EP1668683A1 - Method of forming dielectric layers with low dielectric constants - Google Patents
Method of forming dielectric layers with low dielectric constantsInfo
- Publication number
- EP1668683A1 EP1668683A1 EP04770031A EP04770031A EP1668683A1 EP 1668683 A1 EP1668683 A1 EP 1668683A1 EP 04770031 A EP04770031 A EP 04770031A EP 04770031 A EP04770031 A EP 04770031A EP 1668683 A1 EP1668683 A1 EP 1668683A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- layer
- recited
- wafer
- dielectric
- substrate
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
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Classifications
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02104—Forming layers
- H01L21/02107—Forming insulating materials on a substrate
- H01L21/02109—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates
- H01L21/02112—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer
- H01L21/02123—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer the material containing silicon
- H01L21/02126—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer the material containing silicon the material containing Si, O, and at least one of H, N, C, F, or other non-metal elements, e.g. SiOC, SiOC:H or SiONC
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02104—Forming layers
- H01L21/02107—Forming insulating materials on a substrate
- H01L21/02109—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates
- H01L21/02203—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates the layer being porous
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02104—Forming layers
- H01L21/02107—Forming insulating materials on a substrate
- H01L21/02109—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates
- H01L21/02205—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates the layer being characterised by the precursor material for deposition
- H01L21/02208—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates the layer being characterised by the precursor material for deposition the precursor containing a compound comprising Si
- H01L21/02214—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates the layer being characterised by the precursor material for deposition the precursor containing a compound comprising Si the compound comprising silicon and oxygen
- H01L21/02216—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates the layer being characterised by the precursor material for deposition the precursor containing a compound comprising Si the compound comprising silicon and oxygen the compound being a molecule comprising at least one silicon-oxygen bond and the compound having hydrogen or an organic group attached to the silicon or oxygen, e.g. a siloxane
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02104—Forming layers
- H01L21/02107—Forming insulating materials on a substrate
- H01L21/02225—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer
- H01L21/0226—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process
- H01L21/02282—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process liquid deposition, e.g. spin-coating, sol-gel techniques, spray coating
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02104—Forming layers
- H01L21/02107—Forming insulating materials on a substrate
- H01L21/02296—Forming insulating materials on a substrate characterised by the treatment performed before or after the formation of the layer
- H01L21/02299—Forming insulating materials on a substrate characterised by the treatment performed before or after the formation of the layer pre-treatment
- H01L21/02307—Forming insulating materials on a substrate characterised by the treatment performed before or after the formation of the layer pre-treatment treatment by exposure to a liquid
Definitions
- ILD's inter- level and intra-level dielectrics
- porous Si0 2 formed from hydrosilsesquioxane (HSQ), which is a flowable oxide that may be deposited by spin-on coating techniques. After the spin-on process is complete, the material is baked, and the solvent is removed, leaving silicon dioxide (glass), which is porous.
- the dielectric constant of the porous oxide layer is illustratively on the order of approximately 2.0 to approximately 3.8, and certainly less than 3.9. As can be appreciated, the greater the degree of porosity, the lower the dielectric constant.
- the referenced dielectric materials deposited by spin-coating are often referred to as spin-on-glass (SOG) materials. While these materials have shown promise in providing low-k ILD's, their deposition can be exceedingly costly.
- a method of depositing a dielectric material includes providing a substrate with at least one layer over the substrate. The method further includes pre-wetting a top surface of a top layer with a substance, spin coating the solution and forming the dielectric material.
- a semiconductor structure includes a layer of porous low-k dielectric material disposed over a substrate, wherein the material has a thickness across the layer, and the thickness has a uniformity across a surface with a standard deviation of +0.728%.
- Fig. 1 is a flow-chart of a process 100 of forming a low-k dielectric layer over a semiconductor wafer in accordance with an example embodiment.
- the wafer includes a semiconductor substrate, and at least one other layer formed thereover.
- the layer or layers over the substrate may be the usual layers in an IC, including but not limited to doped and undoped semiconductor layers, dielectric layers metal layers, including patterned metal layers, and other layers within the purview of one of ordinary skill in the art in the semiconductor processing art.
- a wafer is provided.
- a solvent is dispensed over the uppermost surface of the wafer.
