ELECTRODE IN SEMICONDUCTOR DEVICE, CAPACITOR AND METHOD OF FABRICATING THE SAME
A semiconductor device and a method of fabricating the same include an electrode having a nickel layer with impurities. The electrode having a nickel layer with impurities can be a gate electrode or a capacitor electrode. The electrode having a nickel layer with impurities may include a combination of a pure nickel layer and a nickel layer with impurities.
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The present application is a Divisional Application of U.S. patent application Ser. No. 12/344,182, filed Dec. 24, 2008, which claims priority of Korean patent application number 2008-0081575, filed on Aug. 20, 2008, which is incorporated herein by reference in its entirety.
BACKGROUNDThe disclosure relates to a semiconductor device, and more particularly, to an electrode and a capacitor in a semiconductor device, and a method of fabricating the same.
Recently, in a process for fabricating a Metal Insulator Metal (MIM) capacitor, a method for fabricating a dielectric layer with a high dielectric constant (k) or an electrode having a high work function has been proposed to obtain required capacitance even when a semiconductor device is integrated.
However, the dielectric layer with the high dielectric constant (k) cannot be applied to semiconductor devices due to deterioration of current leakage despite the fact that the dielectric layer with the high dielectric constant (k) has a low energy band gap.
To overcome the limitation of the dielectric layer, precious metals are used to form the electrode. However, the precious metal cannot be applied to the process since the precious metal with a high work function has a low adhesion force due to a low coupling force.
Thus, it is required to develop an electrode with the high work function and the high adhesion force.
SUMMARYOne or more embodiments provide a semiconductor device having an electrode and/or a capacitor and method of fabricating the same.
In accordance with one or more embodiments, an electrode for a semiconductor device includes a nickel layer with impurities.
The impurities may include carbon (C) or hydrogen (H). The concentration of the impurities in the nickel layer with impurities may range from approximately 5% to approximately 50%.
In accordance with one or more embodiments, an electrode for a semiconductor device includes a combination of a pure nickel layer and a nickel layer with impurities.
The pure nickel layer and the nickel layer with impurities may be formed to have a stack structure.
The combination of the pure nickel layer and the nickel layer with impurities may have a stack structure of a nickel layer with impurities, a pure nickel layer, and a nickel layer with impurities.
In accordance with one or more embodiments, a capacitor includes: a first electrode; a dielectric layer; and a second electrode, wherein one of the first electrode and the second electrode includes a nickel layer with impurities.
One of the first electrode and the second electrode may include a pure nickel layer and a nickel layer with impurities.
The nickel layer with impurities may be formed to be in contact with the dielectric layer.
One of the first electrode and the second electrode may have a stack structure of a nickel layer with impurities, a pure nickel layer, and a nickel layer with impurities.
One of the first electrode and the second electrode may have a stack structure of a pure nickel layer and a nickel layer with impurities.
The impurities may include carbon (C) or hydrogen (H).
The concentration of the impurities in the nickel layer with impurities may range from approximately 5% to approximately 50% of the nickel layer with impurities.
The first electrode or the second electrode may be of a concave type, a cylinder type, or a pillar type.
In accordance with one or more embodiments, a method of fabricating a capacitor includes: forming a first electrode; forming a dielectric layer over the first electrode; and forming a second electrode over the dielectric layer, wherein one of the first electrode and the second electrode includes a nickel layer with impurities.
The impurities may include carbon (C) or hydrogen (H).
The concentration of the impurities in the nickel layer with impurities may range from approximately 5% to approximately 50%.
One of the first electrode and the second electrode may have a combination of a pure nickel layer and a nickel layer with impurities.
The nickel layer with impurities may be formed to be in contact with the dielectric layer.
One of the first electrode and the second electrode may have a stack structure of a pure nickel and a nickel layer with impurities.
The first electrode or the second electrode may have a stack structure of a nickel layer with impurities, a pure nickel layer, and a nickel layer with impurities.
The pure nickel layer and the nickel layer with impurities may be formed through a Chemical Vapor Deposition (CVD) process or an Atomic Layer Deposition (ALD) process.
The pure nickel layer and the nickel layer with impurities may be formed through the ALD process using a nickel precursor and a reaction gas.
