4.8 Article

Hierarchical Self-Assembly of Perylene Diimide (PDI) Crystals

Journal

JOURNAL OF PHYSICAL CHEMISTRY LETTERS
Volume 11, Issue 10, Pages 3934-3940

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.0c01226

Keywords

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Funding

  1. Leading Foreign Research Institute Recruitment Program through the National Research Foundation of Korea (NRF) - Ministry of Education, Science and Technology (MEST) [NRF-2015K1A4A3047100]
  2. National Research Foundation of Korea (NRF) - Ministry of Science, ICT and Future Planning, Korea (MSIP) [NRF -2019R1A2C4003950, NRF-2015M3A7B6027973, NRF-2017H1A2A1046199]
  3. MSIP
  4. POSTECH
  5. National Research Foundation of Korea [2017H1A2A1046199] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Controlling molecular self-assembly of organic semiconductors is a key factor in enhancing the performance of organic electronics and optoelectronics. However, unlike various p-type organic semiconductors, it has proven elusive to control molecular self-assembly with about tens of nm dimensions using n-type organic semiconductors including perylene diimide (PDI), which is the most promising alternative to fullerene derivatives, without using an additional synthetic method or additives, thus far. Here, we developed a simple self-assembling method for the hierarchical self-assembly of PDI crystals with nanometer-to-micrometer scale features using pristine PDI-C8 without using an additional synthetic method or additive. Interestingly, we observed crystalline and optical properties of self-assembled PDI crystals depending on their size and structural features. In addition, we fabricated p-n junctions composed of PDI and poly(3-hexylthiophene) (P3HT), where the p-n junctions had coassembled and blended nanomorphologies, and confirmed that coassembled nanomorphologies enabled more effective energy transfer than the blended nanomorphologies.

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