This work reports a SO2 derivative-detecting and colorful hyperbranched polymeric ionic liquid （HBPIL） vesicle through aqueous self-assembly. By a simple anion-exchange, we achieved the combination of functional sma...This work reports a SO2 derivative-detecting and colorful hyperbranched polymeric ionic liquid （HBPIL） vesicle through aqueous self-assembly. By a simple anion-exchange, we achieved the combination of functional small-molecule probe of acid fuchsin with HBPILs. The obtained HBPIL vesicle displayed ultraviolet absorption at 544 nm, and was used as a novel SO2 derivative sensor with high sensitivity and visualization. Due to the functional ion pairs enriching on the surface, the SO32 detection limit of the HBPILs vesicles was as low as 0.138 gmol/L, which was about 1.5 orders of magnitude lower than that of acid fuchsin.展开更多
We synthesized one quaternary ammonium polymeric ionic liquids（PILs）P[VBTHEA]Cl and three imidazolium PILs of P[VEIm]Br, P[VEIm]BF, P[VEIm]PFby free-radical polymerization in solution. These PILs were characterized ...We synthesized one quaternary ammonium polymeric ionic liquids（PILs）P[VBTHEA]Cl and three imidazolium PILs of P[VEIm]Br, P[VEIm]BF, P[VEIm]PFby free-radical polymerization in solution. These PILs were characterized by FT-IR,H-NMR,C-NMR, TGA, XRD and SEM. Their COadsorption capacities were measured under different pressures and temperatures by constant-volume technique. It was observed that quaternary ammonium PILs of P[VBTHEA]Cl have higher adsorption capacity for COthan those imidazolium PILs, following P[VBTHEA]Cl > P[VEIm]PF> P[VEIm]BF> P[VEIm]Br, which may be ascribed to higher positive charge density on ammonium cation than that on imidazolium cation and thus stronger interaction with CO, consistent with the results from dual-mode adsorption model that ammonium PILs have much higher CObulk absorption than imidazolium PILs. COadsorption capacity of P[VBTHEA]Cl is 9.02 mg/g under 295 K and 1 bar, which is comparable to that of some other PILs, and is much higher than that of the corresponding ILs monomer. These PILs have good adsorption selectivity for COover Nand regeneration efficiency.展开更多
Solid polymer electrolytes(SPEs)have attracted much attention for their safety,ease of packaging,costeffectiveness,excellent flexibility and stability.Poly-dioxolane(PDOL)is one of the most promising matrix materials ...Solid polymer electrolytes(SPEs)have attracted much attention for their safety,ease of packaging,costeffectiveness,excellent flexibility and stability.Poly-dioxolane(PDOL)is one of the most promising matrix materials of SPEs due to its remarkable compatibility with lithium metal anodes(LMAs)and suitability for in-situ polymerization.However,poor thermal stability,insufficient ionic conductivity and narrow electrochemical stability window(ESW)hinder its further application in lithium metal batteries(LMBs).To ameliorate these problems,we have successfully synthesized a polymerized-ionic-liquid(PIL)monomer named DIMTFSI by modifying DOL with imidazolium cation coupled with TFSI^(-)anion,which simultaneously inherits the lipophilicity of DOL,high ionic conductivity of imidazole,and excellent stability of PILs.Then the tridentate crosslinker trimethylolpropane tris[3-(2-methyl-1-aziridine)propionate](TTMAP)was introduced to regulate the excessive Li^(+)-O coordination and prepare a flame-retardant SPE(DT-SPE)with prominent thermal stability,wide ESW,high ionic conductivity and abundant Lit transference numbers(t_(Li+)).As a result,the LiFePO_(4)|DT-SPE|Li cell exhibits a high initial discharge specific capacity of 149.60 mAh g^(-1)at 0.2C and 30℃with a capacity retention rate of 98.68%after 500 cycles.This work provides new insights into the structural design of PIL-based electrolytes for long-cycling LMBs with high safety and stability.展开更多
Room temperature ionic liquids(RTILs) are non-volatile organic salts. They may replace conventional coalescing agents in latex coating thus reducing volatile organic compounds(VOCs) emission as well as improving perfo...Room temperature ionic liquids(RTILs) are non-volatile organic salts. They may replace conventional coalescing agents in latex coating thus reducing volatile organic compounds(VOCs) emission as well as improving performance of latex coating products such as better thermal stability, conductivity, and antifouling property. The formation of latex coating containing RTILs can be achieved by encapsulation of RTILs inside particles via miniemulsion polymerization. In this study, the role of RTILs and its concentration on stability of miniemulsion during storage and polymerization were investigated. It has been found that, above a critical concentration(10 wt%), adding more RTILs to oil phase may weaken miniemulsion stability during storage as well as polymerization. Such observations were consistent with the zeta potential measurement for miniemulsions prepared at the similar conditions. The results obtained here would be a useful guideline for the development of new waterborne coating products with desirable functions and particle sizes.展开更多
