• 沒有找到結果。

用不同材料修飾改變基板表面特性,由X 光晶格繞射來判定五環素在排列上 並無相變化的產生,但在電性上則有明顯的變化。以電流電壓曲線和電容電壓曲 線互相比較,發現電晶體開啟順序和電荷開始累積的順序是ㄧ樣的,但是數值上 的差異是很明顯的,為了更了解這差異的來源,可使用儀器和引入模型來幫助分 析。

先利用電容的特性曲線計算被捕陷電量。為了分析捕捉陷阱的來源,我們分 為晶粒內部和晶粒邊界(grain boundary)兩部份來探討。晶粒內部可利用X光晶格 繞射的強度來觀察排列的情況,發現強度越強排列越整齊的,捕捉的載子是最少 的。而晶粒邊界必須分成兩個部份討論,X-Y平面與Z軸方向。X-Y平面則是先使 用原子力顯微鏡掃描五環素的表面形貌,之後利用MATLAB程式分析邊界長度,

五環素的厚度有100 Å與 600 Å,由程式分析的結果發現不同厚度可得到相同的 趨勢,邊界長度越長的元件,會越慢開啟;而Z軸方向晶粒有 300 Å,所以Z方向 的晶粒邊界陷阱捕捉是可以忽略的。緊接著利用接觸角量測經修飾之後的表面 能,推測五環素成長的模型。五環素的表面能比PVP和SiNx小,所以會形成層狀 結構,晶粒較大,邊界長度較短;而PMMA和HMDS修飾後表面的表面能比五環 素小,形成島狀結構,晶粒較小,邊界長度較長。邊界長度越長的元件,會使得 載子在傳輸時容易被陷阱捕捉,元件會較慢開啟;反之,邊界長度短的元件,載 子傳輸時不易被捕捉,元件開啟的時間就會較早。

元件經過不同材料修飾後改變整體捕捉陷阱密度,主要是因為五環素排列整 齊度與晶粒邊界多寡,造成元件特性的差異。元件開啟電壓主要是晶粒邊界多寡 決定,由此可知如果想要做出可調變的元件,可以利用不同材料的修飾層來調變 Vto

[參考文獻]

[1] G. Horowitz, “Organic Thin Film Transistors: From Theory to Real Devices”, J.

Mat. Res. 19, pp. 1946, 2004.

[2] T. Dobbertin, M. Kroeger, D. Heithecker, D. Schneider, D. Metzdorf, H. Neuner, E.

Becker, H.-H. Johannes, and W. Kowalsky, “Inverted Top-Emitting Organic Diodes Using Sputter-Deposited Anodes ”, Appl. Phys. Lett. 82, pp. 284, 2003.

[3] C. J. Brabec, N. S. Sariciftci, and J. C. Hummelen, “Plastic Solar Cells”, Adv.

Funct. Mater. 11, pp. 15, 2001.

[4] K. Nomoto, N. Hirai, N. Yoneya, N. Kawashima, M. Noda, M. Wada, and J.

Kasahara, “A High-Performance Short-Channel Bottom-Contact OTFT and Its Application to AM-TN-LCD”, IEEE T. Electron Dev. 52, pp. 1519, 2005.

[5] L. Zhou, S. Park, B. Bai, J. Sun, S. C. Wu, T. N. Jackson, S. Nelson, D. Freeman, and Y. Hong, “Pentacene TFT Driven AM OLED Displays”, IEEE Electron Device Letter. 26, pp.640, 2005.

[6] V. Subramanian, J. M. J. Frechent, P. C. Chang, and S. K. Volkman, ” Progress Toward Development of All-Printed RFID Tags: Materials, Processes, and Devices”, Proceeding Of The IEEE, 93, pp.1330, 2005.

[7] Zheng-Tao Zhu, Jeffery T. Mason, Rudiger Dieckmann, and George G. Malliaras,

“Humidity Sensors Based on Pentacene Thin-Film Transistors”, Appl. Phys. Lett.

21, pp.4643, 2002.

[8] F. Ebisawa, T. Kurokawa, and S. Nara, “Electrical Properties of Polyacetylene/Polysiloxane Interface”, J. Appl. Phys. 54, pp.3255, 1983.

[9] A. Tsumura, H. Koezuka, and T. Ando, ”Macromolecular electronic device : Field-Effect Transistors with a Polythiophene Thin Film”, Appl. Phys. Lett. 49, pp.

1210, 1986.

[10] A. Assadi, C. Svensson, M. Willander, and O. Inganas, “Field-Effect Mobility of Poly(3-hexylthiophene)”, Appl. Phys. Lett. 53, pp.195, 1988.

[11]F. Garnier, G. Horowitz, X. Z. Peng, D. Fichou. Adv. Mater. 2, pp. 592-594, 1990.

[12] G. Horowitz, X. Z. Peng, D. Fichou, and F. Garnier, “Role of Semiconductor/insulator Interface in the Characteristics of -Conjugated-Oligomer-Based Thin-Film Transistors”, Syn. Met. 51, pp.419, 1992.

[13] Y.-Y. Lin, D. J. Gundlach, S. F. Nelson, and T. N. Jackson, “Stacked Pentacene Organic Thin-Film Transistors with Improved Characteristics”, IEEE Electron Device Letters, 18, pp.606, 1997.

[14] M. P. Hong, B. S. Kim, Y. U. Lee, K. K. Song, J. H. Oh, J. H. Kim, T. Y. Choi, M.

