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Related Concept Videos

Precipitation of Ions03:11

Precipitation of Ions

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Predicting Precipitation
The equation that describes the equilibrium between solid calcium carbonate and its solvated ions is:
28.1K
Redox Titration: Iodimetry and Iodometry01:23

Redox Titration: Iodimetry and Iodometry

2.7K
Iodometry and iodimetry are analytical methods used to determine the concentration of oxidizing or reducing agents using iodine. In iodometric titrations, the oxidizing analyte solution is usually acidified and treated with an excess of iodide ions, which generates an equivalent amount of iodine in equilibrium with triiodide. The released iodine is subsequently titrated directly against a standardized reducing agent. As the dilute iodine color becomes pale yellow, a few drops of freshly...
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Alkyl Halides02:45

Alkyl Halides

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Structural Properties
Alkyl halides are halogen-substituted alkanes wherein one or more hydrogen atoms of an alkane is replaced by a halogen atom such as fluorine, chlorine, bromine, or iodine. The carbon atom in an alkyl halide is bonded to the halogen atom, which is sp3-hybridized and exhibits a tetrahedral shape.
Unlike alkyl halides, compounds in which a halogen atom is bonded to an sp2 -hybridized carbon atom of a carbon-carbon double bond (C=C) are called vinyl halides. Whereas aryl...
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Solubility of Ionic Compounds02:55

Solubility of Ionic Compounds

64.1K
Solubility is the measure of the maximum amount of solute that can be dissolved in a given quantity of solvent at a given temperature and pressure. Solubility is usually measured in molarity (M) or moles per liter (mol/L). A compound is termed soluble if it dissolves in water.
64.1K
Solution Formation02:16

Solution Formation

32.8K
There is no one solvent that can dissolve every type of solute. Some substances that readily dissolve in a certain solvent might be insoluble in a different solvent. A simple way to predict which substances dissolve in which solvent is the phrase "like dissolves like". This means that polar substances, such as salt and sugar, dissolve in a polar substance like water. In contrast, non-polar substances are more soluble in non-polar solvents such as carbon tetrachloride.
This selective...
32.8K
Common Ion Effect03:24

Common Ion Effect

42.3K
Compared with pure water, the solubility of an ionic compound is less in aqueous solutions containing a common ion (one also produced by dissolution of the ionic compound). This is an example of a phenomenon known as the common ion effect, which is a consequence of the law of mass action that may be explained using Le Châtelier’s principle. Consider the dissolution of silver iodide:
42.3K

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Related Experiment Video

Updated: Sep 13, 2025

Chemoselective Preparation of 1-Iodoalkynes, 1,2-Diiodoalkenes, and 1,1,2-Triiodoalkenes Based on the Oxidative Iodination of Terminal Alkynes
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Chemoselective Preparation of 1-Iodoalkynes, 1,2-Diiodoalkenes, and 1,1,2-Triiodoalkenes Based on the Oxidative Iodination of Terminal Alkynes

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Balanced Iodophilicity and Solvophilicity Unlocks Fast Iodine Conversion Chemistry.

Tao Xiao1, Jin-Lin Yang1,2, Ruo Jie Xu3

  • 1School of Physical and Mathematical Sciences, Nanyang Technological University, Singapore 637371, Singapore.

Journal of the American Chemical Society
|August 1, 2025
PubMed
Summary

This study introduces a dual single atomic catalyst for aqueous zinc-iodine batteries, balancing polyiodide adsorption and transport. This innovation enhances cathode stability and significantly improves battery performance.

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

  • Electrochemistry
  • Materials Science
  • Catalysis

Background:

  • Aqueous Zn-I2 batteries face challenges from polyiodide shuttling and slow redox kinetics.
  • Existing catalysts often fail to balance polyiodide adsorption with interfacial mass transport, leading to poor iodine utilization and capacity fade.

Purpose of the Study:

  • To develop a novel catalytic interface that optimizes the balance between polyiodide adsorption and mass transport kinetics at the cathode.
  • To enhance the stability and performance of aqueous Zn-I2 batteries by addressing the limitations of current catalytic approaches.

Main Methods:

  • Employed a dual single atomic catalyst featuring Nickel-Nitrogen-Phosphorus (NiN4P) and Iron-Nitrogen-Phosphorus (FeN4P) sites.
  • Investigated the synergistic effects of FeN4 and NiN4 sites on polyiodide immobilization and mass transport, respectively.
  • Utilized phosphorus ligands to tune electronic properties and create favorable interfacial conditions.

Main Results:

  • The dual atomic catalyst achieved a well-balanced solvophilicity and iodophilicity at the cathode interface.
  • FeN4 sites enhanced polyiodide immobilization, while NiN4 sites improved mass transport kinetics.
  • The catalyst demonstrated high cycling stability and an ultralow self-discharge rate under low electrolyte-to-iodine ratios.

Conclusions:

  • The developed dual single atomic catalyst effectively regulates the aqueous halogen cathode interface.
  • This approach offers a promising strategy for achieving long cycle life in aqueous Zn-I2 batteries.
  • The findings provide critical insights for designing advanced catalysts for energy storage systems.