We have developed an optimized deposition condition for sol-gel ZrZnO semiconductor film and succeeded to fabricate a ZrZnO-based transparent thin film transistor with bottom-gate structure. The optimal conditions for depositing the ZrZnO film by spin coater are at room temperature and deposit two layers, each layer is baked on the hotplate at 300°C for 60 minutes. After film deposition, devices are taken one curing step under oxygen ambience at 350°C for 60 minutes. With the development of wet etchants, active regions can be patterned accurately.
We solve the time dependent behaviors of devices and light illumination effect by adding post annealing treatment under nitrogen ambience at 350°C to complete device fabrication. Besides, the oxygen adsorption theory successfully explained the mechanisms of light illumination effect and oxygen pressure effect. ZnO, ZTO and IZO are also discussed to replace the active channel layer in this thesis. Devices with IZO active layer have the best performance, which can compete with traditional a-si TFTs. We also make some measurements to test electrical stability of devices, such as light illumination, oxygen pressure, and bias stress. At last, we successfully demonstrated sol-gel derived ZnO and ZrZnO and IZO based TFTs on glass substrate by spin-on deposition at low temperature. For large area flat-panel display fabrication in the future, the chemical solution deposition process provides a low cost and more efficient way for depositing devices than vacuum deposition techniques.
Reference
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Fig1-1 The wurtzite lattice structure of zinc oxide: small circles represent
zinc atoms, the large circles are oxygen atoms.Fig2-1 The device structure of thin film transistor
VG(V)
Fig2-2 Transfer characteristics of ZrZnO TFTs that are fabricated by
“Standard Manufacturing Processes”
Fig2-3 Time dependent transfer characteristics of ZrZnO TFTs that are
fabricated by “Standard Manufacturing Processes”Fig3-1 Lennard-Jones Model of physisorption and chemisorption; (a)
phtsisorption of a molecule, (b) chemisorption, where at d=∞, enough energy has been introduced to dissociate the moleculeVG-ID (VD=21V)
VG(V)
-60 -40 -20 0 20 40 60 80
ID(A)
10-13 10-12 10-11 10-10 10-9 10-8 10-7 10-6 10-5
10 mins 30 mins 60 mins STD
Fig3-2 Transfer characteristics of ZrZnO TFTs that are annealed under
oxygen ambience with various timeVG-ID (VD=21V)
Fig3-3 Time dependent transfer characteristics of ZrZnO TFTs that are
annealed under oxygen ambience for 60 minutesVG-ID (VD=21V)
Fig3-4 Transfer characteristics of ZrZnO TFTs that are annealed in
VG(V)
Fig3-5 Time dependent transfer characteristics of ZrZnO TFTs that are
annealed in vacuum for 10minutesVG-ID (VD=21V)
Fig3-6 Transfer characteristics of ZrZnO TFTs that are annealed under
nitrogen ambience with various timeVG(V)
Fig3-7 Time independent transfer characteristics of ZrZnO TFTs that are
annealed under nitrogen ambience for 10 minutesVG-ID (VD=21V)
Fig3-8 Transfer characteristics of ZrZnO TFTs with various baking time
VG-ID (VD=21V)
Fig3-9 Transfer characteristics of ZrZnO TFTs which suffer seriously
Drain Induced Barrier Lowering effect (DIBL)VG-ID (VD=21V)
Fig3-10 Transfer characteristics of ZrZnO TFTs with HMDS coating
baked for various timeVG-ID (VD=21V)
Fig3-11 Transfer characteristics of ZrZnO TFTs that are baked for 10
minutes with or without HMDS coatingVG-ID (VD=21V)
Fig3-12 Transfer characteristics of ZrZnO TFTs that are baked for 30
minutes with or without HMDS coatingVG-ID (VD=21V)
