The present application is the U.S. national phase entry of PCT/CN2015/084343, with an international filing date of Jul. 17, 2015, which claims the benefit of Chinese Patent Application No. 201510180005.1, filed on Apr. 16, 2015, the entire disclosures of which are incorporated herein by reference.
The present disclosure relates to the field of display technology and particularly to a metal oxide thin film transistor and a corresponding manufacturing method, a display substrate and a display device.
With the development of information technologies, display technology as a window for acquiring information has been developed rapidly. At present, the thin film transistor liquid crystal display (TFT-LCD) has become the largest display market in the globe instead of the cathode ray tube (CRT) display. As a core element for the currently most popular flat-panel display, the performance of the thin film transistor (TFT) directly impacts on the quality of the display. Development of high mobility materials becomes a focus under increasing requirements on high PPI (pixels per inch) and high refresh rate in the field of display. Although the conventional polysilicon thin film transistor has high mobility, it cannot satisfy the requirement of large-scale production due to its complicated manufacturing process and high manufacturing cost. On the other hand, the oxide thin film transistor is suitable for large-scale production, but it has low mobility which is just 10-30 cm2/Vs currently and needs to be further increased.
It is known that the calculation formula of the mobility μ of the oxide thin film transistor can be expressed as:
wherein m* is an electron effective mass, τ is carrier release time.
Therefore, there are two ways to improve the mobility of the oxide thin film transistor:
(1) Increase the content of metal ions with small molecule effective mass m*. For example, in IGZO (indium gallium zinc oxide), referring to Table 1, electrons have the smallest m* in In2O3, thus In has the most predominant effect on improving the mobility of the thin film transistor. Increasing the content of In3+ ions in the oxide can improve the mobility of the oxide thin film transistor significantly. However, the In3+ ions have the largest orbital radius, and the bond energy between In3+ and O is the smallest, thus the formed In—O bond is easily broken, thereby forming some oxygen dangling bonds or redundant oxygen defects, which in turn influences the stability of the thin film transistor.
(2) Reduce the number of defects in the oxide which impact on carrier transmission. The carrier relaxation time is most affected by the defects. Specifically, reducing the number of defects in the oxide can increase the carrier relaxation time, thereby improving the mobility of the thin film transistor.
The applicant has discovered that particular materials have strong oxygen deficiency adsorptive removal capabilities. By forming an oxygen deficiency adsorptive removal layer between the active layer and the source/drain electrode, redundant oxygen dangling bonds and oxygen defects can be adsorptively removed to increase the carrier relaxation time, thereby reaching the purpose of improving the mobility of the metal oxide thin film transistor. To this end, the oxide of the material acting as the oxygen deficiency adsorptive removal layer should be more stable than the metal oxide in the active layer.
To explore materials suitable for the oxygen deficiency adsorptive removal layer of the oxide thin film transistor, the stabilities of multiple oxides would be determined based on the standard Gibbs free energies of formation of the oxides in a unit volume. The standard Gibbs free energy of formation of a compound is a measure for determining whether it is easy for the compound to decompose into corresponding elementary substances, that is, the larger the standard Gibbs free energy of formation is, the more stable the compound is; contrarily, it is easier for the compound to decompose into corresponding elementary substances.
In view of the above, a first aspect of the present disclosure provides a metal oxide thin film transistor, wherein an oxygen deficiency adsorptive removal layer comprising an oxygen deficiency adsorptive removal material may be provided between the active layer and the source, and/or between the active layer and the drain. The standard Gibbs free energy of formation of the oxide of the oxygen deficiency adsorptive removal material in a unit volume is larger than that of the metal oxide in the active layer.
