Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

Interfacial Electrochemical Methods: Overview01:06

Interfacial Electrochemical Methods: Overview

384
Interfacial electrochemical methods focus on the phenomena occurring at the boundary between an electrode and a solution, as opposed to bulk methods that concentrate on the solution's overall properties. These interfacial methods are classified as either static or dynamic based on the presence of a nonzero current in the electrochemical cell and the consistency of analyte concentrations. Static methods, such as potentiometry, measure the cell's potential without any significant current...
384
Dialysis01:15

Dialysis

803
Dialysis is a diffusion-based purification process that separates analyte molecules from a complex matrix. This is accomplished by allowing molecules in the solution to pass through a semipermeable membrane into a liquid on the other side. The membrane is usually made of cellulose acetate or cellulose nitrate, and the second liquid must be miscible with the solution. Ions (e.g., chloride or sodium) or organic molecules (e.g., glucose) can pass through the membrane pores, which generally have...
803
Electrolytes: van't Hoff Factor03:08

Electrolytes: van't Hoff Factor

33.6K
Colligative Properties of Electrolytes
The colligative properties of a solution depend only on the number, not on the identity, of solute species dissolved. The concentration terms in the equations for various colligative properties (freezing point depression, boiling point elevation, osmotic pressure) pertain to all solute species present in the solution. Nonelectrolytes dissolve physically without dissociation or any other accompanying process. Each molecule that dissolves yields one...
33.6K
Ion-Exchange Chromatography01:09

Ion-Exchange Chromatography

759
Ion-exchange chromatography, or IEC, is a technique for separating ions based on their affinity for the stationary phase. The stationary phase is a cross-linked polymer resin with covalently attached ionic functional groups. The functional groups can be either positively charged (cation exchangers) or negatively charged (anion exchangers). A cation exchanger consists of a polymeric anion and active cations, while an anion exchanger is a polymeric cation with active anions. The choice of...
759
Electrolyte and Nonelectrolyte Solutions02:21

Electrolyte and Nonelectrolyte Solutions

63.8K
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.
63.8K
Introduction to Electrolytes01:33

Introduction to Electrolytes

12.4K
In humans, electrolytes play a vital role in various physiological processes. Balancing electrolyte levels is essential for normal body functions; their imbalance can be life-threatening. The major electrolytes include sodium, potassium, chloride, calcium, phosphate, and bicarbonate. They are primarily involved in physiological processes, such as nerve signal transmission, membrane trafficking, muscle contraction, buffering body fluids, and balancing water levels in the body.
Role of Sodium
One...
12.4K

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Heat Transfer Fluids as Co-Diluents in Localized High-Concentration Electrolytes for High-Rate Lithium Metal Batteries With Enhanced Safety.

Angewandte Chemie (International ed. in English)·2026
Same author

Li diffusion and migration are influenced differently by co-solvents in polymer electrolytes based on poly(ε-caprolactone) and poly(ethylene oxide).

Chemical science·2026
Same author

Mechanism and mitigation of stainless steel dissolution in LiFSI-based lithium-ion battery electrolytes.

Nature communications·2026
Same author

Water in Solvate Ionic Liquids: Preserving Lithium Coordination While Enhancing Ionic Conductivity.

Chemphyschem : a European journal of chemical physics and physical chemistry·2026
Same author

Supramolecular light-switchable triazole-hosts for photoresponsive anion binding.

Organic & biomolecular chemistry·2026
Same author

The Role of Li<sup>+</sup> Ions in Polyzwitterionic Ionogels: Gelator or Mobile Charge Carrier?

The journal of physical chemistry. B·2026
Same journal

Revisiting crossed-correlated baths in open quantum systems simulated by HEOM or T-TEDOPA.

The Journal of chemical physics·2026
Same journal

Vesicle size and membrane composition control monomer transfer pathways in multicomponent lipid vesicles.

The Journal of chemical physics·2026
Same journal

Polaron-mediated exciton dynamics of P(NDI2OD-T2) unveiled by transient absorption spectroscopy under electrochemical conditions.

The Journal of chemical physics·2026
Same journal

Green-Kubo relation in a mesoscale odd fluid model.

