4.8 Article

Synergistic Effects of Self-Doped Nanostructures as Charge Trapping Elements in Organic Field Effect Transistor Memory

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 8, Issue 29, Pages 18969-18977

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.6b03792

Keywords

OFET memory; polymer; conformation; beta-phase; nanostructure

Funding

  1. National Basic Research Program of China [2014CB648300, 2015CB932200]
  2. National Natural Science Foundation of China [61475074, 21274064, 21504041, 61136003]
  3. National Natural Science Funds for Excellent Young Scholar [21322402]
  4. Changjiang Scholars and Innovative Research Team in University [IRT_15R37]
  5. Natural Science Foundation of Jiangsu Province [BM2012010, 14KJB510027]
  6. Synergetic Innovation Center for Organic Electronics and Information Displays
  7. Excellent Science and Technology Innovation Team of Jiangsu Higher Education Institutions
  8. China Postdoctoral Science Foundation [2015M580419]
  9. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD) [YX03001]
  10. Program for Postgraduates Research Innovation in University of Jiangsu Province [KYLX15_0850]

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Despite remarkable advances in the development of organic field-effect transistor (OFET) memories,over recent years, the charge trapping elements remain confined to the critical electrets of polymers, nanoparticles, or ferroelectrics. Nevertheless, rare reports are available on the complementary advantages of different types of trapping elements integrated in one single OFET memory. To address this issue, we fabricated two kinds of pentacene-based OFET memories with solution-processed amorphous and beta-phase poly(9,9-dioctylfluorene) (PFO) films as charge trapping layers, respectively. Compared to the amorphous film, the beta-PFO film has self-doped nanostructures (20-120 nm) and could act as natural charge trapping elements, demonstrating the synergistic effects of combining both merits of polymer and nanoparticles into one electret. Consequently, the OFET memory with beta-PFO showed nearly 26% increment in the storage capacity and a pronounced memory window of similar to 45 V in 20 ms programming time. Besides, the retention time of beta-PFO device extended 2 times to maintain an ON/OFF current ratio of 103, indicating high bias-stress reliability. Furthermore, the beta-PFO device demonstrated good photosensitivity in the 430-700 nm range, which was attributed to the additive effect of smaller bandgap and self-doped nanostructures of beta-phase. In this regard, the tuning of molecular conformation and aggregation in a polymer electret is an effective strategy to obtain a high performance OFET memory.

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