In the metal oxide thin film transistor, the oxygen deficiency adsorptive removal layer having strong oxygen adsorptive removal capability (i.e. the standard Gibbs free energy of formation of the corresponding oxide in a unit volume is large) can adsorptively remove weak oxygen dangling bonds and oxygen defects from the active layer of the metal oxide, thereby effectively improving the mobility of the metal oxide thin film transistor. In embodiments, the oxygen deficiency adsorptive removal layer can be arranged between the source and the active layer, or arranged between the drain and the active layer, or particularly the both to further improve the mobility of the metal oxide thin film transistor.
In accordance with an embodiment of the present disclosure, the oxygen deficiency adsorptive removal layer may have a thickness ranging from 100 to 3000 Å. The thickness of the oxygen deficiency adsorptive removal layer is related to the thickness and material of the active layer, and the concentrations of the oxygen dangling bonds and oxygen defects. When the active layer is relatively thick, the metal oxide in the active layer is relatively stable or the concentrations of the oxygen dangling bonds and oxygen defects are relatively high, the thickness of the oxygen deficiency adsorptive removal layer can be increased accordingly. It is to be noted that those skilled in the art can design and implement oxygen deficiency adsorptive removal layers with different thicknesses based on practical needs.
In accordance with another embodiment of the present disclosure, the oxygen deficiency adsorptive removal material may be selected from the group consisting of Hf, Ti, Be, Al, Si and Ca. It can be seen from
In accordance with a further embodiment of the present disclosure, the oxygen deficiency adsorptive removal material may be identical with the materials of the source and the drain. In this case, oxygen deficiency adsorptive removal layer can be formed simultaneously with the source and drain, which consequently does not involve additional process steps and leads to simple manufacture and reduced cost.
In accordance with yet another embodiment, the metal oxide in the active layer may be selected from oxides of Zn, In, Sn and Ga. It can also be seen from
In addition, in accordance with an embodiment of the present disclosure, the metal oxide in the active layer may comprise a metal nitrogen oxide.
A second aspect of the present disclosure provides a method for manufacturing a metal oxide thin film transistor, which may comprise: forming, on a substrate, a gate layer, a gate insulating layer and an active layer successively, and performing patterning process treatment on each layer; forming, on the active layer, an oxygen deficiency adsorptive removal layer comprising an oxygen deficiency adsorptive removal material; forming a source/drain electrode layer; performing patterning process treatment on the source/drain electrode layer and the oxygen deficiency adsorptive removal layer, wherein the oxygen deficiency adsorptive removal layer is between the active layer and the source, and/or between the active layer and the drain, and the standard Gibbs free energy of formation of the oxide of the oxygen deficiency adsorptive removal material in a unit volume is larger than that of the metal oxide in the active layer.
In the metal oxide thin film transistor prepared by the above method, the oxygen deficiency adsorptive removal layer having strong oxygen adsorptive removal capability (i.e. the standard Gibbs free energy of formation of the corresponding oxide in a unit volume is large) can adsorptively remove weak oxygen dangling bonds and oxygen defects in the active layer of the metal oxide, thereby effectively improving the mobility of the metal oxide thin film transistor. In embodiments, the oxygen deficiency adsorptive removal layer can be arranged between the source and the active layer, or arranged between the drain and the active layer, or particularly the both to further improve the mobility of the metal oxide thin film transistor.
In accordance with an embodiment of the present disclosure, the above method may further comprise an annealing step after forming the source/drain electrode layer. The annealing step can expedite the adsorptive removal of the oxygen defects and oxygen dangling bonds in the active layer by the oxygen deficiency adsorptive removal layer, which is hence more advantageous to carrier transmission and thereby improves the mobility of the metal oxide thin film transistor.
In accordance with another embodiment of the present disclosure, the annealing step may be performed at a temperature ranging from 100 to 350° C. for 30 to 90 minutes. Suitable annealing process can improve the mobility of the device and improve important parameters such as threshold voltage and current on-off ratio so as to improve the performance of the device. However, the annealing temperature should not be too high. If the annealing temperature is too high, the mobility of the metal oxide thin film transistor would decrease as the temperature increases.
