This application is related to the following co-pending and commonly assigned application; application Ser. No. 10/661,100, filed Sep. 12, 2003, entitled “MASKING STRUCTURE HAVING MULTIPLE LAYERS INCLUDING AN AMORPHOUS CARBON LAYER” which is hereby incorporated by reference.
The present invention relates generally to semiconductor devices, more particularly to masking structures in the semiconductor devices.
Semiconductor devices such as memory devices reside in many computers and electronic products to store data. A typical semiconductor device has many layers of different materials formed on a semiconductor wafer.
During manufacturing, the layers go through many processes. For example, a patterning process puts patterns on the layers. Some patterning processes use a mask to transfer patterns from the mask to the layers underneath the mask.
Some conventional masks are made of amorphous carbon. However, an amorphous carbon mask at some thickness may have a high absorption of optical light, causing the amorphous carbon mask inapplicable for some processes.
The present invention provides devices having a masking structure and techniques for forming the masking structure. The masking structure includes an amorphous carbon layer having a low absorption property. The amorphous layer is transparent in visible light range of the electromagnetic radiation.
The following description and the drawings illustrate specific embodiments of the invention sufficiently to enable those skilled in the art to practice the invention. Other embodiments may incorporate structural, logical, electrical, process, and other changes. In the drawings, like numerals describe substantially similar components throughout the several views. Examples merely typify possible variations. Portions and features of some embodiments may be included in or substituted for those of others. The scope of the invention encompasses the full ambit of the claims and all available equivalents.
The visible light range is the range (optical range) of the electromagnetic spectrum having light (electromagnetic radiation) visible to human eyes. The visible light range includes any light having a wavelength between about 400 nm (nanometers) and about 700 nm. The non-visible light range is the range of the entire electromagnetic spectrum minus the visible light range. Some examples of the non-visible light range include electromagnetic radiations with wavelengths between 700 nm and one millimeter (infrared light), wavelengths between 10 nm and 400 nm (ultraviolet light), and wavelengths between 0.01 nm and 10 nm (X-ray).
In this specification, the amorphous carbon layer is transparent in visible light range means that the amorphous carbon layer has a substantially low absorption coefficient (k) in which k has a range between about 0.15 and about 0.001 at wavelength of 633 nm. In some embodiments, the amorphous carbon layer transparent in visible light range is an amorphous carbon layer formed at a temperature from about 200° C. to about 500° C. such that the amorphous carbon layer has an absorption coefficient (k) between about 0.15 and about 0.001 at wavelength of 633 nm.
At box 102 of method 100 in
At box 104, the parameters are set for the process of forming an amorphous carbon layer according to the invention. The parameters include temperature, gas mixture, gas flow rate, power, and pressure. The temperature in the chamber is set to a selected temperature. The selected temperature is any temperature from about 200° C. to about 500° C. In some embodiments, the temperature is set between about 200° C. and below 300° C. In other embodiments, the temperature is set between about 225° C. and about 375° C.
In the process of forming an amorphous carbon layer, a process gas including propylene (C3H6) is introduced into the chamber at a flow rate. In some embodiments, the flow rate of the propylene is set between about 500 standard cubic centimeters per minute (sccm) and about 3000 sccm. An additional gas including helium may be also introduced into the chamber at a flow rate. In some embodiments, the flow rate of the helium is set between about 250 sccm and about 1000 sccm. Further, embodiments exist where at least one of the other hydrocarbon gases is used as the process gas. Examples of the other hydrocarbon gases include CH4, C2H2, C2H4, C2H6, and C3H8. Helium may also be used in combination with at least one of these hydrocarbon gases. Thus, in box 104, a gas mixture is introduced into the chamber.
In this specification, the gas mixture may be either one gas only or a combination of at least two gases. For example, the gas mixture may be either propylene (C3H6) only or a combination of propylene and helium. As another example, the gas mixture may be at least one of the propylene, CH4, C2H2, C2H4, C2H6, and C3H8. As a further example, the gas mixture may be at least one of the propylene, CH4, C2H2, C2H4, C2H6, and C3H8 plus helium.
