Methods for depositing tungsten layers employing atomic layer deposition techniques
Abstract
A method for forming a tungsten layer on a substrate surface is provided. In one aspect, the method includes positioning the substrate surface in a processing chamber and exposing the substrate surface to a soak. A nucleation layer is then deposited on the substrate surface in the same processing chamber by alternately pulsing a tungsten-containing compound and a reducing gas selected from a group consisting of silane, disilane, dichlorosilane and derivatives thereof. A tungsten bulk layer may then be deposited on the nucleation layer using cyclical deposition, chemical vapor deposition, or physical vapor deposition techniques.
Claims
exact text as granted — not AI-modified1 . A method for forming a tungsten layer on a substrate surface, comprising:
positioning the substrate surface in a processing chamber; exposing the substrate surface to a soak for a predetermined time, wherein the soak comprises a soak compound; and depositing a nucleation layer in the same processing chamber by alternately pulsing a tungsten-containing compound and a reducing gas,-wherein the reducing gas comprises a reductant different than the soak compound.
2 . The method of claim 1 , wherein the reductant is selected from the group consisting of hydrogen, silane, disilane, trisilane, dichlorosilane, borane, diborane, derivatives thereof, and combinations thereof.
3 . The method of claim 2 , wherein the nucleation layer is deposited by alternately pulsing tungsten hexafluoride and silane.
4 . The method of claim 2 , wherein the nucleation layer is deposited by alternately pulsing tungsten hexafluoride and diborane.
5 . The method of claim 4 , wherein the nucleation layer has a thickness in a range from about 10 Å to about 200 Å.
6 . The method of claim 2 , wherein the tungsten-containing compound is selected from the group consisting of tungsten hexafluoride and tungsten carbonyl.
7 . The method of claim 6 , wherein the soak compound is selected from the group consisting of hydrogen, borane, diborane, hydrogen, silane, disilane, trisilane, dichlorosilane, derivatives thereof and combinations thereof.
8 . The method of claim 7 , wherein exposing the substrate surface to the soak for the predetermined time is in a range from about 5 seconds to about 90 seconds.
9 . The method of claim 1 , further comprising forming a bulk tungsten deposition film on the nucleation layer using atomic layer deposition, chemical vapor deposition or physical vapor deposition techniques.
10 . The method of claim 7 , wherein exposing the substrate surface to the soak is at a temperature in a range from about 100° C. to about 400° C.
11 . The method of claim 7 , wherein the substrate surface comprises titanium nitride.
12 . A method for forming a tungsten layer on a substrate surface, comprising:
exposing a substrate surface to diborane at a pressure range from about 1 Torr to about 50 Torr and at a temperature range from about 100° C. to about 400° C.; depositing a nucleation layer by alternately pulsing a tungsten-containing compound and silane gas; and forming a bulk tungsten deposition film on the nucleation layer.
13 . The method of claim 12 , wherein exposing the substrate surface to diborane and depositing the nucleation layer occurs in the same chamber.
14 . The method of claim 13 , wherein the nucleation layer has a thickness in a range from about 10 Å to about 200 Å.
15 . The method of claim 14 , wherein the bulk tungsten deposition film has a thickness in a range from about 100 Å to about 5,000 Å.
16 . The method of claim 13 , wherein exposing the substrate surface to diborane for a predetermined time is in a range from about 5 seconds to about 90 seconds.
17 . The method of claim 12 , wherein the substrate surface comprise a barrier layer selected from the group consisting of titanium, titanium nitride, tungsten nitride, tantalum and tantalum nitride.
18 . A method for forming a tungsten layer on a substrate surface, comprising:
positioning the substrate surface in a processing chamber; exposing the substrate surface to a diborane soak for a predetermined time; depositing a nucleation layer in the same processing chamber by alternately pulsing a tungsten-containing compound and a reducing gas, wherein the reducing gas comprises a reductant; and forming a bulk tungsten deposition film on the nucleation layer.
19 . The method of claim 18 , wherein the nucleation layer has a thickness in a range from about 10 Å to about 200 Å.
20 . The method of claim 19 , wherein the bulk tungsten deposition film has a thickness in a range from about 100 Å to about 5,000 Å.
21 . The method of claim 19 , wherein the tungsten-containing compound is selected from the group consisting of tungsten hexafluoride and tungsten carbonyl.
22 . The method of claim 21 , wherein exposing the substrate surface to the diborane soak for the predetermined time is in a range from about 5 seconds to about 90 seconds.
23 . The method of claim 22 , wherein exposing the substrate surface to the diborane soak is at a temperature in a range from about 100° C. to about 400° C.
24 . The method of claim 18 , wherein the reductant is selected from the group consisting of hydrogen, silane, disilane, trisilane, dichlorosilane, borane, diborane, derivatives thereof, and combinations thereof.
25 . The method of claim 24 , wherein the tungsten-containing compound is tungsten hexafluoride and the reductant is silane.
26 . The method of claim 24 , wherein the tungsten-containing compound is tungsten hexafluoride and the reductant is diborane.
27 . A method for forming a tungsten layer on a substrate surface, comprising:
positioning the substrate surface in a processing chamber; exposing the substrate surface to a soak for a predetermined time, wherein the soak comprises a soak compound selected from the group consisting of hydrogen, borane, diborane, hydrogen, silane, disilane, trisilane, dichlorosilane, derivatives thereof and combinations thereof; and depositing a nucleation layer in the same processing chamber by alternately pulsing a tungsten-containing compound and a reducing gas, wherein the reducing gas comprises a reductant different than the soak compound.
28 . The method of claim 27 , wherein the reductant is selected from the group consisting of hydrogen, silane, disilane, trisilane, dichlorosilane, borane, diborane, derivatives thereof, and combinations thereof.
29 . The method of claim 28 , wherein the nucleation layer is deposited by alternately pulsing tungsten hexafluoride and silane.
30 . The method of claim 28 , wherein the nucleation layer is deposited by alternately pulsing tungsten hexafluoride and diborane.
31 . The method of claim 30 , wherein the nucleation layer has a thickness in a range from about 10 Å to about 200 Å.
32 . The method of claim 28 , wherein the tungsten-containing compound is selected from the group consisting of tungsten hexafluoride and tungsten carbonyl.
33 . The method of claim 32 , wherein exposing the substrate surface to the soak for the predetermined time is in a range from about 5 seconds to about 90 seconds.
34 . The method of claim 28 , further comprising forming a bulk tungsten deposition film on the nucleation layer using atomic layer deposition, chemical vapor deposition or physical vapor deposition techniques.
35 . The method of claim 32 , wherein exposing the substrate surface to the soak is at a temperature in a range from about 100° C. to about 400° C.
36 . The method of claim 32 , wherein the substrate surface comprises titanium nitride.Join the waitlist — get patent alerts
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