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  • AIP Publishing  (2)
  • Liu, Yang  (2)
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  • AIP Publishing  (2)
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  • 1
    In: AIP Advances, AIP Publishing, Vol. 9, No. 12 ( 2019-12-01)
    Abstract: A thin layer of single-walled carbon nanotubes (SWCNTs) exhibiting optical anisotropy is prepared by electroactively elongating SWCNT agglomerates. SWCNTs are doped into a reactive mesogen (RM) solution, and the composite solution is spin-coated on an interdigitated-electrode substrate. The spherical shaped SWCNT agglomerates observed in the solution of thin layers are electroactively elongated and aligned along the direction of the external electric field. After elongating the SWCNT agglomerates, the transparency of RM-SWCNT thin composite layers increases by about 14%. In addition, the elongated SWCNT agglomerates present significant optical anisotropy such that an incident light with a polarization direction parallel and perpendicular to the elongated direction of SWCNTs is absorbed and transmitted, respectively. The electroactively elongating strategy adopted to realize the optical anisotropy of SWCNT agglomerates suggests a new way to fabricate an optically anisotropic SWCNT thin layer.
    Type of Medium: Online Resource
    ISSN: 2158-3226
    Language: English
    Publisher: AIP Publishing
    Publication Date: 2019
    detail.hit.zdb_id: 2583909-3
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  • 2
    In: Structural Dynamics, AIP Publishing, Vol. 8, No. 3 ( 2021-05-01)
    Abstract: The mechanisms of 2-(Benzo[d]thiazol-2-yl)phenol-based bifunctional probe (HBT-FS) for detecting fluoride (F−) and sulfite (SO32–) based on excited-state intramolecular proton transfer (ESIPT) and intramolecular charge transfer (ICT) have been theoretically studied. Laplacian bond order of HBT-FS indicates that the F− ion cleaves the Si-O bond and then forms Compound 2 possessing a six-membered ring with a hydrogen bond. Potential energy curves and dynamic simulations confirm that ESIPT in Compound 2 occurs along with this hydrogen bond and forms a keto structure with an emission at 623 nm, which agrees with the observed experimental value (634 nm) after adding F−. Therefore, the fluorescence red-shift (from 498  to 634 nm) of HBT-FS observed in experiment after adding F− is caused by ESIPT. The SO32– ion is added to the C5 site of HBT-FS, which is confirmed by orbital-weighted dual descriptor, and then forms Compound 3 with fluorescence located at 404 nm. The experimentally measured fluorescence at 371 nm after adding SO32– is assigned to Compound 3. Charge transfer analyses indicate that the ICT extent of Compound 3 is relatively weak compared with that of HBT-FS because of the destruction of the conjugated structure by the addition reaction of SO32–, which induces the blue-shift of the fluorescence of HBT-FS from 498 to 371 nm. The different fluorescence responses make HBT-FS a fluorescent probe to discriminatorily detect F− and SO32–.
    Type of Medium: Online Resource
    ISSN: 2329-7778
    Language: English
    Publisher: AIP Publishing
    Publication Date: 2021
    detail.hit.zdb_id: 2758684-4
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