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dc.contributor.author | Gachuz, Edwin J. | es_ES |
dc.contributor.author | Castillo-Santillán, Martín | es_ES |
dc.contributor.author | Juarez-Moreno, Carla | es_ES |
dc.contributor.author | Maya Cornejo, Jose | es_ES |
dc.contributor.author | Martinez-Richa, Antonio | es_ES |
dc.contributor.author | Andrio, Andreu | es_ES |
dc.contributor.author | Compañ Moreno, Vicente | es_ES |
dc.contributor.author | Mota-Morales, Josué D. | es_ES |
dc.date.accessioned | 2021-02-19T04:34:17Z | |
dc.date.available | 2021-02-19T04:34:17Z | |
dc.date.issued | 2020-09-07 | es_ES |
dc.identifier.issn | 1463-9262 | es_ES |
dc.identifier.uri | http://hdl.handle.net/10251/161864 | |
dc.description.abstract | [EN] A series of semi-interpenetrating polymer networks (semi-IPNs) consisting of crosslinked poly(itaconic acid) in the presence of the polysaccharide inulin were prepared by free-radical polymerization, taking advantage of the chemistry of deep eutectic systems (DESs). Up to 14 wt% of the polysaccharide inulin readily dissolves in a nonaqueous DES composed of glycerol (Gly) and choline chloride (ChCl). On the other hand, itaconic acid (IA) mixed with ChCl formed a deep eutectic solvent (DES) monomer, which upon free-radical polymerization in solution aided by multifunctional acrylates allowed the synthesis of highly crosslinked polymer networks. Bringing together both DESs, the DES monomer containing IA and the inert one containing inulin dissolved in it, allowed the synthesis of all-natural (ca.96 wt% of biobased components, excluding crosslinkers) and biocompatible semi-IPNs. Remarkably, the DESs entrapped in the semi-IPNs served as a stable nonaqueous electrolyte in the range of 25-75 degrees C, thus exhibiting a typical Arrhenius dependence of conductivity with temperature (an apparent activation energy of 18 kJ mol(-1)), irrespective of the type of crosslinker used. Following electrode polarization (EP) analysis based on the Macdonald-Trukhan model, the free-ion diffusivity, the mobility, and the number of charge carrier density of the polymeric networks were calculated. The results show that diffusivity and mobility increase along with temperature in all semi-IPNs with a maximum conductivity of 3.2 mS cm(-1)at 65 degrees C in the semi-IPN crosslinked with a trifunctional acrylate. The higher conductivity and diffusivity observed in the semi-IPN crosslinked with the trifunctional acrylate in comparison with the difunctional one are related to the long-translational diffusion, because the diffusive dynamics are dominated by the localized motions that are not strongly affected by the confinement of the DES electrolyte within the polymeric network. In summary, this work furthers the applications of DES chemistry towards the fabrication of greener materials,e.g.natural polymers and biobased feedstocks, with future applications in technologies seeking biocompatible conductive gels. | es_ES |
dc.description.sponsorship | J. D. M.-M. acknowledges the financial support from the National Council of Science and Technology (CONACYT) through grant no. 252774, and PAPIIT-UNAM project no. IA202018 and TA200220, Mexico. All authors kindly acknowledge The National Laboratory for Characterization of Physicochemical Properties and Molecular Structure, CONACYT (Grant No. 123732) for the instrumentation time provided, and technical assistance provided by Beatriz Millan-Malo (CFATA-UNAM) in XRD measurements (Laboratorio Nacional de Caracterizacion de Materiales con Certificacion ISO 9001:2015), and Karla A. Barrera-Rivera (UG) for obtaining DSC thermograms. | es_ES |
dc.language | Inglés | es_ES |
dc.publisher | The Royal Society of Chemistry | es_ES |