Poly(1-butyl-3-vinylimidazolium bromide)is a polymerized ionic liquid(PILs),a relatively new class of materials that combines the attractive properties of ionic liquids(ILs)and polyelectrolytes and finds wide applicat...Poly(1-butyl-3-vinylimidazolium bromide)is a polymerized ionic liquid(PILs),a relatively new class of materials that combines the attractive properties of ionic liquids(ILs)and polyelectrolytes and finds wide applications.The backbone of this PIL is composed of quaternary imidazolium salts,which are among the most promising and popular ILs.However,little is known about the physicochemical characteristics of the aqueous solutions of this PIL.In this study,we synthesized and characterized samples of this PIL and obtained experimental data on the viscosity,static and dynamic light scattering,and nuclear magnetic resonance diffusometry for aqueous and aqueous KBr solutions with varying polymer contents at T=298.15 K.We discuss the effects of the polymer concentration and salinity on the behavior of the solution.展开更多
Polymerizable ionic liquid copolymer P（MMA-co-BVIm-Br） was synthesized by radical polymerization technique, and characterized by Fourier transform infrared spectrometry （FTIR）, 1H Nuclear magnetic resonance （1H-...Polymerizable ionic liquid copolymer P（MMA-co-BVIm-Br） was synthesized by radical polymerization technique, and characterized by Fourier transform infrared spectrometry （FTIR）, 1H Nuclear magnetic resonance （1H-NMR） and gel permeation chromatography （GPC）. The resulting copolymer was used to prepare poly（vinylidene fluoride） （PVDF） blend membranes via a phase inversion method. The effects of the copolymer on the polymorphism, surface wettability and zeta potential （0 of the blend membranes were investigated by ATR-FTIR, contact angle instrument and zeta potential analyzer. Scanning electron microscopy （SEM and SEM-EDS） was also applied to investigate the morphology and the surface element changes of the fabricated membranes. The results indicated that P（MMA-co-BVIm-Br） copolymer existed on the surface of the membrane which made the blend membrane have a positive surface during the experimental pH range. The copolymer was also in favor of the formation of βcrystal phase in PVDF membranes. The contact angle experiment indicated that P（MMA-co-BVIm-Br） copolymer could switch the wettability of the blend membranes from hydrophilic to hydrophobic by exchanging Br- anion with PF6-. Compared with pure PVDF membranes, the water flux and water recovery flux of the blend membranes were enhanced obviously. The results from the flux recovery ratio （FR） and total fouling ratio （Rt） all suggested that the blend membranes had good anti-fouling properties.展开更多
A method of in-situ reduction to prepare Au@Pt core-satellite nanopar- ticles （NPs） is described by using Au NPs coating poly[1-methyl 3-（2-methacryloyloxy propylimidazolium bromine）] （PMMPImB-@-Au NPs） as the t...A method of in-situ reduction to prepare Au@Pt core-satellite nanopar- ticles （NPs） is described by using Au NPs coating poly[1-methyl 3-（2-methacryloyloxy propylimidazolium bromine）] （PMMPImB-@-Au NPs） as the template. After electrostatic complex chloroplatinic acid with PMMPImB shell, the composite NP was directly reduced with N2H4 to produce Au@Pt core-satellite NPs. The characterization of composite and core-satellite NPs under different amounts of chloroplatinic acid were studied by DLS, UV-vis absorption spectrum and TEM. The satellite Pt NPs with a small size （-2 nm） dotted around Au core, and the resulting Au@Pt core-satellite NPs showed a red-shift surface plasmon resonance （SPR） and a good dispersion due to effectively electrostatic repulsion providing by the polymeric ionic liquid （PIL） shell. Finally, Au@Pt core-satellite NPs exhibit an enhanced catalytic activity and cycled catalytic capability for the reduction ofp- nitrophenol with NaBH4.展开更多
Dye-sensitized solar cells （DSSCs） are the most promising, low cost and most extensively investigated solar cells. They are famous for their clean and efficient solar energy conversion. Nevertheless this, long-time ...Dye-sensitized solar cells （DSSCs） are the most promising, low cost and most extensively investigated solar cells. They are famous for their clean and efficient solar energy conversion. Nevertheless this, long-time sta- bility is still to be acquired. In recent years research on solid and quasi-solid state electrolytes is extensively in- creased. Various quasi-solid electrolytes, including composites polymer electrolytes, ionic liquid electrolytes, thermoplastic polymer electrolytes and thermosetting polymer electrolytes have been used. Performance and stability of a quasi-solid state electrolyte are between liquid and solid electrolytes. High photovoltaic performances of QS-DSSCs along better long-term stability can be obtained by designing and optimizing quasi-solid electrolytes. It is a prospective candidate for highly efficient and stable DSSCs.展开更多
