Boundaries and cross-linking densities modulate domain sizes of polydomain nematic elastomers

When nematic liquid crystal elastomers (LCEs) crosslinked at their isotropic phase are quenched to the nematic phase, they show polydomain patterns, in which nematic microdomains with different orientations self-organize into a three-dimensional mosaic with characteristic correlation patterns. The orientational correlation length of the domain, which is usually in the micrometer range, is believed to emerge as a result of a competition between liquid crystalline ordering and frozen network inhomogeneity. Although polydomain patterns show potentials as the basic platform for optical, memory, and mechanical devices, no study exists regarding how they are modulated by experimentally accessible parameters. Here, using confocal polarized fluorescence microscopy, we study the effects of a solid-wall or open boundary on the domain size in conjunction with effects of cross-linking density. The LCE bounded by solid glass shows reduced domain size near the boundary. In contrast, increased domain size appears at the free surface. With increasing cross-linking density, the domain size decreases, also exhibiting the boundary effects. Guided by theoretical considerations, the results are explained by a picture that the effective strength of the inhomogeneity frozen in the polymer network, <i>i.e.</i>, the effective disorder strength, varies depending on the cross-linking density and constrained states at boundaries. The results offer the first experimental approach to global and local modulation of the polydomain pattern in nematic LCEs.

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Publication Details

Journal
Soft Matter
Published
2025-01-01
DOI
https://doi.org/10.1039/d4sm01419g
Citations
3
Primary Topic
Advanced Materials and Mechanics
Type
article
Field-Weighted Citation Impact
2.14

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article

Boundaries and cross-linking densities modulate domain sizes of polydomain nematic elastomers

Nariya Uchida, Kaoru Katoh, Takuya Ohzono
3 citations
Soft Matter
Advanced Materials and Mechanics
2.14
article

Boundaries and cross-linking densities modulate domain sizes of polydomain nematic elastomers

Nariya Uchida, Kaoru Katoh, Takuya Ohzono
article en
3 citations

Abstract

When nematic liquid crystal elastomers (LCEs) crosslinked at their isotropic phase are quenched to the nematic phase, they show polydomain patterns, in which nematic microdomains with different orientations self-organize into a three-dimensional mosaic with characteristic correlation patterns. The orientational correlation length of the domain, which is usually in the micrometer range, is believed to emerge as a result of a competition between liquid crystalline ordering and frozen network inhomogeneity. Although polydomain patterns show potentials as the basic platform for optical, memory, and mechanical devices, no study exists regarding how they are modulated by experimentally accessible parameters. Here, using confocal polarized fluorescence microscopy, we study the effects of a solid-wall or open boundary on the domain size in conjunction with effects of cross-linking density. The LCE bounded by solid glass shows reduced domain size near the boundary. In contrast, increased domain size appears at the free surface. With increasing cross-linking density, the domain size decreases, also exhibiting the boundary effects. Guided by theoretical considerations, the results are explained by a picture that the effective strength of the inhomogeneity frozen in the polymer network, <i>i.e.</i>, the effective disorder strength, varies depending on the cross-linking density and constrained states at boundaries. The results offer the first experimental approach to global and local modulation of the polydomain pattern in nematic LCEs.

Soft MatterVol. 21(6)
Tohoku University (JP), National Institute of Advanced Industrial Science and Technology (JP)
Japan Agency for Medical Research and Development, Ministry of Education, Culture, Sports, Science and Technology, Japan Society for the Promotion of Science
Openalex Percentile: Top 16%
Advanced Materials and Mechanics
2.14
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