- the solvent is chosen to provide an adequate cleaning of the top surface of the wafer. Characteristically, the solvent significantly reduces if not substantially eliminates the surface tension at the surface of the wafer. As described more fully below, the surface tension retards the adhering of the slurry of the SOG to the wafer, thereby impeding the deposition of the slurry.
- the slurry is a solution of hydrosilsequioxane polymer (HSQ) in a solution of hexamethyldisiloxane (Siloxane).
- HSQ hydrosilsequioxane polymer
- Siloxane hexamethyldisiloxane
- the solution is illustratively 80% Siloxane / 20% HSQ by volume.
- the solvent used as the pre- wet is beneficially Siloxane as well.
- approximately 3.0 ml to approximately 5.0 ml of the Siloxane is dispensed onto the wafer as it is rotated at approximately 75 rpm for approximately 2.5 seconds.
- the wafer is spun at a rate of approximately 1000 rpm for approximately 4.0 seconds to spread the solvent more evenly across the entire wafer surface.
- the HSG/Siloxane solution is dispensed onto the wafer by known spin- on techniques.
- the SOG spread step is advantageously increased from approximately 70 rpm to approximately 75 rpm, and the rotation time is changed from 1.5 to 2.0 sec.
- a 'high-speed' rotation step follows the initial slurry deposition step.
- the rotation rate of the wafer in the 'high speed' is adjusted for optimum thickness, depending on the desired thickness of the applied SOG film. For example, for an SOG layer having a mean thickness of 4500 Angstroms the rotation rate of the wafer in high-speed step is approximately 4000 rpm. For a layer with a mean thickness of 2000 Angstroms, the rotation rate is approximately 2000 rpm.
- Fig. 2a shows a wafer 201, which includes a substrate 204, which is illustratively a semiconductor such as monocrystalline silicon.
- the substrate has at least one other layer disposed thereover in this stage of the processing of the wafer.
- These illustrative layers 202 and 203 may be other dielectric layers (e.g., ILD's), other semiconductor layers, metal layers within an oxide, and other layers within the purview of the artisan of ordinary skill. It is also noted that the low-k ILD of the example embodiments may be fabricated over the PHUS03 0336WO ⁇ resort nTM PCT/IB2004/051793
- Fig. 2b shows the rotation 206 of the wafer 201 and the deposition of the pre-wet solvent 205, which is illustratively siloxane. This sequence is substantially the same as that described in connection with step 102 of Fig. 1. After the pre-wet is completed, and as shown in Fig. 2c the slurry 207 is deposited while the pre- wetted wafer 201 is spun as at 206. This sequence is essentially the same as that described at step 103. Fig. 2d shows the slurry 208 deposited over the top surface of the wafer 201.
- the wafer is baked, resulting in the low-k dielectric material layer's 209 being formed over the wafer 201 and as shown in Fig. 2e.
- This layer 209 may be an ILD, or other dielectric layer as needed.
- the wafer may be further processed as needed.
- the processing after the pre-wetting of the wafer as at step 102 of Fig. 1 and Fig. 2b is, for the most part, well-known, and is as described for example in texts such as VLSI Principles and Technology, Silicon and Gallium Arsenide, 2 nd Edition, 1994, by Soreb Ghandi, page 725. The disclosure of this reference is specifically incorporated herein by reference.
- step 103 the deposition of the slurry of step 103, and the heat treatment of step 104 may be well-known
- the pre-wet of the example embodiments of step 102 of Fig. 1 and of Fig. 2b is clearly advantageous compared to known methods.
- the method of the exemplary embodiments results in a significant reduction in the amount of slurry that is required to deposit a layer of slurry of a sufficient thickness to fabricate a low-k ILD of sufficient thickness.
- the amount of slurry required to form a layer having a certain thickness was reduced from 4.0 ml by a known technique, which does not include a pre-wet, to 1.4 ml of slurry when the pre-wet of the example embodiments is used.
- This reduction by nearly 65% of the amount of slurry used results in a significant reduction in wasted slurry.
- the components of the slurry can be among the most expensive in processing semiconductor wafers.
- applicants have determined that by using the prewetting technique of the example embodiments, the uniformity across the wafer of the resultant SOG layer (low-k ILD) is significantly improved compared to known techniques.
- a standard method of depositing the SOG by spin-coating results in a layer having a mean thickness of 4482.73 Angstroms, with a standard deviation in thickness of +39.3589.73 Angstroms, or + 0.878%.
