Related Experiment Video
Updated: May 22, 2025

Characterization of Electrode Materials for Lithium Ion and Sodium Ion Batteries Using Synchrotron Radiation Techniques
Published on: November 11, 2013
Monocarboxylic Acid Structural Analogues Facilitate In Situ Composite of Functional Complexes for Aqueous Batteries
Yichun Su1, Yanfei Zhang1, Wanchang Feng1
1School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou, Jiangsu, 225002, P.R. China.
Abstract:
In situ composite methods have aroused research interest in materials science and acted as a novel strategy to achieve structural tailoring of materials. However, the controllable preparation of composites containing functional groups remains a challenge. Herein, we report an approach based on competitive coordination between structural analogs, by which the functionally composite metal complex (NiSH@Ni-FSA) was synthesized. The introduction of different functional groups allows precise control of the functionality of composites, ranging from NiSH@Ni-ClSA-D, NiSH@Ni-BrSA to NiSH@Ni-CF3SA. More interestingly, the synthesized material retained the microporous and mesoporous structure of the original complexes. The incorporation of hydrophobic functional groups effectively protects the electrode materials from degradation and corrosion. Meanwhile, the presence of intermolecular hydrogen bonding facilitates new composite nanomaterials with better performance for advanced energy storage applications.
More Related Videos
Related Concept Videos
Batteries and Fuel Cells
Nomenclature of Carboxylic Acid Derivatives: Acid Halides, Esters, and Acid Anhydrides
The IUPAC and common names of acid halides are derived from the corresponding carboxylic acids, by changing “ic acid” to “yl halide.” For example, as shown below, the IUPAC name ethanoyl chloride is derived from ethanoic acid, and the common name, acetyl chloride, is obtained from acetic acid.
Ion Exchange
Alkylation of β-Diester Enolates: Malonic Ester Synthesis
Acid Halides to Carboxylic Acids: Hydrolysis
As shown below, the mechanism involves a nucleophilic attack by water at the carbonyl carbon to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen π bond along with the departure of a halide ion. A final proton transfer step yields carboxylic...
Carboxylic Acid Derivatives: Overview

