Embodiment
Below, with reference to accompanying drawing, the flip-chip nitride-based illuminating device will be described in further detail according to the preferred embodiment of the present invention.
Fig. 1 has shown according to the present invention the sectional view of the flip-chip nitride-based illuminating device of first execution mode.
Referring now to Fig. 1, the flip-chip nitride-based illuminating device is formed by following structure, and described structure comprises stacked successively substrate 110, resilient coating 120, n-type coating 130, active layer 140, p-type coating 150, transparent conductive film layer 170 and the reflector 180 on it. Reference marker 190 and 200 is represented p-type electrode pad and n-type electrode pad respectively.
Be equivalent to ray structure from the part of substrate 110 to p-type coating 150, the transparent conductive film layer 170 that is stacked on the p-type coating 150 is equivalent to the ohmic contact structure.
Substrate 110 is preferably by being selected from sapphire (Al
2O
3), any one material of diamond dust (SiC), silicon (Si) and GaAs (GaAs) forms.
Can omit resilient coating 120.
From each layer of resilient coating 120 to p-type coating 150 is to be selected from by general formula: Al
xIn
yGa
zN (0=x=1,0=y=1,0=z=1,0=x+y+z=1) the arbitrary compound in Dai Biao the III group-III nitride based compound is that the basis forms.N-type coating 130 and p-type coating 150 contain adding corresponding dopant wherein.
Thereby can dispose active layer 140 makes it have various known structure for example individual layer or mqw layer.
For example, when using gallium nitride-based compound semiconductor, resilient coating 120 is formed by GaN, for example Si, Ge, Se and Te form n-type coating 130 by add n-type dopant in GaN, active layer 140 is formed by InGaN/GaN MQW or AlGaN/GaN MQW, and p-type coating 150 for example Mg, Zn, Ca, Sr and Ba form by add p-type dopant in GaN.
Can between n-type coating 130 and n-type electrode pad 200, insert n-type ohmic contact layer (not shown), and various known structure for example have the stacked successively titanium (Ti) and the layer structure of aluminium (Al) etc. on it and can be used as n-type ohmic contact layer.
As p-type electrode pad 190, can use have stacked successively on it nickel (Ni)/gold (Au) or the layer structure of silver (Ag) gold/(Au).
Can form each layer by using electron beam evaporation plating device, physical vapor deposition (PVD), chemical vapor deposition (CVD), plasmon deposition (PLD) or the hot evaporator sputter of dimorphism (dual-type) to wait.
Transparent conductive film layer 170 as the ohmic contact structure, be that diffuse by inhibitory reflex layer 180 forms to the material in the p-type coating 150, reflector 180 will form in ensuing process, therefore transparent conductive film layer 170 has served as the diffusion barrier of above-mentioned material, and high transmission rate and conductivity are provided simultaneously.
In addition, for transparent conductive film layer 170, use can increase the material of the efficient carrier concentration of p-type coating 150, and the material that preferably can react with other composition except that nitrogen-atoms in the compound of forming p-type coating 150.For example, contain in the situation of GaN based compound as main component,, use with gallium (Ga) reaction to have more active material than reacting with nitrogen for transparent conductive film layer 170 at light-emitting device.
In this case, for example, because transparent conductive film layer 170 has above-mentioned character, contain gallium nitride (GaN) as the p-type coating 150 of main component by its with transparent conductive film layer 170 between the surface of the p-type that is reflected at coating 150 on formation gallium room.At this, because p-type dopant has been served as in formed gallium room on p-type coating 150, the reaction between p-type coating 150 and the transparent conductive film layer 170 causes p-type coating 150 lip-deep efficient carrier concentration to increase.
In addition, for transparent conductive film layer 170, can use and to reduce gallium oxide (Ga
2O
3) material, described gallium oxide is a kind of natural oxide layer, it is retained on p-type coating 150 surfaces, and serving as the potential barrier that charge carrier flows on the interface between transparent conductive film layer 170 and the p-type coating 150, the material that therefore reduces gallium oxide has reduced the height and the width of Schottky barrier.
Can satisfy above-mentioned condition owing to be used for the material of transparent conductive film layer 170, it can use transparent conductive oxide (TCO) or electrically conducting transparent nitride (TCN).