In accordance with an embodiment of the present disclosure, the above method may further comprise a step of forming a passivation layer above the resultant metal oxide thin film transistor.
The present disclosure further provides a display substrate comprising the metal oxide thin film transistor according to the first aspect of the present disclosure and a display device comprising the display substrate. They have features and advantages similar to those described above for the metal oxide thin film transistor, which are not described here in detail for simplicity.
Other purposes and features of the present disclosure would become apparent from the detailed description below with reference to the drawings. However, it is to be understood that the figures are shown only for illustrative purpose rather than restrictive purpose, and the figures are not necessarily plotted to scale. In the drawings,
Throughout the respective figures, the same reference sign denotes the same portion specifically as follows, 1: gate layer; 2: gate insulating layer; 3: active layer; 4: source; 5: drain; 6: oxygen deficiency adsorptive removal layer; 7: passivation layer; 8: etch stop layer (ESL).
It is to be noted that although
The oxygen deficiency adsorptive removal layer 6 may have a thickness ranging from 100 to 3000 Å, and the oxygen deficiency adsorptive removal material may be selected from the group consisting of Hf, Ti, Be, Al, Si and Ca. In practice, those skilled in the art can design and implement the oxygen deficiency adsorptive removal layer 6 of different thicknesses and materials according to the thicknesses and materials of the active layer 3, the concentrations of the oxygen dangling bonds and oxygen defects, etc.
The metal oxide in the active layer 3 may be selected from oxides or nitrogen oxides of Zn, In, Sn and Ga. In addition, the source 4 and the drain 5 may employ the metal Mo.
The thin film transistor of a top gate structure in
At step 504, an oxygen deficiency adsorptive removal layer 6 is formed on the active layer 3. At step 506, a source/drain electrode layer is to formed on the oxygen deficiency adsorptive removal layer 6. Particularly, the oxygen deficiency adsorptive removal layer 6 and the source/drain electrode layer are formed by the same material. In this case, step 504 and step 506 can be carried out simultaneously. In addition, the oxygen deficiency adsorptive removal layer 6 may also be only present between the active layer 3 and the source or between the active layer 3 and the drain.
At step 508, an annealing process is carried out. As shown in
At step 510, patterning process treatment is performed on the source/drain electrode layer and the oxygen deficiency adsorptive removal layer 6, as shown in
Finally, at step 512, a passivation layer 7 is formed above the device to obtain the structure shown in
It is to be noted that the method disclosed by the present disclosure is not limited to the order recited for the method. Some steps may be performed simultaneously with other steps and some steps may be omitted.
While the disclosure has been illustrated and described in detail in the drawings and foregoing description, such illustration and description are to be considered illustrative or exemplary and not restrictive; the disclosure is not limited to the disclosed embodiments.
Variations to the disclosed embodiments can be understood and effected by the skilled person in practicing the claimed invention, from a study of the drawings, the disclosure, and the appended claims. The mere fact that certain measures are recited in mutually different dependent claims does not indicate that a combination of these measures cannot be used to advantage.
Number | Date | Country | Kind |
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2015 1 0180005 | Apr 2015 | CN | national |
Filing Document | Filing Date | Country | Kind |
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PCT/CN2015/084343 | 7/17/2015 | WO | 00 |
Publishing Document | Publishing Date | Country | Kind |
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WO2016/165224 | 10/20/2016 | WO | A |
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20120256179 | Yamazaki | Oct 2012 | A1 |
20130048978 | Watanabe et al. | Feb 2013 | A1 |
20130134412 | Godo et al. | May 2013 | A1 |
20150270407 | Suzuki | Sep 2015 | A1 |
20150295092 | Misaki | Oct 2015 | A1 |
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101257048 | Sep 2008 | CN |
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102194692 | Sep 2011 | CN |
102709326 | Oct 2012 | CN |
103904125 | Jul 2014 | CN |
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Number | Date | Country | |
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20170092660 A1 | Mar 2017 | US |