Fig3-13 Transfer characteristics of ZrZnO TFTs that are baked for 60
minutes with or without HMDS coatingu/u0 vs Baking Tim e
Mobility Changing Ratio (u/u o)
uo: Before HMDS coating u : After HM DS coating
10m ins 30mins 60mins
Fig3-14 Mobility changing ratio with various baking time
VG-ID (VD=21V)
Fig3-15 Transfer characteristics of ZrZnO TFTs with different numbers
of active layersFig3-16 Transfer characteristics of ZrZnO TFTs that are treated with RTA
under NH3 ambienceVG-ID (VD=21V)
Fig3-17 Transfer characteristics of ZrZnO TFTs that are treated with RTA
under Ar ambienceFig3-18 Transfer characteristics of ZrZnO TFTs before and after SiOx
passivationVG-ID of SiNx Passivation (VD=21V)
Fig3-19 Transfer characteristics of ZrZnO TFTs before and after SiNx
passivationFig3-20 Transfer characteristics of ZrZnO TFTs before and after PC403
passivationVG-ID of ZrZnO TFT
Fig3-21 Transfer characteristics of ZrZnO TFTs that are fabricated by the
optimal conditionsVD-ID of ZrZnO TFT
VG-ID of ZnO TFT
Fig3-23 Transfer characteristics of ZnO TFTs that are fabricated by the
optimal conditions acquired from ZrZnO TFTsVD-ID of ZnO TFT
Fig3-24 I
D-VD of ZnO TFTs that are fabricated by the optimal conditions acquired from ZrZnO TFTsVG-ID of ZTO TFT
Fig3-25 Transfer characteristics of ZTO TFTs
VD-ID of ZTO TFT
VG-ID of IZO TFT
Fig3-27 Transfer characteristics of IZO TFTs
VD-ID of IZO TFT
VG-ID (VD=21V)
Fig4-1 Transfer characteristics of ZrZnO TFTs with light illumination
and hold for 15 minute in dark environmentVG-ID (VD=21V)
Fig4-2 Transfer characteristics of ZrZnO TFTs that are annealed under
nitrogen with light illumination and hold for 1 minute in dark environmentFig4-3 Physical model of oxygen effect on the conductance of ZnO film
and the interaction with lightVG-ID (VD=21V)
VG(V)
-40 -20 0 20 40 60
ID(A)
10-14 10-13 10-12 10-11 10-10 10-9 10-8 10-7 10-6
10-5 1 torr
10 torr 100 torr 760 torr
Fig4-4 Transfer characteristics of ZTO TFTs that are measured under
different oxygen pressureFig4-5 Transfer characteristics of IGZO TFTs that are measured under
different oxygen pressureVG-ID (VD=21V)
VG(V)
-60 -40 -20 0 20 40 60 80
10-14 10-13 10-12 10-11 10-10 10-9 10-8 10-7 10-6 10-5 10-4 10-3
ID(A)
1 torr 10 torr 100 torr 760 torr
Fig4-6 Transfer characteristics of ZTO TFTs with light illumination that
are measured under different oxygen pressureVG-ID (VD=1V)
Fig4-7 Transfer characteristics of ZrZnO TFTs under gate bias stress for
1000s and after relax for 1000s at room pressureVG-ID (VD=1V)
Fig4-8 Transfer characteristics of ZrZnO TFTs under gate bias stress for
1000s and after relax for 1000s in vacuumTable2-1 Experiment flow of in this experiment
Table2-2 Experiment flow of sol-gel precursor preparation
Table2-3 Experiment flow of various ambience and treatment time
Table2-4 Experiment flow of various numbers of active channel layer
Table2-5 Experiment flow of various baking time and with or w/o HMDS
coatingTable2-6 Experiment flow of various RTA and passivation processes
Table3-1 The characteristics of physisorption and chemisorption
Table3-2 The electrical parameters of various TFTs
Table4-1 Experiment flow of devices under light illumination
Table4-2 Experiment flow of devices measured under different oxygen
pressure
Table4-3 Experiment flow of devices measured under gate bias stress
簡 歷
姓 名:郭 豫 杰 ( Yu-Chieh Kuo )
性 別:男
出生年月日:民國 73 年 08 月 26 日
住 址:台北市光復北路103巷36號3樓
學 歷:
國立清華大學工業工程與工程管理學系學士 (91.9-95.6) 國立交通大學光電工程學系顯示科技研究所碩士 (95.9-97.6)
碩士論文題目:
溶膠凝膠金屬氧化物薄膜電晶體之研究
Investigation on Sol-Gel Derived Metal Oxide Semiconductor Thin Film Transistors