Source abstract
Abstract
Aggregation-induced emission (AIE)-based circularly polarized luminescence (CPL) has been recognized as a promising pathway for developing chiroptical materials with high luminescence dissymmetry factors (|glum|). Here, we propose a method for the construction of a thermally tunable CPL-active system based on a supramolecular self-assembly approach that utilizes helical nano- or microfilament templates in conjunction with an AIE dye. The CPL properties of the ensuing ensembles are predominantly determined by the intrinsic geometric differences among the various filament templates such as their overall dimensions (width, height, and helical pitch) and the area fraction of the exposed aromatic segments or sublayers. The proposed mechanism is based on the collective data acquired by absorption, steady state and time-resolved fluorescence, absolute quantum yield, and CPL measurements. The highest |glum| value for the most promising dual-modulated helical nanofilament templates in the present series was further enhanced, reaching up to |glum| = 0.25 by confinement in the appropriate diameter of anodized aluminum oxide (AAO) nanochannels. It is envisioned that this methodology will afford new insights into the design of temperature-rate indicators or anti-counterfeiting tags using a combination of structural color by the nano- and microfilament templates and the AIE property of the guest dye.
Source: openalex_inverted_index · Quality: baseline
Affiliations
Materials Science Graduate Program, Kent State University, Kent, Ohio 44242-0001, United States
Advanced Materials and Liquid Crystal Institute, Kent State University, Kent, Ohio 44242-0001, United States
Univ Rennes, ISCR - UMR 6226, ScanMAT − UAR 2025, F-35000 Rennes, France
Department of Chemistry and Biochemistry, Kent State University, Kent, Ohio 44242-0001, United States
Brain Health Research Institute, Kent State University, Kent, Ohio 44242-0001, United States
Funding
Ohio Department of Higher Education · Division of Materials Research