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Page 10 of 24        Boaretto et al. Energy Mater. 2025, 5, 500040  https://dx.doi.org/10.20517/energymater.2024.203

               Table 3. Selected transport parameters for supported QSPEs and Li|QSPE|Li cells: ionic conductivity at room temperature, Li +
               transference number, Li/QSPE interface resistance in Li||Li cells, and steady-state current by applying a constant polarization ΔV of
               10 mV
                            σ (25 °C)/mS cm -1            T +               R /Ω cm 2          I /µA
                                                                              *
                                                                                               ss
                                                                             int
                QSPE-1      1.2 ± 0.2                     0.09 ± 0.01       240 ± 50           29 ± 5
                QSPE-2      1.4 ± 0.3                     0.12 ± 0.01       140 ± 20           47 ± 6
                QSPE-3      1.2 ± 0.3                     0.14 ± 0.01       107 ± 5            59 ± 2





































                                                                          1
                Figure 1. Chemical, thermal and transport characterization of supported QSPEs: (A)  H NMR spectra of the three QSPEs in DMSO,
                           1
                together with the  H NMR spectra of ethylene carbonate (EC), and methylethylketone (MEK); (B) FTIR spectra of QSPE-2, processed in
                                                -1
                acetone and MEK, between 400 and 2,000 cm ; (C) thermogravimetric profiles, collected under Ar atmosphere, at a heating rate of
                      -1
                10 °C min , between room temperature and 1,000 °C; (D) Derivative TGA profiles, up to 600 °C; (E) DSC profiles, collected at a
                                -1
                heating rate of 2 °C min , between -80 and 100 °C (cycle 2); (F) Ionic conductivity vs. temperature, between 20 and 80 °C (average of
                three cells).
               corrosion phenomena involving the Al foil could contribute to the parasitic current at high voltages. The
                                                                                             -1
               LSV profiles are shown in Figure 2. LSV was conducted at an ultra-low scan rate of 5 µV s  to mimic the
               residence time in the floating current test and avoid any capacitive contribution. The oxidative stability limit
                                                +
               for QSPE-1 is quite low, 4.2 V vs. Li/Li . LSV conducted with SS working electrodes on unsupported QSPEs
               showed a slightly higher oxidation potential of 4.3 V vs. Li/Li  [Supplementary Figure 6]. Addition of LiBOB
                                                                  +
                                                                                               -2
               (QSPE-2) results in an increase of the oxidative stability, with a current density of 0.5 µA cm  at 4.4 V vs.
               Li/Li  and a marked increase from 4.5 V vs. Li/Li . A similar result was also observed in SS||Li cells, in which
                   +
                                                        +
               the electrolyte containing a mixture of LiFSI and LiBOB showed much higher stability than the electrolyte
               containing LiFSI only. QSPE-3 shows intermediate stability, with the current increasing slowly from 4.3 V
               vs. Li/Li  and a steep increase from 4.4 V vs. Li/Li . After the oxidation onset, the current increases much
                                                          +
                      +
               more steeply with the LiNO -containing QSPE-3, indicating that this salt may be deleterious for the
                                        3
               oxidative stability of the electrolyte. LiBOB, on the other hand, is confirmed as a fundamental CEI-forming
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