To enhance the solubility of polyanilines(PANI),polymeric ionic liquid(PIL)was introduced into the polymerization synthesis of PANI with various proportions.The structure and properties of the modified PANIs were char...To enhance the solubility of polyanilines(PANI),polymeric ionic liquid(PIL)was introduced into the polymerization synthesis of PANI with various proportions.The structure and properties of the modified PANIs were characterized by 1H NMR,Fourier transform infrared spectroscopy,thermogravimetric analysis,ultraviolet-visible spectrum,etc.It was found that the obtained PANIs doped with PILs were soluble in various organic solvents such as N,N-dimethyl formamide and acetonitrile.Compared with the pure PANI,the PANIs doped by PILs showed remarkable solubility and their chemical structure and conductivity kept integrated.展开更多
We like to highlight the extension of COSMO-based models(COSMO RS-FV and COSMO SAC-FV)to the prediction of gas solubility in polymers,including polymerized ionic liquids(PILs)for the first time.To verify the applicabi...We like to highlight the extension of COSMO-based models(COSMO RS-FV and COSMO SAC-FV)to the prediction of gas solubility in polymers,including polymerized ionic liquids(PILs)for the first time.To verify the applicability of COSMO-based models,the predicted values for gas solubility in both common polymers(CH_(4)/N_(2)+PEG)and PELs(CO_(2)+P[MATMA][BF_(4)]/P[VATMA][BF_(4)])were evaluated based on previous experimental data.It was confirmed that the COSMO-RS(Klamt)model performs better than the COSMO-SAC model for common polymers,whereas the COSMO-RS(ADF-Lei 2018)exhibits the best predictions for PILs.The moderately accurate predictions of COSMObased models demonstrate the high potential for predicting gas solubility in polymers.展开更多
Palladium nanoparticles immobilized on a cross-linked imidazolium-containing polymer were evaluated as a catalyst for Suzuki carbon-carbon cross-coupling reactions using water as the solvent. The nanocatalysts show go...Palladium nanoparticles immobilized on a cross-linked imidazolium-containing polymer were evaluated as a catalyst for Suzuki carbon-carbon cross-coupling reactions using water as the solvent. The nanocatalysts show good catalytic activities for aryl iodides and aryl bromides and moderate activity with aryl chloride substrates. Coupling of sterically hindered substrates could also be achieved in reasonable yields. The heterogeneous catalyst is stable, can be stored without precautions to exclude air or moisture, and can be easily recycled and reused.展开更多
Electrolytes based on poly(ionic liquid)s(PILs)have attracted great attention in the fields of next-generation solid lithium-ion batteries.However,the low ionic conductivity prevents their practical applications.Herei...Electrolytes based on poly(ionic liquid)s(PILs)have attracted great attention in the fields of next-generation solid lithium-ion batteries.However,the low ionic conductivity prevents their practical applications.Herein,we report novel solid electrolytes based on block copolymers composed of PILs and comb-like poly(ethylene glycol)(PEG),which were synthesized via ring-opening metathesis polymerization of 3-(2-(bicyclo[2.2.1]hept-5-en-2-yl)ethyl)-1-butyl-1H-imidazol-3-ium bis((trifluoromethyl)sulfonyl)amide and poly(ethylene glycol monomethyl ether)bicyclo[2.2.1]hept-5-ene-2-carboxylate.Comb-like PEG acts as plasticizers in block copolymers dominated by PILs to promote the mobility of PILs segments.Effects of the copolymer composition and length of the comb-like PEG chain on ionic conductivity were investigated.The optimized electrolyte delivers the highest ionic conductivity of 1.5×10^(–5)S·cm^(–1)at 30℃,and robust electrochemical stability up to 4.6 V.A solid-state Li/LiFePO4 cell using the optimized electrolyte demonstrates good cycle performance at 0.2 C with high capacity retention of 92%after 70 cycles at 50℃.展开更多
基金supported by the National Basic Research Program(No.2013CB834506)the National Science Fund for Distinguished Young Scholars(No.21225420)+1 种基金the National Natural Science Foundation of China(Nos.91127047,21474062 and 21404070)Program of Shanghai Subject Chief Scientist(No.15XD1502400)
文摘This work reports a SO2 derivative-detecting and colorful hyperbranched polymeric ionic liquid （HBPIL） vesicle through aqueous self-assembly. By a simple anion-exchange, we achieved the combination of functional small-molecule probe of acid fuchsin with HBPILs. The obtained HBPIL vesicle displayed ultraviolet absorption at 544 nm, and was used as a novel SO2 derivative sensor with high sensitivity and visualization. Due to the functional ion pairs enriching on the surface, the SO32 detection limit of the HBPILs vesicles was as low as 0.138 gmol/L, which was about 1.5 orders of magnitude lower than that of acid fuchsin.