- a layer of SOG fabricated using the pre-wet of the example embodiments had a thickness of 4433.09 Angstroms with a standard deviation of ⁇ 32.2566 Angstroms, or +0.728%.
- this standard deviation is merely illustrative, and the standard deviation in the thickness may be less than +0.728%.
- the thickness uniformity and reproducibility may be further improved compared to the example embodiments above, by 'priming' the wafers with hexamethyldisilazane (HMDS) before applying the pre-wet.
- HMDS hexamethyldisilazane
- the HMDS vapor is applied, followed by a vacuum heat treatment (bake) at 120 °C for approximately 10 minutes.
- the example embodiments described so far primarily focus on the use of HSQ in Siloxane solution as the material for the SOG, with Siloxane as the pre-wet.
- octamethyltrisiloxane and decamethyltetrasiloxane may be used as the pre-wet to possibly further improve the process latitude and to possibly further reduce the volume of SOG solution (slurry) required for forming the low-k dielectric for each wafer.
- SOG solution slurry
- octamethyltrisiloxane in concentration of approximately 5 to approximately 50% by volume in combination with hexamethyldisiloxane as the solvent for HSQ instead of Siloxane alone.
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- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- General Physics & Mathematics (AREA)
- Manufacturing & Machinery (AREA)
- Computer Hardware Design (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Power Engineering (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Formation Of Insulating Films (AREA)
- Paints Or Removers (AREA)
- Internal Circuitry In Semiconductor Integrated Circuit Devices (AREA)
Abstract
A method (100) of depositing a dielectric material includes providing (101) a substrate with at least one layer over the substrate. The method further includes pre-wetting (102) a top surface of a top layer with a substance, spin coating (103) the solution and forming (104) the dielectric material. The dielectric material is illustratively SiO2 that is relatively porous, and has a relatively low dielectric constant. The pre-wetting results in a reduction in processing costs due to a reduction in lost solution. Moreover, the dielectric layer (209) has an improved thickness uniformity.
Description
1 METHOD OF FORMING DIELECTRIC LAYERS WITH LOW DIELECTRIC CONSTANTS Interconnection technology is constantly challenged to meet ever- increasing demands for high density of elements and high performance in very large scale and ultra large scale integration integrated circuits, or VLSI IC's and ULSI IC's, respectively. As is well known, the speed of circuits varies inversely with the product of the resistance (R) of the circuit and the capacitance (C) of the interconnections of the IC. This so-called RC time constant must be minimized as much as possible to foster adequate signal transmission and switching speed, and to minimize signal cross-talk. With the ever-increasing demand for greater integration and miniaturization of components in IC's a major limiting factor on the system speed can be the IC's RC limitations. Accordingly, there is a great interest in reducing the resistance and capacitance of the interconnections of the IC. One way to reduce the RC time constants of the interconnections of an IC is to reduce the capacitance created between the various elements of the IC, by using inter- level and intra-level dielectrics (ILD's) that have a comparatively lower dielectric constant (εr or k). These materials usefully have a dielectric constant less than 3.9, the dielectric constant of dense Si02. One type of low-k ILD is porous Si02 formed from hydrosilsesquioxane (HSQ), which is a flowable oxide that may be deposited by spin-on coating techniques. After the spin-on process is complete, the material is baked, and the solvent is removed, leaving silicon dioxide (glass), which is porous. The dielectric constant of the porous oxide layer is illustratively on the order of approximately 2.0 to approximately 3.8, and certainly less than 3.9. As can be appreciated, the greater the degree of porosity, the lower the dielectric constant. The referenced dielectric materials deposited by spin-coating are often referred to as spin-on-glass (SOG) materials. While these materials have shown promise in providing low-k ILD's, their deposition can be exceedingly costly. Moreover, the thickness of the deposited ILD can be non-uniform across the wafer, which can adversely impact the consistency of the electrical characteristics of the devices and circuits formed from the processed wafer. As such, what is needed is a method of forming SOG layers in IC applications that addresses at least the referenced shortfalls of known techniques.