During the process of forming the amorphous carbon layer in method 100, the chamber is subjected to a radio frequency (RF) power and a pressure. In some embodiments, the radio frequency power is set between about 450 Watts and about 1000 Watts, and the pressure is set between about 4 Torr and about 6.5 Torr.
In box 106, an amorphous carbon layer is formed as a deposited layer over the wafer. The amorphous carbon layer is transparent in visible light range. In some embodiments, the amorphous carbon layer formed by method 100 has an absorption coefficient (k) between about 0.15 and about 0.001 at wavelength of 633 nm.
Since the amorphous carbon layer formed by method 100 is transparent in visible light range, the amorphous carbon layer formed by method 100 is also referred to as a transparent amorphous carbon layer. Thus, the transparent amorphous carbon layer refers to an amorphous carbon layer formed according method 100 in which the temperature is set from about 200° C. to about 500° C.
The transparency of the amorphous carbon layer formed by method 100 depends in part on the temperature set during the process. In method 100, the transparency of the amorphous carbon layer formed to a specific thickness at a lower temperature is more transparent than the amorphous carbon layer formed to that specific thickness at a higher temperature. For example, in method 100, the amorphous carbon layer formed to a thickness at 200° C. is more transparent than the amorphous carbon layer formed to the same thickness at 500° C.
The transparent amorphous carbon layer formed by method 100 may be used in semiconductor devices such as memory devices and microprocessors. For example, the transparent amorphous carbon layer formed by method 100 may be included in a structure of semiconductor devices as an insulating layer or an antireflective layer. As another example, the transparent amorphous carbon layer formed by method 100 may also be used as a mask in an etching process during manufacturing of semiconductor devices.
In
In
In
Substrate 210 has a surface 212 in which alignment marks 214 are formed. Alignment marks 214 serves as reference points or coordinates of substrate (wafer) 210. During an alignment process, the alignment marks 214 are used to align or position substrate 210 such that structures and layers on substrate 210 can be accurately aligned with each other or with substrate 210.
Amorphous carbon layer 430 has a thickness T4. T4 can be any thickness. In some embodiments, T4 is at least 4000 Angstroms. Amorphous carbon layer 430 has a low absorption coefficient such that amorphous carbon layer 430 is transparent in visible light range. In some embodiments, amorphous carbon layer 430 has an absorption coefficient (k) between about 0.15 and about 0.001 at wavelength of 633 nm.
Since amorphous carbon layer 430 is transparent in visible light range, amorphous carbon layer 430 does not substantially absorb or reflect the light in the visible light range. Therefore, the transparency in visible light range property of amorphous carbon layer 430 improves the reading of alignment marks 214 (
In comparing amorphous carbon layer 430 with a conventional amorphous carbon layer having a higher absorption coefficient (or less transparent) than that of amorphous carbon layer 430, the conventional amorphous carbon may have a thickness limitation for some processes. For example, some process may require a mask with a specific thickness, using a conventional amorphous carbon layer with the specific thickness may cause difficulty in reading the alignment marks or may result in inaccurate reading because of the high absorption property of the conventional amorphous carbon layer. Therefore, because of the low absorption property, amorphous carbon layer 430 is useful in processes that may require a mask with a specific thickness in which a conventional amorphous carbon mask is unsuitable.
Amorphous carbon layer 430 of device 200 is formed with a thickness sufficient to properly etch a device structure such as device structure 320. For example, amorphous carbon layer 430 is formed with thickness T4 equal to or greater than about 4000 Angstroms to etch device structure 320 with thickness T3 equal to or greater than 40000 Angstroms.
Cap layer 540 can be formed by a deposition process such as a CVD and PECVD process. In some embodiments, cap layer 540 is formed together with amorphous carbon layer 430 in the same process (same processing step) such that cap layer 540 is situ deposited over amorphous carbon layer 430.