dc.relation.ispartof | Green Chemistry | es_ES |
dc.rights | Reserva de todos los derechos | es_ES |
dc.subject.classification | MAQUINAS Y MOTORES TERMICOS | es_ES |
dc.title | Electrical conductivity of an all-natural and biocompatible semi-interpenetrating polymer network containing a deep eutectic solvent | es_ES |
dc.type | Artículo | es_ES |
dc.identifier.doi | 10.1039/d0gc02274h | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/CONACyT//123732/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/CONACyT//252774/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/UNAM//IA202018/MX/Nanocompositos macroporosos jerárquicos a partir de emulsiones gel “Pickering” estabilizados por biopolímeros usando disolventes eutécticos no acuosos/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/UNAM//TA200220/ | es_ES |
dc.rights.accessRights | Abierto | es_ES |
dc.contributor.affiliation | Universitat Politècnica de València. Departamento de Termodinámica Aplicada - Departament de Termodinàmica Aplicada | es_ES |
dc.description.bibliographicCitation | Gachuz, EJ.; Castillo-Santillán, M.; Juarez-Moreno, C.; Maya Cornejo, J.; Martinez-Richa, A.; Andrio, A.; Compañ Moreno, V.... (2020). Electrical conductivity of an all-natural and biocompatible semi-interpenetrating polymer network containing a deep eutectic solvent. Green Chemistry. 22(17):5785-5797. https://doi.org/10.1039/d0gc02274h | es_ES |
dc.description.accrualMethod | S | es_ES |
dc.relation.publisherversion | https://doi.org/10.1039/d0gc02274h | es_ES |
dc.description.upvformatpinicio | 5785 | es_ES |
dc.description.upvformatpfin | 5797 | es_ES |
dc.type.version | info:eu-repo/semantics/publishedVersion | es_ES |
dc.description.volume | 22 | es_ES |
dc.description.issue | 17 | es_ES |
dc.relation.pasarela | S\424072 | es_ES |
dc.contributor.funder | Universidad Nacional Autónoma de México | es_ES |
dc.contributor.funder | Consejo Nacional de Ciencia y Tecnología, México | es_ES |
dc.description.references | Baumgartner, M., Hartmann, F., Drack, M., Preninger, D., Wirthl, D., Gerstmayr, R., … Kaltenbrunner, M. (2020). Resilient yet entirely degradable gelatin-based biogels for soft robots and electronics. Nature Materials, 19(10), 1102-1109. doi:10.1038/s41563-020-0699-3 | es_ES |
dc.description.references | Le Bideau, J., Viau, L., & Vioux, A. (2011). Ionogels, ionic liquid based hybrid materials. Chem. Soc. Rev., 40(2), 907-925. doi:10.1039/c0cs00059k | es_ES |
dc.description.references | Chakraborty, P., Das, S., & Nandi, A. K. (2019). Conducting gels: A chronicle of technological advances. Progress in Polymer Science, 88, 189-219. doi:10.1016/j.progpolymsci.2018.08.004 | es_ES |
dc.description.references | Abbott, A. P., Bell, T. J., Handa, S., & Stoddart, B. (2005). O-Acetylation of cellulose and monosaccharides using a zinc based ionic liquid. Green Chemistry, 7(10), 705. doi:10.1039/b511691k | es_ES |
dc.description.references | Abbott, A. P., Capper, G., Davies, D. L., Rasheed, R. K., & Tambyrajah, V. (2002). Novel solvent properties of choline chloride/urea mixturesElectronic supplementary information (ESI) available: spectroscopic data. See http://www.rsc.org/suppdata/cc/b2/b210714g/. Chemical Communications, (1), 70-71. doi:10.1039/b210714g | es_ES |
dc.description.references | Smith, E. L., Abbott, A. P., & Ryder, K. S. (2014). Deep Eutectic Solvents (DESs) and Their Applications. Chemical Reviews, 114(21), 11060-11082. doi:10.1021/cr300162p | es_ES |
dc.description.references | Mota-Morales, J. D., Sánchez-Leija, R. J., Carranza, A., Pojman, J. A., del Monte, F., & Luna-Bárcenas, G. (2018). Free-radical polymerizations of and in deep eutectic solvents: Green synthesis of functional materials. Progress in Polymer Science, 78, 139-153. doi:10.1016/j.progpolymsci.2017.09.005 | es_ES |
