Nonvolatile resistive memory devices based on ferrocene‐terminated hyperbranched polyimide derived from different dianhydrides

ABSTRACT A series of ferrocene‐terminated hyperbranched polyimides (HBPI‐Fcs) were synthesized from a tetra‐amine, bis(4‐(3,5‐bis (4‐amino‐2‐(trifluoromethyl) phenoxy) phenoxy) phenyl) methanon, and various dianhydrides, followed by termination with (4‐amino) phenyl ferrocene. All the HBPI‐Fcs posse...

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Veröffentlicht in:Journal of polymer science. Part A, Polymer chemistry Polymer chemistry, 2018-03, Vol.56 (5), p.505-513
Hauptverfasser: Tan, Haiwei, Yu, Huaxuan, Song, Ying, Zhu, Shiyang, Zhang, Bo, Yao, Hongyan, Guan, Shaowei
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Sprache:eng
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Zusammenfassung:ABSTRACT A series of ferrocene‐terminated hyperbranched polyimides (HBPI‐Fcs) were synthesized from a tetra‐amine, bis(4‐(3,5‐bis (4‐amino‐2‐(trifluoromethyl) phenoxy) phenoxy) phenyl) methanon, and various dianhydrides, followed by termination with (4‐amino) phenyl ferrocene. All the HBPI‐Fcs possessed good organo‐solubility and high thermal stability. The devices based on HBPI‐Fcs exhibited bipolar and nonvolatile write‐once‐read‐many times (WORM) memory performance with various threshold voltages and the same ON/OFF current ratio of 104. Moreover, the devices possessed excellent bistability under a constant bias of −1.00 V during a test period of 104 s. The different charge trapping ability of the electron‐accepting moiety endowed the devices with different the threshold voltages. Mechanism analysis showed that the switching behavior was dominated by the charge trapping effect and the charge transfer was well fitted with the space‐current‐limited‐current (SCLC) and ohmic model. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2018, 56, 505–513 A series of ferrocene‐terminated hyperbranched polyimides (HBPI‐Fcs) were synthesized from a tetra‐amine and various dianhydrides and terminated with (4‐amino) phenyl ferrocene. All the memory devices based on HBPI‐Fc exhibited bipolar WORM behavior and the threshold voltage can be tuned by the chemical structure of the dianhydride.
ISSN:0887-624X
1099-0518
DOI:10.1002/pola.28920