Two step oxide removal for memory cells

Semiconductor device manufacturing: process – Chemical etching – Vapor phase etching

Reexamination Certificate

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C438S704000, C438S712000, C438S714000, C438S720000

Reexamination Certificate

active

06174817

ABSTRACT:

FIELD OF INVENTION
The invention relates generally to the field of semiconductor processing and more specifically to removing oxide from semiconductor wafers.
BACKGROUND OF INVENTION
Silicon dioxide, SiO
2
, is commonly used as a dielectric material in semiconductor manufacturing. The dielectric may be formed by various methods, such as by plasma deposition, TEOS decomposition and thermal growth. Regardless of the manner of oxide formation, it is necessary to remove or pattern the oxide. One way to pattern oxide is by plasma etching, also known as dry etching, as described in
Plasma Etching,
by Manos and Flamm, copyright 1989, pages 159-165. Another way to pattern oxide is by wet etching as described in
Semiconductor Integrated Circuit Processing Technology,
by Runyan and Bean, copyright 1990, pages 264-266. Hydrofluoric acid (HF) mixed with water and often buffered with ammonium fluoride is a standard silicon dioxide wet etchant. Typically, the semiconductor wafer is immersed into a tank containing the wet etchant and thereafter removed where it may be dipped into other tanks for rinsing or cleaning the wet etchant from the wafer.
A problem with wet etching silicon dioxide and subsequent tank rinsing is particle generation. Particles are small minute bits or pieces of silicon dioxide that remain on the surface of the semiconductor wafer after rinsing. Sometimes, the particles do not necessarily cause problems. However, as linewidths continue to shrink, small particles that may not have affected larger linewidth devices, become more problematical as they do affect smaller linewidth devices. As an example, dynamic random access memories (DRAMs) of the 16 megabit variety are typically manufactured with around 0.5 micron design rules. 64 megabit DRAMs are typically manufactured with around 0.35 micron design rules. 256 megabit DRAMs will be manufactured with around 0.25 micron linewidths and 1 gigabit DRAMs will have even smaller linewidths. See
Semiconductor Memories,
by Prince, copyright 1991, page 114.
Particle control is a problem regardless of the type of memory cell architecture used for the DRAM. Two commonly used types of memory cell architectures are trench type and stack type. These are described in
Semiconductor Memories,
by Prince, copyright 1991, pages 138-141. Another relatively new type of memory cell architecture is the crown. Crown type memory cells are described in the following papers:
1. Crown-Shaped Stacked-Capacitor Cell for 1.5-V Operation 64-Mb DRAM's, by Kaga et al., IEEE Transactions On Electron Devices, Vol. 38 No. 2, February 1991, pages 255-261; and
2. Fabrication Process for Container and Crown Electrodes in Memory Devices, by Kotecki et al., IBM Technical Disclosure Bulletin, Vol. 38 No. 11, November 1995.
Crown type memory cells are discussed in the following U.S. patents:
1. U.S. Pat. No. 5,612,241, issued Mar. 18, 1997 to Arima and assigned to Mitsubishi;
2. U.S. Pat. No. 5,545,582, issued Aug. 13, 1996 to Roh and assigned to Samsung;
3. U.S. Pat. No. 5,491,103, issued Feb. 13, 1996 to Ahn et al. and assigned to Samsung;
4. U.S. Pat. No. 5,354,705, issued Oct. 11, 1994 to Mathews et al. and assigned to Micron;
5. U.S. Pat. No. 5,278,091, issued Jan. 11, 1994 to Fazan et al. and assigned to Micron;
6. U.S. Pat. No. 5,270,241, issued Dec. 14, 1993 to Dennison et al. and assigned to Micron;
7. U.S. Pat. No. 5,238,862, issued Aug. 24, 1993 to Blalock et al. and assigned to Micron; and
8. U.S. Pat. No. 5,162,248m issued Nov. 10, 1992 to Dennison et al. and assigned to Micron.
Prior art FIGS.
1
a-f
show a sequence of manufacturing steps used to make a crown type memory cell. Prior art FIGS.
1
a-f
correspond respectively to FIGS.
7
a-f
of the Kaga et al. IEEE article described in publication 1 above. The following manufacturing description also comes from the Kaga et al. article. To be noted is that a HF solution is used to remove SiO
