The present disclosure relates to a plasma reactor for generating radicals of gas for injection onto a substrate.
Plasma is partially ionized gas consisting of large concentrations of excited atomic, molecular, ionic, and free-radical species. The reactive species or radicals generated by plasma can be used for various purposes, including (i) chemically or physically modifying the characteristics of a surface of substrate by exposing the surface to the reactive species or radicals, (ii) performing chemical vapor deposition (CVD) by causing reaction of the reactive species or radicals and source precursor in a vacuum chamber, and (iii) performing atomic layer deposition (ALD) by exposing a substrate adsorbed with source precursor molecules to the reactive species or radicals.
There are two different types of plasma reactors: (i) a direct plasma reactor, and (ii) a remote plasma reactor. The direct plasma reactor generates plasma that comes into contact directly with the substrate. The direct plasma reactor may generate energetic particles (e.g., free radicals, electrons and ions) and radiation that directly come into contact with the substrate. Such contact may cause damage to the surface of the substrate and also disassociate source precursor molecules adsorbed in the substrate. Hence, the direct plasma reactor has limited use in fabrication of semiconductor devices or organic light emitting diode (OLED) devices.
A remote plasma device generates plasma at a location remote from the substrate. Hence, the remote plasma device is less likely to cause damage to the substrate. However, in a remote plasma device, the radicals or reactive species generated by the plasma needs to travel across a certain distance to the substrate. While traveling, the radicals or the reactive species may revert back to low reactive state or dissipate. Therefore, the amount of radicals or reactive species generated in the remote plasma device tends to be smaller than a comparable direct plasma reactor.
Embodiments relate to a remote plasma reactor with a plurality of sub-plasma reactors cascaded to increase the amount or reactivity of radicals or reactive species generated in the remote plasma reactor. Each sub-plasma reactor includes a chamber for generating plasma. By applying energy to gas within a first sub-plasma reactor, plasma is formed in the plasma chamber to generate a first excited gas. The first excited gas is then injected into a second sub-plasma reactor to generate a second excited gas that is more reactive or excited than the first excited gas.
In one embodiment, the first sub-plasma reactor includes a first inner electrode and a first outer electrode defining a first chamber of the first sub-plasma reactor. A voltage difference is applied between the first inner electrode and the first outer electrode to generate plasma in the first chamber to excite gas within the first chamber. The second sub-plasma reactor includes a second inner electrode and a second outer electrode defining a second chamber of the second sub-plasma reactor. A voltage difference is applied between the second inner electrode and the second outer electrode to excite gas within the second chamber.
In one embodiment, the first sub-plasma reactor and the second sub-plasma reactor include a body formed with at least one channel for circulating cooling medium to cool the plasma reactor.
In one embodiment, the second sub-plasma reactor is formed with an exposure chamber open towards the substrate and having a width larger than a gap between the second sub-plasma reactor and the substrate.
In one embodiment, the first and second sub-plasma reactors are capacitively coupled plasma (CCP) type sub-plasma reactors.
In one embodiment, the first sub-plasma reactor and the second sub-plasma reactor are of different types.
In one embodiment, the first sub-plasma reactor is an inductively coupled plasma (ICP) type sub-plasma reactor and the second sub-plasma reactor is a capacitively coupled plasma (CCP) type sub-plasma reactor.
In one embodiment, the first sub-plasma reactor includes a coil surrounding the first chamber and electric current passes the coil to induce plasma within the first chamber.
In one embodiment, the plasma reactor includes a third sub-plasma reactor connected to the first sub-plasma reactor to receive the first excited gas. The third sub-plasma reactor is formed with a third chamber and is configured to generate a third excited gas that is more reactive or excited than the first excited gas. The third sub-plasma reactor injects the third excited gas onto the substrate.
In one embodiment, the second sub-plasma reactor and the third sub-plasma reactor are placed in tandem.
In one embodiment, different portions of the substrate are successively injected with the second excited gas as the substrate passes the second sub-plasma reactor.
Embodiments are described herein with reference to the accompanying drawings. Principles disclosed herein may, however, be embodied in many different forms and should not be construed as being limited to the embodiments set forth herein. In the description, details of well-known features and techniques may be omitted to avoid unnecessarily obscuring the features of the embodiments.
In the drawings, like reference numerals in the drawings denote like elements. The shape, size and regions, and the like, of the drawing may be exaggerated for clarity.
Embodiments relate to a remote plasma reactor including two or more sub-plasma reactors connected in series to generate an increased amount of radicals and reactive species or increase the reactivity of excited gas. The two or more sub-plasma reactors may be of the same type or a different type. The plasma reactor including two or more sub-plasma reactors connected in series is advantageous, among other reasons, because smaller space is used to generate more reactive or more excited gas compared to using multiple plasma reactors placed on tandem.
