TY - JOUR
T1 - Ionic Liquid Analogs of AlCl3 with Urea Derivatives as Electrolytes for Aluminum Batteries
AU - Angell, Michael
AU - Zhu, Guanzhou
AU - Lin, Meng Chang
AU - Rong, Youmin
AU - Dai, Hongjie
N1 - Funding Information:
This work was supported by DOE DE-SC0016165. The authors would like to acknowledge help with viscosity and conductivity data collection from Ms. Yung-Yu Hsiao. M.A. would also like to acknowledge Stephen R. Lynch for assistance with, and useful conversations pertaining to, NMR experiments, and Mohammad Hasani for useful conversations pertaining to ionic liquid analogs.
Publisher Copyright:
© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2020/1
Y1 - 2020/1
N2 - The ionic liquid analog, formed through the mixture of urea and AlCl3, has previously shown to serve as a low-cost electrolyte for an aluminum-graphite battery, while maintaining good performance and achieving high Coulombic efficiency. Undesirable are the relatively high viscosity and low conductivity of this electrolyte, when compared to chloroaluminate ionic liquids with organic cations. In this work, the fundamental changes to the electrolyte resulting from using derivatives of urea (N-methyl urea and N-ethyl urea), again mixed with AlCl3, are examined. These electrolytes are shown to have significantly lower viscosities (η = 45, 67, and 133 cP when using N-ethyl urea, N-methyl urea, and urea, respectively, at 25 °C). The associated batteries exhibit higher intrinsic discharge voltages (2.04 and 2.08 V for N-methyl urea and N-ethyl urea electrolytes, respectively, vs 1.95 V for urea system@100 mA g−1 specific current for ≈5 mg cm−2 loading), due to changes in concentrations of ionic species. Aluminum deposition is directly observed to primarily occur through reduction of Al2Cl7 − when AlCl3 is present in excess, in contrast to previously suggested cationic Al-containing species, via operando Raman spectroscopy performed during cyclic voltammetry.
AB - The ionic liquid analog, formed through the mixture of urea and AlCl3, has previously shown to serve as a low-cost electrolyte for an aluminum-graphite battery, while maintaining good performance and achieving high Coulombic efficiency. Undesirable are the relatively high viscosity and low conductivity of this electrolyte, when compared to chloroaluminate ionic liquids with organic cations. In this work, the fundamental changes to the electrolyte resulting from using derivatives of urea (N-methyl urea and N-ethyl urea), again mixed with AlCl3, are examined. These electrolytes are shown to have significantly lower viscosities (η = 45, 67, and 133 cP when using N-ethyl urea, N-methyl urea, and urea, respectively, at 25 °C). The associated batteries exhibit higher intrinsic discharge voltages (2.04 and 2.08 V for N-methyl urea and N-ethyl urea electrolytes, respectively, vs 1.95 V for urea system@100 mA g−1 specific current for ≈5 mg cm−2 loading), due to changes in concentrations of ionic species. Aluminum deposition is directly observed to primarily occur through reduction of Al2Cl7 − when AlCl3 is present in excess, in contrast to previously suggested cationic Al-containing species, via operando Raman spectroscopy performed during cyclic voltammetry.
KW - aluminum battery
KW - aluminum deposition
KW - ionic liquids
KW - N-ethyl urea
KW - urea electrolyte
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U2 - 10.1002/adfm.201901928
DO - 10.1002/adfm.201901928
M3 - Article
AN - SCOPUS:85074711640
SN - 1057-9257
VL - 30
JO - Advanced Materials for Optics and Electronics
JF - Advanced Materials for Optics and Electronics
IS - 4
M1 - 1901928
ER -