US2005287747A1PendingUtilityA1
Doped nitride film, doped oxide film and other doped films
Est. expiryJun 29, 2024(expired)· nominal 20-yr term from priority
Inventors:Ashima B. ChakravartiJudson R. HoltKevin K. ChanSadanand V. DeshpandeRangarajan Jagannathan
H10P 14/69433H10P 14/6927H10P 14/6922H10P 14/6682H10P 14/6336H10P 14/6334H10W 20/077H10W 20/074H10W 20/071C23C 16/308C23C 16/401C23C 16/34H10D 30/601H10D 30/6745H10D 30/6731H10D 30/792
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Claims
Abstract
Adding at least one non-silicon precursor (such as a germanium precursor, a carbon precursor, etc.) during formation of a silicon nitride, silicon oxide, silicon oxynitride or silicon carbide film improves the deposition rate and/or makes possible tuning of properties of the film, such as tuning of the stress of the film. Also, in a doped silicon oxide or doped silicon nitride or other doped structure, the presence of the dopant may be used for measuring a signal associated with the dopant, as an etch-stop or otherwise for achieving control during etching.
Claims
exact text as granted — not AI-modified1 . A method of producing a doped silicon nitride film, doped silicon oxide film, doped silicon oxynitride film or doped silicon carbide film, the method comprising at least:
providing at least one silicon precursor, providing at least one of: a nitrogen precursor (which may be the same as or different from the silicon precursor) or an oxygen precursor, further providing at least one non-silicon precursor (which may be the same as or different from the silicon precursor, the nitrogen precursor and/or the oxygen precursor), wherein a doped silicon nitride film, a doped silicon oxide film, a doped silicon oxynitride film or a doped silicon carbide film is formed (provided that when the film is a doped oxide, the non-silicon precursor is not boron and not phosphorous).
2 . The method of claim 1 , wherein the providing of at least one silicon precursor and the providing of at least one non-silicon precursor occurs simultaneously and is in a form of providing flow of a gas.
3 . The method of claim 1 , wherein the non-silicon precursor is a germanium precursor.
4 . The method of claim 1 , wherein the non-silicon precursor is selected from the group consisting of a carbon precursor; a boron precursor; an aluminum precursor; an arsenic precursor; a hafnium precursor; a gallium precursor and an indium precursor.
5 . The method of claim 1 , wherein a produced film is a silicon nitride film.
6 . The method of claim 1 , wherein a produced film is germanium- and/or carbon-doped silicon nitride or silicon oxide.
7 . The method of claim 1 , wherein a produced film has a tunable stress.
8 . The method of claim 1 , wherein the non-silicon precursor is an organogermanium compound or a germanium precursor selected from the group consisting of GeH 4 and GeH 3 CH 3 ;
diborane; trimethyl aluminum (TMA); a C 2 H 4 carbon precursor; trimethyl Ga; trimethyl In; trialkyl amino Ga; trialkyl amino In; GaH 3 ; InH 3 ; AlH and aluminum isopropoxide.
9 . The method of claim 1 , wherein the non-silicon precursor is an alkyl hydride or an alkyl amino hydride of germanium, carbon, aluminum, boron, arsenic, hafnium, gallium or indium.
10 . The method of claim 1 , including applying a precursor modification to tune at least one chemical or physical property of a produced film.
11 . The method of claim 10 , wherein the precursor modification is a mixture of at least two precursors.
12 . The method of claim 10 , wherein the at least one chemical or physical property is stress of a produced film.
13 . The method of claim 10 , wherein the at least one chemical or physical property is selected from the group consisting of: wet etch rate; dry etch rate; etch end point; deposition rate; and physical, electrical and/or optical property.
14 . The method of claim 1 , wherein deposition is at a lower temperature than if the non-silicon precursor were omitted.
15 . The method of claim 1 , conducted at a temperature below about 700° C.
16 . The method of claim 1 , wherein the deposition is RTCVD, PECVD, LPCVD, remote plasma nitride or ALD.
17 . The method of claim 1 , including adding germane to a mixture of silane and ammonia, and forming a Ge-doped Si nitride film.
18 . The method of claim 1 , further comprising a step of measuring a signal for a non-silicon dopant from the non-silicon precursor, said signal measuring for controlling an etch.
19 . The method of claim 1 , wherein the produced film is a Ge-doped silicon nitride film having a uniformly distributed Ge concentration.
20 . A silicon nitride or silicon oxide film, having a tunable stress in a range of about 3 G Pa (compressive) to 3 G Pa (tensile).
21 . The film of claim 20 , wherein the film is germanium doped
22 . The film of claim 20 , wherein the film is boron-doped, aluminum-doped, carbon-doped, arsenic-doped, hafnium-doped, gallium-doped and/or indium-doped.
23 . The film of claim 20 , including two or more dopants
24 . The film of claim 20 , wherein the film is Ge-doped and wherein the Ge-doped film has a stress that is at least about 1.0 G Pa greater than a film that has been made by a same process except without Ge-doping.
25 . An aluminum-doped silicon oxide film.
26 . A germanium-doped silicon nitride film.
27 . The film of claim 26 , wherein the film is a Ge-doped silicon nitride film with uniformly distributed Ge.
28 . The method of claim 1 , wherein the deposition is conducted at room temperature.Join the waitlist — get patent alerts
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