基金financially supported by State Key Laboratory of Organic-Inorganic Composites(oic-201601012)the International Scientific Partnership Program ISPP at King Saud University for funding this research work through ISPP#0080
文摘We synthesized one quaternary ammonium polymeric ionic liquids（PILs）P[VBTHEA]Cl and three imidazolium PILs of P[VEIm]Br, P[VEIm]BF, P[VEIm]PFby free-radical polymerization in solution. These PILs were characterized by FT-IR,H-NMR,C-NMR, TGA, XRD and SEM. Their COadsorption capacities were measured under different pressures and temperatures by constant-volume technique. It was observed that quaternary ammonium PILs of P[VBTHEA]Cl have higher adsorption capacity for COthan those imidazolium PILs, following P[VBTHEA]Cl > P[VEIm]PF> P[VEIm]BF> P[VEIm]Br, which may be ascribed to higher positive charge density on ammonium cation than that on imidazolium cation and thus stronger interaction with CO, consistent with the results from dual-mode adsorption model that ammonium PILs have much higher CObulk absorption than imidazolium PILs. COadsorption capacity of P[VBTHEA]Cl is 9.02 mg/g under 295 K and 1 bar, which is comparable to that of some other PILs, and is much higher than that of the corresponding ILs monomer. These PILs have good adsorption selectivity for COover Nand regeneration efficiency.
基金financially supported by the National Key R&D Program of China(Grant No.2022YFE0207300)National Natural Science Foundation of China(Grant Nos.22179142 and 22075314)+1 种基金Jiangsu Funding Program for Excellent Postdoctoral Talent(Grant No.2024ZB051 and 2023ZB836)the technical support for Nano-X from Suzhou Institute of Nano-Tech and Nano-Bionics,Chinese Academy of Sciences(SINANO).
文摘Solid polymer electrolytes(SPEs)have attracted much attention for their safety,ease of packaging,costeffectiveness,excellent flexibility and stability.Poly-dioxolane(PDOL)is one of the most promising matrix materials of SPEs due to its remarkable compatibility with lithium metal anodes(LMAs)and suitability for in-situ polymerization.However,poor thermal stability,insufficient ionic conductivity and narrow electrochemical stability window(ESW)hinder its further application in lithium metal batteries(LMBs).To ameliorate these problems,we have successfully synthesized a polymerized-ionic-liquid(PIL)monomer named DIMTFSI by modifying DOL with imidazolium cation coupled with TFSI^(-)anion,which simultaneously inherits the lipophilicity of DOL,high ionic conductivity of imidazole,and excellent stability of PILs.Then the tridentate crosslinker trimethylolpropane tris[3-(2-methyl-1-aziridine)propionate](TTMAP)was introduced to regulate the excessive Li^(+)-O coordination and prepare a flame-retardant SPE(DT-SPE)with prominent thermal stability,wide ESW,high ionic conductivity and abundant Lit transference numbers(t_(Li+)).As a result,the LiFePO_(4)|DT-SPE|Li cell exhibits a high initial discharge specific capacity of 149.60 mAh g^(-1)at 0.2C and 30℃with a capacity retention rate of 98.68%after 500 cycles.This work provides new insights into the structural design of PIL-based electrolytes for long-cycling LMBs with high safety and stability.
