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Novel Oxide Thin Film Transistors for Transparent AMOLED

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25-3 / D.-H. Cho

IMID/IDMC/ASIA DISPLAY ‘08 DIGEST •

Abstract

We have fabricated the transparent TFTs using new oxide material (AZTO: Al-doped zinc tin oxide) as an active layer. The AZTO TFT showed good performance without post-annealing. The electrical characteristics were improved by the post-annealing up to 300. The AZTO TFTs exhibited a mobility of 8~12 cm2/Vs, a sub- threshold swing of 0.2~0.6 V/dec, and an on/off ratio of more than 109.

1. Introduction

Flexible displays based on organic light emitting diodes (OLED) have attracted interests because they are considered to create new applications of electronics. The reliable transparent TFT array showing good electrical performance is indispensable and it should be manufactured at low temperature for the flexible displays which are commercially available.

In recent time, the flat panel display televisions demand high resolution, large size, fast response, and low power consumption. As the display size and resolution increases, the TFT back-plane with good uniformity, low cost and high stability is required.[1]

Conventional a-Si (amorphous silicon) TFT can be fabricated with high uniformity and low cost, however, its mobility and bias stability are poor. LTPS (low temperature poly silicon) TFT has disadvantages for large size production due to relatively poor uniformity and high cost.[2] For these reasons, oxide TFTs are considered as prominent candidate for the driving device of AMOLED.[3] The transparent oxide TFTs using ZnO[4], In-Zn-O[5-6], Zn-Sn-O[7-8] and IGZO[9-10]

as an active channel material have been widely studied. Most oxide TFT is required high temperature (>200oC) processing to represent a good electrical performance. Several studies concerning about the oxide TFT processed at low temperature (<150oC) were reported, however the electrical performances were relatively poor.[11] In order to use plastic

substrates for flexible displays, the processing temperature lower than 180oC for all manufacturing process is desirable.

2. Experimental

We have fabricated the inverse co-planar type bottom gate TFTs with the AZTO active layer sputtered at room temperature. Sputtering method has advantages on low cost and large area uniformity among various deposition methods. The active material was composed of Al2O3-ZnO-SnO2. The schematic diagram of the AZTO TFT structure is shown in figure 1. A 100x100 mm2 alkaline-free glass

Fig. 1. Schematic diagram of bottom gate AZTO TFT structure

was used as a substrate after the ultrasonic cleaning with acetone, iso-propyl alcohol and DI water in sequence. Gate and source/drain electrodes were constituted with 150 nm thick ITO. A gate insulator of Al2O3 was formed by atomic layer deposition (ALD) method at 150ଇ and its thickness was 185 nm. An AZTO layer was formed by co- sputtering of an AlOx-ZnO (AlOx 2 wt%) target and a SnO2 target (ANP Co.) with an off-axis type RF magnetron sputter at room temperature. The sputtering was performed in the atmosphere of Ar and O2 mixed gas with the chamber pressure of 0.2 Pa. All patterning processes were performed with photo-

Novel Oxide Thin Film Transistors for Transparent AMOLED

Doo-Hee Cho, Shinhyuk Yang, Chunwon Byun, Jeong Ik Lee, Chi-Sun Hwang, Sang-Hee Ko Park, Hye-Yong Chu, and Kyoung Ik Cho

Transparent Electronics Team, ETRI, Daejeon 305-350, Korea TEL:82-2-860-6035, e-mail:chodh@etri.re.kr.

Keywords : oxide, TFT, transparent, OLED

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25-3 / D.-H. Cho

• IMID/IDMC/ASIA DISPLAY ‘08 DIGEST

lithographic method and wet etching process. The post-annealing was performed in vacuum using electric ovens. The electrical characteristics of the TFTs were measured with the semiconductor parameter analyzer (Agilent B1500A). X-ray diffraction (XRD) spectra of the AZTO films were recorded with a Rigaku RU-200BH diffractometer XVLQJ &X.Į UDGLDWLRQ The chemical composition of AZTO thin film was analyzed by Auger electron spectroscopy method.

3. Results and discussion

The AZTO thin film deposited by RF magnetron sputtering at room temperature was amorphous.

Figure 2 shows XRD spectra of AZTO thin films having composition of about 4 mol% AlOx, 66 mol%

ZnO, and 30 mol% SnO2 before and after annealing at 300oC for 1 hour. There was no diffraction peak of crystalline phase in the XRD spectra even after the 300oC annealing. Thus, the AZTO active layers on the TFTs were considered as very stable amorphous oxide material. Amorphous oxide active layer has an advantage on large area uniformity and long-term reliability because it has no grain boundary.[10]

Fig. 2. XRD spectra of AZTO thin film deposited at room temperature (upper) and annealed at 300oC (lower)

Figure 3 shows the transfer characteristics of the

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layer deposited at room temperature before annealing and after 150oC and 180oC annealing in vacuum.