The Journal of chemical physics·2026
Same journal

Nitrogenation of microscopic MoS2 surfaces by oxidation scanning probe lithography.

The Journal of chemical physics·2026
Same journal

Molecular structure, binding, and disorder in TDBC-Ag plexcitonic assemblies.

The Journal of chemical physics·2026
查看所有相关文章

相关实验视频

Updated: Sep 9, 2025

On-chip Isotachophoresis for Separation of Ions and Purification of Nucleic Acids
10:32

On-chip Isotachophoresis for Separation of Ions and Purification of Nucleic Acids

Published on: March 2, 2012

24.7K

在局部高度电解质中分析内部接口

Anne Hockmann1,2, Monika Schönhoff1, Diddo Diddens1,3

  • 1Institute of Physical Chemistry, University of Münster, Corrensstraße 28/30, 48149 Münster, Germany.

The Journal of chemical physics
|August 29, 2025
PubMed
概括
此摘要是机器生成的。

具有不同阴离子的局部高度电解质 (LHCE) 显示出不同的界面行为. TFSI- 离子丰富了接口,增强了离子解离,而FSI- 则消耗了它,对离子运输产生了不同的影响.

更多相关视频

Merging Ion Concentration Polarization between Juxtaposed Ion Exchange Membranes to Block the Propagation of the Polarization Zone
08:06

Merging Ion Concentration Polarization between Juxtaposed Ion Exchange Membranes to Block the Propagation of the Polarization Zone

Published on: February 23, 2017

8.6K
Functional Characterization of Na+/H+ Exchangers of Intracellular Compartments Using Proton-killing Selection to Express Them at the Plasma Membrane
07:38

Functional Characterization of Na+/H+ Exchangers of Intracellular Compartments Using Proton-killing Selection to Express Them at the Plasma Membrane

Published on: March 30, 2015

9.3K

相关实验视频

Last Updated: Sep 9, 2025

On-chip Isotachophoresis for Separation of Ions and Purification of Nucleic Acids
10:32

On-chip Isotachophoresis for Separation of Ions and Purification of Nucleic Acids

Published on: March 2, 2012

24.7K
Merging Ion Concentration Polarization between Juxtaposed Ion Exchange Membranes to Block the Propagation of the Polarization Zone
08:06

Merging Ion Concentration Polarization between Juxtaposed Ion Exchange Membranes to Block the Propagation of the Polarization Zone

Published on: February 23, 2017

8.6K
Functional Characterization of Na+/H+ Exchangers of Intracellular Compartments Using Proton-killing Selection to Express Them at the Plasma Membrane
07:38

Functional Characterization of Na+/H+ Exchangers of Intracellular Compartments Using Proton-killing Selection to Express Them at the Plasma Membrane

Published on: March 30, 2015

9.3K

科学领域:

  • 电化学
  • 材料科学
  • 计算化学

背景情况:

  • 局部化高度电解质 (LHCE) 由于相不混合性而表现出复杂的微观结构.
  • 了解LHCE的界面特性和离子传输机制对于先进的电池应用至关重要.

研究的目的:

  • 通过分子动力学模拟来研究LHCE的协调结构和界面特性.
  • 分析不同离子 (TFSI和FSI) 对离子传输和界面组成的影响.
  • 探索增加盐度对LHCE微观结构和离子动态的影响.

主要方法:

  • 使用 LiFSI 和 LiTFSI 盐进行分子动力学模拟.
  • 分析内部接口的尺寸和组成.
  • 为了评估离子传输特性,评估了Onsager系数.

主要成果:

  • 表面活性TFSI- 离子形成了丰富的离子接口,促进离子解离和反相关离子运动.
  • 具有局部电荷的FSI-离子导致界面耗尽和不同的离子传输特性.
  • 增加的LiFSI度会导致富含溶剂的接口,较少的扩散边界和改变的离子相关性.

结论:

  • 阴离子结构和度在很大程度上决定了LHCE的界面特性和离子传输.
  • 具有TFSI-的LHCE表现出增强的离子解离,而具有FSI-的LHCE表现出不同的界面行为.
  • 这些发现提供了设计电解质与量身定制的微观结构以提高电化学性能的见解.