dc.description.references | Li, R., Fan, T., Chen, G., Zhang, K., Su, B., Tian, J., & He, M. (2020). Autonomous Self-Healing, Antifreezing, and Transparent Conductive Elastomers. Chemistry of Materials, 32(2), 874-881. doi:10.1021/acs.chemmater.9b04592 | es_ES |
dc.description.references | Ren’ai, L., Zhang, K., Chen, G., Su, B., Tian, J., He, M., & Lu, F. (2018). Green polymerizable deep eutectic solvent (PDES) type conductive paper for origami 3D circuits. Chemical Communications, 54(18), 2304-2307. doi:10.1039/c7cc09209a | es_ES |
dc.description.references | Li, R., Chen, G., He, M., Tian, J., & Su, B. (2017). Patternable transparent and conductive elastomers towards flexible tactile/strain sensors. Journal of Materials Chemistry C, 5(33), 8475-8481. doi:10.1039/c7tc02703f | es_ES |
dc.description.references | Mukesh, C., Gupta, R., Srivastava, D. N., Nataraj, S. K., & Prasad, K. (2016). Preparation of a natural deep eutectic solvent mediated self polymerized highly flexible transparent gel having super capacitive behaviour. RSC Advances, 6(34), 28586-28592. doi:10.1039/c6ra03309a | es_ES |
dc.description.references | Qin, H., & Panzer, M. J. (2017). Chemically Cross‐Linked Poly(2‐hydroxyethyl methacrylate)‐Supported Deep Eutectic Solvent Gel Electrolytes for Eco‐Friendly Supercapacitors. ChemElectroChem, 4(10), 2556-2562. doi:10.1002/celc.201700586 | es_ES |
dc.description.references | Logan, M. W., Langevin, S., Tan, B., Freeman, A. W., Hoffman, C., Trigg, D. B., & Gerasopoulos, K. (2020). UV-cured eutectic gel polymer electrolytes for safe and robust Li-ion batteries. Journal of Materials Chemistry A, 8(17), 8485-8495. doi:10.1039/d0ta01901a | es_ES |
dc.description.references | Imre, B., García, L., Puglia, D., & Vilaplana, F. (2019). Reactive compatibilization of plant polysaccharides and biobased polymers: Review on current strategies, expectations and reality. Carbohydrate Polymers, 209, 20-37. doi:10.1016/j.carbpol.2018.12.082 | es_ES |
dc.description.references | Moradali, M. F., & Rehm, B. H. A. (2020). Bacterial biopolymers: from pathogenesis to advanced materials. Nature Reviews Microbiology, 18(4), 195-210. doi:10.1038/s41579-019-0313-3 | es_ES |
dc.description.references | Klein, R. J., Zhang, S., Dou, S., Jones, B. H., Colby, R. H., & Runt, J. (2006). Modeling electrode polarization in dielectric spectroscopy: Ion mobility and mobile ion concentration of single-ion polymer electrolytes. The Journal of Chemical Physics, 124(14), 144903. doi:10.1063/1.2186638 | es_ES |
dc.description.references | Bandara, T. M. W. J., Dissanayake, M. A. K. L., Albinsson, I., & Mellander, B.-E. (2011). Mobile charge carrier concentration and mobility of a polymer electrolyte containing PEO and Pr4N+I− using electrical and dielectric measurements. Solid State Ionics, 189(1), 63-68. doi:10.1016/j.ssi.2011.03.004 | es_ES |
dc.description.references | Qi, X., Watanabe, M., Aida, T. M., & Smith Jr., R. L. (2010). Efficient one-pot production of 5-hydroxymethylfurfural from inulin in ionic liquids. Green Chemistry, 12(10), 1855. doi:10.1039/c0gc00141d | es_ES |
dc.description.references | Hu, S., Zhang, Z., Song, J., Zhou, Y., & Han, B. (2009). Efficient conversion of glucose into 5-hydroxymethylfurfural catalyzed by a common Lewis acid SnCl4 in an ionic liquid. Green Chemistry, 11(11), 1746. doi:10.1039/b914601f | es_ES |
dc.description.references | Hu, S., Zhang, Z., Zhou, Y., Song, J., Fan, H., & Han, B. (2009). Direct conversion of inulin to 5-hydroxymethylfurfural in biorenewable ionic liquids. Green Chemistry, 11(6), 873. doi:10.1039/b822328a | es_ES |
