucidate the interface formation mechanism.

Main Results:

  • The additive 2-(2,2,2-trifluoroethoxy)-1,3,2-dioxaphospholane 2-oxide (TFEOP) significantly improved capacity retention in NMC532/graphite cells cycled at high voltages.
  • XPS and NMR analysis indicated that TFEOP forms a protective passivation layer on the NMC532 cathode surface through a sacrificial polymerization reaction.
  • The proposed cathode-electrolyte-interface formation pathway involves the polymerizable cyclic ring and electron-withdrawing fluorinated alkyl group of the additive.

Conclusions:

  • Cyclic fluorinated phosphate esters are effective electrolyte additives for stabilizing high-voltage NMC532 cathodes.
  • The combination of a polymerizable ring and fluorinated groups in the additive molecule enhances cathode protection.
  • A new design principle for electrolyte additives, integrating functionalities from various existing additives into a single molecule, is validated.