The combination of amorphous carbon layer 430, cap layer 540, and photoresist layer 550 forms a masking structure 560. In some embodiments, cap layer 540 is omitted from masking structure 560. In other embodiments, besides amorphous carbon layer 430, cap layer 540, and photoresist layer 550, masking structure 560 further includes an additional layer formed between photoresist layer 550 and cap layer 540. The additional layer serves as an antireflective layer to further enhance the photo processing performance.
Layer 322 is etched to a level 902. Level 902 is any level above surface 212 of substrate 210. In embodiments represented by
In the above description of
In embodiments where an amorphous carbon layer exists within device structure 320, the amorphous carbon layer within device structure 320 may be used for insulating purposes, antireflection purposes, or for other purposes. Hence, in embodiments where device structure 320 includes an amorphous carbon layer similar to amorphous carbon layer 430, the amorphous carbon layer of device structure 320 still remains in device 200 after amorphous carbon layer 430 of masking structure 560 is removed from device 200.
After amorphous carbon layer 430 is removed as shown in
Memory device 1100 also includes an insulating layer 1130 and a number of contacts 1140 (1140.1 through 1140.3) extending through insulating layer 1130. Each of the contacts 1140 connects to one of the diffusion regions 1106. A barrier layer 1145 separates surface structures 1105 from insulating layer 1130 and contacts 1140. Contacts 1140 are made of conducting material to provide electrical connections for diffusion regions 1106. Barrier layer 1145 can be oxide, or nitrite, or other non-conducting materials to prevent cross-diffusion of materials between surface structures 1105 and insulating layer 1130. In some embodiments, barrier layer 1145 is omitted. Insulating layer 1130 provides insulation between the contacts 1140. Insulating layer 1130 can be a layer of silicate glass doped with one or more dopants such as boron and phosphorous or other types of doped glasses. For example, insulating layer 1130 can be Boronsilicate glass (BSG), or Phosphosilicate glass (PSG). In embodiments represented by
In embodiments represented by
Each of the gate structures 1105 includes a number of elements: a gate dielectric (gate oxide) 1109, a doped polysilicon layer 1112, a silicide layer 1114, a capping dielectric layer 1116, and dielectric spacers 1118. Silicide layer 1114 can include a compound of metal and silicon such as titanium silicide, tungsten silicide, and others. All dielectrics in gate structures 1105 can include material such as silicon oxide. Each of the gate structures 1105 is also referred to as a word line. The structure of
Since amorphous carbon layer 430 is transparent in visible light range, amorphous carbon layer 1330 may be formed at a selected thickness to properly etch device structure 1220 without substantially affecting the reading of the alignment marks 1104 during an alignment of device 1100. Amorphous carbon layer 1330 has a thickness T13, which can be selected at an appropriate value to properly etch device structure 1220. T13 can be any thickness. In some embodiments, T13 is at least 4000 Angstroms.
In some embodiments, after amorphous carbon layer 1330 is patterned, the combination of layers 1330, 1440, and 1450 of masking structure 1460 may remain and is used as a mask to etch the layers of device structure 1220. In other embodiments, after amorphous carbon layer 1330 is patterned, either photoresist layer 1450 or a combination of both photoresist layer 1450 and cap layer 1440 is removed. The remaining (not removed) layer, or layers, of masking structure 1220 is used as a mask to etch device structure 1220.
Memory device 1110 includes access transistors T1 and T2. Gate structure 1105.2 and diffusion regions 1106.1–1106.2 form access transistor T1. Gate structure 1105.3 and diffusion regions 1106.2–1106.3 form access transistor T2. Access transistor T1 and storage capacitor C1 form a memory CELL1. Access transistor T2 and storage capacitor C2 form a memory CELL2.