dc.description.references | Zuo, M., Le, K., Li, Z., Jiang, Y., Zeng, X., Tang, X., … Lin, L. (2017). Green process for production of 5-hydroxymethylfurfural from carbohydrates with high purity in deep eutectic solvents. Industrial Crops and Products, 99, 1-6. doi:10.1016/j.indcrop.2017.01.027 | es_ES |
dc.description.references | Maugeri, Z., & Domínguez de María, P. (2012). Novel choline-chloride-based deep-eutectic-solvents with renewable hydrogen bond donors: levulinic acid and sugar-based polyols. RSC Adv., 2(2), 421-425. doi:10.1039/c1ra00630d | es_ES |
dc.description.references | Sapir, L., Stanley, C. B., & Harries, D. (2016). Properties of Polyvinylpyrrolidone in a Deep Eutectic Solvent. The Journal of Physical Chemistry A, 120(19), 3253-3259. doi:10.1021/acs.jpca.5b11927 | es_ES |
dc.description.references | Stefanovic, R., Webber, G. B., & Page, A. J. (2019). Polymer solvation in choline chloride deep eutectic solvents modulated by the hydrogen bond donor. Journal of Molecular Liquids, 279, 584-593. doi:10.1016/j.molliq.2019.02.004 | es_ES |
dc.description.references | Chen, Z., McDonald, S., FitzGerald, P., Warr, G. G., & Atkin, R. (2017). Small angle neutron scattering study of the conformation of poly(ethylene oxide) dissolved in deep eutectic solvents. Journal of Colloid and Interface Science, 506, 486-492. doi:10.1016/j.jcis.2017.07.068 | es_ES |
dc.description.references | Zdanowicz, M., Wilpiszewska, K., & Spychaj, T. (2018). Deep eutectic solvents for polysaccharides processing. A review. Carbohydrate Polymers, 200, 361-380. doi:10.1016/j.carbpol.2018.07.078 | es_ES |
dc.description.references | Ramírez-Wong, D. G., Ramírez-Cardona, M., Sánchez-Leija, R. J., Rugerio, A., Mauricio-Sánchez, R. A., Hernández-Landaverde, M. A., … Luna-Bárcenas, G. (2016). Sustainable-solvent-induced polymorphism in chitin films. Green Chemistry, 18(15), 4303-4311. doi:10.1039/c6gc00628k | es_ES |
dc.description.references | Kim, Y., Faqih, M. ., & Wang, S. . (2001). Factors affecting gel formation of inulin. Carbohydrate Polymers, 46(2), 135-145. doi:10.1016/s0144-8617(00)00296-4 | es_ES |
dc.description.references | Mota-Morales, J. D., Gutiérrez, M. C., Ferrer, M. L., Sanchez, I. C., Elizalde-Peña, E. A., Pojman, J. A., … Luna-Bárcenas, G. (2013). Deep eutectic solvents as both active fillers and monomers for frontal polymerization. Journal of Polymer Science Part A: Polymer Chemistry, 51(8), 1767-1773. doi:10.1002/pola.26555 | es_ES |
dc.description.references | Bednarz, S., Fluder, M., Galica, M., Bogdal, D., & Maciejaszek, I. (2014). Synthesis of hydrogels by polymerization of itaconic acid-choline chloride deep eutectic solvent. Journal of Applied Polymer Science, 131(16), n/a-n/a. doi:10.1002/app.40608 | es_ES |
dc.description.references | Bednarz, S., Kowalski, G., & Konefał, R. (2019). Unexpected irregular structures of poly(itaconic acid) prepared in Deep Eutectic Solvents. European Polymer Journal, 115, 30-36. doi:10.1016/j.eurpolymj.2019.03.021 | es_ES |
dc.description.references | Sánchez-Leija, R. J., Torres-Lubián, J. R., Reséndiz-Rubio, A., Luna-Bárcenas, G., & Mota-Morales, J. D. (2016). Enzyme-mediated free radical polymerization of acrylamide in deep eutectic solvents. RSC Advances, 6(16), 13072-13079. doi:10.1039/c5ra27468k | es_ES |
dc.description.references | Castelli, F., Sarpietro, M. G., Micieli, D., Ottimo, S., Pitarresi, G., Tripodo, G., … Giammona, G. (2008). Differential scanning calorimetry study on drug release from an inulin-based hydrogel and its interaction with a biomembrane model: pH and loading effect. European Journal of Pharmaceutical Sciences, 35(1-2), 76-85. doi:10.1016/j.ejps.2008.06.005 | es_ES |
dc.description.references | Izawa, K., Akiyama, K., Abe, H., Togashi, Y., & Hasegawa, T. (2013). Inulin-based glycopolymer: Its preparation, lectin-affinity and gellation property. Bioorganic & Medicinal Chemistry, 21(11), 2895-2902. doi:10.1016/j.bmc.2013.03.066 | es_ES |
