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High anchoring photoalignment material based on new photo‐induced hole dipoles' mechanism
Flat nonprofiled surface of photoalignment AtA‐2 azo‐dye layer possesses simultaneously low molecular orientation anisotropy and strong azimuthal anchoring energy. We explain how flat surface of alignment layer orients nematic liquid crystal and show the existence of the new photoalignment mechanism...
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Published in: | Journal of the Society for Information Display 2021-11, Vol.29 (11), p.833-839 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Flat nonprofiled surface of photoalignment AtA‐2 azo‐dye layer possesses simultaneously low molecular orientation anisotropy and strong azimuthal anchoring energy. We explain how flat surface of alignment layer orients nematic liquid crystal and show the existence of the new photoalignment mechanism based on photo‐induced hole dipole moments in the azo‐dye layer. The dependence of anchoring energy coefficient on the square of dipole moments of the alignment layer and the liquid crystal layer is formulated, grounding the idea of chemical modification of AtA‐2 azo‐dye with molecular dipole moment ~16D to obtain novel high anchoring photoalignment material. The new AtA‐0042 azo‐dye with molecular dipole moment ~27.5D is synthesized and experimentally verified. Strong azimuthal anchoring energy over >1.4 × 10−4 J/m2 is obtained for AtA‐0042 photoalignment material layer with ~40 mJ/cm2 exposure dose.
New photo‐induced hole dipoles' photoalignment mechanism grounds idea of chemical modification of the high anchoring azo‐dye photoalignment materials. The anchoring energy coefficient (Wa) has square dependence on the values of dipole moments of alignment (μAL) and liquid crystal (μLC) layers. Strong azimuthal anchoring energy over >1.4 × 10−4 J/m2 is obtained for AtA‐0042 photoalignment material layer with >40 mJ/cm2 exposure dose. |
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ISSN: | 1071-0922 1938-3657 |
DOI: | 10.1002/jsid.1020 |