Open AccessCCS ChemistryRESEARCH ARTICLES18 Jan 2023Dynamic Photo-responsive Ultralong Phosphorescence from 1D Halide Microrods Towards Multi-level Information Storage Chang Xing, Bo Zhou, Dongpeng Yan and Wei-Hai Fang Chang Xing Google Scholar More articles by this author , Bo Zhou Google Scholar More articles by this author , Dongpeng Yan Google Scholar More articles by this author and Wei-Hai Fang Google Scholar More articles by this author https://doi.org/10.31635/ccschem.023.202202605 SectionsSupplemental MaterialAboutPDF ToolsAdd to favoritesDownload CitationsTrack Citations ShareFacebookTwitterLinked InEmail Ultralong room temperature phosphorescence (RTP) has drawn much attention in fields such as optical imaging, sensors, information security, and so on. To meet the need of intelligent systems, the development of photoresponsive ultralong RTP materials is highly desirable, however it remains a challenge due to the lack of rational design strategies that can leverage RTP and photochromism effectively. Herein, we report a new type of onedimensional (1D) metal-organic halides (MOHs) that simultaneously exhibited dynamic ultralong RTP and photochromic optical waveguide with a large switching ratio, obvious visualization contrast, and robust reversibility. These properties facilitate future applications for multi-color photonic barcodes and optical logic gates. Moreover, benefiting from the color-time-space multi-dimensional tunable ultralong RTP, this 1D microrod displayed a multi-mode luminescent signal output, with significantly higher information storage capacity than typical fluorescent systems. Therefore, this work demonstrates a new 1D color-tunable optical waveguide and photo-responsive ultralong RTP based on molecular self-assembly of MOHs, and extends frontier photonic applications as multi-level data encryption and information storage at the micro/nanoscale. Download figure Download PowerPoint Previous articleNext article FiguresReferencesRelatedDetails Issue AssignmentNot Yet AssignedSupporting Information Copyright & Permissions© 2023 Chinese Chemical Society Downloaded 0 times PDF downloadLoading ...