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Effect of the Thickness of Insulator Polymeric Films on the Memory Behavior: The Case of the Polymethylmethacrylate and the Polystyrene

DOI: 10.1155/2011/702464

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Abstract:

The effect of thickness variation on the memory behavior of the polymethylmethacrylate-(PMMA)-based devices has been investigated. The PMMA film thicknesses have been varied between 5 to 300?nm, and we have found that the film thickness determines the type of behavior: ohmic, write-once-read-many-times (WORM) memory with two ON states, WORM memory with a negative differential resistance (NDR) region, and WORM memory without NDR region. The fact that similar results were obtained using different solvents to dilute PMMA (chlorobenzene, chloroform, and dimethyl sulfoxide), as well as using an other insulating polymer such as polystyrene (PS), leads to the conclusion that the phenomenon of memory depends on the aluminum electrodes, organic film thickness, and the compliance current used during the electroformation whereas the type of organic layer (PMMA or PS) has minor influence. From here, we conclude that the conductivity switching of the insulator organic film is due to the injection of aluminum particles into the film during the first voltage cycle. 1. Introduction Since the last decade, there has been an intensive research in the field of organic electronics, the organic memory devices being one of the emerging research areas in this field. A considerable number of architectures as well as materials for the development of devices with memory effect has been proposed [1–3]. Among the principal thin-film structures that have been reported are metal-organic insulator-metal (MIM) [4–14], metal–organic–metal–organic–metal [15–17], metal nanoparticles embedded in the organic layer in MIM architecture [18], devices where the embedded metal nanoparticles are replaced with organic particles such as fullerenes [19–21], and carbon nanoshells [22]. From all, the simplest architecture and one of the first to show memory behavior was the MIM architecture. One of the pioneer works was realized by Simmons and Verderber [23], who used a thin film of SiO2 inorganic insulator with a thickness in the order of nanometers between two metallic electrodes. The authors explained this phenomenon as the creation of charge traps in the inorganic film due to an electric field. However, different theories have been proposed in order to explain such phenomena, one of them by Thurstans and Oxley [24] who proposed the effect of electroformation. They mentioned that once a voltage was applied on the device, an electric field was induced and this field moves the metal particles coming from the electrodes into the organic film, where they form metallic islands. These islands are