As transparent conductive oxide, can use by at least a composition of indium (In), tin (Sn), zinc (Zn), gallium (Ga), cadmium (Cd), magnesium (Mg), beryllium (Be), silver (Ag), molybdenum (Mo), vanadium (V), copper (Cu), iridium (Ir), rhodium (Rh), ruthenium (Ru), tungsten (W), cobalt (Co), nickel (Ni), manganese (Mn), palladium (Pd), platinum (Pt) and lanthanum (La) and the material of oxygen combination of being selected from.
In addition, the electrically conducting transparent nitride comprise those have low sheet resistance and high transmission rate and contain the nitride of titanium (Ti) and nitrogen (N) at least.For example, can mention titanium nitride (TiN) or titanium oxynitrides (Ti-N-O).
In order to improve electrology characteristic, can in transparent conductive oxide or electrically conducting transparent nitride, add metallic element at least a periodic table as dopant.
Preferably, join the ratio of the dopant in transparent conductive oxide or the electrically conducting transparent nitride in the scope of 0.001-20wt%.Herein, wt% is meant the weight ratio between the material of adding.
By considering work function that purposes determined and sheet resistance, select the material of transparent conductive film layer 170 by light-emitting device.
In order to have suitable light transmittance and conductivity, the thickness of transparent conductive film layer 170 is preferably at 1nm-1, in the 000nm scope.
This transparent conductive film layer 170 is individual layer or by form two-layer or the more multi-layered sandwich construction of forming preferably.Fig. 5 has shown its example.
Reflector 180 is to be formed by the material with high reflectance, for example, and at least a silver (Ag), the silver oxide (Ag of being selected from
2O), the material of aluminium (Al), zinc (Zn), titanium (Ti), rhodium (Rh), magnesium (Mg), palladium (Pd), ruthenium (Ru) and platinum (Pt).
According to another aspect of the present invention, reflector 180 is to form by containing alloy or its solid solution of silver (Ag) as main component, and wherein contains at least a aluminium (Al), the silver oxide (Ag of being selected from that is less than 5wt% in the silver
2O), the element of zinc (Zn), titanium (Ti), rhodium (Rh), magnesium (Mg), palladium (Pd), ruthenium (Ru), platinum (Pt) and iridium (Ir).The basic alloy of this silver (Ag) has alleviated independent low tack and the thermal instability that occurs when using silver (Ag), therefore good contact and thermal endurance is provided and has kept high light reflectivity.
Reflector 180 is formed so that suitable reflectivity to be provided by the thick film with 100nm-1000nm thickness.Preferably, use above-mentioned material to be deposited as reflector 180 then with its annealing.
In having the light-emitting device of this structure, when using above-mentioned material to form transparent conductive film layer 170 and following it when suitable temperature is annealed in oxygen or air ambient, described layer 170 becomes the transparent conductive material of have high transmission rate (promptly transmittance surpasses 90% under the 400nm wavelength) and low sheet resistance value (less than 10 Ω/unit are), simultaneously described layer 170 minimizing gallium oxide (Ga
2O
3), gallium oxide is a kind of natural oxide layer, it is retained on p-type coating 150 surfaces, and serve as the potential barrier that charge carrier flows on the interface between transparent conductive film layer 170 and the p-type coating 150, therefore described layer 170 has reduced the height and the width of Schottky barrier, therefore caused the tunnel effect that helps forming ohmic contact, improved electrology characteristic, and had and approach 100% light transmittance.
In addition, when reflector 180 is when being formed by above-mentioned material, the diffuse that transparent conductive film layer 170 suppresses to form reflector enters p-type coating 150/ contact p-type coating 150.
Fig. 2 has shown according to the present invention the sectional view of the flip-chip nitride-based illuminating device of another execution mode.For with the figure that formerly shows in have the element of identical function, below identical numeral be meant identical element.
Referring now to Fig. 2, light-emitting device is formed by following structure, and described structure comprises stacked successively substrate 110, resilient coating 120, n-type coating 130, active layer 140, p-type coating 150, interface modification layer 160, transparent conductive film layer 170 and the reflector 180 on it.
Interface modification layer 160 is used to improve the ohmic contact between p-type coating 150 and the transparent conductive film layer 170.
As interface modification layer 160, its employed material has conductivity, and under less than 800 ℃ temperature when all gases environment is for example annealed in oxygen, nitrogen and the argon gas, can easily be decomposed into electrical-conductive nanometer phase oxide particle, or can form the transparent conductive film layer, and simultaneously described material reduces the natural oxide layer that is formed at p-type coating 150 tops thinly, i.e. gallium oxide (Ga
2O
3), perhaps change the gallium oxide layer into conductive oxide layer.℃
The material that satisfies above-mentioned condition that is used for interface modification layer 160 can be selected from following various materials:
1) arbitrary element that is selected from indium (In), tin (Sn), zinc (Zn), magnesium (Mg), silver (Ag), iridium (Ir), ruthenium (Ru), rhodium (Rh), platinum (Pt), nickel (Ni) and palladium (Pd), contain at least a alloy that is selected from above-mentioned element, and their solid solution.
