Reference will now be made to the drawings to describe preferred and exemplary embodiments of the present invention in detail.
The substrate 20 is transparent, and can for example be made of glass. The substrate 20 includes an upper surface (not labeled) and a bottom surface (not labeled). The bottom surface is configured to be a light emitting surface of the OLED 200. That is, images displayed by the OLED 200 are viewed at the bottom surface.
The first electrode layer 22 is configured to be an anode layer, and is made of transparent, electrically conductive material such as indium tin oxide (ITO) or indium zinc oxide (IZO). The first electrode layer 22 is disposed on the upper surface of the substrate 20. A thickness of the first electrode layer 22 is in the range from 25 nanometers (nm) to 100 nm.
The organic layer 23 has a triple-layer structure. The triple-layer structure includes a hole transport layer (HTL) 232, an emitting layer (EML) 230, and an electron transport layer (ETL) 231 stacked on the first electrode layer 22 in that sequence. An overall thickness of the organic layer 23 is in the range from 80 nm to 150 nm.
The HTL 232 is made of transparent P-type organic material having high hole mobility, such as n-propyl bromide (NPB). A highest occupied molecule orbital (HOMO) of the HTL 232 is close to that of the first electrode layer 22, so as to lower the potential barrier between the THL 232 and the first electrode layer 22. Thus, holes provided by the first electrode layer 22 can transmit to the THL 232 easily.
The EML 230 and the ETL 231 are both made of transparent N-type organic material having high electron mobility, such as aluminum-tris-quinolate (Alq3). Fluorescent organic material is doped into the EML 230, such that the fluorescent organic material occupies about 1% to 10% by volume of the doped N-type organic material. The fluorescent organic material is doped into the EML 230 to control the optical spectrum, as well as to increase the luminous efficiency. A lowest unoccupied molecule orbital (LUMO) of each of the EML 230 and the ETL 231 is much greater than the HOMO of the HTL 232, so that the potential barrier between the EML 230 and the HTL 232 is sufficiently great. Thus, it is very difficult for electrons in the EML 230 to transmit into the HTL 232.
The second electrode layer 21 is configured to be a cathode layer, and has a triple-layer structure. The triple-layer structure includes a photic layer 210, an absorbing layer 211, and a metal layer 212 stacked on the ETL 231 in that sequence.
The photic layer 210 is made of metal or alloy having a low work function, so as to reduce the potential barrier between the organic layer 23 and the second electrode layer 21. The photic layer 210 is a thin electrically conductive film with a thickness less than the skin depth of visible light. The skin depth is defined as a depth at which the amplitude of the electromagnetic field provided by visible light beams drops to 1/e of the source amplitude. The skin depth depends on the frequency of light beams, and on the magnetic permeability and conductivity of the photic layer 210. Thus, visible light beams can transmit through the photic layer 210. Typically, the thickness of the photic layer 210 is in the range from 2 nm to 12 nm. A material of the photic layer 210 can be one of calcium (Ca), magnesium (Mg), and lithium fluoride (LiF).
The absorbing layer 211 is configured to absorb light beams passing through the photic layer 210. The absorbing layer 211 is made of electrically conductive material capable of absorbing visible light beams; for example, graphite. A thickness of the absorbing layer 211 is in the range from 5 nm to 10 nm.
The metal layer 212 is mainly configured to be a conductive electrode, as well as to protect the absorbing layer 211 and the photic layer 210 of the second electrode layer 21. The metal layer 212 is made of metal having high electrical conductivity, such as silver (Ag) or aluminum (Al). A thickness of the metal layer 212 is in the range from 100 nm to 150 nm.
In operation, a direct current voltage is applied to the first electrode layer 22 and the metal layer 212 for driving the OLED 200 to display images. Due to the direct current voltage, a plurality of holes are provided by the first electrode layer 22, and a plurality of electrons are provided by the second electrode layer 21, respectively. The holes emit from the first electrode layer 22, pass through the HTL 232, and then arrive at the EML 230. Simultaneously, the electrons emit from the second electrode layer 21, pass through the ETL 231, and then also arrive at the EML 230. The electrons are obstructed from transmitting into the HTL 232 because of the potential barrier caused by the difference between the HOMO of the HTL 232 and the LUMO of the EML 230. Therefore, almost all of the electrons stay in the EML 230.
In the EML 230, recombination is induced between each of the electron-hole pairs. During the recombination, the electron transits from an energy band having a higher energy level to an energy band having a lower energy level. Thus, the energy of the recombined electrons is reduced, and energy is released via generation of photons. Due to the optical spectrum control function of the fluorescent organic material in the EML 230, emitting light beams having a corresponding frequency are thereby generated.
