US2022115232A1PendingUtilityA1
Methods for depositing a transition metal chalcogenide film on a substrate by a cyclical deposition process
Est. expiryNov 16, 2038(~12.3 yrs left)· nominal 20-yr term from priority
H10P 14/6929H10P 14/6334H10P 14/3466H10P 14/24H10P 14/3436H10P 14/203H10D 30/481H10D 62/883H10D 62/405H10D 62/80H10D 30/675H10D 99/00C23C 16/45527C23C 16/305C23C 16/52C23C 16/56H01L 29/045H01L 29/78681H01L 21/0262H01L 21/02568H01L 29/24H01L 21/02609H01L 21/02145H01L 21/02271H10P 95/90H10P 14/6928H10P 14/668H10P 14/69395H10P 14/69392H10D 64/01342H10P 14/418
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Claims
Abstract
Systems for depositing a transition metal chalcogenide film on a substrate by cyclical deposition process are disclosed. The methods may include, contacting the substrate with at least one transition metal containing vapor phase reactant comprising at least one of a hafnium precursor, or a zirconium precursor, and contacting the substrate with at least one chalcogen containing vapor phase reactant. Semiconductor device structures including a transition metal chalcogenide film deposited by the methods of the disclosure are also provided.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method for depositing a transition metal chalcogenide film on a substrate by a cyclical deposition process, the method comprising:
contacting the substrate with at least one transition metal containing vapor phase reactant comprising at least one of a hafnium precursor and a zirconium precursor; and contacting the substrate with at least one chalcogen containing vapor phase reactant.
2 . The method of claim 1 , wherein the cyclical deposition process comprises atomic layer deposition.
3 . The method of claim 1 , wherein the cyclical deposition process comprises cyclical chemical vapor deposition.
4 . The method of claim 1 , wherein at least one of the hafnium precursor and the zirconium precursor comprises at least one of a halide precursor and a metalorganic precursor.
5 . The method of claim 4 , wherein the halide precursor comprises at least one of hafnium tetrachloride (HfCl 4 ) and zirconium tetrachloride (ZrCl 4 ).
6 . The method of claim 4 , wherein the metalorganic precursor comprises at least one of an alkylamide precursor and a cyclopentadienyl-ligand containing precursor.
7 . The method of claim 6 , wherein the alkylamide precursor comprises at least one of tetrakis(ethylmethylamido)hafnium (Hf(NEtMe) 4 ), and tetrakis(ethylmethylamido)zirconium (Zr(NEtMe) 4 ).
8 . The method of claim 6 , wherein the cyclopentadienyl-ligand containing precursor comprises at least one of tris(dimethylamido)cyclopentadienylhafnium (HfCp(NMe 2 ) 3 ), bis(methylcyclopentadienyl)methoxymethylhafnium ((MeCp) 2 Hf(CH) 3 (OCH 3 )), tris(dimethylamido)cyclopentadienylzirconium (ZrCp(NMe 2 ) 3 ), and bis(methylcyclopentadienyl)methoxymethylzirconium ((MeCp) 2 Zr(CH) 3 (OCH 3 )).
9 . The method of claim 1 , wherein the at least one chalcogen containing vapor phase reactant comprises hydrogen sulfide (H 2 S), hydrogen selenide (H 2 Se), dimethyl sulfide ((CH 3 ) 2 S), and dimethyl telluride (CH 3 ) 2 Te.
10 . The method of claim 1 , further comprising flowing the chalcogen containing vapor phase reactant through a gas purifier prior to entering the reaction chamber to reduce a concentration of at least one of water and oxygen within the chalcogen containing vapor phase reactant.
11 . The method of claim 10 , wherein the concentration of at least one of water and oxygen within the chalcogen containing vapor phase reactant is reduced to less than 1 part per million.
12 . The method of claim 1 , further comprising flowing a carrier gas through a vessel containing a source of the transition metal containing vapor phase reactant to transport the transition metal containing vapor phase reactant to the reaction chamber and further comprising flowing the carrier gas through a gas purifier prior to entering the source of the transition metal containing vapor phase reactant to reduce a concentration of at least one of water and oxygen within the carrier gas.
13 . The method of claim 12 , wherein the concentration of at least one of water and oxygen within the carrier gas is reduced to less than 1 part per million.
14 . The method of claim 1 , further comprising pre-annealing the reaction chamber prior to film deposition.
15 . The method of claim 1 , wherein the transition metal chalcogenide film comprises a predominant (001) crystallographic orientation.
16 . The method of claim 1 , further comprising in-situ depositing a capping layer over the transition metal chalcogenide film.
17 . The method of claim 16 , wherein in-situ depositing a capping layer over the transition metal chalcogenide film comprises depositing the capping layer utilizing non-oxidative precursors or non-oxygen reactants.
18 . The method of claim 16 , wherein the capping layer comprises a metal silicate film.
19 . The method of claim 18 , wherein the metal silicate film comprises an aluminum silicate film (Al x Si y O z ).
20 . A semiconductor device structure comprising a transition metal chalcogenide film deposited by the method of claim 1 .Join the waitlist — get patent alerts
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