Healable Ionoelastomer Designed from Polymeric Ionic Liquid and Vitrimer Chemistry
The growing demand for all-solid flexible, stretchable, and wearable devices has boosted the need for liquid-free and stretchable ionoelastomers. These ionic conducting materials are subjected to repeated deformations during functioning, making them susceptible to damage. Thus, imparting cross-linke...
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Veröffentlicht in: | ACS applied polymer materials 2023-01, Vol.5 (1), p.529-541 |
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description | The growing demand for all-solid flexible, stretchable, and wearable devices has boosted the need for liquid-free and stretchable ionoelastomers. These ionic conducting materials are subjected to repeated deformations during functioning, making them susceptible to damage. Thus, imparting cross-linked materials with healing ability seems particularly promising to improve their durability. Here, a polymeric ionic liquid (PIL) bearing allyl functional groups was synthesized based on the quaternization of N-allylimidazole with a copolymer rubber of poly(epichlorohydrin) and poly(ethylene oxide) (PEO). The resulting PIL was then cross-linked with dynamic boronic ester cross-linkers 2,2′-(1,4-Phenylene)-bis[4-mercaptan-1,3,2-dioxaborolane] (BDB) through thiol–ene “click” photoaddition. PEO dangling chains were additionally introduced for acting as free volume enhancers. The properties of the resulting all-solid PIL networks were investigated by tuning dynamic cross-linkers and dangling chain contents. Adjusting the cross-linker and dangling chain quantities yielded soft (0.2 MPa), stretchable (300%), and highly conducting ionoelastomers (1.6 × 10–5 S·cm–1 at 30 °C). The associative exchange reaction between BDB endowed these materials with vitrimer properties such as healing and recyclability. The recycled materials were able to retain their original mechanical properties and ionic conductivity. These healable PIL networks display a great potential for applications requiring solid electrolytes with high ionic conductivity, healing ability, and reprocessability. |
doi_str_mv | 10.1021/acsapm.2c01635 |
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T. M. ; Vancaeyzeele, Cédric ; Vidal, Frédéric ; Plesse, Cédric</creator><creatorcontrib>Li, Fengdi ; Nguyen, Giao. T. M. ; Vancaeyzeele, Cédric ; Vidal, Frédéric ; Plesse, Cédric</creatorcontrib><description>The growing demand for all-solid flexible, stretchable, and wearable devices has boosted the need for liquid-free and stretchable ionoelastomers. These ionic conducting materials are subjected to repeated deformations during functioning, making them susceptible to damage. Thus, imparting cross-linked materials with healing ability seems particularly promising to improve their durability. Here, a polymeric ionic liquid (PIL) bearing allyl functional groups was synthesized based on the quaternization of N-allylimidazole with a copolymer rubber of poly(epichlorohydrin) and poly(ethylene oxide) (PEO). The resulting PIL was then cross-linked with dynamic boronic ester cross-linkers 2,2′-(1,4-Phenylene)-bis[4-mercaptan-1,3,2-dioxaborolane] (BDB) through thiol–ene “click” photoaddition. PEO dangling chains were additionally introduced for acting as free volume enhancers. The properties of the resulting all-solid PIL networks were investigated by tuning dynamic cross-linkers and dangling chain contents. Adjusting the cross-linker and dangling chain quantities yielded soft (0.2 MPa), stretchable (300%), and highly conducting ionoelastomers (1.6 × 10–5 S·cm–1 at 30 °C). The associative exchange reaction between BDB endowed these materials with vitrimer properties such as healing and recyclability. The recycled materials were able to retain their original mechanical properties and ionic conductivity. These healable PIL networks display a great potential for applications requiring solid electrolytes with high ionic conductivity, healing ability, and reprocessability.</description><identifier>ISSN: 2637-6105</identifier><identifier>EISSN: 2637-6105</identifier><identifier>DOI: 10.1021/acsapm.2c01635</identifier><identifier>PMID: 36686061</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Chemical Sciences</subject><ispartof>ACS applied polymer materials, 2023-01, Vol.5 (1), p.529-541</ispartof><rights>2022 The Authors. Published by American Chemical Society</rights><rights>2022 The Authors. Published by American Chemical Society.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>2022 The Authors. 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T. M.</creatorcontrib><creatorcontrib>Vancaeyzeele, Cédric</creatorcontrib><creatorcontrib>Vidal, Frédéric</creatorcontrib><creatorcontrib>Plesse, Cédric</creatorcontrib><title>Healable Ionoelastomer Designed from Polymeric Ionic Liquid and Vitrimer Chemistry</title><title>ACS applied polymer materials</title><addtitle>ACS Appl. Polym. Mater</addtitle><description>The growing demand for all-solid flexible, stretchable, and wearable devices has boosted the need for liquid-free and stretchable ionoelastomers. These ionic conducting materials are subjected to repeated deformations during functioning, making them susceptible to damage. Thus, imparting cross-linked materials with healing ability seems particularly promising to improve their durability. Here, a polymeric ionic liquid (PIL) bearing allyl functional groups was synthesized based on the quaternization of N-allylimidazole with a copolymer rubber of poly(epichlorohydrin) and poly(ethylene