4.8 Article

Electroluminescence from Spontaneously Generated Single-Vesicle Aggregates Using Solution-Processed Small Organic Molecules

期刊

ACS NANO
卷 10, 期 1, 页码 998-1006

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.5b06261

关键词

supramolecular chemistry; soft matter; biuret; molecular electronics

资金

  1. LabEx AMADEus [ANR-10-LABX-0042-AMADEUS through grant ANR-10-IDEX-0003-02)]
  2. Agence Nationale de la Recherche Ministry of Science and Technology (MOST) Taiwan [ANR-13-IS07-0001 EVOLVE, 103-2923-M-002-001-MY3]
  3. [ANR-13-BS-07-0004 CrystOS]
  4. Agence Nationale de la Recherche (ANR) [ANR-13-IS07-0001] Funding Source: Agence Nationale de la Recherche (ANR)

向作者/读者索取更多资源

Self-assembled aggregates offer great potential for tuning the morphology of organic semiconductors, thereby controlling their size and shape. This is particularly interesting for applications in electroluminescent (EL) devices, but there has been, to date, no reports of a functional EL device in which the size and color of the emissive domains could be controlled using self assembly. We now report a series of molecules that spontaneously self-organize into small EL domains of sub-micrometer dimensions. By tailoring the emissive chromophores in solution, spherical aggregates that have an average size of 300 mu in diameter and emit any one color, including CIE D65 white, are spontaneously formed in solution. We show that the individual aggregates can be used in EL devices built either using small patterned electrodes or using a sandwich architecture to produce devices emitting in the blue, green, red, and white. Furthermore, sequential deposition of the three primary colors yields an RGB device in which single aggregates of each color are present in close proximity.

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