The present disclosure generally relates to a semiconductor device and method. More particularly, the invention relates to a light emitting diode device and method for manufacturing a light emitting diode device and a method for fabricating the light emitting diode device.
ITO (indium-tin oxide) has been widely used as a current diffusion layer in fabrication of an LED (light emitting diode) device. To achieve a light extraction efficiency enhancement, a commonly used method is to roughen the surface of an ITO layer. In the prior art, the method for roughening the surface of the ITO layer mainly comprises a dry etching method and a wet etching method. A dry etching method may comprise steps of forming the ITO layer, forming a pattern using a photoresist, and etching an ITO region which is not protected by the photoresist using ICP (inductive couple plasmas), so as to roughen the surface of the ITO layer. A wet etching method may comprise steps of coating a layer of nanoparticles on at least a portion of surface of the ITO layer as a protective layer and etching a region which is not covered by the nanoparticles using a corrosion solution, such as an acid solution, so as to roughen the surface of the ITO layer.
According to one exemplary embodiment of the subject disclosure, a method is described. The method comprises providing an epitaxial wafer. The method further comprises depositing ITO source material on the epitaxial wafer to form a base ITO layer by a direct current electron gun and depositing ZnO source material, during simultaneous deposition of the ITO source material, on the base ITO layer to form a ZnO doped ITO layer by a pulse current electron gun. The ZnO source material may be deposited at a deposition rate higher than the rate at which the ITO source material is deposited. Generation and termination of current may be controlled by adjusting a duty cycle of pulse current provided by the pulse current electron gun and result in discontinuous deposition of the ZnO source material. The method further comprises depositing the ITO source material on the ZnO doped ITO layer to cover the ZnO doped ITO layer and form a finished ITO layer.
According to another exemplary embodiment of the subject disclosure, a method is described. The method comprises providing a current diffusion layer, forming a photoresist protective layer on the finished ITO layer to cover a step region, removing the finished ITO layer and the ZnO doped ITO layer from a mesa region, removing the photoresist protective layer, and depositing conductive material on the surface of the cover ITO layer in the step region to form a positive electrode and on the surface of the n-type nitride layer in the mesa region to form a negative electrode.
These and other aspects and advantages of embodiments of the present disclosure will become apparent and more readily appreciated from the following descriptions made with reference to the accompanying drawings, in which:
Reference will be made in detail to embodiments of the present disclosure. The embodiments described herein with reference to drawings are explanatory, illustrative, and used to generally understand the present disclosure. The embodiments shall not be construed to limit the present disclosure or claims thereto. The same or similar elements and the elements having same or similar functions are denoted by like reference numerals throughout the descriptions.
A photoresist protective layer 211 having a pattern may be formed by applying a lithography process. The photoresist protective layer 211 may be applied to a surface of the p-type nitride layer 208, as shown in
To form a current diffusion layer, ITO source material may be deposited on the epitaxial wafer 200, as shown in
During the deposition of the ITO source material, ZnO source material may be deposited, such as using a physical vapor deposition method, such as electron beam physical vapor deposition, at step S12. For convenience and brevity, the ITO layer formation prior to deposition of the ZnO is referred as base ITO layer 212. The ZnO source material and ITO source material may be deposited simultaneously using their respective deposition method resulting in dispersion of ZnO 214 in the base ITO layer. The deposition of ITO source material and ZnO source material may use the same method or different methods. ZnO source material may be deposited at a deposition rate higher than the deposition rate at which the ITO source material is deposited. As a result of the simultaneous deposition of ZnO source material and ITO source material, a ZnO doped ITO layer may be formed. In one embodiment, the ITO source material may be deposit at a rate of about 0.5 Å/s to about 1.2 Å/s. The ZnO source material may be deposited at a rate of about 20 Å/s to about 30 Å/s.
When electron beam physical vapor deposition method is used to deposit ZnO source material into the ITO layer, current generation and termination may be controlled by adjusting the pulse duty cycle of the beam current of the electron gun. In one embodiment, the duty cycle may be about 20%-30%. Current generation and termination may control deposition of the ZnO source material on the base ITO layer 212, thus resulting in discontinuous deposition. The discontinuous deposition may form a ZnO layer 214 on the base ITO layer 212 with an uneven surface. For example, the ZnO layer 214 may include a plurality of grooves such as grooves 214A, as shown in
After deposition of ZnO source material concludes, ITO source material may continue to be heated and deposited at step S13 until the surface of the doped ZnO and the plurality of grooves (e.g., 214A) are covered by ITO source material. ITO source material that covers the doped ZnO may be about 10 nanometers to about 15 nanometers thick. For convenience and brevity, the ITO source material that covers the doped ZnO layer may be referred as cover ITO layer 216. The process of depositing ITO source material may form a finished ITO layer having a desired thickness of about 285 nanometers to about 290 nanometers. ZnO source material may be deposited when thickness of the base ITO layer reaches about 85%-90% of the desired thickness, such as when the thickness of the base ITO layer 212 is about 250 nanometers to about 260 nanometers.
The method may further comprise depositing a passivation layer 224 without covering at least one surface of the positive electrode 220 and without covering at least one surface of the negative electrode 222, such as a surface of a top wall or a surface of a sidewall. As illustrated in
The ZnO source material may comprise at least one of In doped ZnO, Ga doped ZnO, and aluminum doped ZnO and a mixture of Indium oxide and ZnO. Because the conductivity of one of the ZnO source material is similar to the conductivity of ITO, when a current diffusion layer is formed from ITO and the ZnO source material, the current may diffuse uniformly. The ZnO source material and ITO are both transparent compounds. So the refractive index of the ZnO source material and the refractive index of ITO are approximate. For example, the refractive index of the ZnO source material is about 2.0. Light may not be easily refracted when penetrating through the ITO layer 216 and the ZnO doped ITO layer, thus reducing the loss of light.
Although explanatory embodiments have been shown and described, it would be appreciated by those skilled in the art that the above embodiments cannot be construed to limit the present disclosure, and changes, alternatives, and modifications can be made in the embodiments without departing from spirit, principles and scope of the present disclosure.
| Number | Date | Country | Kind |
|---|---|---|---|
| 201110163904.2 | Jun 2011 | CN | national |
| PCT/CN2012/077035 | Jun 2012 | CN | national |
This application is a continuation of PCT/CN2012/077035, which claims priority to Chinese Patent Application Serial No. 201110163904.2, filed with the State Intellectual Property Office of P. R. China on Jun. 17, 2011, the entire content each of which are incorporated herein by reference in their entireties.