The process chamber enclosed by walls may be maintained in a vacuum state to prevent contaminants from affecting the deposition process. The process chamber 110 contains a susceptor 128 which receives a substrate 120. The susceptor 128 is placed on a support plate 124 for a sliding movement. The support plate 124 may include a temperature controller (e.g., a heater or a cooler) to control the temperature of the substrate 120.
The linear deposition device 100 may also include lift pins (not shown) that facilitate loading of the substrate 120 onto the susceptor 128 or dismounting of the substrate 120 from the susceptor 128.
In one embodiment, the susceptor 128 is secured to brackets 210 that move across an extended bar 138 with screws formed thereon. The brackets 210 have corresponding screws formed in their holes receiving the extended bar 138. The extended bar 138 is secured to a spindle of a motor 114, and hence, the extended bar 138 rotates as the spindle of the motor 114 rotates. The rotation of the extended bar 138 causes the brackets 210 (and therefore the susceptor 128) to make a linear movement on the support plate 124. By controlling the speed and rotation direction of the motor 114, the speed and the direction of the linear movement of the susceptor 128 can be controlled. The use of a motor 114 and the extended bar 138 is merely an example of a mechanism for moving the susceptor 128. Various other ways of moving the susceptor 128 (e.g., use of gears and pinion or a linear motor at the bottom, top or side of the susceptor 128). Moreover, instead of moving the susceptor 128, the susceptor 128 may remain stationary and the reactors 136 may be moved.
One or more of the reactors 320, 334, 364, 368 are connected to gas pipes (not shown) to provide source precursor, reactant precursor, purge gas and/or other materials. The materials provided by the gas pipes may be (i) injected onto the substrate 314 directly by the reactors 320, 334, 364, 368, (ii) after mixing in a chamber inside the reactors 320, 334, 364, 368, or (iii) after conversion into radicals by plasma generated within the reactors 320, 334, 364, 368. After the materials are injected onto the substrate 314, the redundant materials may be exhausted through outlets 330, 338. The interior of the rotating deposition device 300 may also be maintained in a vacuum state.
The reactors 136 of
Plasma Reactor with Serially Connected Plasma Chambers
A body 510 of the plasma reactor 400 is made of a conductive material such as aluminum, stainless steel or nickel. Materials such as aluminum, stainless steel and nickel are stable and tend to have negligible reaction of radicals or reactive species generated in the plasma reactor. The body 510 is formed with a gas channel 518, cooling medium channels 522, gas holes 526, a first plasma chamber 528, a second plasma chamber 583 and an exposure chamber 515.
The reactivity of radicals or reactive species may drop if their temperature is excessively high. Therefore, the cooling medium channels 522 are provided to circulate cooling water or other cooling medium through the body 510 to cool the body 510, if needed.
Gas is injected into the first plasma chamber 528 of a first sub-plasma reactor 542 via gas holes 526. The first plasma chamber 528 is defined by an inner electrode 546 extending across the plasma reactor 400 and an outer electrode 541 surrounding the inner electrode 546. The outer electrode 541 may be part of the body 510. In one embodiment, the body 510 (and hence, the first electrode) is connected to ground whereas the electrode 546 is connected to a voltage source. As voltage pulse is applied across the electrode 546 and the body 510, plasma of the injected gas is generated in the plasma chamber 528. A first excited gas including radicals or reactive species is generated in the plasma chamber 528 as a result.
The first excited gas from the plasma chamber 528 travels to a second plasma chamber 538 of the second sub-plasma reactor 550 via radical exit 552. The second plasma chamber 538 is defined by an inner electrode 556 extending across the plasma reactor 400 and an outer electrode 549 surrounding the inner electrode 556. The outer electrode 549 may be part of the body 510. As voltage pulses are applied across the inner electrode 556 and the outer electrode 549, plasma is generated in the second plasma chamber 538. As a result, a second excited gas is generated in the second plasma chamber 538. The second excited gas has increased reactivity compared to the first excited gas by having more radicals or reactive species.
To induce the flow of the first excited gas from the first plasma chamber 528 to the second plasma chamber 538, the pressure in the first plasma chamber 528 is higher than the pressure in the second plasma chamber 538.
The second excited gas generated in the second plasma chamber 538 are injected via radical exit 560 into the exposure chamber 515 where the second excited gas travels to substrate 412 for reaction with the substrate 412. The radicals, reactive species in the second excited gas or gas remaining after the second excited gas comes into contact with the substrate 412 travel across gaps 568, 570 for discharge. It is advantageous to set the width w of the exposure chamber 515 to be larger than heights h1, h2 of gaps 568, 570 to enable sufficient exposure of the substrate 412 to the second excited gas before the second excited gas is discharged via the gaps 568, 570. In one embodiment, the height of gaps 568, 570 between the body 510 and the substrate 412 is 10 mm to 80 mm. To discharge the second excited gas remaining after injection onto the substrate 412 from the exposure chamber 515 to one side or both sides of the body 510 via one of the gaps 568, 570, the pressure in the exposure chamber 515 is maintained at a higher level than in the gaps 568, 570.