References

[1]  J. C. Scott and L. D. Bozano, “Nonvolatile memory elements based on organic materials,” Advanced Materials, vol. 19, no. 11, pp. 1452–1463, 2007.
[2]  Q. D. Ling, D. J. Liaw, E. Y. H. Teo et al., “Polymer memories: bistable electrical switching and device performance,” Polymer, vol. 48, no. 18, pp. 5182–5201, 2007.
[3]  Y. Yang, J. Y. Ouyang, L. Ma, R. J. H. Tseng, and C. W. Chu, “Electrical switching and bistability in organic/polymeric thin films and memory devices,” Advanced Functional Materials, vol. 16, no. 8, pp. 1001–1014, 2006.
[4]  D. Tondelier, K. Lmimouni, D. Vuillaume, C. Fery, and G. Haas, “Metal/organic/metal bistable memory devices,” Applied Physics Letters, vol. 85, no. 23, pp. 5763–5765, 2004.
[5]  M. C?lle, M. Büchel, and D. M. de Leeuw, “Switching and filamentary conduction in non-volatile organic memories,” Organic Electronics, vol. 7, no. 5, pp. 305–312, 2006.
[6]  F. Verbakel, S. C. J. Meskers, R. A. J. Janssen et al., “Reproducible resistive switching in nonvolatile organic memories,” Applied Physics Letters, vol. 91, no. 19, Article ID 192103, 2007.
[7]  Y. S. Lai, C. H. Tu, D. L. Kwong, and J. S. Chen, “Bistable resistance switching of poly(N-vinylcarbazole) films for nonvolatile memory applications,” Applied Physics Letters, vol. 87, no. 12, Article ID 122101, pp. 1–3, 2005.
[8]  H. S. Majumdar, A. Bolognesi, and A. J. Pal, “Memory applications of a thiophene-based conjugated polymer: capacitance measurements,” Journal of Physics D, vol. 36, no. 2, pp. 211–215, 2003.
[9]  M. Beinhoff, L. D. Bozano, J. C. Scott, and K. R. Carter, “Design and synthesis of new polymeric materials for organic nonvolatile electrical bistable storage devices: poly(biphenylmethylene)s,” Macromolecules, vol. 38, no. 10, pp. 4147–4156, 2005.
[10]  M. Lauters, B. McCarthy, D. Sarid, and G. E. Jabbour, “Multilevel conductance switching in polymer films,” Applied Physics Letters, vol. 89, no. 1, Article ID 013507, 2006.
[11]  A. R. Elsharkawi and K. C. Kao, “Switching and memory phenomena in anthracene thin films,” Journal of Physics and Chemistry of Solids, vol. 38, no. 1, pp. 95–96, 1977.
[12]  C. H. Tu, Y. S. Lai, and D. L. Kwong, “Memory effect in the current—voltage characteristic of 8-hydroquinoline aluminum salt films,” IEEE Electron Device Letters, vol. 27, no. 5, pp. 354–356, 2006.
[13]  M. Terai, K. Fujita, and T. Tsutsui, “Electrical bistability of organic thin-film device using Ag electrode,” Japanese Journal of Applied Physics, vol. 45, no. 4, pp. 3754–3757, 2006.
[14]  S. Baek, D. Lee, J. Kim, S. H. Hong, O. Kim, and M. Ree, “Novel digital nonvolatile memory devices based on semiconducting polymer thin films,” Advanced Functional Materials, vol. 17, no. 15, pp. 2637–2644, 2007.
[15]  L. P. Ma, J. Liu, and Y. Yang, “Organic electrical bistable devices and rewritable memory cells,” Applied Physics Letters, vol. 80, no. 16, pp. 2997–2999, 2002.
[16]  T. Ouisse and O. Stéphan, “Electrical bistability of polyfluorene devices,” Organic Electronics, vol. 5, no. 5, pp. 251–256, 2004.
[17]  L. D. Bozano, B. W. Kean, V. R. Deline, J. R. Salem, and J. C. Scott, “Mechanism for bistability in organic memory elements,” Applied Physics Letters, vol. 84, no. 4, pp. 607–609, 2004.
[18]  J. Y. Ouyang, C. W. Chu, C. R. Szmanda, L. Ma, and Y. Yang, “Programmable polymer thin film and non-volatile memory device,” Nature Materials, vol. 3, no. 12, pp. 918–922, 2004.
[19]  C. W. Chu, J. Y. Ouyang, J. H. Tseng, and Y. Yang, “Organic donor-acceptor system exhibiting electrical bistability for use in memory devices,” Advanced Materials, vol. 17, no. 11, pp. 1440–1443, 2005.
[20]  J. K. Baral, H. S. Majumdar, A. Laiho et al., “Organic memory using [6,6]-phenyl-C61 butyric acid methyl ester: morphology, thickness and concentration dependence studies,” Nanotechnology, vol. 19, no. 3, Article ID 035203, 2008.
[21]  H. S. Majumdar, J. K. Baral, R. ?sterbacka, O. Ikkala, and H. Stubb, “Fullerene-based bistable devices and associated negative differential resistance effect,” Organic Electronics, vol. 6, no. 4, pp. 188–192, 2005.
[22]  J. A. ávila-Ni?o, E. Segura-Cárdenas, A. O. Sustaita, I. Cruz-Cruz, R. López-Sandoval, and M. Reyes-Reyes, “Nonvolatile write-once-read-many-times memory device with functionalized-nanoshells/PEDOT:PSS nanocomposites,” Materials Science and Engineering B, vol. 176, no. 5, pp. 462–466, 2011.
[23]  G. Simmons and R. R. Verderber, “New conduction and reversible memory phenomena in thin insulating films,” Proceedings The Royal Society A, vol. 301, no. 1464, pp. 77–102, 1967.
[24]  R. E. Thurstans and D. P. Oxley, “The electroformed metal-insulator-metal structure: a comprehensive model,” Journal of Physics D, vol. 35, no. 8, pp. 802–809, 2002.
[25]  H. Carchano, R. Lacoste, and Y. Segui, “Bistable electrical switching in polymer thin films,” Applied Physics Letters, vol. 19, no. 10, pp. 414–415, 1971.
[26]  Y. Segui, B. Ai, and H. Carchano, “Switching in polystyrene films: transition from on to off state,” Journal of Applied Physics, vol. 47, no. 1, pp. 140–143, 1976.
[27]  L. F. Pender and R. J. Fleming, “Memory switching in glow discharge polymerized thin films,” Journal of Applied Physics, vol. 46, no. 8, pp. 3426–3431, 1975.
[28]  W. J. Joo, T. L. Choi, J. Lee et al., “Metal filament growth in electrically conductive polymers for nonvolatile memory application,” Journal of Physical Chemistry B, vol. 110, no. 47, pp. 23812–23816, 2006.
[29]  G. Dearnaley, A. M. Stoneham, and D. V. Morgan, “Electrical phenomena in amorphous oxide films,” Reports on Progress in Physics, vol. 33, no. 3, pp. 1129–1191, 1970.
[30]  S. Pyo, L. Ma, J. He, Q. Xu, Y. Yang, and Y. Gao, “Experimental study on thickness-related electrical characteristics in organic/metal-nanocluster/organic systems,” Journal of Applied Physics, vol. 98, no. 5, Article ID 054303, 6 pages, 2005.
[31]  D. C. Prime, Switching mechanisms, electrical characterization and fabrication of nanoparticle based non-volatile polymer polymer memory devices, Ph.D. thesis, De Montfort University, Leicester, UK, 2010.
[32]  W. L. Kwan, B. Lei, Y. Shao, S. V. Prikhodko, N. Bodzin, and Y. Yang, “Direct observation of localized conduction pathways in photocross-linkable polymer memory,” Journal of Applied Physics, vol. 105, no. 12, Article ID 124516, 2009.

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