Titolo | Recent developments in the ENEA lithium metal battery project |
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Tipo di pubblicazione | Articolo su Rivista peer-reviewed |
Anno di Pubblicazione | 2005 |
Autori | Shin, J.-H., Henderson W.A., Appetecchi Giovanni Battista, Alessandrini F., and Passerini S. |
Rivista | Electrochimica Acta |
Volume | 50 |
Paginazione | 3859-3865 |
ISSN | 00134686 |
Parole chiave | Electrochemistry, Ionic liquid, Lithium batteries, Lithium battery project, Organic solvents, Phase separation, Plastic films, Polyelectrolytes, Pyrrolidinium, Room temperature ionic liquid (RTIL), TFSI, Thermal effects |
Abstract | Solvent-free P(EO)20LiTFSI + PYR14TFSI polymer electrolyte films with PYR14+/Li+ mole ratios ranging from 0.96 to 3.22 were prepared by hot-pressing mixtures composed of PEO, LiTFSI and PYR14TFSI of selected stoichiometries. The PYR 14TFSI room temperature ionic liquid (RTIL) is homogeneously incorporated into the P(EO)20LiTFSI membrane without phase separation. For a PYR14+/Li+ mole ratio of 3.22, the ionic conductivity was about 2 × 10-4 S/cm at 20 °C, i.e., more than one order of magnitude higher than that of the RTIL-free electrolyte. The electrochemical stability window of the polymer electrolyte containing the RTIL was about 6 V (versus Ag/Ag+). Li/V 2O5 cells with the polymer electrolyte (PYR 14+/Li+ = 1.92) showed a 60% capacity retention after 80 cycles at 40 °C (the initial capacity was 210 mA h/g). Li/V 2O5 cells (PYR14+/Li+ = 1.28) held at 30 °C delivered about 93 mA h/g (at 0.057 mA/cm2), which corresponds to approximately 34% utilization of the active material. These results suggest that the incorporation of the RTILs into PEO-based polymer electrolytes is very promising for the future realization of solid-state lithium metal polymer batteries operating near ambient temperatures. © 2005 Elsevier Ltd. All rights reserved. |
Note | cited By 91 |
URL | https://www.scopus.com/inward/record.uri?eid=2-s2.0-20444424536&doi=10.1016%2fj.electacta.2005.02.049&partnerID=40&md5=27900b11d3af4bc3186bc18920976656 |
DOI | 10.1016/j.electacta.2005.02.049 |
Citation Key | Shin20053859 |