Most of the emitting light beams 240 transmit down through the HTL 232, the first electrode layer 22, and the substrate 20 sequentially, and then emit from the bottom surface of the substrate 20. Thereby, the OLED 200 is able to display images. The rest of the emitting light beams 241 transmit up, pass through the ETL 231 and the photic layer 210, and then are absorbed by the absorbing layer 211. Further, ambient light beams 250 enter the OLED 200 via the bottom surface, pass through the substrate 20, the first electrode layer 22, the organic layer 23, and the photic layer 210 sequentially, and then are also absorbed by the absorbing layer 211.
As described above, the light beams 241 and 250 that transmit to the second electrode layer 21 are absorbed by the absorbing layer 211 therein. Therefore, no reflected light beams emit from the bottom surface of the substrate 20 of the OLED 200. Thus, any interference phenomenon that would otherwise exist is substantially reduced or even eliminated, because the light beams 241, 250 are not able to reflect back down and interfere with the emitting light beams 240. Accordingly, the display quality of the OLED 200 can be improved. Moreover, when the OLED 200 displays a black or dark image, because there are substantially no reflected light beams, the brightness of the OLED 200 can be maintained at a suitable lower level, so that the contrast ratio of the OLED 200 is improved.
In step S1, a substrate 20 is provided. The substrate 20 is transparent, and is typically made of glass.
In step S2, a first electrode layer 22 is deposited on the substrate 20 via physical vapor deposition (PVD). The material of the first electrode layer 22 is transparent, electrically conductive material such as ITO or IZO. A thickness of the first electrode layer 22 is controlled to be in the range from 25 nm to 100 nm, by controlling the deposition time.
Step S3 includes the following steps: forming a hole transport layer (HTL) 232 on the first electrode layer 22; forming an emitting layer (EML) 230 on the HTL 232; and forming an electron transport layer (ETL) 231 on the EML 230.
In detail, firstly, the HTL 232 is deposited on the first electrode layer 22. The HTL 232 is made of transparent P-type organic material having high hole mobility, such as NPB.
Secondly, a transparent N-type organic layer having high electron mobility is deposited on the HTL 232, and then fluorescent organic material is doped into the N-type organic layer. The material of the N-type organic layer can be Alq3, and the fluorescent organic material can occupy about 1% to 10% by volume of the doped N-type organic material. After that, the EML 230 is deposited on the HTL 232.
Thirdly, the ETL 231 is deposited on the EML 230, so that the organic layer 23 including the HTL 232, the EML 230, and the ETL 231 is formed on the first electrode layer 22. The ETL 231 is a transparent N-type organic material such as Alq3. An overall thickness of the organic layer 23 is controlled to be in the range from 80 nm to 150 nm. The HTL 232, the EML 230, and the ETL 231 can each be formed by a selected one of the following methods: PVD, spin coating, and printing.
Step S4 includes the following steps: forming a photic layer 210 on the ETL 231; forming an absorbing layer 211 on the photic layer 210; and forming a metal layer 212 on the absorbing layer 211.
In detail, firstly, the photic layer 210 is deposited on the ETL 231. The photic layer 210 is made of material having a low work function, such as a selected one of Ca, Mg, and LiF. A thickness of the photic layer 210 is controlled to be in the range from 2 nm to 12 nm.
Secondly, the absorbing layer 211 capable of absorbing visible light beams is deposited on the photic layer 210. A thickness of the absorbing layer 211 is controlled to be in the range from 5 nm to 10 nm. The material of the absorbing layer 211 can be graphite.
Thirdly, the metal layer 212 having a thickness in the range from 100 nm to 150 nm is deposited on the absorbing layer 211. The material of the metal layer 212 can be Ag or Al. After that, the second electrode layer 21 is deposited on the organic layer 23. The photic layer 210, the absorbing layer 211, and the metal layer 212 can all be formed via PVD.
Furthermore, a passivation layer can be formed on the second electrode layer 21, to protect the OLED 200 from being oxidized.
It is to be understood, however, that even though numerous characteristics and advantages of preferred and exemplary embodiments have been set out in the foregoing description, together with details of the structures and functions of the embodiments, the disclosure is illustrative only; and that changes may be made in detail within the principles of present invention to the full extent indicated by the broad general meaning of the terms in which the appended claims are expressed.
Number | Date | Country | Kind |
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95137304 | Oct 2006 | TW | national |