Method of Etching MTJ Using CO Process Chemistries

Abstract
A method for fabricating a magnetic film structure is provided. The method comprises forming a magnetic structure on a bottom electrode layer, the magnetic structure comprising at least one pinned bottom magnetic film layer having a fixed magnetic orientation; at least one top magnetic film layer whose magnetic orientation can be manipulated by a current; and a tunneling layer between the bottom magnetic film layer and the top magnetic film layer; forming a metallic hard mask atop the magnetic structure; patterning and etching the metallic hard mask to define exposed areas of the magnetic structure; selectively etching the exposed areas of the magnetic structure by a chemical etch process based on a CO etch chemistry to form discrete magnetic bits.
Description
FIELD

Embodiments of the invention relate to MRAM (Magnetic Random Access Memory) semiconductor devices.


BACKGROUND

Nonvolatile solid state memory can be fabricated based on MRAM chips which have the potential to replace Flash memory and Electronically Programmable Read-Only Memory (EEPROM).


MRAM fabrication techniques include sputter etching and chemical etching. In the case of sputter etching (also known as Ion Beam Etching) a high energy ion beam is used to etch/pattern metallic/magnetic materials. The by-products created by this physical sputtering technique are involatile and are susceptible to redeposition on the side-walls of etched structures. This is undesirable.


Chemical etching, e.g. with chlorine based plasma chemistries may be operated under high density conditions to provide practical etch rates for most alloys. However, there is always a concern with corrosion caused by plasma residues that remain on feature sidewalls upon removal from the reactor.





BRIEF DESCRIPTION OF THE DRAWINGS

The following drawings are illustrative of particular embodiments and therefore do not limit the scope of the invention, but are presented to assist in providing a proper understanding. The drawings are not to scale and are intended for use in conjunction with the explanations in the following detailed description. The present invention will hereinafter be described in conjunction with the appended drawings, wherein like reference numerals denote like elements.



FIGS. 1-6 illustrate steps for producing a MRAM circuit, in accordance with one embodiment of the invention.





DETAILED DESCRIPTION OF THE INVENTION

In the following description, for purposes of explanation, numerous specific details are set forth in order to provide a thorough understanding of the invention. It will be apparent, however, to one of ordinary skill in the art that the invention may be practiced without these specific details.


Reference in this specification to “one embodiment” or “an embodiment” means that a particular feature, structure, or characteristic described in connection with the embodiment is included in at least one embodiment of the invention. The appearances of the phrase “in one embodiment” in various places in this specification are not necessarily all referring to the same embodiment, nor are separate or alternative embodiments mutually exclusive of other embodiments. Moreover, various features are described which may be exhibited by some embodiments and not by others. Similarly, various requirements are described which may be requirements for some embodiments but not other embodiments.


The shortcomings of the conventional physical sputter or chlorine etch can be resolved by using a method that can etch the multi-layer materials without re-depositions on the sidewalls by using a Carbonyl reactive ion etch (RIE) process. The etched devices are also corrosion free under these carbon monoxide (CO) based gas chemistries. An electro conductive material is used as the hard mask such as titanium nitride (TiN) for etching the Magnetic-Tunneling-Junction (MTJ) and for allowing self aligned via for the following bottom electrode (BELT) etch step. Carbonyl reactive ion etch has good selectivity of TiN to MTJ.


It has been well known in the steel industry that iron will form iron carbonyl Fe(CO)5 when reacted with CO at a boiling point of 103° C. Subsequently it was found that most metals will form carbonyls at elevated temperatures. On that basis NiFe can be etched reactively in a plasma reactive ion etch chamber into Ni(CO)4 and Fe(CO)5, where the byproducts are volatile and may be pumped away.


Embodiments of the present invention disclose a method for etching multi-layer metallic stacks in MRAM devices utilizing CO based etch chemistries to form volatile carbonyl byproducts. In one embodiment NH3 is added into the CO gas mixture to prevent to certain extent the dissociation of CO into non-reactive carbon and oxygen. As a result, C to O bonding was preserved as the reactive etching species, and the formation of carbide and oxide on the surface was avoided. An alternative gas chemistry for producing carbonyl by-products effectively is methanol (CH3OH), where CO reactive species can be generated in a plasma without the need for the additional ammonia. Typical etch rates were ˜300 Å·min-1 for Ni0.8Fe0.2, a factor of about three higher than purely physical Ar+ sputtering as in ion milling at similar RF power and pressure ratios. The method includes utilizing a metallic hard mask that is in-volatile to the CO/NH3 or CH3OH process chemistry such as Ta, TiN or Al2O3. The disclosed process may be operated at 100° C. to 200° C., below temperatures that could alter the magnetic properties of the MTJ. The disclosed process may be run at an inductively-coupled-plasma (ICP) reactor (may include capacitively-coupled (CCP), transformer-coupled (TCP) reactors and electron cyclotron resonance (ECR)) and run at a substrate bias power level that does cause electrical damage (ESD) to the sensitive device layers. Advantageously, the CO/NH3 or methanol chemistries do not cause corrosion upon wafer removal from the reactor since no residue is left behind on feature sidewalls.



