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Ji Lan,1 Bo Zhou,1 Chenxiao Yin,1 Lin Weng,1 Wei Ni,2 and Ling-Ying Shi1,*
1
College of Polymer Science and Engineering, Sichuan University, Chengdu 610065, China
2
State Key Laboratory of Vanadium and Titanium Resources Comprehensive Utilization, ANSTEEL Research
Institute of Vanadium & Titanium (Iron & Steel), Chengdu 610031, China
1
Table S1. The formulation of DN ion gels.
Note: The mixed solution of DMAPS, DESs and photoinitiator (0.2 mol% to monomer DMAPS) is precursor
solution A. The mixed solution of precursor solution A after photopolymerization, HEMA, photoinitiator (0.2 mol%
to monomer HEMA) and crosslinking agent (0.1 mol% to monomer HEMA) constitutes precursor solution B.
2
Table S2. The formulation of SN ion gels.
SN
0.280 1.170 2.900
1
SN
0.280 0.520 1.600
2
0.1 mol% to monomer 0.2 mol% to monomer
DMAPS and HEMA DMAPS and HEMA
SN
0.560 0.606 2.332
3
SN
0.560 0.390 1.900
4
3
Fig. S2. (a) The dissipated energy during cyclic tensile of DN ion gel under different
strains. (b) Dissipative energy of tensile cycle with different recovery time at 200%
strain.
Fig. S4. SEM image and Elemental (S, N and Cl) mapping images of the DN4 ion gel
surface.
4
Fig. S5. TGA curves of DN ion gel and DN hydrogel.
Fig. S6. EIS plots of a series of SN ion gels at room temperature, with corresponding
conductivity shown in the illustration.
Ionic
(S m−1)
5
Fig. S7. LSV curve of DN hydrogel with the potential range of 0–1.5V and scanning
speed of 10 mV s−1 at room temperature.