基金the Low Carbon Automation Manufacture Innovation Team 2011B81006 for the PhD studentshipNingbo Natural Science Foundation funding 2012A610094
文摘Room temperature ionic liquids(RTILs) are non-volatile organic salts. They may replace conventional coalescing agents in latex coating thus reducing volatile organic compounds(VOCs) emission as well as improving performance of latex coating products such as better thermal stability, conductivity, and antifouling property. The formation of latex coating containing RTILs can be achieved by encapsulation of RTILs inside particles via miniemulsion polymerization. In this study, the role of RTILs and its concentration on stability of miniemulsion during storage and polymerization were investigated. It has been found that, above a critical concentration(10 wt%), adding more RTILs to oil phase may weaken miniemulsion stability during storage as well as polymerization. Such observations were consistent with the zeta potential measurement for miniemulsions prepared at the similar conditions. The results obtained here would be a useful guideline for the development of new waterborne coating products with desirable functions and particle sizes.
基金financially supported by the Russian Science Foundation(No.20-13-00038).
文摘Poly(1-butyl-3-vinylimidazolium bromide)is a polymerized ionic liquid(PILs),a relatively new class of materials that combines the attractive properties of ionic liquids(ILs)and polyelectrolytes and finds wide applications.The backbone of this PIL is composed of quaternary imidazolium salts,which are among the most promising and popular ILs.However,little is known about the physicochemical characteristics of the aqueous solutions of this PIL.In this study,we synthesized and characterized samples of this PIL and obtained experimental data on the viscosity,static and dynamic light scattering,and nuclear magnetic resonance diffusometry for aqueous and aqueous KBr solutions with varying polymer contents at T=298.15 K.We discuss the effects of the polymer concentration and salinity on the behavior of the solution.
基金financially supported by the National Natural Science Foundation of China(Nos.51103130 and 21004051)Qianjiang Talents Project of Technology Office in Zhejiang Province(No.2013R10070)
文摘Polymerizable ionic liquid copolymer P（MMA-co-BVIm-Br） was synthesized by radical polymerization technique, and characterized by Fourier transform infrared spectrometry （FTIR）, 1H Nuclear magnetic resonance （1H-NMR） and gel permeation chromatography （GPC）. The resulting copolymer was used to prepare poly（vinylidene fluoride） （PVDF） blend membranes via a phase inversion method. The effects of the copolymer on the polymorphism, surface wettability and zeta potential （0 of the blend membranes were investigated by ATR-FTIR, contact angle instrument and zeta potential analyzer. Scanning electron microscopy （SEM and SEM-EDS） was also applied to investigate the morphology and the surface element changes of the fabricated membranes. The results indicated that P（MMA-co-BVIm-Br） copolymer existed on the surface of the membrane which made the blend membrane have a positive surface during the experimental pH range. The copolymer was also in favor of the formation of βcrystal phase in PVDF membranes. The contact angle experiment indicated that P（MMA-co-BVIm-Br） copolymer could switch the wettability of the blend membranes from hydrophilic to hydrophobic by exchanging Br- anion with PF6-. Compared with pure PVDF membranes, the water flux and water recovery flux of the blend membranes were enhanced obviously. The results from the flux recovery ratio （FR） and total fouling ratio （Rt） all suggested that the blend membranes had good anti-fouling properties.
基金We acknowledge the financial support from the National Natural Science Foundation of China （Grant Nos. 51103035 and 51403055）.
文摘A method of in-situ reduction to prepare Au@Pt core-satellite nanopar- ticles （NPs） is described by using Au NPs coating poly[1-methyl 3-（2-methacryloyloxy propylimidazolium bromine）] （PMMPImB-@-Au NPs） as the template. After electrostatic complex chloroplatinic acid with PMMPImB shell, the composite NP was directly reduced with N2H4 to produce Au@Pt core-satellite NPs. The characterization of composite and core-satellite NPs under different amounts of chloroplatinic acid were studied by DLS, UV-vis absorption spectrum and TEM. The satellite Pt NPs with a small size （-2 nm） dotted around Au core, and the resulting Au@Pt core-satellite NPs showed a red-shift surface plasmon resonance （SPR） and a good dispersion due to effectively electrostatic repulsion providing by the polymeric ionic liquid （PIL） shell. Finally, Au@Pt core-satellite NPs exhibit an enhanced catalytic activity and cycled catalytic capability for the reduction ofp- nitrophenol with NaBH4.