2
in conjunction with FIGS.
1
e
and
1
f.
Prior art FIG.
1
a
shows a semiconductor substrate
10
having word lines
12
covered by a SiO
2
layer
14
. After removal of the thin SiO
2
layer
14
at the data line contact region
16
, polycyrstalline Si
18
, WSi
2
20
and SiO
2
22
are deposited on the surface of the wafer using a chemical vapor deposition (CVD) technique as illustrated in prior art FIG.
1
b.
In the step of prior art FIG.
1
b,
the polycrystalline Si surface
18
is planarized using an etch-back method to make a planar WSi
2
surface
20
.
Next, the data lines are formed by anisotropic dry etching. Then a sidewall SiO
2
region
24
is formed using CVD and an anisotropic dry etching method as illustrated in prior art FIG.
1
c.
During this step, capacitor contacts are automatically formed on the Si surface. Then, selective polycrystalline Si layers
26
are formed on the contacts.
In FIG.
1
d,
a Si
3
N
4
layer
28
and a SiO
2
layer
30
are deposited using CVD. The Si
3
N
4
layer
28
(about 200 nm) fills both the word-line spaces and data-line spaces. Because these spaces are approximately 0.3 &mgr;m, almost a flat Si
3
N
4
surface can be created.
After SiO
2
/Si
3
N
4
layer deposition, the SiO
2
/Si
3
N
4
layer is etched using anisotropic dry etching. Then a 100 nm thick n-type polycrystalline Si layer
32
is deposited using a phosphorus doped CVD technique as illustrated in FIG.
1
e.
After filling the holes with SiO
2
by using CVD and an etch-back method, the polycrystalline Si layer
32
is anisotropically etched. Then the filled SiO
2
and the SiO
2
layer
30
on the Si
3
N
4
layer
28
are removed using a HF solution. Next, a crown-shaped polycrystalline Si electrode is formed. Then, a Ta
2
O
5
film
34
is deposited using CVD. In this step, a two-step oxygen-ambient annealing method is applied to reduce current leakage and to improve film reliability. Finally, a tungsten film
36
is sputtered as illustrated in FIG.
1
f.
Kaga et al. is silent as to how the SiO
2
layer
30
is removed using a HF solution. Possibly, the wafer was dipped into a solution of HF followed by dipping the wafer into a rinse as described above. However, such technique could possibly generate thousands of particles which could settle back onto the wafer surface. It is also possible that the wafer was put into a vapor HF chamber to remove the oxide.
FSI Corporation of Chaska, Minn., United States of America manufactures an anhydrous vapor HF etcher called the “Excaliber ISR-200”. U.S. Pat. No. 4,749,440, issued on Jun. 7, 1988 to Blackwood et al. and assigned to both FSI and Texas Instruments describes an apparatus and process for anhydrous vapor HF processing. Among the advantages provided over wet etching, are uniform, repeatable and controllable etching and smooth surfaces. However, even the advantageous techniques described in the patent may not be enough to successfully minimize particle disruption for ULSI devices such as DRAMS having complex topographies. What is needed is a new technique for advanced wafer oxide cleaning which greatly minimizes particles.
It is accordingly an object of the invention to provide a new method for etching oxide from semiconductor wafer surfaces which minimizes particle defects.
Other objects and advantages of the invention will be apparent to those of ordinary skill in the art having the benefit of the following specification.
SUMMARY OF INVENTION
A two step insitu oxide strip significantly reduces particles and minimizes defective memory cells. Following an inital exposure to vapor HF for oxide removal, a first insitu water rinse occurs. A second exposure to vapor HF then occurs and is followed by a second insitu water rinse. During both the first water rinse and the second water rinse, the wafer may be rotated at increasing speeds which aids in sweeping particles off the wafer surface. Water, rather than water vapor, aids in freeing particles from the wafer surface which may contain complex topographies. The process may be practiced in a commercially available reactor, such as one manufactured by FSI, and is particularly suitable for ULS

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