S. Ryu, and K. Chung, S. Y. Lee, B. W. Koo, J. H. Shin, E. J. Jeong, and L. S. Pu,

“Recent Process in Large Sized & High Performance Organic TFT Array”, SID 05 DIGEST, 23, 2005.

[15]Oana D. Jurchescu, Jacob Baas, and Thomas T. M. Palstra, Appl. Phys. Lett. 84, pp. 3061, 2004.

[16] A.Tsumura, H. Koezuka, T. Ando, Appl. Phys. Lett. 49, pp. 1210, 1986.

[17] A.Assadi, C. Svensson, M. Willander, O. Ingans, Appl. Phys. Lett. 1988.

[18] J. Paloheimo, E. Punkka, H. Stubb, P.Kuivalainen, in Lower Dimensional Systems and Molecular Devices, Proceedings of NATO ASI, Spetses, Greece (Ed:

R. M. Mertzger), Plenum, New York, 1989.

[19] Z. Bao, A. Dodabalapur, A. J. Lovinger, Appl. Phys. Lett. 69, pp. 4108, 1996.

[20] H. Sirringhaus, N. Tessler, R. H. Friend, Science, 280, pp. 1741, 1998.

[21] F. Ebisawa, T. Kurokawa, S. Nara, J. Appl. Phys., 54, pp. 3255, 1983.

[22] J. H. Burroughes, C. A. Jones, R. H. Friend, Nature, 335, pp. 137, 1988.

[23] G. M. Wang, J. Swensen, D. Moses, and A. J. Heeger, “Increased mobility from regioregular poly (3-hexylthiophene) field-effect transistors”, J. Appl. Phys, 93, pp

6137, 2003.

[24] R. Hajlaoui, G. Horowitz, F. Garnier, A. Arce-Brouchet, L. Laigre, A. Elkassmi, F. Demanze, F. Kouki, Adv. Mater. 9, pp. 389, 1997.

[25] J. H. Schn, C. Kloc, B. Batlogg, Org. Electron., 1, pp. 57, 2000.

[26] Y. Y. Lin, D. J. Gundlach, S. Nelson, T. N. Lett., 18, pp. 606, 1997.

[27] C. D. Dimitrakopoulos, A. R. Brown, A. Pomp, J. Appl. Phys., 80, pp. 2501, 1996.

[28] Y. Y. Lin, D. J. Gundlach, T. N. Jackson, 54th Annual Device Research Conference Digest 1996, p.80. 1991.

[29] G. Horowitz, X. Peng, D. Fichou, F. Garnier, Synth. Met., 51, pp. 419, 1992.

[30] R. C. Haddon, A. S. Perel, R. C. Morris, T. T. M. Palstra, A. F. Hebard, R. M.

Fleming, Appl. Phys. Lett., 67, pp. 121, 1995.

[31] J. Kastner, J. Paloheimo, H. Kuzmany, in Solid State Sciences(Eds:H. Huzmany, M. Mehring, J. Fink), Springer, New York, pp. 515-521, 1993.

[32] G. Guillaud, M. Al Sadound, M. Maitrot, Chem. Phys. Lett., 167, pp. 503, 1990.

[33] Z. Bao, A. J. Lovinger, J. Brown, J. Am. Chem. Soc., 120, pp. 207, 1998.

[34] H. Fuchigami, A. Tsumura, H. Koezuka, Appl. Phys. Lett., 63, pp. 1372, 1993.

[35] A. R. Brown, D. M. de Leeuw, E. J. Lous, E. E. Havinga, Synth. Met., 66, pp. 257, 1994.

[36] G. Horowitz, “Organic Field-Effect Transistors”, Adv. Mater. 10, pp. 365, 1998.

[37] R. B. Campbell, J. Monteath Robertson, and J. Trotter, “The crystal and molecular structure of pentacene” ,Acta Cryst. 14, pp.705, 1961.

[38] L. Sebastian, G. Weiser, and H. Bassler, “Charge transfer transitions in solid tetracene and pentacene studied by electroabsorption”, Chemical Physics, 61, pp 125-135, 1981.

[39] E. M. Suuberg, J. Chem. Eng. Data, 43, pp. 486–492, 1998.

[40] D. Knipp,a) R. A. Street,b) A. Vo¨ lkel, and J. Ho, J. Appl. Phys., vol. 93, pp. 347, 2003.

[41] Christine C. Mattheus, Anne B. Dros, Jacob Baas, Auke Meetsma, Jan L. de Boer and Thomas T. M. Palstra, “Polymorphism in pentacene”, Acta Cryst. C57, pp.939 2001.

[42] Christine C. Mattheus, Gilles A. de Wijs, Robert A. de Groot, and Thomas T. M.

Palstra, “Modeling the polymorphism of pentacene”, J. Am. Chem. Soc. 125, pp.

6323, 2003.

[43] C. D. Dimitrakopoulos, and P. L. Malenfant, “Organic Thin Film Transistors for Large Area Electronics”, Adv. Mater. 14, pp.99, 2002.

[44] D. A. Neamen, “Semiconductor Physics and Devices :Basic Principles”, 3rd, McGraw-Hill, 2003.

[45]M. A. Lampert, Physical Review, 103, pp. 1648-1656, 1956.

[46]D. K. Schroder, “Semiconductor Material and Device Characterization”, (Wiley-Interscience, New York, 1998)

[47] A. Wang, I. Kymissis, V. Bulović, and A. I. Akintunde, “Tunable threshold voltage and flatband voltage in pentacene field effect transistors”, Appl. Phys. Lett. 89, pp.

112109, (2006).

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