Low-Threshold Wavelength-Switchable Organic Nanowire Lasers Based on Excited-State Intramolecular Proton Transfer

Coherent light signals generated at the nanoscale are crucial to the realization of photonic integrated circuits. Self‐assembled nanowires from organic dyes can provide both a gain medium and an effective resonant cavity, which have been utilized for fulfilling miniaturized lasers. Excited‐state int...

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Published inAngewandte Chemie International Edition Vol. 54; no. 24; pp. 7125 - 7129
Main Authors Zhang, Wei, Yan, Yongli, Gu, Jianmin, Yao, Jiannian, Zhao, Yong Sheng
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 08.06.2015
WILEY‐VCH Verlag
Wiley Subscription Services, Inc
EditionInternational ed. in English
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Summary:Coherent light signals generated at the nanoscale are crucial to the realization of photonic integrated circuits. Self‐assembled nanowires from organic dyes can provide both a gain medium and an effective resonant cavity, which have been utilized for fulfilling miniaturized lasers. Excited‐state intramolecular proton transfer (ESIPT), a classical molecular photoisomerization process, can be used to build a typical four‐level system, which is more favorable for population inversion. Low‐power driven lasing in proton‐transfer molecular nanowires with an optimized ESIPT energy‐level process has been achieved. With high gain and low loss from the ESIPT, the wires can be applied as effective FP‐type resonators, which generated single‐mode lasing with a very low threshold. The lasing wavelength can be reversibly switched based on a conformation conversion of the excited keto form in the ESIPT process. Low‐threshold single‐mode lasing was achieved via excited‐state intramolecular proton transfer (ESIPT)‐assisted population inversion in crystal organic nanowires fabricated by the self‐assembly of proton‐transfer dye molecules. The lasing wavelength can be reversibly switched based on the photoinduced conformation conversion of the excited keto form in the ESIPT process.
Bibliography:Strategic Priority Research Program of the Chinese Academy of Sciences - No. XDB12020300
Ministry of Science and Technology of China - No. 2012YQ120060
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ArticleID:ANIE201502684
This work was supported by the National Natural Science Foundation of China (21125315, 21221002), the Ministry of Science and Technology of China (2012YQ120060), and the Strategic Priority Research Program of the Chinese Academy of Sciences (XDB12020300).
National Natural Science Foundation of China - No. 21125315; No. 21221002
ObjectType-Article-1
SourceType-Scholarly Journals-1
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ISSN:1433-7851
1521-3773
DOI:10.1002/anie.201502684