The nickel precursor may flow at a rate of approximately 50 sccm to 1,000 sccm. The reaction gas may flow at a rate of approximately 100 sccm to approximately 3,000 sccm for formation of the nickel layer with impurities, and the reaction gas may flow at a rate of approximately 3,000 sccm to approximately 5,000 sccm for formation of the pure nickel layer.
The reaction gas may include H2 or NH3.
H2 plasma or NH3 plasma may be applied during the ALD process.
The ALD process may be performed at a temperature of approximately 200° C. to approximately 500° C.
The pure nickel layer and the nickel layer with impurities may be formed In-situ or Ex-situ.
The first electrode or the second electrode may be of a concave type, a cylinder type or a pillar type.
One or more embodiments relate to an electrode and/or a capacitor electrode in a semiconductor device, and a method of fabricating the same. In accordance with one or more embodiments, an electrode includes a nickel layer containing impurities, such as carbon (C) or hydrogen (H), to improve adhesion force. Furthermore, leakage current characteristics and crystallization characteristics of a dielectric layer can be improved.
The advantages, features and aspects of one or more embodiments will become apparent from the following description of the embodiments with reference to the accompanying drawings.
In the drawings, the illustrated thicknesses of layers and regions are exaggerated to facilitate explanation. It will also be understood that when a layer is referred to as being “on/under” another layer or substrate, it can be directly on/under the other layer or substrate, or intervening layers may also be present. In addition, when a layer is referred to as being ‘between’ two layers, it can be the only layer between the two layers, or one or more intervening layers may also be present. Furthermore, the same or like reference numerals represent the same or like elements throughout the drawings.
Referring to
The nickel layer has a high work function of approximately 4.8 eV to approximately 5.15 eV and exhibits excellent adhesion force with other layers. Thus, when the nickel layer is used as an electrode of the device with the high dielectric layer, current leakage characteristics can be improved.
A pure nickel layer has poor roughness because of a three-dimensional structure growth and may be oxidized during a process of depositing a dielectric layer over the pure nickel layer. According to an embodiment, a nickel layer 101 containing impurities can improve the roughness and prevent the oxidation.
The impurities in the nickel layer 101 do not affect the characteristics of the pure nickel layer. Preferably, the impurities may be carbon (C) or hydrogen (H). The impurities may range from approximately 5% to approximately 50% of the nickel layer 101.
The nickel layer 101 containing impurities, for example, a nickel layer 101 containing carbon (C), is formed to have Ni—C coupling and grows in a two-dimensional direction so that the nickel layer 101 has a planar surface. The Ni—C coupling enables Ni and C to combine with each other and therefore, the nickel layer 101 containing carbon (C) has less crystallization characteristics than the pure nickel layer, and carbon (C) is randomly distributed and deposited in the nickel layer 101. Thus, the nickel layer 101 firstly grows in the second-dimensional direction to form the planar surface and then a deposition process is performed forming a film layer with the planar surface.
Since the nickel layer 101 containing the impurities has relatively less chemical bondings between Ni and C than the pure nickel layer due to the presence of the impurities, the oxidation is prohibited.
Referring to
The pure nickel layer 202 has a high work function of approximately 4.8 eV to approximately 5.15 eV and exhibits excellent adhesion force with other layers. Thus, when the nickel layer is employed as an electrode of the device with the high dielectric layer, current leakage characteristics can be improved.
The first nickel layer 201 containing impurities and the second nickel layer 203 containing impurities are formed to improve the roughness and prevent the oxidation.
The impurities in the first and second nickel layers 201 and 203 containing impurities do not affect the quality of the pure nickel layer 202. Preferably, the impurities may be carbon (C) or hydrogen (H). When a ratio of C to Ni is 1:3, that is, when a compound contains C of approximately 25% and Ni of approximately 75%, the compound is called a Nickel carbide (Ni3C).
Since the pure nickel layer 202 grows in a three-dimensional direction, the surface roughness is not excellent. However, the first and second nickel layers 201 and 203 containing the impurities, for example, having a Ni—C coupling, grow in a second-dimensional direction, forming a planar surface.
In the Ni—C coupling, Ni and C are combined with each other. Therefore, the first and second nickel layers 201 and 203 containing the impurities have less crystallization than the pure nickel layer 202 and the impurities are randomly distributed. Thus, the nickel layer 201 firstly grows in the second-dimensional direction to form a planar surface and then a deposition process is performed. Thus, a film layer with the planar surface is formed.