There was no heat treatment on the active layer before annealing because the active layer is deposited in the final process. The AZTO TFT showed the field effect mobilit\ ȝFET) of 1.9 cm2/Vs, the turn-on voltage (Von) of near -1.0 V, the on-off current ratio (Ion/Ioff) of more than 107 before annealing. The sub-threshold swing (S/S) was relatively large and the off-current level was under 10-12 A. The 150oC annealed TFT H[KLELWHGWKHȝFET of 6.2 cm2/Vs, the Von of 0.9 V, the Ion/Ioff of about 109, and the S/S of 0.60 V/dec. The 180o&DQQHDOHG7)7H[KLELWHGWKHȝFET of 10.1 cm2/Vs, the Von of 0.9 V, the Ion/Ioff of more than 109, and the S/S of 0.58 V/dec. It can be seen that the mobility increased with increase of annealing temperature. The sub-threshold swing and the on-off current ratio were sufficiently good for the application to active matrix displays just by post-annealing at 150oC. The turn-on voltage shifted to near 0 V by the low temperature annealing.

Fig. 3. Transfer characteristics of AZTO TFT without heat treatment, annealed at 150oC, and 180oC in vacuum for 1 hr.

Figure 4 shows the transfer characteristics of the bottom gate AZTO TFT (W/L ȝPȝP ZKLFK

is composed of about 5 mol% of AlOx, 79 mol% of ZnO, and 16 mol% of SnO2 with and without passivation layer. The passivation was performed with poly-imide polymer by spin coating and baking method. The turn-on voltage was shifted by gate bias field before the passivation as shown in figure 4. The turn-on voltage shift and the sub-threshold swing were reduced by the poly-imide passivation. The field effect mobility was not degraded by the passivation.

The mobility changes with SnO2 content are shown

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25-3 / D.-H. Cho

IMID/IDMC/ASIA DISPLAY ‘08 DIGEST • in figure 5. The mobilities in figure 5 were measured

for the AZTO TFTs with the composition of xSn(1- x)(Al0.06Zn0.94)Oy. The mobility increased with SnO2

content. The mobility change was large until 16 mol%

of SnO2, from then, the mobility increment became slowdown. Below 10 mol% of SnO2, the AZTO thin films did not show the field effect transistor characteristics.

Fig. 4. Transfer characteristics of non-passivated AZTO TFT annealed at 180oC in vacuum and poly-imide passivated AZTO TFT

Fig. 5. The field effect mobility change of AZTO TFTs with SnO2 content in AZTO active layer

The AZTO TFTs with bottom gate structure showed good electrical characteristics, however, they had relatively poor stability and showed hysteresis between up and down transfer curve. Figure 6 shows the transfer curve shift under the +20 V gate bias stresses for the 250oC annealed bottom gate AZTO TFT. The gate bias stress experiments were carried out in order to examine bias stabilities of the non- passivated AZTO TFT with the bottom gate structure.

The turn-on voltage of the bottom gate TFT shifted by 7.5 V for 3 hours. The turn-on voltage of the AZTO TFT significantly shifted to positive side with positive gate bias. It can be thought that the main origin of the gate bias instability is the charge trapping at the gate insulator-active channel interface. A number of charge trapping sites are supposed to be near the gate insulator-active channel interface even after the post- annealing due to the surface damage of the gate insulators during the active layer sputtering.

Therefore, we fabricated the top gate structured AZTO TFT with the same composition of active layer to the bottom gate TFT. Figure 7 shows the turn-on voltage shift under the +20 V gate bias for the 300oC annealed top gate AZTO TFT. The turn-on voltage of the top gate TFT shifted by just 0.2 V for 14 hours.

The gate bias stability was remarkably improved in the top gate structure. It is thought that the gate insulator-active interface was scarcely damaged due to the ALD process of the gate insulator.