dc.description.references | Pitarresi, G., Triolo, D., Giorgi, M., Fiorica, C., Calascibetta, F., & Giammona, G. (2012). Inulin-Based Hydrogel for Oral Delivery of Flutamide: Preparation, Characterization, and in vivo Release Studies. Macromolecular Bioscience, 12(6), 770-778. doi:10.1002/mabi.201200003 | es_ES |
dc.description.references | Stevens, C. V., Meriggi, A., & Booten, K. (2001). Chemical Modification of Inulin, a Valuable Renewable Resource, and Its Industrial Applications. Biomacromolecules, 2(1), 1-16. doi:10.1021/bm005642t | es_ES |
dc.description.references | Chen, W., Bai, X., Xue, Z., Mou, H., Chen, J., Liu, Z., & Mu, T. (2019). The formation and physicochemical properties of PEGylated deep eutectic solvents. New Journal of Chemistry, 43(22), 8804-8810. doi:10.1039/c9nj02196e | es_ES |
dc.description.references | Ahmed Rahma, W. S., Mjalli, F. S., Al-Wahaibi, T., & Al-Hashmi, A. A. (2017). Polymeric-based deep eutectic solvents for effective extractive desulfurization of liquid fuel at ambient conditions. Chemical Engineering Research and Design, 120, 271-283. doi:10.1016/j.cherd.2017.02.025 | es_ES |
dc.description.references | Mielczarek, K., Łabanowska, M., Kurdziel, M., Konefał, R., Beneš, H., Bujok, S., … Bednarz, S. (2020). High‐Molecular‐Weight Polyampholytes Synthesized via Daylight‐Induced, Initiator‐Free Radical Polymerization of Renewable Itaconic Acid. Macromolecular Rapid Communications, 41(4), 1900611. doi:10.1002/marc.201900611 | es_ES |
dc.description.references | Afinjuomo, F., Barclay, T. G., Song, Y., Parikh, A., Petrovsky, N., & Garg, S. (2019). Synthesis and characterization of a novel inulin hydrogel crosslinked with pyromellitic dianhydride. Reactive and Functional Polymers, 134, 104-111. doi:10.1016/j.reactfunctpolym.2018.10.014 | es_ES |
dc.description.references | El Hariri El Nokab, M., & van der Wel, P. C. A. (2020). Use of solid-state NMR spectroscopy for investigating polysaccharide-based hydrogels: A review. Carbohydrate Polymers, 240, 116276. doi:10.1016/j.carbpol.2020.116276 | es_ES |
dc.description.references | Hackney, J. ., Atalla, R. ., & VanderHart, D. . (1994). Modification of crystallinity and crystalline structure of Acetobacter xylinum cellulose in the presence of water-soluble β-1,4-linked polysaccharides: 13C-NMR evidence. International Journal of Biological Macromolecules, 16(4), 215-218. doi:10.1016/0141-8130(94)90053-1 | es_ES |
dc.description.references | Dan, A., Ghosh, S., & Moulik, S. P. (2009). Physicochemical studies on the biopolymer inulin: A critical evaluation of its self-aggregation, aggregate-morphology, interaction with water, and thermal stability. Biopolymers, 91(9), 687-699. doi:10.1002/bip.21199 | es_ES |
dc.description.references | Lee, S. J., Kim, S. S., & Lee, Y. M. (2000). Interpenetrating polymer network hydrogels based on poly(ethylene glycol) macromer and chitosan. Carbohydrate Polymers, 41(2), 197-205. doi:10.1016/s0144-8617(99)00088-0 | es_ES |
dc.description.references | Teacă, C.-A., Bodîrlău, R., & Spiridon, I. (2013). Effect of cellulose reinforcement on the properties of organic acid modified starch microparticles/plasticized starch bio-composite films. Carbohydrate Polymers, 93(1), 307-315. doi:10.1016/j.carbpol.2012.10.020 | es_ES |
dc.description.references | Song, M., Hourston, D. J., Pollock, H. M., Schäfer, F. U., & Hammiche, A. (1997). Modulated differential scanning calorimetry: XI. A characterisation method for interpenetrating polymer networks. Thermochimica Acta, 304-305, 335-346. doi:10.1016/s0040-6031(97)00124-x | es_ES |