Since the first and second nickel layers 201 and 203 containing the impurities has relatively less chemical bondings than the pure nickel layer because of the Ni—C coupling, the oxidation is prevented.
The electrode with a stack structure comprising the first nickel layer 201 containing impurities, the pure nickel layer 202, and the second nickel layer 203 containing impurities is formed in a planar type. However, the electrode with a stack structure comprising the first nickel layer 201 containing impurities, the pure nickel layer 202, and the second nickel layer 203 containing impurities can be formed to have a plate type, a concave type, a cylinder type, a pillar type and a combination thereof.
The first nickel layer 201 containing impurities, the pure nickel layer 202, and the second nickel layer 203 containing impurities are formed through a Chemical Vapor Deposition (CVD) process or an Atomic Layer Deposition (ALD) process. The formation method through the ALD process will be described in more detail later by referring to
Referring to
Referring to
According to the ALD process, a source gas is provided to be chemically adsorbed to a surface of a substrate, and a purge gas flows to purge the physically extra-adsorbed sources. A reaction gas is provided to a source in one layer to cause a chemical reaction between the source in one layer and the reaction gas to thereby deposit an atomic film layer. The ALD process is performed in a surface reaction mechanism to form a stable and even film layer. Thus, the method can be applied to a process for forming a structure with high step coverage (or a big height difference) and a low design rule.
Furthermore, since the source gas and the reaction gas are separated, sequentially provided and purged, the ALD process generates less particles caused by a gas phase reaction than the CVD process.
Referring to
Herein, each layer is formed in-situ or ex-situ. Particularly, when the layer is formed in-situ, the quantity of the reaction gas for forming the layer is controlled to form the pure nickel layer, the first nickel layer containing the impurities and the second nickel layer containing the impurities. For instance, when the source gas flows at a rate of approximately 50 sccm to approximately 1,000 sccm, the reaction gas is controlled to flow at a rate of approximately 3,000 to approximately 5,000 sccm to form the pure nickel layer and at a rate of approximately 100 sccm to approximately 3,000 sccm to form the first and the second nickel layers.
First to third unit cycles are sequentially performed to form the first nickel layer containing the impurities, the pure nickel layer, and the second nickel layer containing impurities. Particularly, each unit cycle is repeatedly performed X, Y, and Z times, respectively to adjust thicknesses of the above layers.
The ALD process may be performed at a temperature of approximately 200° C. to approximately 500° C.
Each of the first to third unit cycles is performed in a sequence of source gas/purge gas/reaction gas/purge gas.
The first unit cycle for forming the first nickel layer containing the impurities includes injection of nickel source gas 301, injection of purge gas 302, injection of reaction gas 303, and injection of purge gas 302.
The injection of the nickel source gas 301 flows nickel organic precursor at a rate of approximately 50 sccm to approximately 1,000 sccm for approximately 0.1 second to approximately 10 seconds by using carrier gas such as nitrogen (N2) or argon (Ar). Here, the nickel organic precursor may be NiCO3.
The injection of the purge gas 302 is performed after the injection of the source gas 301 and the injection of the reaction gas 303. In the injection of the purge gas 302, the N2 gas flows into a deposition chamber at a rate of approximately 100 sccm to approximately 2,000 sccm for approximately 1 second to approximately 10 seconds to remove the remaining nickel source gas or reaction gas in the chamber.
The injection of the reaction gas 303 is performed to form the first nickel layer containing the impurities. The reaction gas, that is, H2 or NH3 flows into the deposition chamber at rate of approximately 100 sccm to approximately 3,000 sccm for 1 second to 10 seconds to form the first nickel layer containing the impurities. Particularly, the reaction gas is adjusted to form the first nickel layer containing the impurities. Here, the reaction gas is injected less than that required for forming the pure nickel layer to prevent the reaction of the impurities in the nickel source gas. A portion of the impurities is removed and the remaining impurities are included in the film layer. Thus, the first nickel layer containing the impurities is formed.
As described above, the first unit cycle is repeatedly performed X times to form the first nickel layer containing the impurities with a desired thickness.
The second unit cycle for forming the pure nickel layer includes injection of nickel source gas 301, injection of purge gas 302, injection of reaction gas 303, and injection of purge gas 302.
