Electrochemical Behavior of Rechargeable Al–Ni Battery Systems in Concentrated [EMIm]Cl-AlCl3 ElectrolyteClick to copy article linkArticle link copied!
- Bing Wu*Bing Wu*Email: [email protected]Department of Inorganic Chemistry, University of Chemistry and Technology Prague, Technická 5, 166 28 Prague 6, Czech RepublicMore by Bing Wu
- Lukas DekanovskyLukas DekanovskyDepartment of Inorganic Chemistry, University of Chemistry and Technology Prague, Technická 5, 166 28 Prague 6, Czech RepublicMore by Lukas Dekanovsky
- Mazanek VlastimilMazanek VlastimilDepartment of Inorganic Chemistry, University of Chemistry and Technology Prague, Technická 5, 166 28 Prague 6, Czech RepublicMore by Mazanek Vlastimil
- Shuangying WeiShuangying WeiDepartment of Inorganic Chemistry, University of Chemistry and Technology Prague, Technická 5, 166 28 Prague 6, Czech RepublicMore by Shuangying Wei
- Zdenek Sofer*Zdenek Sofer*Email: [email protected]Department of Inorganic Chemistry, University of Chemistry and Technology Prague, Technická 5, 166 28 Prague 6, Czech RepublicMore by Zdenek Sofer
Abstract

In this work, the electrochemical behavior of the Al–Ni battery system in electrolyte composed of aluminum chloride (AlCl3) and 1-ethyl-3-methylimidazolium chloride ([EMIm]Cl) with a molar ratio of 1.3 is investigated. The results reveal that the reversible capacity, which is based on the de/alloying process of Al on a Ni cathode, can be triggered only once the Ni electrode has been chlorinated. The value of reversible capacity is related to the chlorination degree of the nickel electrode. However, because the produced nickel chloride is soluble in the [EMIm]Cl-based electrolyte, the dissolved Ni2+ can migrate to the Al anode side and spontaneously react with the Al electrode, causing the battery to fail drastically. To safeguard the Al anode, an interlayer composed of Al powder is inserted between the separators to react with the dissolved Ni ions. The upgraded Al–Ni battery system can provide significantly improved performance, with cycling stability increasing from 84 to over 580 cycles in an 8 min controlled galvanostatic charge procedure.
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