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  4. Novel Authentic and Ultrafast Organic Photorecorders Enhanced by AIE-Active Polymer Electrets via Interlayer Charge Recombination
 
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Novel Authentic and Ultrafast Organic Photorecorders Enhanced by AIE-Active Polymer Electrets via Interlayer Charge Recombination

Journal
Advanced Functional Materials
Journal Volume
31
Journal Issue
28
Date Issued
2021
Author(s)
Ke C.-Y
Chen M.-N
Chen M.-H
Li Y.-T
Chiu Y.-C
GUEY-SHENG LIOU  
DOI
10.1002/adfm.202101288
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85109397313&doi=10.1002%2fadfm.202101288&partnerID=40&md5=8ca9edeffc8519dbab5462f37732f8cb
https://scholars.lib.ntu.edu.tw/handle/123456789/600318
Abstract
Organic photonic memory, featuring a variety of glamorously light-driven characteristics, is rapidly growing into an indispensable building block for next-generation optical communication systems. However, the ambiguity of their operating mechanism associated with the limitation of photoadaptive materials as an electronics promoter results in the slow development of photonic transistor-based devices. In this study, the conjugated polymers composed of donor–acceptor motifs with typical aggregation-induced emission (AIE) behaviors are designed and successfully discover high-performance photoprogrammable memory. Moreover, the mechanism of photoboosted recording behavior, attributed to the recombination of the formed interlayer excitons right after simultaneous excitation without applying vertical and parallel electric-field at the interface in-between active semiconductor and AIE polymers, is cautiously corroborated by steady-state PL and pulse PL measurements. The AIE-polymer memory devices perform ultrafast photoresponse time of 0.1?ms, an outstanding current switch ratio up to 106, and retention stability over 40?000 s without significant dissipation. Furthermore, photoresponsive AIE-polymer electrets not only modulate the memory performance through the emission wavelength but easily switch storage behavior of nonvolatile memory from flash to WORM by adjusting the torsion-angle through the motif of the donor and acceptor moieties. These findings open an avenue for designing conjugated polymer electret for ultrafast optical storage devices. ? 2021 Wiley-VCH GmbH
Subjects
AIE polymers
interlayer exciton
photonic transistor memory
polymer electrets
pulse PL
Electrets
Electric excitation
Electric fields
Excited states
Flash memory
Interface states
Laser recording
Nonvolatile storage
Optical communication
Virtual storage
Aggregation-induced emissions
Charge recombinations
Emission wavelength
Non-volatile memory
Optical storage devices
Parallel electric fields
Photonic transistors
Ultrafast photoresponse
Conjugated polymers
SDGs

[SDGs]SDG7

Type
journal article

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