A critical barrier to overcome in the development of solid‐state electrolytes for lithium batteries is the trade‐off between sacrificing ionic conductivity for enhancement of mechanical stiffness. Here, a physically cross‐linked, polymer‐supported gel electrolyte consisting of a lithium salt/ionic liquid solution featuring a fully zwitterionic (ZI) copolymer network is introduced for rechargeable lithium‐based batteries. The ZI scaffold is synthesized using a 3:1 molar ratio of 2‐methacryloyloxyethyl phosphorylcholine and sulfobetaine vinylimidazole, and the total polymer content is varied between 1.1 and 12.5 wt%. Room‐temperature ionic conductivity values comparable to the base liquid electrolyte (≈1 mS cm−1) are achieved in ZI copolymer‐supported gels that display compressive elastic moduli as large as 14.3 MPa due to ZI dipole–dipole cross‐links. Spectroscopic characterization suggests a change in the Li+coordination shell upon addition of the zwitterions, indicative of strong Li+···ZI group interactions. Li+transference number measurements reveal an increase in Li+conductivity within a ZI gel electrolyte (
Lignin is an aromatic‐rich biomass polymer that is cheap, abundant, and sustainable. However, its application in the solid electrolyte field is rare due to challenges in well‐defined polymer synthesis. Herein, the synthesis of lignin‐graft‐poly(ethylene glycol) (PEG) and its conductivity test for a solid electrolyte application are demonstrated. The main steps of synthesis include functionalization of natural lignin's hydroxyl to alkene, followed by graft‐copolymerization of PEG thiol to the lignin via photoredox thiol‐ene reaction. Two lignin‐graft‐PEGs are prepared having 22 wt% lignin (lignin‐graft‐PEG 550) and 34 wt% lignin (lignin‐graft‐PEG 2000). Then, new polymer electrolytes for conductivity tests are prepared via addition of lithium bis‐trifluoromethanesulfonimide. The polymer graft electrolytes exhibit ionic conductivity up to 1.4 × 10−4 S cm−1 at 35 °C. The presence of lignin moderately impacts conductivity at elevated temperature compared to homopolymer PEG. Furthermore, the ionic conductivity of lignin‐graft‐PEG at ambient temperature is significantly higher than homopolymer PEG precedents.
more » « less- Award ID(s):
- 1804871
- NSF-PAR ID:
- 10453952
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Macromolecular Rapid Communications
- Volume:
- 42
- Issue:
- 3
- ISSN:
- 1022-1336
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
more » « less
Abstract nearly doubles). ZI gels display enhanced stability against Li metal, dendrite suppression, and suitable charge–discharge performance in a graphite|lithium nickel cobalt manganese oxide cell. Fully ZI polymer networks in nonvolatile, ionic liquid‐based electrolytes represent a promising approach toward realizing highly conductive, mechanically rigid gels for lithium battery technologies. -
The use of highly conductive solid-state electrolytes to replace conventional liquid organic electrolytes enables radical improvements in the reliability, safety and performance of lithium batteries. Here, we report the synthesis and characterization of a new class of nonflammable solid electrolytes based on the grafting of ionic liquids onto octa-silsesquioxane. The electrolyte exhibits outstanding room-temperature ionic conductivity (∼4.8 × 10 −4 S cm −1 ), excellent electrochemical stability (up to 5 V relative to Li + /Li) and high thermal stability. All-solid-state Li metal batteries using the prepared electrolyte membrane are successfully cycled with high coulombic efficiencies at ambient temperature. The good cycling stability of the electrolyte against lithium has been demonstrated. This work provides a new platform for the development of solid polymer electrolytes for application in room-temperature lithium batteries.more » « less
-
more » « less
Abstract Additive manufacturing of solid-state batteries is advantageous for improving the power density by increasing the geometric complexity of battery components, such as electrodes and electrolytes. In the present study, bulk three-dimensional Li1+