The injection of the nickel source gas 301 flows nickel organic precursor at a rate of approximately 50 sccm to approximately 1,000 sccm for approximately 0.1 second to approximately 10 seconds by using carrier gas such as N2 or Ar. Here, the nickel organic precursor may be NiCO3.
The injection of the purge gas 302 is performed after the injection of the source gas 301 and the injection of the reaction gas 303. In the injection of the purge gas 302, the N2 gas flows into a deposition chamber at a rate of approximately 100 sccm to approximately 2,000 sccm for approximately 1 second to approximately 10 seconds to remove the remaining nickel source gas or reaction gas in the chamber.
The injection of the reaction gas 303 is performed to form the pure nickel layer. The reaction gas, which is H2 or NH3, flows into the deposition chamber at rate of approximately 3,000 sccm to approximately 5,000 sccm for 1 second to 10 seconds to form the pure nickel layer containing the impurities. Particularly, the reaction gas is adjusted sufficiently to form the pure nickel layer. Here, the reaction gas is injected in a sufficient amount that all the impurities in the nickel source gas react off. Therefore, the reaction gas is injected in a rate of approximately 3,000 sccm to approximately 5,000 sccm.
A second unit cycle described above is repeatedly performed Y times to form the pure nickel layer with a desired thickness.
The second nickel layer containing the impurities is formed in the same order that the first nickel layer containing the impurities is formed.
The second nickel layer containing the impurities is formed by repeatedly performing a third unit cycle Z times.
Particularly, each of the first to third unit cycles is repeatedly performed X, Y, and Z times to adjust the thickness of each layer and sequentially performed in order of stack.
Furthermore, in the ALD process, N2 or NH3 plasma may be applied to increase the deposition speed.
Referring to
Here, the impurities include carbon (C) or hydrogen (H). The impurities occupy approximately 5% to approximately 50% of the nickel layer.
The first and the second electrodes 401 and 403 are formed through the CVD process or the ALD process.
The first and the second electrodes 401 and 403 can be formed to have a plate type, a pillar type, a concave type, a cylinder type, or a combination thereof.
Referring to
The cylinder type lower electrode 507A and the first upper electrode 509 are formed of the nickel layer containing the impurities described above referring to
The dielectric layer 508 may include a high-k material. The high-k material may include TiO2, SrTiO2, or BaSbTiO3. Here, the lower electrode 507A is preferably formed to have the structure illustrated in
Referring to
A storage node contact plug 503 through the inter-layer dielectric layer 502 is formed to be connected to a region in the substrate 501. To be specific, the inter-layer dielectric layer 502 is etched to form a contact hole exposing the substrate 501. A conductive material is formed to fill the contact hole and then an etch process is performed until the surface of the inter-layer dielectric layer 502 is exposed.
The conductive material may include a transition metal layer, a rare earth metal layer, a transition metal silicide, a rare earth metal silicide, or an alloy thereof. The conductive material may include a polysilicon layer doped with impurity ions or have a stack structure of multi-layers. The conductive material may include a stack structure of at least two materials including the above conductive materials. When the storage node contact plug 503 includes a metal layer (which is the transition layer or the rare earth metal), a barrier metal layer (not shown) may be formed between the metal layer of storage node contact plug 503 and the contact hole.
An etch stop layer 504 is formed over the inter-layer dielectric layer 502. When the contact hole for a subsequent lower electrode is formed, the etch stop layer 504 stops the etch process to prevent the inter-layer dielectric layer 502 from being damaged. Furthermore, when a dip-out process for forming the cylinder type capacitor is performed, the etching solution is prevented from flowing into the inter-layer dielectric layer 502 by the etch stop layer 504. Thus, the etch stop layer 504 includes a material having an etch selectivity ratio with a subsequent sacrificial layer. The etch stop layer 504 may include a nitride layer such as a silicon nitride (SiN, Si3N4).
A sacrificial layer 505 is formed over the etch stop layer 504. In the sacrificial layer 505, a contact hole for the lower electrode is formed. The sacrificial layer 505 may include an oxide layer and may comprise one or more layers. The oxide layer may be an HDP oxide layer, a BPSG layer, a PSG layer, a BSG layer, a TEOS layer, an USG layer, an FSG layer, a CDO layer, an OSG layer or a combination thereof such as a stack structure of the foregoing. The oxide layer may include a layer coated by a spin coating method such as an SOD layer.
