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Self-Assembly of Charged Diblock Copolymers with Reduced Backbone Polarity AITranslate

University of Minnesota; University of Minnesota; University of Minnesota; University of Minnesota
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Publisher: ACS
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Abstract AITranslate

Charged block copolymers that can self-assemble into a host of nanostructures offer a great opportunity as next-generation battery electrolytes with outstanding ionic conductivity and mechanical robustness. The impact of ions on the self-assembly of charged block copolymers, however, remains to be fully understood. In this article, we report the phase behavior of charged-neutral block copolymers where a relatively nonpolar matrix was employed in the charged block to boost the strength of electrostatic interaction. The phase behavior was established using small-angle X-ray scattering (SAXS). We found that the overall shape of the phase boundary between ordered and disordered states is asymmetric, tilting toward the charged block-lean side of the phase portrait. However, the composition windows of the ordered phases, such as lamellae and hexagonally packed cylinders observed in this study, are comparable to those of neutral diblock copolymers and are not obviously affected by the incorporation of charges. The results obtained in this work provide insight into the impact of ions on the self-assembly of charged block copolymers as well as the design of nanostructured polymer electrolytes.

KeyWords AITranslate

charged block copolymers ionomers singleion conductors polymer electrolytes selfassembly phase behavior Xray scattering
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Basic Information:

DOI:https://doi.org/10.1021/acsapm.2c02220

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Citation Information:

Charged block copolymers that can self-assemble into a host of nanostructures offer a great opportunity as next-generation battery electrolytes with outstanding ionic conductivity and mechanical robustness. The impact of ions on the self-assembly of charged block copolymers, however, remains to be fully understood. In this article, we report the phase behavior of charged-neutral block copolymers where a relatively nonpolar matrix was employed in the charged block to boost the strength of electrostatic interaction. The phase behavior was established using small-angle X-ray scattering (SAXS). We found that the overall shape of the phase boundary between ordered and disordered states is asymmetric, tilting toward the charged block-lean side of the phase portrait. However, the composition windows of the ordered phases, such as lamellae and hexagonally packed cylinders observed in this study, are comparable to those of neutral diblock copolymers and are not obviously affected by the incorporation of charges. The results obtained in this work provide insight into the impact of ions on the self-assembly of charged block copolymers as well as the design of nanostructured polymer electrolytes.

quote

GB/T 7714-2015 [1] Bo Zhang, Caini Zheng, Frank S. Bates, et al. ACS Applied Polymer Materials, 2023(5). DOI:10.1021/acsapm.2c02220.
MLA [1] Bo Zhang, et al., ACS Applied Polymer Materials, no. 5, 2023, https://doi.org/10.1021/acsapm.2c02220.
APA [1] Bo Zhang, Caini Zheng, Frank S. Bates, & Timothy P. Lodge. (2023). ACS Applied Polymer Materials(5). https://doi.org/10.1021/acsapm.2c02220
IEEE [1] Bo Zhang, Caini Zheng, Frank S. Bates, and Timothy P. Lodge, ACS Applied Polymer Materials, no. 5, 2023, doi: 10.1021/acsapm.2c02220. keywords: {charged block copolymers;ionomers;singleion conductors;polymer electrolytes;selfassembly;phase behavior;Xray scattering}