Related Experiment Video
Updated: Nov 26, 2025

A Protocol for Electrochemical Evaluations and State of Charge Diagnostics of a Symmetric Organic Redox Flow Battery
Published on: February 13, 2017
Rechargeable Aqueous Aluminum Organic Batteries
Jiangchun Chen1, Qiaonan Zhu1, Li Jiang2
1School of Chemistry, Beijing Advanced Innovation Center for Biomedical Engineering, Beihang University, Beijing, 100191, China.
This study introduces phenazine as an organic cathode for aqueous aluminum-ion batteries (AABs). It demonstrates improved performance through anion co-intercalation, overcoming limitations of traditional inorganic materials.
Area of Science:
- Electrochemistry
- Materials Science
- Energy Storage
Background:
- Aqueous aluminum-ion batteries (AABs) are promising energy storage systems.
- Current inorganic cathodes face challenges like sluggish kinetics and poor stability due to strong Al3+ interactions.
- Limited lattice spacing and rigid structures hinder ion diffusion in conventional materials.
Purpose of the Study:
- To explore organic compounds as cathode materials for AABs.
- To investigate the potential of phenazine (PZ) as a high-performance cathode.
- To understand the mechanism of anion co-intercalation in organic cathodes for AABs.
Main Methods:
- Utilizing phenazine (PZ) as a redox-active organic cathode material in AABs.
- Investigating the Al-complex co-intercalation mechanism facilitated by the flexible organic structure.
- Analyzing the electrochemical performance, including capacity and cyclability.
Main Results:
- Phenazine enables large-size Al-complex co-intercalation, reducing desolvation penalty and Coulombic repulsion.
- The organic cathode exhibits high capacity and excellent cyclability, surpassing most reported AAB cathode materials.
- Demonstrated the viability of anion co-intercalation chemistry in redox-active organic materials.
Conclusions:
- Organic materials, specifically phenazine, offer a promising alternative to inorganic cathodes in AABs.
- Anion co-intercalation is an effective strategy to enhance electrochemical performance in AABs.
- This research paves the way for developing advanced multivalent-ion battery systems.
More Related Videos
Related Concept Videos
Batteries and Fuel Cells
Acid Halides to Alcohols: LiAlH4 Reduction
The mechanism proceeds in three steps. First, the nucleophilic hydride ion attacks the carbonyl carbon of the acid halide to form a tetrahedral intermediate. Next, the carbonyl group is re-formed, and the halide ion departs as a leaving group, generating an aldehyde. A second nucleophilic attack by the hydride yields an alkoxide ion, which, upon protonation, gives a primary alcohol as...
Voltaic/Galvanic Cells
Spontaneous redox reactions occur abundantly in nature. The chemical reaction occurring in a disposable AA battery powering our remote controls is one such example of a spontaneous redox reaction. Another example is the immersion of coiled copper wire into an aqueous silver nitrate solution. The reaction shows a gradual, visually impressive color change from colorless to bright blue and the formation of a grey precipitate on the copper wire. In this experiment,...
Preparation of Aldehydes and Ketones from Nitriles and Carboxylic Acids
Reducing carboxylic acid derivatives like acyl chlorides (RCOCl), esters (RCO2R′), and nitriles (RCN) using milder aluminum hydride agents like lithium tri-tert-butoxyaluminum hydride [LiAlH(O-t-Bu)3] and diisobutylaluminum hydride [DIBAL-H]...
Nitriles to Amines: LiAlH4 Reduction
As shown below, the mechanism involves three steps. Firstly, the hydride ion acting as a nucleophile attacks the nitrile carbon to form an anion. In the second step, a second equivalent of the hydride ion attacks the anion to...
Acid Halides to Alcohols: Grignard Reaction
Grignard reagents are a source of carbanions and function as nucleophiles. The mechanism begins with the nucleophilic attack by the carbanion at the carbonyl carbon of the acid halide to form a tetrahedral intermediate. Next, the carbonyl group is re-formed, and the halide ion departs,...