The sacrificial layer 505 and the etch stop layer 504 are etched to form a storage node hole 506 exposing the storage node contact hole 503. The storage node hole 506 defines a region where the lower electrode is formed. In detail, mask patterns are formed over the sacrificial layer 505, then the sacrificial layer 505 and the etch stop layer 504 are etched using the mask patterns as an etch barrier to form the storage node hole. For mask patterns, a photoresist layer is coated over the sacrificial layer 505 and patterned to open the region where the storage node contact hole is formed. A hard mask layer may be additionally formed before the photoresist layer is formed to secure an etch margin, which may not be sufficient only with the photoresist layer.
Referring to
The lower electrode 507 containing the impurities includes a first nickel layer containing impurities, a pure nickel layer, and a second nickel layer containing impurities as the structure illustrated in
A thermal treatment process is performed on the lower electrode 507 to increase crystallinity. The thermal treatment process may be a rapid thermal treatment process or furnace annealing process. A temperature for the thermal treatment process varies according to equipment. In this embodiment, the thermal treatment process is performed at a temperature of approximately 400 to approximately 800.
Referring to
Referring to
Referring to
Thereafter, a first upper electrode 509 and a second upper electrode 510 are formed over the dielectric layer 508. The first upper electrode 509 is formed by the same manner as that for forming the lower electrode pattern 507A. That is, the first upper electrode 509 is formed to include the nickel layer containing the impurities. After the formation of the first upper electrode 509, a thermal treatment process can be performed for the same reason as the thermal treatment of the lower electric 507A.
The second upper electrode 510 includes a titanium nitride (TiN) layer to be electrically connected. The second upper electrode 510 may be formed through the CVD process. The upper electrode may comprise only the first upper electrode 509 without forming the second upper electrode 510.
Referring to
The pillar type lower electrode 607A and the upper electrode 609 may be formed to have the structure illustrated in
The dielectric layer 608 may include a high-k material. The high-k material may include TiO2, SrTiO2, or BaSbTiO3. Here, the lower electrode 607A is formed to have the structure illustrated in
Referring to
A storage node contact plug 603 through the inter-layer dielectric layer 602 is formed to be connected to a region in the substrate 601. To be specific, the inter-layer dielectric layer 602 is etched to form a contact hole exposing the substrate 601. A conductive material is formed to fill the contact hole and then an etch process is performed until a surface of the inter-layer dielectric layer 602 is exposed.
The conductive material may include a transition metal layer, a rare earth metal layer, a transition metal silicide, a rare earth metal silicide, or an alloy thereof. The conductive material may include a polysilicon layer doped with impurity ions or have a stack structure of multi-layers. When the storage node contact plug 603 includes a metal layer (the transition metal, the rare earth metal), a barrier metal layer (not shown) may be additionally formed between the storage node contact 603 and the contact hole.
An etch stop layer 604 is formed over the inter-layer dielectric layer 602. When the contact hole for a subsequent lower electrode is formed, the etch stop layer 604 stops the etch process to prevent the inter-layer dielectric layer 602 from being damaged. Furthermore, when a dip-out process for forming the pillar type capacitor is performed, the etching solution is prevented from flowing into the inter-layer dielectric layer 602 by the etch stop layer 605. Thus, the etch stop layer 604 includes a material having an etch selectivity ratio with a subsequent sacrificial layer. The etch stop layer 604 may be a nitride layer including a silicon nitride such as SiN, Si3N4.
A sacrificial layer 605 is formed over the etch stop layer 604. In the sacrificial layer 605, a contact hole for the lower electrode is formed. The sacrificial layer 605 may include an oxide layer and may comprise one layer or multi-layers. The oxide layer may be an HDP oxide layer, a BPSG layer, a PSG layer, a BSG layer, a TEOS layer, an USG layer, an FSG layer, a CDO layer, an OSG layer or a combination thereof such as a stack structure of the foregoing. The oxide layer may include a layer coated by a spin coating method such as an SOD layer.
The sacrificial layer 605 and the etch stop layer 604 are etched to form a storage node hole 606 exposing the storage node contact hole 603. The storage node hole 606 defines a region where the lower electrode is formed. In detail, mask patterns are formed over the sacrificial layer 605, then the sacrificial layer 605 and the etch stop layer 604 are etched using the mask patterns as an etch barrier to form the storage node hole. For mask patterns, a photoresist layer is coated over the sacrificial layer 605 and patterned to open the region where the storage node contact hole is formed. A hard mask layer may be additionally formed before the photoresist layer is formed to secure an etch margin which may not be sufficient only with the photoresist layer.