文摘Dye-sensitized solar cells （DSSCs） are the most promising, low cost and most extensively investigated solar cells. They are famous for their clean and efficient solar energy conversion. Nevertheless this, long-time sta- bility is still to be acquired. In recent years research on solid and quasi-solid state electrolytes is extensively in- creased. Various quasi-solid electrolytes, including composites polymer electrolytes, ionic liquid electrolytes, thermoplastic polymer electrolytes and thermosetting polymer electrolytes have been used. Performance and stability of a quasi-solid state electrolyte are between liquid and solid electrolytes. High photovoltaic performances of QS-DSSCs along better long-term stability can be obtained by designing and optimizing quasi-solid electrolytes. It is a prospective candidate for highly efficient and stable DSSCs.
基金The authors gratefully acknowledge the valuable help and great support from the Fundamental Research Funds for the Central Universities(Nos.2232018D3-07,2232018D3-24 and 2232019G-02)China Postdoctoral Science Foundation(No.2016M591573)+1 种基金the National Natural Science Foundation of China(Grant No.21404024)Changsha Science and Technology Project.
文摘To enhance the solubility of polyanilines(PANI),polymeric ionic liquid(PIL)was introduced into the polymerization synthesis of PANI with various proportions.The structure and properties of the modified PANIs were characterized by 1H NMR,Fourier transform infrared spectroscopy,thermogravimetric analysis,ultraviolet-visible spectrum,etc.It was found that the obtained PANIs doped with PILs were soluble in various organic solvents such as N,N-dimethyl formamide and acetonitrile.Compared with the pure PANI,the PANIs doped by PILs showed remarkable solubility and their chemical structure and conductivity kept integrated.
基金support of the AMS(Amsterdam Modeling Suite)2020 for free use provided by Software for Chemistry&Materials(SCM)
文摘We like to highlight the extension of COSMO-based models(COSMO RS-FV and COSMO SAC-FV)to the prediction of gas solubility in polymers,including polymerized ionic liquids(PILs)for the first time.To verify the applicability of COSMO-based models,the predicted values for gas solubility in both common polymers(CH_(4)/N_(2)+PEG)and PELs(CO_(2)+P[MATMA][BF_(4)]/P[VATMA][BF_(4)])were evaluated based on previous experimental data.It was confirmed that the COSMO-RS(Klamt)model performs better than the COSMO-SAC model for common polymers,whereas the COSMO-RS(ADF-Lei 2018)exhibits the best predictions for PILs.The moderately accurate predictions of COSMObased models demonstrate the high potential for predicting gas solubility in polymers.
基金supported by the Ecole Polytechnique Fédérale de Lausanne and the Iranian Ministry of Science,Research and Technology(to S.G.-E.)
文摘Palladium nanoparticles immobilized on a cross-linked imidazolium-containing polymer were evaluated as a catalyst for Suzuki carbon-carbon cross-coupling reactions using water as the solvent. The nanocatalysts show good catalytic activities for aryl iodides and aryl bromides and moderate activity with aryl chloride substrates. Coupling of sterically hindered substrates could also be achieved in reasonable yields. The heterogeneous catalyst is stable, can be stored without precautions to exclude air or moisture, and can be easily recycled and reused.
基金supported by the National Natural Science Foundation of China(Grant No.52130307).
文摘Electrolytes based on poly(ionic liquid)s(PILs)have attracted great attention in the fields of next-generation solid lithium-ion batteries.However,the low ionic conductivity prevents their practical applications.Herein,we report novel solid electrolytes based on block copolymers composed of PILs and comb-like poly(ethylene glycol)(PEG),which were synthesized via ring-opening metathesis polymerization of 3-(2-(bicyclo[2.2.1]hept-5-en-2-yl)ethyl)-1-butyl-1H-imidazol-3-ium bis((trifluoromethyl)sulfonyl)amide and poly(ethylene glycol monomethyl ether)bicyclo[2.2.1]hept-5-ene-2-carboxylate.Comb-like PEG acts as plasticizers in block copolymers dominated by PILs to promote the mobility of PILs segments.Effects of the copolymer composition and length of the comb-like PEG chain on ionic conductivity were investigated.The optimized electrolyte delivers the highest ionic conductivity of 1.5×10^(–5)S·cm^(–1)at 30℃,and robust electrochemical stability up to 4.6 V.A solid-state Li/LiFePO4 cell using the optimized electrolyte demonstrates good cycle performance at 0.2 C with high capacity retention of 92%after 70 cycles at 50℃.