Memory cells CELL1 and CELL2 store data in form of charge in storage capacitors C1 and C2. The charges are transferred to and from doped regions 1106.1 and 1106.3 of capacitors C1 and C2 via contact 1140.2. In some embodiments, contact 1140.2 is a buried bit line contact, which connects to a bit line of memory device 1100.
In other embodiments, other elements having structures different from the structures of the layers 1902, 1904, and 1906 can be formed in openings 1701 (
Memory device 1100 may be a dynamic random access memory (DRAM) device. Examples of DRAM devices include synchronous DRAM commonly referred to as SDRAM, SDRAM II, SGRAM (Synchronous Graphics Random Access Memory), DDR SDRAM (Double Data Rate SDRAM), DDR II SDRAM, DDR III SDRAM, GDDR III SDRAM (Graphic Double Data Rate), and Rambus DRAMs. Memory device 1100 includes other elements, which are not shown for clarity.
Wafer 2020 includes a number of alignment marks 2014 and a number of dice 2030. In some embodiments, alignment marks 2014 represent alignment marks 214 (
At least one of the dice 2030 includes elements according to embodiments described in FIG. 2–
A die such as one of the dice 2030 is a pattern on a semiconductor wafer such as wafer 2020. A die contains circuitry to perform a specific function. For, example, at least one of the dice 2030 contains circuitry for a device such as a processor, or memory device such as memory device 1100 (FIG. 11–
Various embodiments of the invention provide technique to form a transparent amorphous carbon layer. The transparent amorphous carbon layer can be used as a mask for etching certain structure of the device. The amorphous carbon layer can also be a part of a structure of the device for other purposes. Although specific embodiments are described herein, those skilled in the art recognize that other embodiments may be substituted for the specific embodiments shown to achieve the same purpose. This application covers any adaptations or variations of the present invention. Therefore, the present invention is limited only by the claims and all available equivalents.
Number | Name | Date | Kind |
---|---|---|---|
H566 | Nyaiesh et al. | Jan 1989 | H |
4849642 | Katsumi | Jul 1989 | A |
4971853 | Chaiken et al. | Nov 1990 | A |
4975144 | Yamazaki et al. | Dec 1990 | A |
5096791 | Yahalom | Mar 1992 | A |
5198263 | Stafford et al. | Mar 1993 | A |
5324365 | Niwa | Jun 1994 | A |
5346729 | Pitts et al. | Sep 1994 | A |
5358880 | Lebby et al. | Oct 1994 | A |
5369040 | Halvis et al. | Nov 1994 | A |
5420043 | Kaisha | May 1995 | A |
5431800 | Kirchhoff | Jul 1995 | A |
5437961 | Yano et al. | Aug 1995 | A |
5470661 | Bailey et al. | Nov 1995 | A |
5496752 | Nasu et al. | Mar 1996 | A |
5514885 | Myrick | May 1996 | A |
5578501 | Niwa | Nov 1996 | A |
5589307 | Tacheuchi | Dec 1996 | A |
5629532 | Myrick | May 1997 | A |
5669644 | Kaihotsu et al. | Sep 1997 | A |
5723029 | Shimoyama | Mar 1998 | A |
5733713 | Yano et al. | Mar 1998 | A |