The substrate 412 moves below the body 510 to expose different parts of the substrate 412 to the second excited gas. Due to the increased reactivity of the second excited gas, the exposure of the substrate 412 for a short amount of time is sufficient to process the substrate 412. Hence, the substrate 412 can move across the reaction chamber 515 at a higher speed compared to using a plasma reactor with a single plasma chamber. The plasma reactor 400 advantageously produces the second excited gas with increased reactivity while occupying the same horizontal area as other plasma reactor with a single plasma chamber, and therefore, the plasma reactor 400 enables more efficient use of space in facilities where the plasma reactor 400 is installed.
The plasma reactors 600, 700 of
Plasma Reactors with CCP Sub-Plasma Reactors
By including the dielectric tubes 812, 816 or coating the electrodes 546, 556 with the dielectric material, more stable plasma can be generated. The dielectric material for coating or forming the dielectric tubes 812, 816 may include, among others, ceramic material such as alumina, Mg-doped alumina, magnesia, zirconia or yttria, monocrystalline sapphire without grain boundary or amorphous quartz. To prevent arc from forming, the dielectric tubes 812, 816 may be grinded to have a smooth surface.
A first excited gas is generated in the first plasma chamber 528 and then injected into the second plasma chamber 538. A second excited gas is then generated in the second plasma chamber 538 by further applying voltage between the electrode 556 and the body of the plasma reactor 800.
The plasma reactor of
Plasma is formed in the plasma chamber 934 of the CCP type sub-plasma reactor 916, increasing the reactivity of the injected radicals or reactive species injected via the radical exit 932.
The CCP type sub-plasma reactor 916 is formed with cooling medium channel 938, the plasma chamber 934 and an exposure chamber 950. The reactivity of radicals or reactive species may drop if their temperature is excessively high. Therefore, the cooling medium channels 938 are provided to circulate cooling water or other coolants through the CCP type sub-plasma reactor 916 to cool the CCP type sub-plasma reactor 916.
The plasma chamber 934 is defined by an electrode 942 extending across the plasma reactor 900 and the body 944 (which functions as another electrode). In one embodiment, the body 944 is connected to ground whereas the electrode 942 is connected to a voltage source. Dielectric tube 946 is placed in the plasma chamber 934. Instead of using dielectric tube 946, dielectric material may be coated on the electrode 942. As voltage pulse is applied across the electrode 942 and the body 944, plasma of the injected gas is generated in the plasma chamber 934. As a result, radicals or reactive species are generated in the plasma chamber 934.
The radicals and reactive species generated in the plasma chamber 934 are injected via radical exit 948 into the exposure chamber 950 where the radicals and the reactive species travel to substrate 412 for reaction with the substrate 412. The radicals, reactive species or gas remaining after the contact with the substrate 412 travel across gaps 968, 970 for discharge. In one embodiment, the height of gaps 968, 970 between the body 944 and the substrate 412 is configured in the same manner as gaps 568, 570 described in detail above with reference to
In the embodiment of
In one embodiment, cooling medium may be provided via the coil 924. The coil 924 may be formed with a passage for the cooling medium to pass through. The cooling medium may cool the ICP type sub-plasma reactor 912. The coil 924 may be made of copper tubing, for example.
In one embodiment, paths between the ICP type sub-plasma reactor 1120 and the CCP-type sub-plasma reactors 1130, 1140 are cooled down to extend the time that the radicals or reactive species remain active.
Although only two CCP-type sub-plasma reactors 1130, 1140 are described in
The sub-plasma reactors of the cascaded plasma reactor generate plasma at lower power than a single large plasma with capacity for generating the same or similar amounts of radicals. Hence, the electrodes of the cascaded plasma reactor will suffer less abrasion and/or resputtering compared to electrodes in a single large plasma reactor. Also, when the cascade plasma reactor is injected with oxygen, the cascade plasma reactor generates more O* radicals than a single large plasma reactor because the first sub-plasma reactor generate O3 and second sub-plasma reactor amplify or multiply the number of O* radicals by the contributions of ozone molecules.
To perform depositing of Al2O3 film by using radical assisted atomic layer deposition (ALD) and the cascaded plasma reactor, trimethylaluminium (TMA) may be used as a source precursor and O2 gas may be used as a reactant precursor. By moving the substrate 412, TMA molecule layer chemisorbed on substrate 412 reacts with the O* radicals and forms ALD Al2O3 film. According to an experiment, Al2O3 film deposited using the cascaded plasma reactor exhibited increased breakdown voltage and reduced leakage current compared to Al2O3 film deposited using a single large plasma reactor.
Although embodiments are described above with reference to linear or rotational deposition apparatus, the plasma reactors may be used in other devices for performing various operations.
This application claims priority under 35 U.S.C. §119(e) to co-pending U.S. Provisional Patent Application No. 61/755,353, filed on Jan. 22, 2013, which is incorporated by reference herein in its entirety.
Number | Date | Country | |
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61755353 | Jan 2013 | US |