1-1) material that is used for the interface modification layer preferably by the indium of above-mentioned element, add to have to add element and contain indium and formed as the alloy of main component and in their solid solution any one.Herein, join in the indium as the interpolation element that is used for the material of interface modification layer and comprise at least a element that is selected from tin (Sn), zinc (Zn), gallium (Ga), cadmium (Cd), magnesium (Mg), beryllium (Be), silver (Ag), molybdenum (Mo), vanadium (V), copper (Cu), iridium (Ir), rhodium (Rh), ruthenium (Ru), tungsten (W), cobalt (Co), nickel (Ni), manganese (Mn), palladium (Pd), platinum (Pt) and lanthanum (La).The interpolation element that is added not is special the qualification with respect to the ratio of indium, but preferred in the scope of 0.001-50wt%.
1-2) material that is used for the interface modification layer also preferably by the tin of above-mentioned element, add to have to add element and contain tin and formed as the alloy of main component and in their solid solution any one.Herein, join in the tin as the interpolation element that is used for the material of interface modification layer and comprise at least a element that is selected from indium (In), zinc (Zn), gallium (Ga), cadmium (Cd), magnesium (Mg), beryllium (Be), silver (Ag), molybdenum (Mo), vanadium (V), copper (Cu), iridium (Ir), rhodium (Rh), ruthenium (Ru), tungsten (W), cobalt (Co), nickel (Ni), manganese (Mn), palladium (Pd), platinum (Pt) and lanthanum (La).The interpolation element that is added is not special the qualification with respect to the ratio of tin, but preferred in the scope of 0.001-50wt%.
2) p-type transparent conductive oxide
For interface modification layer 160, the material of its use can provide 10
15-10
18/ cm
3The hole concentration of p-type transparent conductive oxide, described p-type transparent conductive oxide is formed at the top of p-type coating 150, can reduce the height and the width of the Schottky barrier that forms between p-type coating 150 and interface modification layer 160 like this.
2-1) as the example of p-type transparent conductive oxide, preferably by at least a formed binary of element or the ternary oxide that is selected from the II family element that comprises magnesium (Mg), zinc (Zn) and beryllium (Be).
2-2) as the example of p-type oxide, preferably any one is selected from Ag
2O, CuAlO
2, SrCu
2O
2, LaMnO
3, LaNiO
3And In
xO
1-xOxide.
Can in p-type oxide, suitably add p-type dopant, can control the concentration and the work function of p-type transparent conductive oxide like this, and reduce the height and the width of Schottky barrier simultaneously.
In addition, except above-mentioned p-type transparent conductive oxide, can also use following material, this material can the value of providing be 10
15-10
17/ cm
3Transparent conductive nano phase particle or the electron concentration of thin layer, described nanophase particle or thin layer are formed at p-type coating 150 tops, can be reduced between p-type coating 150 and the interface modification layer 160 height and the width of the Schottky barrier that forms like this.
2-3) in above-mentioned material, preferred indium base oxide, tin-based oxide or zinc-base oxide.
Under the situation of indium base oxide, preferably to main component indium oxide (In
2O
3) in adding can regulate indium oxide (In
2O
3) concentration and work function and simultaneously can reduce the height of Schottky barrier and the interpolation element of width.As adding element, can mention at least a composition that is selected from gallium (Ga), magnesium (Mg), beryllium (Be), molybdenum (Mo), vanadium (V), copper (Cu), iridium (Ir), rhodium (Rh), ruthenium (Ru), tungsten (W), cobalt (Co), nickel (Ni), manganese (Mn) and lanthanum (La).
Under the situation of tin-based oxide, preferably in tin oxide further adding can regulate the concentration of tin oxide and work function and can reduce the height of Schottky barrier and the interpolation element of width simultaneously.As adding element, can mention at least a composition that is selected from zinc (Zn), gallium (Ga), magnesium (Mg), beryllium (Be), molybdenum (Mo), vanadium (V), copper (Cu), iridium (Ir), rhodium (Rh), ruthenium (Ru), tungsten (W), cobalt (Co), nickel (Ni), manganese (Mn) and lanthanum (La).