dc.description.references | Şahiner, N., Pekel, N., & Güven, O. (1999). Radiation synthesis, characterization and amidoximation of N-vinyl-2-pyrrolidone/acrylonitrile interpenetrating polymer networks. Reactive and Functional Polymers, 39(2), 139-146. doi:10.1016/s1381-5148(97)00150-8 | es_ES |
dc.description.references | Yue, Y.-M., Xu, K., Liu, X.-G., Chen, Q., Sheng, X., & Wang, P.-X. (2008). Preparation and characterization of interpenetration polymer network films based on poly(vinyl alcohol) and poly(acrylic acid) for drug delivery. Journal of Applied Polymer Science, 108(6), 3836-3842. doi:10.1002/app.28023 | es_ES |
dc.description.references | Hernández, R., Pérez, E., Mijangos, C., & López, D. (2005). Poly(vinyl alcohol)–poly(acrylic acid) interpenetrating networks. Study on phase separation and molecular motions. Polymer, 46(18), 7066-7071. doi:10.1016/j.polymer.2005.05.108 | es_ES |
dc.description.references | Sánchez-Leija, R. J., Pojman, J. A., Luna-Bárcenas, G., & Mota-Morales, J. D. (2014). Controlled release of lidocaine hydrochloride from polymerized drug-based deep-eutectic solvents. J. Mater. Chem. B, 2(43), 7495-7501. doi:10.1039/c4tb01407c | es_ES |
dc.description.references | Hamcerencu, M., Desbrieres, J., Popa, M., & Riess, G. (2012). Original stimuli-sensitive polysaccharide derivatives/N-isopropylacrylamide hydrogels. Role of polysaccharide backbone. Carbohydrate Polymers, 89(2), 438-447. doi:10.1016/j.carbpol.2012.03.026 | es_ES |
dc.description.references | Micic, M., & Suljovrujic, E. (2013). Network parameters and biocompatibility of p(2-hydroxyethyl methacrylate/itaconic acid/oligo(ethylene glycol) acrylate) dual-responsive hydrogels. European Polymer Journal, 49(10), 3223-3233. doi:10.1016/j.eurpolymj.2013.06.026 | es_ES |
dc.description.references | Shoaib, M., Shehzad, A., Omar, M., Rakha, A., Raza, H., Sharif, H. R., … Niazi, S. (2016). Inulin: Properties, health benefits and food applications. Carbohydrate Polymers, 147, 444-454. doi:10.1016/j.carbpol.2016.04.020 | es_ES |
dc.description.references | Nuss, P., & Gardner, K. H. (2012). Attributional life cycle assessment (ALCA) of polyitaconic acid production from northeast US softwood biomass. The International Journal of Life Cycle Assessment, 18(3), 603-612. doi:10.1007/s11367-012-0511-y | es_ES |
dc.description.references | Zhong, M., Tang, Q. F., Zhu, Y. W., Chen, X. Y., & Zhang, Z. J. (2020). An alternative electrolyte of deep eutectic solvent by choline chloride and ethylene glycol for wide temperature range supercapacitors. Journal of Power Sources, 452, 227847. doi:10.1016/j.jpowsour.2020.227847 | es_ES |
dc.description.references | Zhen, F., Percevault, L., Paquin, L., Limanton, E., Lagrost, C., & Hapiot, P. (2020). Electron Transfer Kinetics in a Deep Eutectic Solvent. The Journal of Physical Chemistry B, 124(6), 1025-1032. doi:10.1021/acs.jpcb.9b09022 | es_ES |
dc.description.references | Navarro-Suárez, A. M., & Johansson, P. (2020). Perspective—Semi-Solid Electrolytes Based on Deep Eutectic Solvents: Opportunities and Future Directions. Journal of The Electrochemical Society, 167(7), 070511. doi:10.1149/1945-7111/ab68d3 | es_ES |
dc.description.references | Z. Xue , W.Zhao and T.Mu , Deep Eutectic Solventes: Synthesis, Properties, and Applications , ed. J. R. Diego and G. Gabriela , Wiley-VCH Verlag GmbH & Co. KGaA , Weinheim, Germany , 1st edn, 2020 , Electrochemistry, pp. 335–360 | es_ES |
dc.description.references | Hong, S., Yuan, Y., Liu, C., Chen, W., Chen, L., Lian, H., & Liimatainen, H. (2020). A stretchable and compressible ion gel based on a deep eutectic solvent applied as a strain sensor and electrolyte for supercapacitors. Journal of Materials Chemistry C, 8(2), 550-560. doi:10.1039/c9tc05913j | es_ES |
