Binary/ternary memory behavior of organo-solubility polyimides containing flexible imide linkages and pendent triphenylamine or 3, 4, 5-trifluobenzene moieties. (15th February 2020)
- Record Type:
- Journal Article
- Title:
- Binary/ternary memory behavior of organo-solubility polyimides containing flexible imide linkages and pendent triphenylamine or 3, 4, 5-trifluobenzene moieties. (15th February 2020)
- Main Title:
- Binary/ternary memory behavior of organo-solubility polyimides containing flexible imide linkages and pendent triphenylamine or 3, 4, 5-trifluobenzene moieties
- Authors:
- Ye, Qingqing
Zhang, Baozhong
Yang, Yanhua
Hu, Xiaoyu
Shen, Yingzhong - Abstract:
- Graphical abstract: Two novel aromatic diamines containing flexible imide linkages were synthesized via a Suzuki coupling reaction. Then the four corresponding functional polyimides (PI-a, PI-b, PI-c, and PI-d) were prepared. The devices of PI-a and PI-b displayed non-volatile binary WORM and Flash behaviors with turn-on voltages of −1.13 V and −1.54 V, respectively. However, the PI-c-based and PI-d-based devices showed non-volatile ternary WORM and Flash behaviors with turn-on voltages of −0.77 V, as well as −1.77 V, respectively. Highlights: Two novel aromatic diamine containing flexible imide linkages moiety and different substituent moieties were synthesized via Suzuki coupling reaction. Four functional polyimides were prepared by chemical imidization. The memory devices based on these polyimides exhibited binary and ternary memory behaviors, respectively. Abstract: Two different aromatic diamines monomers (3, 5-diamino-N-(4'-phenyl-4''-triphenylamino)-N-(4''-benzyl-4'''-triphenylamino)benzamide (DPTBTB) and 3, 5-diamino-N-(4'-3'', 4'', 5''-trifluorobiphenyl)-N-(4''-benzyl-3''', 4''', 5'''-trifluorophenyl)benzamide (DTBTB)) containing flexible linkages were designed and synthesized, respectively. Four organo-solubility polyimides (PI-a, PI-b, PI-c, and PI-d) were prepared via a two-step procedure with pyromellitic dianhydride (PMDA) and 3, 3', 4, 4'-biphenyltetracarboxylic dianhydride (BPDA), respectively. The four PIs performed excellent thermal stability with theGraphical abstract: Two novel aromatic diamines containing flexible imide linkages were synthesized via a Suzuki coupling reaction. Then the four corresponding functional polyimides (PI-a, PI-b, PI-c, and PI-d) were prepared. The devices of PI-a and PI-b displayed non-volatile binary WORM and Flash behaviors with turn-on voltages of −1.13 V and −1.54 V, respectively. However, the PI-c-based and PI-d-based devices showed non-volatile ternary WORM and Flash behaviors with turn-on voltages of −0.77 V, as well as −1.77 V, respectively. Highlights: Two novel aromatic diamine containing flexible imide linkages moiety and different substituent moieties were synthesized via Suzuki coupling reaction. Four functional polyimides were prepared by chemical imidization. The memory devices based on these polyimides exhibited binary and ternary memory behaviors, respectively. Abstract: Two different aromatic diamines monomers (3, 5-diamino-N-(4'-phenyl-4''-triphenylamino)-N-(4''-benzyl-4'''-triphenylamino)benzamide (DPTBTB) and 3, 5-diamino-N-(4'-3'', 4'', 5''-trifluorobiphenyl)-N-(4''-benzyl-3''', 4''', 5'''-trifluorophenyl)benzamide (DTBTB)) containing flexible linkages were designed and synthesized, respectively. Four organo-solubility polyimides (PI-a, PI-b, PI-c, and PI-d) were prepared via a two-step procedure with pyromellitic dianhydride (PMDA) and 3, 3', 4, 4'-biphenyltetracarboxylic dianhydride (BPDA), respectively. The four PIs performed excellent thermal stability with the temperature of 5% weight loss in range of 370–420 ℃ at N2 atmosphere. The Al/PI-a/ITO and Al/PI-b/ITO memory devices exhibited binary write-once-many-read (WORM) and rewritable (Flash) behavior, respectively. But the Al/PI-c/ITO and Al/PI-d/ITO memory devices showed ternary WORM and Flash behavior due to the deeper charge traps came from the fluorinated groups in the structure of PI-c and PI-d, respectively. The memory switching mechanism could be demonstrated through molecular simulation. The results gave an effective strategy that adjusting the structure of PI to achieve different memory effects. … (more)
- Is Part Of:
- European polymer journal. Volume 125(2020)
- Journal:
- European polymer journal
- Issue:
- Volume 125(2020)
- Issue Display:
- Volume 125, Issue 2020 (2020)
- Year:
- 2020
- Volume:
- 125
- Issue:
- 2020
- Issue Sort Value:
- 2020-0125-2020-0000
- Page Start:
- Page End:
- Publication Date:
- 2020-02-15
- Subjects:
- Organo-solubility polyimides -- Memory device -- Binary/ternary behaviors
Polymers -- Periodicals
Polymerization -- Periodicals
Polymères -- Périodiques
Polymérisation -- Périodiques
Polymerization
Polymers
Periodicals
Electronic journals
547.705 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00143057 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.eurpolymj.2020.109473 ↗
- Languages:
- English
- ISSNs:
- 0014-3057
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3829.791000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 12737.xml