Under zinc-base oxide ground situation, preferably in zinc oxide further adding can regulate oxidation zinc concentration and work function and can reduce the height of Schottky barrier and the interpolation element of width simultaneously.As the interpolation element that can add, can mention at least a composition that is selected from indium (In), tin (Sn), gallium (Ga), magnesium (Mg), beryllium (Be), molybdenum (Mo), vanadium (V), copper (Cu), iridium (Ir), rhodium (Rh), ruthenium (Ru), tungsten (W), cobalt (Co), nickel (Ni), manganese (Mn) and lanthanum (La).
In this respect, the interpolation element that is added not is special the qualification with respect to the ratio of above-mentioned main component, but preferred in the scope of 0.001-50wt%.Herein, wt% is meant the weight ratio between the material that is added.
The interface modification layer of being made up of above-mentioned material 160 preferably forms with the thickness of 0.1nm-100nm, under this thickness in when annealing, interface modification layer 160 can be decomposed into the electrical-conductive nanometer phase oxide at an easy rate or can form thin layer, and the quantum tunneling of charge carrier can be by described nanophase oxide or thin layer onset.
Transparent conductive oxide 170 is formed by above-mentioned material.
This structure in many ohmic contact layers and reflector 180 prevents from above under 200 ℃ the temperature superficial degradation taking place oxidation to be stable and still to have high reflectance, so it makes the high efficiency light-emitting device of realization become possibility.
Below, have according to the present invention the preparation method of the light-emitting device of first and second execution mode structure with reference to Fig. 1 and 2 explanation.
At first, stacked successively resilient coating 120, n-type coating 130, active layer 140 and p-type coating 150 on substrate 110.
Secondly, in order to ensure the formation space of n-type electrode pad 200, partially-etched zone from p-type coating 150 to n-type coating 130 is to form the MESA structure.
Then, when application drawing 1 structure, on p-type coating 150, only form transparent conductive film layer 170, when application drawing 2 structures, on p-type coating 150, form interface modification layer 160 and transparent conductive film layer 170 successively.
By using known deposition process, for example electron beam evaporation plating, physical vapor deposition (PVD), chemical vapor deposition (CVD), plasmon deposition (PLD) or the hot evaporator sputter of dimorphism etc. form transparent conductive film layer 170 or interface modification layer 160 and transparent conductive film layer 170.
Depositing temperature is 20 ℃-1500 ℃, and the interior pressure of evaporator is an atmospheric pressure to 10
-12Holder.
After forming transparent conductive film layer 170 or interface modification layer 160 and transparent conductive film layer 170 on the p-type coating 150, resulting structures preferably containing the gaseous environment of oxygen, is for example annealed in oxygen atmosphere or the air.
Under 100 ℃-800 ℃ temperature, in reactor, anneal 10 seconds to 3 hour.
After this, on transparent conductive film layer 170, form reflector 180.By above-mentioned known deposition methods deposition of reflective layer 180.
180 form the back in order to improve its tack and thermal stability in the reflector, 10 seconds to 3 hour of in reactor ray structure being annealed in vacuum, nitrogen or argon gas environment under 100 ℃-800 ℃ temperature.
Experiment showed, the degeneration that reflector 180 annealing in the environment except that vacuum, nitrogen and argon gas can be caused its characteristic.
Fig. 3 has shown according to the present invention the sectional view of the flip-chip nitride-based illuminating device of the 3rd execution mode.For with the figure of previous demonstration in have the element of identical function, below identical numeral be meant identical element.
Referring now to Fig. 3, the flip-chip light emitting device is formed by following structure, described structure comprise stacked successively on it substrate 110, resilient coating 120, n-type coating 130, active layer 140, p-type coating 150, interface modification layer 160, insert metal level 165, transparent conductive film layer 170 and reflector 180.
Herein, interface modification layer 160, insertion metal level 165 and transparent conductive film layer 170 are corresponding to many ohmic contact layers.
Inserting metal level 165 is formed between interface modification layer 160 and the transparent conductive film layer 170.
Insert metal level 165 preferably by being converted into transparent conductive oxide easily when the annealing and can regulating the electricity of interface modification layer 160 or transparent conductive film layer 170 simultaneously or the metal of optical characteristics is formed, described transparent conductive film layer 170 is formed at the top of interface improving layer 160 in step subsequently.