dc.description.references | Abbott, A. P., Capper, G., & Gray, S. (2006). Design of Improved Deep Eutectic Solvents Using Hole Theory. ChemPhysChem, 7(4), 803-806. doi:10.1002/cphc.200500489 | es_ES |
dc.description.references | Kusuma, V. A., Macala, M. K., Liu, J., Marti, A. M., Hirsch, R. J., Hill, L. J., & Hopkinson, D. (2018). Ionic liquid compatibility in polyethylene oxide/siloxane ion gel membranes. Journal of Membrane Science, 545, 292-300. doi:10.1016/j.memsci.2017.09.086 | es_ES |
dc.description.references | Balo, L., Shalu, Gupta, H., Kumar Singh, V., & Kumar Singh, R. (2017). Flexible gel polymer electrolyte based on ionic liquid EMIMTFSI for rechargeable battery application. Electrochimica Acta, 230, 123-131. doi:10.1016/j.electacta.2017.01.177 | es_ES |
dc.description.references | Zhu, M., Yu, L., He, S., Hong, H., Liu, J., Gan, L., & Long, M. (2019). Highly Efficient and Stable Cellulose-Based Ion Gel Polymer Electrolyte for Solid-State Supercapacitors. ACS Applied Energy Materials, 2(8), 5992-6001. doi:10.1021/acsaem.9b01109 | es_ES |
dc.description.references | Sørensen, T. S., Compañ, V., & Diaz-Calleja, R. (1996). Complex permittivity of a film of poly[4-(acryloxy)phenyl-(4-chlorophenyl)methanone] containing free ion impurities and the separation of the contributions from interfacial polarization, Maxwell–Wagner–Sillars effects and dielectric relaxations of the polymer chains. J. Chem. Soc., Faraday Trans., 92(11), 1947-1957. doi:10.1039/ft9969201947 | es_ES |
dc.description.references | Coelho, R. (1991). On the static permittivity of dipolar and conductive media — an educational approach. Journal of Non-Crystalline Solids, 131-133, 1136-1139. doi:10.1016/0022-3093(91)90740-w | es_ES |
dc.description.references | Coelho, R. (1983). Sur la relaxation d’une charge d’espace. Revue de Physique Appliquée, 18(3), 137-146. doi:10.1051/rphysap:01983001803013700 | es_ES |
dc.description.references | Macdonald, J. R., Evangelista, L. R., Lenzi, E. K., & Barbero, G. (2011). Comparison of Impedance Spectroscopy Expressions and Responses of Alternate Anomalous Poisson−Nernst−Planck Diffusion Equations for Finite-Length Situations. The Journal of Physical Chemistry C, 115(15), 7648-7655. doi:10.1021/jp200737z | es_ES |
dc.description.references | Wübbenhorst, M., & van Turnhout, J. (2002). Analysis of complex dielectric spectra. I. One-dimensional derivative techniques and three-dimensional modelling. Journal of Non-Crystalline Solids, 305(1-3), 40-49. doi:10.1016/s0022-3093(02)01086-4 | es_ES |
dc.description.references | Choi, U. H., Mittal, A., Price, T. L., Gibson, H. W., Runt, J., & Colby, R. H. (2013). Polymerized Ionic Liquids with Enhanced Static Dielectric Constants. Macromolecules, 46(3), 1175-1186. doi:10.1021/ma301833j | es_ES |
dc.description.references | Sørensen, T. S., & Compañ, V. (1995). Complex permittivity of a conducting, dielectric layer containing arbitrary binary Nernst–Planck electrolytes with applications to polymer films and cellulose acetate membranes. J. Chem. Soc., Faraday Trans., 91(23), 4235-4250. doi:10.1039/ft9959104235 | es_ES |
dc.description.references | Wagle, D. V., Baker, G. A., & Mamontov, E. (2015). Differential Microscopic Mobility of Components within a Deep Eutectic Solvent. The Journal of Physical Chemistry Letters, 6(15), 2924-2928. doi:10.1021/acs.jpclett.5b01192 | es_ES |
dc.description.references | Faraone, A., Wagle, D. V., Baker, G. A., Novak, E. C., Ohl, M., Reuter, D., … Mamontov, E. (2018). Glycerol Hydrogen-Bonding Network Dominates Structure and Collective Dynamics in a Deep Eutectic Solvent. The Journal of Physical Chemistry B, 122(3), 1261-1267. doi:10.1021/acs.jpcb.7b11224 | es_ES |
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