4.6 Article

π-Conjugation-interrupted hyperbranched polymer electrets for organic nonvolatile transistor memory devices

Journal

JOURNAL OF MATERIALS CHEMISTRY C
Volume 2, Issue 19, Pages 3738-3743

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c3tc32441a

Keywords

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Funding

  1. National Natural Science Funds for Excellent Young Scholar [21322402]
  2. National Natural Science Foundation of China [21274064, 21144004, 60876010, 61177029, 20974046]
  3. Program for New Century Excellent Talents in University [NCET-11-0992]
  4. Doctoral Fund of Ministry of Education of China [20133223110007]
  5. Excellent science and technology innovation team of Jiangsu Higher Education Institutions
  6. Natural Science Foundation of Jiangsu Province, China [BK2011761, BK2008053, SJ209003, BM2012010]
  7. Program for Postgraduates Research Innovation in University of Jiangsu Province [CXLX11_0413, CXLX11_0423]
  8. Priority Academic Program Development of Jiangsu Higher Education Institutions, PAPD [YX03001]

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By means of the limited conjugation length, the intrinsic 3-dimensional conformations and the potential nanoporous structures, pi-conjugation-interrupted hyperbranched polymers (CIHPs) were demonstrated as polymer electrets for the application of organic transistor memory devices. As models of CIHPs, PPF and PPF8 were synthesized via Friedel-Crafts C-H polymerization for investigation of the structure-performance relationship according to four-element theory. They exhibited good solubility in organic solvents, excellent thermal stability and film-forming ability. The preliminary as-fabricated transistors showed memory effects with large hysteresis windows and reliable programming/erasing cycles. Furthermore, devices based on PPF exhibited higher mobility, larger ON/OFF ratio and better data retention capability than those based on PPF8. The negative effect of the substitution of alkoxyl groups on the device performance suggests that charge trapping and storage are highly sensitive with electrets' molecular orbital energy levels, vibration relaxation mode, chain aggregates, and surface energy. Soluble organic framework polymers will be potential advanced organic nanomaterials for plastic electronics and mechatronics.

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