5750316 | Kawamura et al. | May 1998 | A |
5800878 | Yao | Sep 1998 | A |
5830332 | Babich et al. | Nov 1998 | A |
5998100 | Azuma | Dec 1999 | A |
6035803 | Robles et al. | Mar 2000 | A |
6107734 | Taneka et al. | Aug 2000 | A |
6128868 | Ohtsuka et al. | Oct 2000 | A |
6136160 | Hrkut et al. | Oct 2000 | A |
6140570 | Kariya | Oct 2000 | A |
6140652 | Shlepr et al. | Oct 2000 | A |
6211065 | Xi et al. | Apr 2001 | B1 |
6221535 | Cox et al. | Apr 2001 | B1 |
6291334 | Somekh | Sep 2001 | B1 |
6300631 | Shofner | Oct 2001 | B1 |
6313896 | Samant et al. | Nov 2001 | B1 |
6316329 | Hirota et al. | Nov 2001 | B1 |
6323119 | Xi et al. | Nov 2001 | B1 |
6331380 | Ye et al. | Dec 2001 | B1 |
6346184 | Sano et al. | Feb 2002 | B1 |
6350997 | Saeki | Feb 2002 | B1 |
6394109 | Somekh | May 2002 | B1 |
6420095 | Kawamura et al. | Jul 2002 | B1 |
6423384 | Khazeni et al. | Jul 2002 | B1 |
6427703 | Somekh | Aug 2002 | B1 |
6444899 | Kubota et al. | Sep 2002 | B1 |
6447891 | Veerasamy et al. | Sep 2002 | B1 |
6461950 | Yin et al. | Oct 2002 | B1 |
6483127 | Saeki | Nov 2002 | B1 |
6508911 | Han et al. | Jan 2003 | B1 |
6541397 | Bencher | Apr 2003 | B1 |
6551941 | Yang et al. | Apr 2003 | B1 |
6566757 | Banerjee | May 2003 | B1 |
6573030 | Fairbairn et al. | Jun 2003 | B1 |
6583481 | Itoh | Jun 2003 | B1 |
6613603 | Sano | Sep 2003 | B1 |
6621535 | Fukada | Sep 2003 | B1 |
6624064 | Sahin et al. | Sep 2003 | B1 |
6627532 | Gaillard | Sep 2003 | B1 |
6649469 | Wilson | Nov 2003 | B1 |
6653735 | Yang et al. | Nov 2003 | B1 |
6668752 | Yao | Dec 2003 | B1 |
6780753 | Latchford et al. | Aug 2004 | B1 |
6784119 | Gaillard et al. | Aug 2004 | B1 |
6795636 | Cronk et al. | Sep 2004 | B1 |
6803313 | Gao et al. | Oct 2004 | B1 |
6821571 | Huang | Nov 2004 | B1 |
6825114 | Fisher et al. | Nov 2004 | B1 |
6841341 | Fairbairn et al. | Jan 2005 | B1 |
6852647 | Bencher | Feb 2005 | B1 |
6864556 | You et al. | Mar 2005 | B1 |
6875664 | Huang et al. | Apr 2005 | B1 |
6875687 | Weidman | Apr 2005 | B1 |
6884733 | Dakshina-Murthy et al. | Apr 2005 | B1 |
20010006837 | Kwon et al. | Jul 2001 | A1 |
20010011730 | Saeki | Aug 2001 | A1 |
20010017153 | Kubota et al. | Aug 2001 | A1 |
20020001778 | Latchford et al. | Jan 2002 | A1 |
20020003239 | Ramdani et al. | Jan 2002 | A1 |
20020086547 | Mui et al. | Jul 2002 | A1 |
20020100696 | Sano et al. | Aug 2002 | A1 |
20030198814 | Khieu et al. | Oct 2003 | A1 |
20030207207 | Li | Nov 2003 | A1 |
20040092098 | Sudijono et al. | May 2004 | A1 |
20050056835 | Yin et al. | Mar 2005 | A1 |
20050056940 | Sandhu et al. | Mar 2005 | A1 |
20060001175 | Sandhu | Jan 2006 | A1 |
20060003237 | Yin et al. | Jan 2006 | A1 |
Number | Date | Country |
---|---|---|
0531232 | Mar 1993 | EP |
1154468 | Nov 2001 | EP |
58-204534 | Nov 1983 | JP |
WO-03038875 | May 2003 | WO |
WO-2004012246 | Feb 2004 | WO |
WO-2005034216 | Apr 2005 | WO |
WO-2005034229 | Apr 2005 | WO |
Number | Date | Country | |
---|---|---|---|
20050059262 A1 | Mar 2005 | US |