Referring to
The lower electrode 607 containing the impurities includes a first nickel layer containing impurities, a pure nickel layer, and a second nickel layer containing impurities as the structure illustrated in
A thermal treatment process is performed on the lower electrode 607 to increase crystallinity. The thermal treatment process may be a rapid thermal treatment process or furnace annealing process. A temperature for the thermal treatment process varies according to equipment. In this embodiment, the thermal treatment process is performed at a temperature of approximately 400 to approximately 800.
Referring to
Referring to
Referring to
Thereafter, an upper electrode 609 is formed over the dielectric layer 608. The upper electrode 609 is formed by the same manner with that for forming the lower electrode 607A. That is, the upper electrode 609 is formed to include the nickel layer containing the impurities. After the upper electrode 609 is formed, a thermal treatment process is performed for the same reason as the thermal treatment of the lower electrode pattern 607A.
While embodiments have been described with reference to the pillar type and the cylinder type capacitors and the method for fabricating the same, changes and modifications can be made to be applied to a planar type capacitor and a concave type capacitor. Furthermore, changes and modifications can be made to be applied to any other electrodes in the devices applying a high-k layer, improving the leakage current characteristics, as well as any other electrodes requiring a low resistivity and a high work function.
While one or more embodiments been described it will be apparent to those skilled in the art that various changes and modifications may be made.
Claims
1. An electrode for a semiconductor device, comprising:
- a nickel layer with impurities.
2. The electrode of claim 1, wherein the impurities include carbon (C) or hydrogen (H).
3. The electrode of claim 1, wherein a concentration of the impurities in the nickel layer with impurities ranges from approximately 5% to approximately 50%.
4. The electrode of claim 1, wherein the electrode is a gate electrode.
5. An electrode for a semiconductor device, comprising:
- a combination of a pure nickel layer and a nickel layer with impurities.
6. The electrode of claim 5, wherein the pure nickel layer and the nickel layer with impurities are formed to have a stack structure.
7. The electrode of claim 5, wherein the combination of the pure nickel layer and the nickel layer with impurities has a stack structure of a first nickel layer with impurities, a pure nickel layer, and a second nickel layer with impurities.
8. The electrode of claim 5, wherein the impurities include carbon (C) or hydrogen (H).
9. The electrode of claim 5, wherein a concentration of the impurities in the nickel layer with impurities ranges from approximately 5% to approximately 50% of the nickel layer.
10. The electrode of claim 5, wherein the electrode is a gate electrode.
11. A capacitor, comprising:
- a first electrode;
- a dielectric layer; and
- a second electrode,
- wherein one of the first electrode and the second electrode includes a nickel layer with impurities.
12. The capacitor of claim 11, wherein one of the first electrode and the second electrode includes a pure nickel layer and a nickel layer with impurities.
13. The capacitor of claim 12, wherein the nickel layer with impurities is formed to be in contact with the dielectric layer.
14. The capacitor of claim 12, wherein one of the first electrode and the second electrode has a stack structure of a first nickel layer with impurities, a pure nickel layer, and a second nickel layer with impurities.
15. The capacitor of claim 11, wherein the impurities include carbon (C) or hydrogen (H).
16. The capacitor of claim 11, wherein a concentration of the impurities in the nickel layer with impurities ranges from approximately 5% to approximately 50% of the nickel layer with impurities.
17. The capacitor of claim 11, wherein the first electrode or the second electrode is a plate type, a concave type, a cylinder type, or a pillar type.
Type: Application
Filed: Feb 23, 2012
Publication Date: Jun 14, 2012
Applicant: HYNIX SEMICONDUCTOR INC. (Icheon-si)
Inventors: Kwan-Woo DO (Icheon-si), Kee-Jeung LEE (Icheon-si), Deok-Sin KIL (Icheon-si), Young-Dae KIM (Icheon-si), Jin-Hyock KIM (Icheon-si), Kyung-Woong PARK (Icheon-si), Jeong-Yeop LEE (Icheon-si)
Application Number: 13/403,541
International Classification: H01G 4/008 (20060101); H01L 23/482 (20060101);