oxide) (PEO). The resulting PIL was then cross-linked with dynamic boronic ester cross-linkers 2,2′-(1,4-Phenylene)-bis[4-mercaptan-1,3,2-dioxaborolane] (BDB) through thiol–ene “click” photoaddition. PEO dangling chains were additionally introduced for acting as free volume enhancers. The properties of the resulting all-solid PIL networks were investigated by tuning dynamic cross-linkers and dangling chain contents. Adjusting the cross-linker and dangling chain quantities yielded soft (0.2 MPa), stretchable (300%), and highly conducting ionoelastomers (1.6 × 10–5 S·cm–1 at 30 °C). The associative exchange reaction between BDB endowed these materials with vitrimer properties such as healing and recyclability. The recycled materials were able to retain their original mechanical properties and ionic conductivity. These healable PIL networks display a great potential for applications requiring solid electrolytes with high ionic conductivity, healing ability, and reprocessability.</description><subject>Chemical Sciences</subject><issn>2637-6105</issn><issn>2637-6105</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp1kd1LwzAUxYMoOqavPkofVdhM0jRtXwSZHxMGiqivIW1vXUbbzKQd7L_3js6hgi9JuPmdk3tzCDlldMwoZ1c693pZj3lOmQyjPTLgMoxHktFo_8f5iJx4v6AUFVzwiB-So1DKRFLJBuRlCrrSWQXBo20sVNq3tgYX3II3Hw0UQelsHTzbao1Vk28oXGfmszNFoJsieDetMxvFZA618a1bH5ODUlceTrb7kLzd371OpqPZ08Pj5GY20iJK21FKQxoDdiKEzGKqQwlplJV5FIqSA08zmaWpQCbnPNERlniBXYfIZzotdDgk173vsstqKHJoWqcrtcR2tFsrq436fdOYufqwK5UmQnAm0OCiN5j_kU1vZmpTo4LGMedixZA93z7m7GcHvlU4bA5VpRuwnVc8lknCBLoiOu7R3FnvHZQ7b0bVJjfV56a2uaHg7OcgO_w7JQQuewCFamE71-C__uf2BYZyogA</recordid><startdate>20230113</startdate><enddate>20230113</enddate><creator>Li, Fengdi</creator><creator>Nguyen, Giao. T. M.</creator><creator>Vancaeyzeele, Cédric</creator><creator>Vidal, Frédéric</creator><creator>Plesse, Cédric</creator><general>American Chemical Society</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>1XC</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-9227-9544</orcidid><orcidid>https://orcid.org/0000-0003-2097-7321</orcidid><orcidid>https://orcid.org/0000-0001-9803-0918</orcidid></search><sort><creationdate>20230113</creationdate><title>Healable Ionoelastomer Designed from Polymeric Ionic Liquid and Vitrimer Chemistry</title><author>Li, Fengdi ; Nguyen, Giao. T. M. ; Vancaeyzeele, Cédric ; Vidal, Frédéric ; Plesse, Cédric</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a459t-90307e366446b70a36e95bfc534f2e29b6b994307c228a52e22d6863644ba9da3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Chemical Sciences</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Fengdi</creatorcontrib><creatorcontrib>Nguyen, Giao. T. M.</creatorcontrib><creatorcontrib>Vancaeyzeele, Cédric</creatorcontrib><creatorcontrib>Vidal, Frédéric</creatorcontrib><creatorcontrib>Plesse, Cédric</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>ACS applied polymer materials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Fengdi</au><au>Nguyen, Giao. T. M.</au><au>Vancaeyzeele, Cédric</au><au>Vidal, Frédéric</au><au>Plesse, Cédric</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Healable Ionoelastomer Designed from Polymeric Ionic Liquid and Vitrimer Chemistry</atitle><jtitle>ACS applied polymer materials</jtitle><addtitle>ACS Appl. Polym. Mater</addtitle><date>2023-01-13</date><risdate>2023</risdate><volume>5</volume><issue>1</issue><spage>529</spage><epage>541</epage><pages>529-541</pages><issn>2637-6105</issn><eissn>2637-6105</eissn><abstract>The growing demand for all-solid flexible, stretchable, and wearable devices has boosted the need for liquid-free and stretchable ionoelastomers. These ionic conducting materials are subjected to repeated deformations during functioning, making them susceptible to damage. Thus, imparting cross-linked materials with healing ability seems particularly promising to improve their durability. Here, a polymeric ionic liquid (PIL) bearing allyl functional groups was synthesized based on the quaternization of N-allylimidazole with a copolymer rubber of poly(epichlorohydrin) and poly(ethylene oxide) (PEO). The resulting PIL was then cross-linked with dynamic boronic ester cross-linkers 2,2′-(1,4-Phenylene)-bis[4-mercaptan-1,3,2-dioxaborolane] (BDB) through thiol–ene “click” photoaddition. PEO dangling chains were additionally introduced for acting as free volume enhancers. The properties of the resulting all-solid PIL networks were investigated by tuning dynamic cross-linkers and dangling chain contents. Adjusting the cross-linker and dangling chain quantities yielded soft (0.2 MPa), stretchable (300%), and highly conducting ionoelastomers (1.6 × 10–5 S·cm–1 at 30 °C). The associative exchange reaction between BDB endowed these materials with vitrimer properties such as healing and recyclability. The recycled materials were able to retain their original mechanical properties and ionic conductivity. These healable PIL networks display a great potential for applications requiring solid electrolytes with high ionic conductivity, healing ability, and reprocessability.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>36686061</pmid><doi>10.1021/acsapm.2c01635</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0001-9227-9544</orcidid><orcidid>https://orcid.org/0000-0003-2097-7321</orcidid><orcidid>https://orcid.org/0000-0001-9803-0918</orcidid><oa>free_for_read</oa></addata></record> |
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title | Healable Ionoelastomer Designed from Polymeric Ionic Liquid and Vitrimer Chemistry |
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