Fig. 6. Transfer curve shift of the bottom gate AZTO TFT under the +20V gate bias voltage

Fig. 7. Transfer curve shift of the top gate AZTO TFT under the +20V gate bias voltage

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25-3 / D.-H. Cho

• IMID/IDMC/ASIA DISPLAY ‘08 DIGEST

Amorphous oxides composed of heavy-metal cations show high electron mobilities because heavy- PHWDO FDWLRQ QV Q•  RUELWDOV ZLWK VSKHULFDO

symmetry overlap between adjacent orbitals and lead conduction band dispersion.[7, 12] In our AZTO thin film, Sn4+ is supposed to control the field effect mobility as seen from figure 6. Al3+ is not heavy-metal ion, thus, the addition of AlOx is considered not to enhance the electron transport. However, the AZTO TFTs showed relatively good mobility without high temperature annealing, while Zn-Sn-O(ZTO) TFT prepared by the same process to the AZTO TFT did not show the transistor characteristics. The active layer of the ZTO TFT was prepared with the same sputtering condition to the AZTO thin film except the target change from Al2O3-ZnO to ZnO. The electron transport properties of the as-deposited films fabricated at the inadequate condition are known to be improved by thermal annealing to a level which is almost the same as that in the films deposited at the optimized condition.[13] It is considered that the addition of AlOx enhanced the electrical properties of active layer near to those of optimized condition even by the room temperature sputtering.

We have manufactured the AMOLED panel using the AZTO TFT back-plane as shown in figure 8. The AMOLED panel size was 2.5 inch and its resolution QCIF+ (176 X 220, MONO).

Fig. 7. AMOLED panel using the AZTO TFT back-plane

4. Summary

We have manufactured the AMOLED panel with the new oxide TFT back-plane composed of the AZTO active layer which was deposited at room temperature and annealed at low temperature. The room temperature deposition and the low temperature process are significant advantages for the fabrication

of flexible electronics. The AZTO layer was deposited by sputtering which is convenient for large size commercial production so that the AZTO TFT is considered to be a prominent candidate for the driving device of large size flexible displays.

5. References

1. J.-H. Lee, D.-H. Kim, D.-J. Yang, S.-Y. Hong, K.-S.

Yoon, P.-S. Hong, C.-O. Jeong, H.-S. Park, S. Y.

Kim, S. K. Lim, S. S. Kim, K.-S. Son, T.-S. Kim, J.-Y. Kwon, S.-Y. Lee, SID 08 Digest, p.625 (2008).

2. K.-S. Son, T.-S. Kim, J.-S. Jung, M.-K. Ryu, K.-B.

Park, B.-W. Yoo, J.-W. Kim, Y.-G. Lee, J.-Y. Kwon, S.-Y. Lee, and J.-M. Kim, SID 08 Digest, p.633 (2008).

3. M. Kim, J. H. Jeong, H. J. Lee, T. K. Ahn, H. S.

Shin, J.-S. Park, J. K. Jeong, Y.-G. Mo, and H. D.

Kim, Appl. Phys. Lett. 90, 212114 (2007)

4. E. Fortunato, P. Barquinha, A. Pimentel, A.

Gonsalves, A. Marques, L. Pereira, and R. Martins, Adv. Mater. 17, 590 (2005).

5. P. Barquinha, A. Pimentel, A. Marques, L. Pereira, R. Martins, and E. Fortunato, J. Non-Cryst. Solids 352, 1749 (2006).

6. J.-I. Song, J.-S. Park, H. Kim, Y.-W. Heo, J.-H. Lee, J.-J. Kim, G. M. Kim, B. D. Choi, Appl. Phys. Lett.

90, 022106 (2007).

7. H. Q. Chiang, J. F. Wager, R. L. Hoffman, J. Jeong, and D. A. Keszler, Appl. Phys. Lett. 86, 013503 (2005).

8. W.B. Jackson, G.S. Herman, R.L. Hoffman, C.

Taussig, S. Braymen, F. Jeffery, J. Hauschildt, J.

Non-Cryst. Solids 352, 1753 (2006).

9. Y. Park, C. J. Kim, S. I. Kim, I. Song, J. C. Park, H.

/LP6:.LP(/HH,':¶'LJHVWAMD9-1, p.1775 (2007)

10. K. Nomura, A. Takagi, T. Kamiya, H. Ohta, M.

Hirano, and H. Hosono, Jpn. Appl. Phys. 45, 4303 (2006).

11. P. F. Carcia, R. S. McLean, M. H. Reilly, and G.

Nunes, Jr., Appl. Phys. Lett. 82, 1117 (2003).

12. H. Hosono, J. Non-Cryst. Solids 352, 851 (2006).

13. H. Hosono, K. Nomura, Y. Ogo, T. Uruga, T.

Kamiya, J. Non-Cryst. Solids 354 ,2796 (2008)

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