IP Library Granted Patent US 12,701,935
Granted Patent B2
US 12,701,935 · App. 17/824,774 · Granted Aug 4, 2026

Method of depositing material and semiconductor devices

Inventors: Johanna Henrica Deijkers (Eindhoven, NL); Adriaan Jacobus Martinus Mackus (Eindhoven, NL); Ageeth Anke Bol (Nuenen, NL); Wilhelmus M. M. Kessels (Tilburg, NL); Hessel Sprey (Leuven, BE); Jan Willem Maes (Wilrijk, BE)
Assignee: ASM IP Holding B.V.
H10P14/418C23C16/305C23C16/45536H10W20/033H10W20/425
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Quick Facts
Patent No.
US 12,701,935
App. No.
17/824,774
Filed
May 25, 2022
Granted
Aug 4, 2026
Kind
B2
Art Unit
2813
USPC
257/570
Abstract

The current disclosure relates to deposition of a transition metal chalcogenide barrier layer. The method of depositing a transition metal chalcogenide barrier layer comprises providing a substrate having an opening into a reaction chamber, providing a transition metal precursor in the reaction chamber in vapor phase and providing an reactive chalcogen species in the reaction chamber. The method may be a plasma-enhanced atomic layer deposition method. The disclosure further relates to an interconnect comprising a transition metal chalcogenide barrier layer.

Claims (24)

1 . A method of depositing a transition metal chalcogenide barrier layer, the method comprising:

providing a substrate having an opening within a dielectric material, into a reaction chamber;

providing a transition metal precursor in the reaction chamber in vapor phase; and

providing a reactive chalcogen species in the reaction chamber, to thereby deposit the transition metal chalcogenide barrier layer on the dielectric material and within the opening,

wherein the transition metal chalcogenide barrier layer is between the dielectric material and a conductive metal,

wherein the chalcogenide comprises one or more of S, Se, and Te,

wherein the transition metal chalcogenide barrier layer mitigates diffusion between the conductive metal and the dielectric material, and

wherein the transition metal precursor comprises a transition metal halide or a transition metal oxyhalide.

2 . The method of claim 1 , wherein the transition metal precursor comprises the transition metal oxyhalide.

3 . The method of claim 1 , wherein the transition metal precursor comprises MoCl 4 , MoCl 5 , MoF 6 , TiCl 4 , ZrCl 4 , ZrI 4 , HfCl 4 , HfI 4 , VCl 4 , NbCl 5 , NbF 5 , TaCl 5 , TaF 5 , TaI 5 , WCl 5 , WCl 6 , or WF 6 .

4 . The method of claim 1 , wherein the method further comprises providing a second transition metal precursor in the reaction chamber.

5 . The method of claim 4 , wherein the second transition metal precursor comprises a metal organic compound comprising at least one of an amido group and an imido group.

6 . The method of claim 5 , wherein the metal organic compound comprises at least one of a tert-butylimido group and a dimethylamido group.

7 . The method of claim 1 , wherein the metal of the transition metal precursor is a group 4 to group 6 transition metal.

8 . The method of claim 1 , wherein the metal of the transition metal precursor is selected from a group consisting of molybdenum (Mo), tungsten (W), tantalum (Ta), niobium (Nb), titanium (Ti), zirconium (Zr), hafnium (Hf) and rhenium (Re).

9 . The method of claim 1 , wherein the reactive chalcogen species comprises (NH 4 ) 2 S, ((CH 3 ) 2 SO), (CH 3 ) 2 Se, (CH 3 ) 2 Te, elemental or atomic S, Se, Te, or chalcogenols with the formula R—Y—H, wherein R is a C1-C8 substituted or unsubstituted hydrocarbon, and Y is S, Se, or Te.

10 . The method of claim 1 , wherein the transition metal precursor and the reactive chalcogen species are provided in the reaction chamber alternatively and sequentially.

11 . The method of claim 1 , wherein the reactive chalcogen species is generated by plasma.

12 . The method of claim 11 , wherein the method comprises using at least two different plasmas.

13 . The method of claim 1 , wherein the temperature of the reaction chamber during providing the precursors in the reaction chamber is from about 50° C. to about 500° C.

14 . The method of claim 1 , wherein the transition metal chalcogenide barrier layer is substantially continuous and has a thickness of 3 nm or less.

15 . The method of claim 1 , further comprising applying substrate bias to affect a morphology of the transition metal chalcogenide barrier layer.

16 . The method of claim 1 , wherein the transition metal chalcogenide barrier layer is crystalline after deposition.

17 . The method of claim 1 , wherein the method further comprises the deposition of a second barrier layer material comprising a second metal chalcogenide, wherein a metal of the transition metal chalcogenide barrier layer and a metal of the second metal chalcogenide differ.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 30, 2022
From: DEIJKERS, JOHANNA HENRICA; MACKUS, ADRIAAN JACOBUS MARTINUS; BOL, AGEETH ANKLE; KESSELS, WILHELMUS M.M.; SPREY, HESSEL; MAES, JAN WILLEM
To: ASM IP HOLDING B.V.
Reel/Frame 060046/0846 →
Continuity (2)
Provisional Application 63194278 · May 28, 2021
Related Publication 20220384197A1 · Dec 1, 2022
References Cited (23)
US 9353139B2 · Sundermeyer · 2016 [cited by examiner]
US 9461134B1 · Xie · 2016 [cited by examiner]
US 10163644B2 · Lin · 2018 [cited by applicant]
US 10170322B1 · Cheng · 2019 [cited by applicant]
US 10847366B2 · Mattinen et al. · 2020 [cited by applicant]
US 11043454B2 · Hedge et al. · 2021 [cited by applicant]
US 11047042B2 · McKee et al. · 2021 [cited by applicant]
US 11756828B2 · Wong et al. · 2023 [cited by applicant]
US 20130267082A1 · Gatineau · 2013 [cited by examiner]
US 20160233322A1 · Yeh et al. · 2016 [cited by applicant]
US 20160372351A1 · Singh et al. · 2016 [cited by applicant]
US 20180108587A1 · Jiang · 2018 [cited by examiner]
US 20190006586A1 · Maes · 2019 [cited by examiner]
US 20200312775A1 · Lee et al. · 2020 [cited by applicant]
US 20210032749A1 · Trinh · 2021 [cited by examiner]
US 20210066080A1 · Mattinen et al. · 2021 [cited by applicant]
US 20220139775A1 · Naylor · 2022 [cited by examiner]
US 20220238324A1 · Good · 2022 [cited by examiner]
GB 2548628A · 2017 [cited by examiner]
WO 2015117150A1 · 2015 [cited by applicant]
WO 2018004587A1 · 2018 [cited by applicant]
Lo, Chun-Li et al. “BEOL Compatible Sub-nm Diffusion Barrier for Advanced Cu Interconnects”; 2018. [cited by applicant]
Sharma, Akhil et al. “Low-temperature plasma-enhanced atomic layer deposition of 2-D MoS2: large area, thickness control and tuneable morphology”; Nanoscale; The Royal Society of Chemistry; Apr. 2018. [cited by applicant]