According to an example embodiment, a method of depositing a dielectric material includes providing a substrate with at least one layer over the substrate. The method further includes pre-wetting a top surface of a top layer with a substance, spin coating the solution and forming the dielectric material. According to another example embodiment, a semiconductor structure includes a layer of porous low-k dielectric material disposed over a substrate, wherein the material has a thickness across the layer, and the thickness has a uniformity across a surface with a standard deviation of +0.728%. The invention is best understood from the following detailed description when read with the accompanying drawing figures. It is emphasized that the various features are not necessarily drawn to scale. In fact, the dimensions may be arbitrarily increased or decreased for clarity of discussion. Fig. 1 is a flow-chart of a process of fabricating a dielectric layer in accordance with an example embodiment. Figs. 2a-2e shows cross-sectional views of an integrated circuit during a fabrication sequence of forming a dielectric layer in accordance with an example embodiment. In the following detailed description, for purposes of explanation and not limitation, example embodiments disclosing specific details are set forth in order to provide a thorough understanding of the present invention. However, it will be apparent to one having ordinary skill in the art having had the benefit of the present disclosure, that the present invention may be practiced in other embodiments that depart from the specific details disclosed herein. Moreover, descriptions of well-known devices, methods and materials may be omitted so as to not obscure the description of the present invention. Fig. 1 is a flow-chart of a process 100 of forming a low-k dielectric layer over a semiconductor wafer in accordance with an example embodiment. Illustratively, the wafer includes a semiconductor substrate, and at least one other layer formed thereover. The layer or layers over the substrate may be the usual layers in an IC, including but not limited to doped and undoped semiconductor layers, dielectric layers metal layers, including patterned metal layers, and other layers within the purview of one of ordinary skill in the art in the semiconductor processing art. At step 101, a wafer is provided. At step 102, a solvent is dispensed over the uppermost surface of the wafer. Advantageously, the solvent is chosen to provide an adequate cleaning of the top surface of the wafer. Characteristically, the solvent significantly reduces
if not substantially eliminates the surface tension at the surface of the wafer. As described more fully below, the surface tension retards the adhering of the slurry of the SOG to the wafer, thereby impeding the deposition of the slurry. In accordance with an illustrative embodiment, the slurry is a solution of hydrosilsequioxane polymer (HSQ) in a solution of hexamethyldisiloxane (Siloxane). The solution is illustratively 80% Siloxane / 20% HSQ by volume. In this example embodiment, the solvent used as the pre- wet is beneficially Siloxane as well. At step 102, approximately 3.0 ml to approximately 5.0 ml of the Siloxane is dispensed onto the wafer as it is rotated at approximately 75 rpm for approximately 2.5 seconds. Next, the wafer is spun at a rate of approximately 1000 rpm for approximately 4.0 seconds to spread the solvent more evenly across the entire wafer surface. At step 103, the HSG/Siloxane solution is dispensed onto the wafer by known spin- on techniques. For optimum uniformity the SOG spread step is advantageously increased from approximately 70 rpm to approximately 75 rpm, and the rotation time is changed from 1.5 to 2.0 sec. A 'high-speed' rotation step follows the initial slurry deposition step. The rotation rate of the wafer in the 'high speed' is adjusted for optimum thickness, depending on the desired thickness of the applied SOG film. For example, for an SOG layer having a mean thickness of 4500 Angstroms the rotation rate of the wafer in high-speed step is approximately 4000 rpm. For a layer with a mean thickness of 2000 Angstroms, the rotation rate is approximately 2000 rpm. After spin step is completed, and, as shown at step 104, the wafer is subjected to a heat treatment (baked) according to known methods. This results in the fabrication of a porous low-k Si02 layer. Finally, the wafer may be further processed at step 105. This further processing may include metallization processing and device fabrication per known techniques. The fabrication sequence of the illustrative method is shown in Figs. 2a-2f, where an illustrative wafer is processed to form a low-k ILD by an exemplary method. Fig. 2a shows a wafer 201, which includes a substrate 204, which is illustratively a semiconductor such as monocrystalline silicon. The substrate has at least one other layer disposed thereover in this stage of the processing of the wafer. These illustrative layers 202 and 203 may be other dielectric layers (e.g., ILD's), other semiconductor layers, metal layers within an oxide, and other layers within the purview of the artisan of ordinary skill. It is also noted that the low-k ILD of the example embodiments may be fabricated over the