FIGS. 1-6 illustrate embodiments of the disclosed technique for fabricating a MRAM circuit/chip. Referring to FIG. 1, a Magnetic Tunnel Junction (MTJ) deposition step is shown. The MTJ deposition step include deposition of a Bottom Electrode Layer (BELT) 12; deposition of a MTJ stack 14; and deposition of a capping layer 16. In one embodiment, the capping layer may comprise ruthenium. All of the aforementioned deposition steps are on a pre-fabricated structure 10 comprising pre-fabricated circuitry on a substrate using techniques known to one of ordinary skill in the art. The MTJ stack may comprise a fixed or pinned bottom magnetic layer; and a top free magnetic layer. The two layers may be separated by a tunneling layer. A magnetic orientation of the fixed magnetic layer is fixed, whereas a magnetic orientation of the top free magnetic layer may be changed through application of a switching field.


Turning now to FIG. 2, there is shown a Hard Mask (HM) deposition and MTJ lithography step. This step includes deposition of a metallic hard mask 18; deposition of a Bottom Antireflective Coating 20; and deposition and patterning (lithography) of a photoresist 22. All of using techniques known to one of ordinary skill in the art. In one embodiment, the metallic hard mask may comprise titanium. In other embodiments the metallic hard mask may be selected from the group consisting of one of titanium, tantalum, titanium nitride, silicon dioxide, aluminum, and amorphous carbon. In other embodiments, the hard mask 18 may be of any suitable material that does not form carbonyls.


Turning now to FIG. 3, there is shown a Hard Mask Magnetic Sack Etch step. Under this step, the metallic hard mask 18 is etched followed by etching of photoresist 22. In one embodiment, a fluorine based chemistry may be used for this etching step.



FIG. 4 illustrates deposition of an oxide spacer 24.



FIG. 5 illustrates a BELT lithography step. This step include deposition of BARC layer 28 and photoresist 28 followed by a lithography step to pattern the layer 28.



FIG. 6. illustrates a BELT etch step wherein the oxide spacer 24 has been etched.


One of ordinary skill in the art would appreciate that the above outlined processing steps may be used to fabricate a MRAM circuit/chip with a plurality of discrete magnetic bits.


The etch chemistries that may be used in the above outlined steps, in accordance with one embodiment of the invention, are provided below.














TABLE 1





CO
NH3
Press
Bias Power
Source Power
Temp


sccm
sccm
mTorr
Watt
Watt
° C.







6 to 20
10 to 30
1 to 10
100 to 300
500 to 2000
100 to 200









CO/NH3 Etch Chemistry for Magnetic Materials

Table 2 below indicates process parameters of a CH3OH etch chemistry, in accordance with one embodiment.













TABLE 2





CH3OH
Press
Bias Power
Source Power
Temp


sccm
mTorr
Watt
Watt
° C.







10 to 30
1 to 10
100 to 300
500 to 2000
100 to 200









CH3OH Etch Chemistry for Magnetic Materials

Table 3 below shows process parameters for deposition of the hard mask layer 18, in accordance with one embodiment.


















TABLE 3










Dep



AR-
ARH-



Tool

Thick
Time
Press
Temp
Power
TIW
TIW
Dep Rate

















Endura
Material
A
sec
mT
° C.
W
sccm
sccm
A/sec
A/min





Endura
Columnar Ti
550
70
4.5
40
8000
80
15
7.9
471









Table 4 below shows process parameters for patterning of the MTJ stack, in accordance with one embodiment.














TABLE 4





Tool
BARC
RESIST
Illumination
Exp Eng
FOV







ASM
650A AR77
3500A TOK
Conventional
21 mJ
−0.1


193 nm


Scanner









Table 5 below shows process parameters for etching the hard mask, in accordance with one embodiment.






















TABLE 5











Etch


Pwr
Pwr







Tool

Thick

Time
Press
Temp
kHz
MHz
Cl2
BCl3
N2
Ar
Etch Rate





















LAM9600
Material
A
ME/OE
sec
mTor
° C.
Watt
Watt
cc
cc
cc
cc
A/sec
A/min





LAM9600
Ti
500
ME
30
8.0
65
100
500
20
10
5
5
41.7
2500









Table 6 below shows process parameters for etching the MTJ stack, in accordance with one embodiment.




















TABLE 8











Etch


Pwr
Pwr





Tool

Thick

Time
Press
Temp
kHz
MHz
CO
NH3
Etch Rate



















Tegal3-PM2
Material
A
ME/OE
sec
mTor
° C.
Watt
Watt
cc
cc
A/sec
A/min






















Tegal3-PM2
MTJ
450
ME
250
3.5
170
250
1000
12
20
1.8
108


Tegal3-PM2
MTJ

OE
250
10
170
75
500
12
20









In the Table 6 ME denoted a main etch step whereas OE denotes a over etch step. In one embodiment, the end points for these etch steps is based on spectral analysis of the plasma within the etching chamber. In particular, spectral signature of the plasm is monitored during the ME step which is ended when a the etching is stopped when a drop in Signal Intensity at 420 nm is observed.


