Viscoelasticity‐Induced Controllable Periodic Meso‐Textures of Liquid Crystal Polymers in Additive Manufacturing

ABSTRACT Liquid crystalline polymers (LCPs) are nematic polymers composed of rod‐like molecular segments that self‐assemble into anisotropic alignment at melt. In material extrusion additive manufacturing, this molecular ordering significantly enhances tensile properties along the printing direction, which is seldom observed in conventional polymers. In this work, we investigate the formation of viscoelasticity‐driven periodic meso‐scale textures during LCP printing, and demonstrate their tunability through control of processing parameters. These textures emerge spontaneously without the need for complex toolpath design, driven by the intrinsic anisotropy of the material. Although this anisotropy can hinder interlayer adhesion, we show that natural cooling improves bonding between layers and increases puncture energy absorption. Beyond structural advantages, the resulting controllable textures offer functional utility: they enable terahertz wave manipulation for photonic devices and the regulation of nerve cell alignment, opening new possibilities for biomedical implants and multifunctional printed systems.

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Publication Details

Journal
Advanced Functional Materials
Published
2025-12-30
DOI
https://doi.org/10.1002/adfm.202521254
Primary Topic
Advanced Materials and Mechanics
Type
article
Field-Weighted Citation Impact
0.00
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article

Viscoelasticity‐Induced Controllable Periodic Meso‐Textures of Liquid Crystal Polymers in Additive Manufacturing

Amy Jin, George G. Malliaras, Sebastian W. Pattinson, Ronan Daly et al.
Advanced Functional Materials
Advanced Materials and Mechanics
article

Viscoelasticity‐Induced Controllable Periodic Meso‐Textures of Liquid Crystal Polymers in Additive Manufacturing

Amy Jin, George G. Malliaras, Sebastian W. Pattinson, Ronan Daly, Dick Ferieno Firdaus, Andrew Gleadall, Xudong Tao, M. Kotter, Christos Margadji, Zehao Ji, Miaomiao Zou, J. Axel Zeitler, Jiongyi Yan, Ran Chen, Zichen Wang, Shushan Wang, Jiaxuan Li, Yi Liu
article en

Abstract

ABSTRACT Liquid crystalline polymers (LCPs) are nematic polymers composed of rod‐like molecular segments that self‐assemble into anisotropic alignment at melt. In material extrusion additive manufacturing, this molecular ordering significantly enhances tensile properties along the printing direction, which is seldom observed in conventional polymers. In this work, we investigate the formation of viscoelasticity‐driven periodic meso‐scale textures during LCP printing, and demonstrate their tunability through control of processing parameters. These textures emerge spontaneously without the need for complex toolpath design, driven by the intrinsic anisotropy of the material. Although this anisotropy can hinder interlayer adhesion, we show that natural cooling improves bonding between layers and increases puncture energy absorption. Beyond structural advantages, the resulting controllable textures offer functional utility: they enable terahertz wave manipulation for photonic devices and the regulation of nerve cell alignment, opening new possibilities for biomedical implants and multifunctional printed systems.

Advanced Functional Materials
Loughborough University (GB), University of Cambridge (GB), Bridge University (SS)
Affordable and clean energy
Openalex Percentile: Top 43%
Advanced Materials and Mechanics
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