Preferably, inserting metal level 165 is formed by at least a composition that is selected from zinc (Zn), indium (In), tin (Sn), nickel (Ni), magnesium (Mg), gallium (Ga), copper (Cu), beryllium (Be), iridium (Ir), ruthenium (Ru) and molybdenum (Mo).
Certainly, inserting metal level 165 can form by a plurality of layers that enumerate material more than using.
Preferably, insert the thickness formation of metal level 165 with 1nm-100nm.
Below, explanation has the preparation method of the light-emitting device of the 3rd execution mode structure according to the present invention with reference to Fig. 3.
At first, on substrate 110, deposit resilient coating 120, n-type coating 130, active layer 140 and p-type coating 150 successively, form ray structure thus.
Secondly, in order to ensure the formation space of n-type electrode pad 200, partially-etched zone from p-type coating 150 to n-type coating 130 is to form the MESA structure.
Then, form many ohmic contact layers, described many ohmic contact layers comprise interface modification layer 160, insertion metal level 165 and the transparent conductive film layer 170 that is stacked in successively on the p-type coating 150.
By using known deposition process, for example electron beam evaporation plating, physical vapor deposition (PVD), chemical vapor deposition (CVD), plasmon deposition (PLD) or the hot evaporator sputter of dimorphism etc. form interface modification layer 160, insert metal level 165 and transparent conductive film layer 170.
In addition, the depositing temperature that is used for forming successively each layer from interface modification layer 160 to transparent conductive film layer 170 is 20 ℃-1500 ℃, and the interior pressure of evaporator is an atmospheric pressure to 10
-12Holder.
Preferably, behind each layer that forms from interface modification layer 160 to transparent conductive film layer 170, then carry out annealing process.
In reactor, in vacuum or suitable gaseous environment, annealing 10 seconds to 3 hour under 100 ℃-800 ℃ the temperature.
Gas as introducing when annealing in the reactor can use at least a gas that is selected from nitrogen, argon gas, helium, oxygen, hydrogen and air.
After the annealing, use previously described material on transparent conductive film layer 170, to form reflector 180.
Come deposition of reflective layer 180 by above-mentioned deposition process.
180 form the back in order to improve its tack and thermal stability in the reflector, by the method for above explanation ray structure are annealed.
Perhaps, on p-type coating 150, deposit successively from interface modification layer 160 to the reflector each layer of 180, then can only need once anneal to ray structure.
Experimental results show that, when annealing for the first time up to carrying out after each layer formation of transparent conductive film layer 170 and annealing for the second time when after reflector 180 forms, carrying out, the light transmittance of many ohmic contact layers further is enhanced and the reflectivity in reflector 180 also is enhanced.
Below, explanation has the preparation method of the light-emitting device of the 4th and the 5th execution mode structure according to the present invention with reference to Figure 4 and 5.
Fig. 4 has shown according to the present invention the sectional view of the flip-chip light emitting device of the 4th execution mode.Referring now to Fig. 4, the flip-chip light emitting device is formed by following structure, and described structure comprises that stacked successively substrate 210, resilient coating 220, n-type coating 230, active layer 240, p-type coating 250, many ohmic contact layers 260 and the reflector 270 on it forms.Reference marker 280 and 290 is represented p-type electrode pad and n-type electrode pad respectively.
Since the composition of above-mentioned flip-chip light emitting device except that many ohmic contact layers 260 basically with first execution mode in identical, so omitted detailed description to them.Below, will describe many ohmic contact layers 260.
Many ohmic contact layers 260 are to form by repeating stacked interface modification layer 260a/ transparent conductive film layer 260b as stacked unit.Fig. 4 has shown the example of this repetition stacked structure.
Referring now to Fig. 4, many ohmic contact layers 260 are that following structure forms, and this structure comprises the stacked successively first interface modification layer 260a/, the first transparent conductive film layer 260b/ second contact surface modified layer 260c/, the second transparent conductive film layer 260d on it.
The first interface modification layer 260a and the first transparent conductive film layer 260b can be according to first forms interface modification layer 160 and transparent conductive film layer 170 described method to the 3rd execution mode in the present invention.
When annealing, provide oxygen by the first transparent conductive film layer 260b or by the second transparent conductive film layer 260d that will in later step, form to second contact surface modified layer 260c, and form the transparent conductive oxide film layer, and further increased simultaneously, the carrier concentration of the first and second transparent conductive film layer 260b and 260d.
In order to reduce sheet resistance, the material that is used for second contact surface modified layer 260c can be identical or different with the composition of the first interface modification layer 260a.