Table 7 below shows process parameters for deposition of the spacer oxide, in accordance with one embodiment.



















TABLE 7










Dep









Tool

Thick
Time
Press
Temp
HF
LF
O2
TEOS
Dep Rate


















Novellus 3
Material
A
sec
Torr
° C.
kW
kW
ml/min
ml/min
A/sec
A/min





Novellus 3
TEOS
2500
18
1.6
350
0.40
0.50
7
1.5
28.4
1704









Table 8 below shows process parameters for the BELT lithography step, in accordance with one embodiment.














TABLE 8





Tool
BARC
RESIST
Illumination
Exp Enc
FOV







ASM248
800A AR
7000A UV6
Conventional
13 mJ
−0.1









Table 9 below shows process parameters for the BELT etch and subsequent steps, in accordance with one embodiment.



















TABLE 9









Etched
Etch


Pwr
Pwr






Thick
Time
Press
Temp
kHz
MHz
CF4
Ar
Etch Rate


















Tegal3-PM-ICP
Material
A
sec
mTor
° C.
Watt
Watt
cc
cc
A/sec
A/min





















Tool













Tegal3-PM1-ICP
Oxide
2500
370
3.5
30
26
400
15
15
6.76
405


Semitool


Tegal3-PM1-ICP
Oxide +
1000
150
10
30
26
400
20
30
5.00
300



BELT









Although the present embodiments have been described with reference to specific example embodiments, it will be evident that various modifications and changes may be made to these embodiments without departing from the broader spirit and scope of the various embodiments.

Claims
  • 1. A method for fabricating a magnetic film structure, wherein the method comprises: forming a magnetic structure on a bottom electrode layer, the magnetic structure including: at least one pinned bottom magnetic film layer having a fixed magnetic orientation;at least one top magnetic film layer having a magnetic orientation that can be manipulated by a current; anda tunneling layer between the at least one pinned bottom magnetic film layer and the at least one top magnetic film layer;forming a metallic hard mask above the magnetic structure;etching, by inductively-coupled plasma etching, the metallic hard mask, but not the magnetic structure, using a first chemistry;starting etching of the magnetic structure using a second chemistry to form at least one magnetic bit;monitoring a signal of a spectral signature of a plasma at a predetermined wavelength while etching the magnetic structure;stopping etching the magnetic structure when a drop in the signal is observed; andover-etching, by inductively-coupled plasma etching, at least one sidewall of the at least one magnetic bit,wherein the second chemistry is different from the first chemistry.
  • 2. The method of claim 1, wherein the metallic hard mask comprises at least one of titanium, tantalum, titanium nitride, silicon dioxide, aluminum, or amorphous carbon.
  • 3-7. (canceled)
  • 8. The method of claim 2, wherein the metallic hard mask comprises titanium nitride.
  • 9. The method of claim 2, wherein the metallic hard mask comprises titanium.
  • 10. The method of claim 1, wherein the second chemistry comprises carbon monoxide.
  • 11. The method of claim 10, wherein the second chemistry comprises a mixture of carbon monoxide and ammonia.
  • 12. The method of claim 1, wherein the second chemistry comprises methanol.
  • 13. The method of claim 1, wherein the first chemistry comprises a fluorine-based chemistry.
  • 14. The method of claim 13, wherein the second chemistry comprises carbon monoxide.
  • 15. The method of claim 14, wherein the second chemistry comprises a mixture of carbon monoxide and ammonia.
  • 16. The method of claim 13, wherein the second chemistry comprises methanol.
  • 17. The method of claim 1, further comprising forming a capping layer above the magnetic structure, and wherein the metallic hard mask is formed above the capping layer.
  • 18. The method of claim 17, wherein the capping layer comprises ruthenium.
  • 19. The method of claim 1, further comprising forming a bottom antireflective coating above the metallic hard mask.
  • 20. The method of claim 1, further comprising forming and etching an oxide spacer above the magnetic bit.
  • 21. The method of claim 1, wherein said starting etching of the magnetic structure is performed at a higher power than said over-etching.
  • 22. The method of claim 1, wherein said starting etching of the magnetic structure is performed at a higher frequency than said over-etching.
  • 23. The method of claim 1, wherein said starting etching of the magnetic structure is performed at a lower pressure than said over-etching.
  • 24. The method of claim 1, wherein: said starting etching of the magnetic structure is performed at a higher power than said over-etching;said starting etching of the magnetic structure is performed at a higher frequency than said over-etching; andsaid starting etching of the magnetic structure is performed at a lower pressure than said over-etching.
  • 25. The method of claim 1, wherein said over-etching is performed using the second chemistry.
Parent Case Info

This application claims the benefit of priority to U.S. Provisional Patent Application No. 61/375,218 filed on Aug. 19, 2010, the entire specification of which is hereby incorporated by reference.

Provisional Applications (1)
Number Date Country
61375218 Aug 2010 US