Related Experiment Video
Updated: Jun 9, 2025

Synthesis and Purification of Iodoaziridines Involving Quantitative Selection of the Optimal Stationary Phase for Chromatography
Published on: May 16, 2014
Azopyridine Aqueous Electrochemistry Enables Superior Organic AZIBs
Yihui Xie1, Ming Li1, Yijian Ma1
1School of Chemistry and Chemical Engineering, Zhejiang Sci-Tech University, Hangzhou 310000, P. R. China.
Azopyridine isomers enable the first azo compound (AZO)-based aqueous zinc-ion batteries (AZIBs) with a 1.4 V output. This breakthrough clarifies the energy storage mechanism, significantly enhancing AZIB performance.
Area of Science:
- Electrochemistry
- Materials Science
- Energy Storage
Background:
- Azo compounds (AZO) are explored as organic electrode materials for aqueous zinc-ion batteries (AZIBs).
- Azobenzene cathodes in AZIBs offer low voltage (~0.7 V) and unclear energy storage mechanisms.
- Low voltage and mechanism ambiguity limit practical AZO cathode applications in AZIBs.
Purpose of the Study:
- To investigate azopyridine isomers as AZO cathodes in AZIBs.
- To elucidate the energy storage mechanism of azopyridine cathodes in AZIBs.
- To develop high-voltage AZO-based AZIBs.
Main Methods:
- Aqueous electrochemical studies of azopyridine isomers as cathodes.
- In situ electrochemical characterizations.
- Theoretical computations.
Main Results:
- Azopyridine cathodes exhibit an uplifted redox potential due to electron-withdrawing pyridyl groups and H+-involved redox reactions.
- The first AZO-based AZIB was successfully developed, achieving a 1.4 V output.
- The developed AZIBs are air-stable, offering high energy/power density and a capacity of ~200 mAh g-1.
- Distinct azopyridine electrochemistry was observed in aqueous versus organic electrolytes.
Conclusions:
- Azopyridine isomers represent a promising class of AZO materials for high-performance AZIBs.
- Understanding the electrochemical mechanism is key to designing advanced AZO cathodes.
- This research significantly advances AZO-based energy storage, outperforming previous AZO materials in AZIBs.
Related Concept Videos
Preparation of 1° Amines: Azide Synthesis
Azide ions act as good nucleophiles and react with unhindered alkyl halides to form alkyl azides. Alkyl azides do not participate in further nucleophilic substitution reactions, thereby eliminating the chances of polyalkylated products. Alkyl azides are reduced by hydride-based reducing agents, like lithium aluminum...
Aryldiazonium Salts to Azo Dyes: Diazo Coupling
Basicity of Heterocyclic Aromatic Amines
Nucleophilic Aromatic Substitution of Aryldiazonium Salts: Aromatic SN1
In the Sandmeyer reaction, for example, the diazonio group is replaced by a chloro, bromo,...
Electrophilic Aromatic Substitution: Fluorination and Iodination of Benzene
Diazonium Group Substitution with Halogens and Cyanide: Sandmeyer and Schiemann Reactions

