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Development of long lifespan high-energy aqueous organic||iodine rechargeable batteries
Rechargeable aqueous metal||I(2) electrochemical energy storage systems are a cost-effective alternative to conventional transition-metal-based batteries for grid energy storage. However, the growth of unfavorable metallic deposition and the irreversible formation of electrochemically inactive by-pr...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9618581/ https://www.ncbi.nlm.nih.gov/pubmed/36310178 http://dx.doi.org/10.1038/s41467-022-34303-8 |
Sumario: | Rechargeable aqueous metal||I(2) electrochemical energy storage systems are a cost-effective alternative to conventional transition-metal-based batteries for grid energy storage. However, the growth of unfavorable metallic deposition and the irreversible formation of electrochemically inactive by-products at the negative electrode during cycling hinder their development. To circumvent these drawbacks, herein we propose 3,4,9,10-perylenetetracarboxylic diimide (PTCDI) as negative electrode active material and a saturated mixed KCl/I(2) aqueous electrolyte solution. The use of these components allows for exploiting two sequential reversible electrochemical reactions in a single cell. Indeed, when they are tested in combination with an active carbon-enveloped I(2) electrode in a glass cell configuration, we report an initial specific discharge capacity of 900 mAh g(−1) (electrode mass of iodine only) and an average cell discharge voltage of 1.25 V at 40 A g(−1) and 25[Formula: see text] 1 °C. Finally, we also report the assembly and testing of a PTCDI|KCl-I(2)|carbon paper multilayer pouch cell prototype with a discharge capacity retention of about 70% after 900 cycles at 80 mA and 25[Formula: see text] 1 °C. |
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