PHUS03 0336WO π^„n™ PCT/IB2004/051793
substrate directly and other layers, including those mentioned above and at least one low-k ILD the example embodiments may be formed over the first low-k ILD. Fig. 2b shows the rotation 206 of the wafer 201 and the deposition of the pre-wet solvent 205, which is illustratively siloxane. This sequence is substantially the same as that described in connection with step 102 of Fig. 1. After the pre-wet is completed, and as shown in Fig. 2c the slurry 207 is deposited while the pre- wetted wafer 201 is spun as at 206. This sequence is essentially the same as that described at step 103. Fig. 2d shows the slurry 208 deposited over the top surface of the wafer 201. After the slurry is deposited, the wafer is baked, resulting in the low-k dielectric material layer's 209 being formed over the wafer 201 and as shown in Fig. 2e. This layer 209 may be an ILD, or other dielectric layer as needed. After the fabrication of the low-k dielectric layer 209, the wafer may be further processed as needed. The processing after the pre-wetting of the wafer as at step 102 of Fig. 1 and Fig. 2b is, for the most part, well-known, and is as described for example in texts such as VLSI Principles and Technology, Silicon and Gallium Arsenide, 2nd Edition, 1994, by Soreb Ghandi, page 725. The disclosure of this reference is specifically incorporated herein by reference. However, it is noted that differences between known processing sequences and those of example embodiments will be readily apparent to one skilled in the semiconductor processing arts. While the deposition of the slurry of step 103, and the heat treatment of step 104 may be well-known, the pre-wet of the example embodiments of step 102 of Fig. 1 and of Fig. 2b is clearly advantageous compared to known methods. For purposes of illustration and not limitation, the method of the exemplary embodiments results in a significant reduction in the amount of slurry that is required to deposit a layer of slurry of a sufficient thickness to fabricate a low-k ILD of sufficient thickness. To this end, by performing a pre-wet as described in connection with an exemplary embodiment, the amount of slurry required to form a layer having a certain thickness was reduced from 4.0 ml by a known technique, which does not include a pre-wet, to 1.4 ml of slurry when the pre-wet of the example embodiments is used. This reduction by nearly 65% of the amount of slurry used results in a significant reduction in wasted slurry. Because the components of the slurry can be among the most expensive in processing semiconductor wafers.
In addition to the cost savings, applicants have determined that by using the prewetting technique of the example embodiments, the uniformity across the wafer of the resultant SOG layer (low-k ILD) is significantly improved compared to known techniques. To this end, a standard method of depositing the SOG by spin-coating results in a layer having a mean thickness of 4482.73 Angstroms, with a standard deviation in thickness of +39.3589.73 Angstroms, or + 0.878%. Contrastingly, and while reducing the waste of the slurry, a layer of SOG fabricated using the pre-wet of the example embodiments had a thickness of 4433.09 Angstroms with a standard deviation of ±32.2566 Angstroms, or +0.728%. Of course, this standard deviation is merely illustrative, and the standard deviation in the thickness may be less than +0.728%. This improvement in uniformity in the thickness of the layer results in, among other benefits, electrical characteristics across circuits formed from the wafer that are more uniform and consistent. According to another example embodiment, the thickness uniformity and reproducibility may be further improved compared to the example embodiments above, by 'priming' the wafers with hexamethyldisilazane (HMDS) before applying the pre-wet. To wit, before step 102 or the sequence of Fig. 2b, the HMDS vapor is applied, followed by a vacuum heat treatment (bake) at 120 °C for approximately 10 minutes. The example embodiments described so far primarily focus on the use of HSQ in Siloxane solution as the material for the SOG, with Siloxane as the pre-wet. It is noted that other materials may be used as the pre-wet and the SOG slurry. For example, octamethyltrisiloxane and decamethyltetrasiloxane may be used as the pre-wet to possibly further improve the process latitude and to possibly further reduce the volume of SOG solution (slurry) required for forming the low-k dielectric for each wafer. In yet other example embodiments, in order to achieve further economy in the amount of slurry required and in the uniformity of the films deposited, octamethyltrisiloxane (in concentration of approximately 5 to approximately 50% by volume) in combination with hexamethyldisiloxane as the solvent for HSQ instead of Siloxane alone. The example embodiments having been described in detail in connection through a discussion of exemplary embodiments, it is clear that modifications of the invention will be apparent to one having ordinary skill in the art having had the benefit of the present disclosure. Such modifications and variations are included in the scope of the appended claims.
