Self-Healable, Stretchable, and Super-Soft Bottlebrush Polyester Elastomers for Highly Sensitive Flexible Sensors AITranslate
Abstract AITranslate
While much effort has been devoted to the creation of super-soft elastomers, there is a dearth of research aimed at self-healable and super-soft renewable elastomers. Herein, self-healing and super-soft renewable elastomers are developed based on bottlebrush architecture design and dynamic associative transesterification. The bottlebrush polymer precursors are generated by ring-opening metathesis polymerization (ROMP) of the norbornene-terminated macromonomer poly(ε-caprolactone-co-l-lactide) (PCLLA) (NB-PCLLA). After introducing alkyne groups onto the end of PCLLA side chains, the bottlebrush polymers are cross-linked to achieve elastomer networks via a UV-induced “click” thiol-yne reaction between the terminal alkyne groups and the dithiothreitol (DTT) additive. The resulting materials exhibit a shear modulus as low as 17 kPa, high stretchability with breaking strains as large as 315%, and a self-healing efficiency of 95.6% at an elevated temperature of 80 °C. Taking the super-softness advantage, flexible sensor devices are assembled based on the prepared elastomer, which are highly sensitive to deformation with a gauge factor of 0.347. This work demonstrates that high-performance biodegradable materials with unique properties that conventional linear polymers impossibly possess can be easily constructed by molecular architecture design using bottlebrush polymers as building blocks.
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DOI:https://doi.org/10.1021/acsapm.3c00017
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While much effort has been devoted to the creation of super-soft elastomers, there is a dearth of research aimed at self-healable and super-soft renewable elastomers. Herein, self-healing and super-soft renewable elastomers are developed based on bottlebrush architecture design and dynamic associative transesterification. The bottlebrush polymer precursors are generated by ring-opening metathesis polymerization (ROMP) of the norbornene-terminated macromonomer poly(ε-caprolactone-co-l-lactide) (PCLLA) (NB-PCLLA). After introducing alkyne groups onto the end of PCLLA side chains, the bottlebrush polymers are cross-linked to achieve elastomer networks via a UV-induced “click” thiol-yne reaction between the terminal alkyne groups and the dithiothreitol (DTT) additive. The resulting materials exhibit a shear modulus as low as 17 kPa, high stretchability with breaking strains as large as 315%, and a self-healing efficiency of 95.6% at an elevated temperature of 80 °C. Taking the super-softness advantage, flexible sensor devices are assembled based on the prepared elastomer, which are highly sensitive to deformation with a gauge factor of 0.347. This work demonstrates that high-performance biodegradable materials with unique properties that conventional linear polymers impossibly possess can be easily constructed by molecular architecture design using bottlebrush polymers as building blocks.
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| GB/T 7714-2015 | [1] Xiaohui Yu, Yufei Wang, Mengke Li, et al. ACS Applied Polymer Materials, 2023(5). DOI:10.1021/acsapm.3c00017. |
| MLA | [1] Xiaohui Yu, et al., ACS Applied Polymer Materials, no. 5, 2023, https://doi.org/10.1021/acsapm.3c00017. |
| APA | [1] Xiaohui Yu, Yufei Wang, Mengke Li, Yingxin Zhang, Yufan Huang, Qi Qian, Yong Zheng, Qiaozhi Hou, & Xiaoshan Fan. (2023). ACS Applied Polymer Materials(5). https://doi.org/10.1021/acsapm.3c00017 |
| IEEE | [1] Xiaohui Yu, Yufei Wang, Mengke Li, Yingxin Zhang, Yufan Huang, Qi Qian, Yong Zheng, Qiaozhi Hou, and Xiaoshan Fan, ACS Applied Polymer Materials, no. 5, 2023, doi: 10.1021/acsapm.3c00017. keywords: {bottlebrush polymer;supersoft elastomer;selfhealable;biodegradable;flexible sensors} |
