Ko Yong-Gi, Kim Dong Min, Kim Kyungtae, Jung Sungmin, Wi Dongwoo, Michinobu Tsuyoshi, Ree Moonhor
Department of Chemistry, Division of Advanced Materials Science, Center for Electro-Photo Behaviors in Advanced Molecular Systems, Pohang Accelerator Laboratory, Polymer Research Institute, and BK School of Molecular Science, Pohang University of Science & Technology (POSTECH) , Pohang 790-784, Republic of Korea.
ACS Appl Mater Interfaces. 2014 Jun 11;6(11):8415-25. doi: 10.1021/am5013134. Epub 2014 May 7.
The fully π-conjugated donor-acceptor hybrid polymers Fl-TPA, Fl-TPA-TCNE, and Fl-TPA-TCNQ, which are composed of fluorene (Fl), triphenylamine (TPA), dimethylphenylamine, alkyne, alkyne-tetracyanoethylene (TCNE) adduct, and alkyne-7,7,8,8-tetracyanoquinodimethane (TCNQ) adduct, were synthesized. These polymers are completely amorphous in the solid film state and thermally stable up to 291-409 °C. Their molecular orbital levels and band gaps vary with their compositions. The TCNE and TCNQ units, despite their electron-acceptor characteristics, were found to enhance the π-conjugation lengths of Fl-TPA-TCNE and Fl-TPA-TCNQ (i.e., to produce red shifts in their absorption spectra and significant reductions in their band gaps). These changes are reflected in the electrical digital memory behavior of the polymers. Moreover, the TCNE and TCNQ units were found to diversify the digital memory modes and to widen the active polymer layer thickness window. In devices with aluminum top and bottom electrodes, the Fl-TPA polymer exhibits stable unipolar permanent memory behavior with high reliability. The Fl-TPA-TCNE and Fl-TPA-TCNQ devices exhibit stable unipolar permanent memory behavior as well as dynamic random access memory behavior with excellent reliability. These polymer devices were found to operate by either hole injection or hole injection along with electron injection, depending on the polymer composition. Overall, this study demonstrated that the incorporation of π-conjugated cyano moieties, which control both the π-conjugation length and electron-accepting power, is a sound approach for the design and synthesis of high-performance digital memory polymers. The TCNE and TCNQ polymers synthesized in this study are highly suitable active materials for the low-cost mass production of high-performance, polarity-free, programmable, volatile, and permanent memory devices that can be operated with very low power consumption, high ON/OFF current ratios, and high reliability.
合成了由芴(Fl)、三苯胺(TPA)、二甲基苯胺、炔烃、炔烃 - 四氰基乙烯(TCNE)加合物和炔烃 - 7,7,8,8 - 四氰基对苯二醌二甲烷(TCNQ)加合物组成的全π共轭供体 - 受体杂化聚合物Fl - TPA、Fl - TPA - TCNE和Fl - TPA - TCNQ。这些聚合物在固体薄膜状态下完全无定形,热稳定性高达291 - 409℃。它们的分子轨道能级和带隙随组成而变化。尽管TCNE和TCNQ单元具有电子受体特性,但发现它们可增强Fl - TPA - TCNE和Fl - TPA - TCNQ的π共轭长度(即导致其吸收光谱发生红移并使其带隙显著减小)。这些变化反映在聚合物的电数字存储行为中。此外,发现TCNE和TCNQ单元使数字存储模式多样化并拓宽了活性聚合物层厚度窗口。在具有铝顶电极和底电极的器件中,Fl - TPA聚合物表现出具有高可靠性的稳定单极永久存储行为。Fl - TPA - TCNE和Fl - TPA - TCNQ器件也表现出稳定的单极永久存储行为以及具有优异可靠性的动态随机存取存储行为。发现这些聚合物器件根据聚合物组成通过空穴注入或空穴注入与电子注入一起操作。总体而言,本研究表明,引入控制π共轭长度和电子接受能力的π共轭氰基部分是设计和合成高性能数字存储聚合物的合理方法。本研究中合成的TCNE和TCNQ聚合物是低成本大规模生产高性能、无极性、可编程、易失性和永久性存储器件的高度合适的活性材料,这些器件可在非常低的功耗、高开关电流比和高可靠性下运行。