Related Experiment Video
Updated: Jun 26, 2025

Synthesis of Ionic Liquid Based Electrolytes, Assembly of Li-ion Batteries, and Measurements of Performance at High Temperature
Published on: December 20, 2016
Starch Gel Electrolyte and its Interaction with Trivalent Aluminum for Aqueous Aluminum-Ion Batteries: Enhanced Low
Saraswathi Ramakrishnan1, Sajan Raj Sasirajan Little Flower1, Desai Prashant Hanamantrao1
1Electrochemical Energy Storage and Conversion Laboratory (EESCL), Department of Chemistry, Faculty of Engineering and Technology, SRM Institute of Science and Technology (SRMIST), Kattankulathur, Tamil Nadu, 603203, India.
Abstract:
This study explores trivalent Al interaction with aqueous starch gel in the presence of two different anions through salting effect. Salting-out nature of Al2(SO4)3·18H2O with starch gel causes precipitation of starch; this happens due to competitive anion-water complex formation over starch-water interaction, thereby reducing polymer solubility. Salting-in effect of AlCl3 with starch gel happens through Al3+ cation interaction with hydroxyl group of starch and increases polymer solubility, making gel electrolyte viable for battery applications. Prepared gel electrolyte exhibits ionic conductivity of 1.59 mS cm-1 and a high tAl 3+ value of 0.77. The gel electrolyte's performance is studied using two different cathodes, the Al|MoO3 cell employing starch gel electrolyte achieves discharge capacity of 193 mA h g-1 and Al|MnO2 cell achieves discharge capacity of 140 mA h g-1 @0.1 A g-1 for first cycle. The diffusion coefficient of both cells using starch gel electrolyte is calculated and found to be 2.1 × 10-11 cm2 s-1 for Al|MoO3 and 3.1 × 10-11 cm2 s-1 for Al|MnO2 cells. The Al|MoO3 cell at lower temperature shows improved electrochemical performance with a specific capacity retention of ≈87.8% over 90 cycles. This kind of aqueous gel electrolyte operating at low temperature broadens the application for next generation sustainable batteries.
Related Concept Videos
Ionic Strength: Effects on Chemical Equilibria
In this solution, the primary...
Qualitative Analysis
For instance, group IV...
Colloidal precipitates
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...