Claims
CLAIMS What is claimed is: 1. A method 100 of depositing a dielectric material, the method comprising: providing 101 a substrate with at least one layer over the substrate; pre-wetting 102 a top surface of a top layer with a substance; spin coating 103 a solution and forming 104 the dielectric material. 2. The method as recited in claim 1, wherein the substance includes hexamethyldisiloxane (Siloxane). 3. The method as recited in claim 1, wherein the solution includes hydrosilsesquioxane (HSQ). 4. The method of claim 3, wherein a solvent of the solution is Siloxane. 5. The method as recited in claim 1, wherein the pre-wetting further comprises spinning the wafer while depositing the substance. 6. The method as recited in claim 1, wherein the dielectric material is Si0 . 7. The method as recited in claim 2, wherein the method further comprises, before the pre-wetting, priming the wafer with a vapor of hexamethyldisilazane (HMDS), and after said priming, but before said pre-wetting, applying heat to the substrate. 8. The method as recited in claim 1, wherein the substance is octamethyltrisiloxane. 9. The method as recited in claim 1, wherein the substance is decamethytetrasiloxane. 10. The method as recited in claim 2, wherein the substance includes octamethyltrisiloxane. 11. A semiconductor structure 201, comprising: a layer of porous low-k dielectric material 209 disposed over a substrate 202,203,204, wherein the material has a thickness across the layer, and the thickness has a uniformity across a surface with a standard deviation of +0.728%. 12. A semiconductor structure as recited in claim 11, wherein the surface is a top surface of a wafer. 13. A semiconductor structure as recited in claim 11, wherein the layer is an inter- layer dielectric layer. 14. A semiconductor structure as recited in claim 11, wherein the layer is an intra- layer dielectric layer.
15. A semiconductor structure as recited in claim 11, wherein the layer has a dielectric constant in the range of approximately 2.0 to approximately 3.8.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US50445203P | 2003-09-19 | 2003-09-19 | |
PCT/IB2004/051793 WO2005029567A1 (en) | 2003-09-19 | 2004-09-18 | Method of forming dielectric layers with low dielectric constants |
Publications (1)
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EP1668683A1 true EP1668683A1 (en) | 2006-06-14 |
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EP04770031A Withdrawn EP1668683A1 (en) | 2003-09-19 | 2004-09-18 | Method of forming dielectric layers with low dielectric constants |
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EP (1) | EP1668683A1 (en) |
JP (1) | JP2007506276A (en) |
KR (1) | KR20060096996A (en) |
CN (1) | CN1883038A (en) |
WO (1) | WO2005029567A1 (en) |
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EP2267080A1 (en) * | 2008-04-02 | 2010-12-29 | Mitsui Chemicals, Inc. | Composition and method for production thereof, porous material and method for production thereof, interlayer insulating film, semiconductor material, semiconductor device, and low-refractive-index surface protection film |
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US5429673A (en) * | 1993-10-01 | 1995-07-04 | Silicon Resources, Inc. | Binary vapor adhesion promoters and methods of using the same |
US6008540A (en) * | 1997-05-28 | 1999-12-28 | Texas Instruments Incorporated | Integrated circuit dielectric and method |
US6066578A (en) * | 1997-12-01 | 2000-05-23 | Advanced Micro Devices, Inc. | Method and system for providing inorganic vapor surface treatment for photoresist adhesion promotion |
US6218020B1 (en) * | 1999-01-07 | 2001-04-17 | Alliedsignal Inc. | Dielectric films from organohydridosiloxane resins with high organic content |
US6541367B1 (en) * | 2000-01-18 | 2003-04-01 | Applied Materials, Inc. | Very low dielectric constant plasma-enhanced CVD films |
JP2002324745A (en) * | 2001-04-25 | 2002-11-08 | Tokyo Ohka Kogyo Co Ltd | Method for forming resist film |
JP2003257836A (en) * | 2002-03-05 | 2003-09-12 | Matsushita Electric Ind Co Ltd | Method of forming organic film |
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2004
- 2004-09-18 EP EP04770031A patent/EP1668683A1/en not_active Withdrawn
- 2004-09-18 KR KR1020067005506A patent/KR20060096996A/en not_active Application Discontinuation
- 2004-09-18 CN CNA2004800341848A patent/CN1883038A/en active Pending
- 2004-09-18 WO PCT/IB2004/051793 patent/WO2005029567A1/en active Application Filing
- 2004-09-18 JP JP2006526795A patent/JP2007506276A/en not_active Withdrawn
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WO2005029567A1 (en) | 2005-03-31 |
CN1883038A (en) | 2006-12-20 |
JP2007506276A (en) | 2007-03-15 |
KR20060096996A (en) | 2006-09-13 |
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