Preferably, the first and second interface modification layer 260a and 260c form with the thickness of 0.1nm-100nm respectively, and these layers can easily decompose and be oxidized to electrical-conductive nanometer phase particle when annealing in this thickness range.
In addition, the first transparent conductive film layer 260b and the second transparent conductive film layer 260d also can be formed by above-mentioned material, but in order to reduce sheet resistance, what the composition of the first transparent conductive film layer 260b can be with the second transparent conductive film layer 260d is identical or different.
As mentioned above, the first transparent conductive film layer 260b and the second transparent conductive film layer 260d also form with the thickness of 1nm-1000nm independently.
Simultaneously, Fig. 5 has shown the light-emitting device of having used another many ohmic contact layers.For with the figure of previous demonstration in have the element of identical function, below identical numeral be meant identical element.
Referring now to Fig. 5, many ohmic contact layers 260 are formed by the structure that comprises the stacked successively first interface modification layer 260a/, the first transparent conductive film layer 260b/, the second transparent conductive film layer 260d on it.
Herein, stacked repetitive is the first interface modification layer 260a/, the first transparent conductive film layer 260b/, the second transparent conductive film layer 260d.
In having many ohmic contact layers 260 of this structure, can use foregoing material and method to form the first interface modification layer 260a/, the first transparent conductive film layer 260b/, the second transparent conductive film layer 260d.
Below, explanation has the preparation method of the light-emitting device of the 4th and the 5th execution mode structure according to the present invention with reference to Figure 4 and 5.
At first, on substrate 210, deposit resilient coating 220, n-type coating 230, active layer 240 and p-type coating 250 successively, form ray structure thus.
Secondly, for guaranteeing the formation space of n-type electrode pad 290, partially-etched each layer from p-type coating 250 to n-type coating 230 is with formation MESA structure.
Then, on the p-of ray structure type coating 250, form many ohmic contact layers 260.
Each layer of forming many ohmic contact layers 260 can lead to the known deposition process of use, and for example electron beam evaporation plating, physical vapor deposition (PVD), chemical vapor deposition (CVD), plasmon deposition (PLD), the hot evaporator sputter of dimorphism form.
In addition, the depositing temperature that is used for forming successively each layer of many ohmic contact layers 260 is 20 ℃-1500 ℃, and the interior pressure of evaporator is an atmospheric pressure to 10
-12Holder.
Preferably, after forming, many ohmic contact layers 260 carry out annealing process.
In reactor, in vacuum or suitable gaseous environment, annealing 10 seconds to 3 hour under 100 ℃-800 ℃ the temperature.
Gas as introduce reactor when annealing can use at least a gas that is selected from nitrogen, argon gas, helium, oxygen, hydrogen and air.
After the annealing, use the material of before having enumerated, on many ohmic contact layers 260, form reflector 270.
By previously mentioned deposition reflector 270.
270 form the back in order to improve its tack and thermal stability in the reflector, by previously described method ray structure are annealed.
Perhaps, after forming many ohmic contact layers 260 and reflector 270 successively on the p-type coating 250, can only once anneal to the gained ray structure.
Experiment showed, when annealing for the first time and after many ohmic contact layers 260 form, carry out and annealing for the second time when after reflector 270 forms, carrying out that the light transmittance of many ohmic contact layers 260 further increases, and the reflectivity in reflector 270 increases.
Fig. 6 and 7 has shown the experimental result of measuring the light-emitting device characteristic, and described light-emitting device is according to method preparation of the present invention described above.
Fig. 6 is the figure that has shown the I-E characteristic result that following light-emitting device is measured, and described light-emitting device is by at the stacked successively Ag/ITO in p-type coating top, annealing and preparation in air ambient under 330 ℃-530 ℃ temperature then.
Fig. 7 is the figure that has shown the I-E characteristic result that following light-emitting device is measured, described light-emitting device is by at the stacked successively Ag/ITO in p-type coating top, under 330 ℃-530 ℃ temperature, in air ambient, anneal then, and then anneal in a vacuum under 330 ℃ of temperature and prepare in the deposition of aluminum reflector.
By comparison diagram 6 and 7 as can be seen, by further forming the then ray structure for preparing of annealing of reflector with aluminium, demonstrate the current-voltage drive characteristic of having improved.
Though the purpose of property discloses preferred implementation of the present invention presented for purpose of illustration, those skilled in the art can understand, and can carry out various improvement, dose and replace and do not deviate from as disclosed scope and spirit of the present invention in the appended claims.