x Alx Ti2−x (PO4)3(LATP) electrolyte samples were prepared using the laser powder bed fusion (L-PBF) additive manufacturing method. Li3PO4(LPO) was added to LATP to compensate for lithium vaporization during processing. Chemical compositions included 0, 1, 3, and 5 wt. % LPO. Resulting ionic conductivity values ranged from 1.4 × 10−6–6.4 × 10−8S cm−1, with the highest value for the sample with a chemical composition of 3 wt. % LPO. Microstructural features were carefully measured for each chemical composition and correlated with each other and with ionic conductivity. These features and their corresponding ranges include: porosity (ranging from 5% to 19%), crack density (0.09–0.15 mm mm−2), concentration of residual LPO (0%–16%), and concentration and Feret diameter of secondary phases, AlPO4 (11%–18%, 0.40–0.61µ m) and TiO2 (9%–11%, 0.50–0.78). Correlations between the microstructural features and ionic conductivity ranged from −0.88 to 0.99. The strongest negative correlation was between crack density and ionic conductivity (−0.88), confirming the important role that processing defects play in limiting the performance of bulk solid-state electrolytes. The strongest positive correlation was between the concentration of AlPO4 and ionic conductivity (0.99), which is attributed to AlPO4 acting as a sintering aid and the role it plays in reducing the crack density. Our results indicate that additions of LPO can be used to balance competing microstructural features to design bulk three-dimensional LATP samples with improved ionic conductivity. As such, refinement of the chemical composition offers a promising approach to improving the processability and performance of functional ceramics prepared using binderless, laser-based additive manufacturing for solid-state battery applications. -
more » « less
Abstract Solid polymer electrolytes have shown to be a promising solution to suppressing dendrite growth for safer and higher performance lithium batteries. This article reports the fabrication and characterization of a series of nanostructured polymer electrolyte membranes (PEMs) comprised of poly(ethylene glycol)/bis(trifluoromethane)sulfonimide lithium electrolyte and acrylate–thiol‐ene crosslinked resin using a holographic polymerization (HP). Nanoscale long‐range order is observed and this unique structure imposes intriguing mechanical and ion‐conducting properties of the PEMs. The modulus of the holographically polymerized PEMs can be tuned to vary from 150 to 1300 MPa while room temperature conductivities of ≈2 × 10−5S cm−1and 90 °C conductivity of ≈5 × 10−4S cm−1are achieved. The HP nanostructure is also capable of directing ion transport either parallel or perpendicular to the membrane surface; an unprecedented ionic conductivity anisotropy as high as 3 × 105is achieved. It is anticipated that these PEMs may be excellent candidates for lithium battery applications.
-
more » « less
Tantalum‐doped lithium lanthanum zirconate garnet (Li7−
x La3Zr2−x Tax O12[LLZTO]) has received interest as a solid electrolyte for solid‐state lithium batteries due to its good electrochemical properties and ionic conductivity. However, the source of discrepancies for reported values of ionic conductivity in nominally or nearly equivalent compositions of LLZTO is not completely clear. Herein, synthesis‐related factors that may contribute to the differences in performance of garnet electrolytes are systematically characterized. The conductivity of samples with composition Li6.4La3Zr1.4Ta0.6O12prepared by various methods including solid‐state reaction (SSR), combustion, and molten salt synthesis is compared. Varying levels of elemental inhomogeneity, comprising a variation in Ta and Zr content on the level of individual LLZTO particles, are identified. The elemental inhomogeneity is found to be largely preserved even after high‐temperature sintering and correlated with reduced ionic conductivity. It is shown that the various synthesis and processing‐related variables in each of the preparation methods play a role in these compositional variations, and that even LLZTO synthesized via conventional, high‐temperature SSR can exhibit substantial variability in local composition. However, by improving reagent mixing and using LLZTO powder with low agglomeration and small particle size distribution, the compositional uniformity, and hence, ionic conductivity, of sintered garnet electrolytes can be improved.
