Synthesis and use of precursors for ALD of tellurium and selenium thin films
US-9783563-B2 · Oct 10, 2017 · US
US10062568B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10062568-B2 |
| Application number | US-201715587551-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 5, 2017 |
| Priority date | May 13, 2016 |
| Publication date | Aug 28, 2018 |
| Grant date | Aug 28, 2018 |
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A method of synthesis of two-dimensional metal chalcogenide monolayers, such as WSe 2 and MoSe 2 , is based on a chemical vapor deposition approach that uses H 2 Se or alkyl or aryl selenide precursors to form a reactive gas. The gaseous selenium precursor may be introduced into a tube furnace containing a metal precursor at a selected temperature, wherein the selenium and metal precursors react to form metal chalcogenide monolayers.
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What is claimed is: 1. A method of synthesizing a metal chalcogenide nanosheet comprising: placing a solid metal precursor in a receptacle; placing the solid-metal precursor-containing receptacle in a reaction chamber; transmitting a gaseous selenium precursor through the reaction chamber; reacting the gaseous selenium precursor with the metal precursor; and forming the metal chalcogenide nanosheet on a substrate, the substrate being independent of the receptacle. 2. The method of claim 1 , wherein the metal chalcogenide nanosheet is selected from the group consisting of: WSe 2 ; MoSe 2 ; NbSe 2 ; PtSe 2 ; ReSe 2 ; TaSe 2 ; TiSe 2 ; ZrSe 2 ; ScSe 2 ; VSe 2 ; GaSe; Ga 2 Se 3 ; Bi 2 Se 3 ; GeSe; InSe; In 2 Se 3 ; SnSe 2 ; SnSe; SbSe 3 ; ZrSe 3 ; MnIn 2 Se 4 ; MgIn 2 Se 4 ; Pb 2 Bi 2 Se 5 ; SnPSe 3 ; and PdPSe; and alloys and doped derivatives thereof. 3. The method of claim 1 , wherein the metal precursor is selected from the group consisting of: a metal; a metal diselenide bulk powder; a metal oxide; an inorganic precursor; an organometallic precursor; a metal alkyl precursor; an ethylhexanoate salt; and bis(ethylbenzene)molybdenum. 4. The method of claim 1 , wherein the gaseous selenium precursor is selected from the group consisting of: H 2 Se; an alkyl selenide; and an aryl selenide. 5. The method of claim 1 , further comprising reacting the gaseous selenium precursor with the metal precursor in the presence of a reducing gas. 6. The method of claim 1 , further comprising reacting the gaseous selenium precursor with the metal precursor in the presence of H 2 S. 7. The method of claim 1 , wherein the gaseous selenium precursor is mixed with a ligand. 8. The method of claim 7 , wherein the ligand is selected from the group consisting of: an alkane thiol; an alkane selenol; and a combination of an alkane thiol and an alkane selenol. 9. The method of claim 1 , wherein the reaction chamber is a chemical vapor deposition reactor. 10. The method of claim 1 , further comprising reacting the gaseous selenium precursor and the metal precursor at a temperature, or a range of temperatures, between 100° C. and 550° C. 11. The method of claim 1 , further comprising reacting the gaseous selenium precursor and the metal precursor at a temperature, or a range of temperatures, above 550° C. 12. The method of claim 1 , further comprising reacting the gaseous selenium precursor and the metal precursor in the presence of an inert carrier gas. 13. The method of claim 1 , wherein the nanosheet has lateral dimensions less than 10 nm. 14. The method of claim 1 , wherein the nanosheet has lateral dimensions between 10 nm and 100 μm. 15. The method of claim 1 , wherein the nanosheet has lateral dimensions greater than 100 μm. 16. The method of claim 1 , wherein reacting the gaseous selenium precursor with the metal precursor is conducted at a pressure below atmospheric pressure. 17. The method of claim 1 , wherein reacting the gaseous selenium precursor with the metal precursor is conducted at atmospheric pressure. 18. The method of claim 1 , wherein reacting the gaseous selenium precursor with the metal precursor is conducted at a pressure above atmospheric pressure.
using chemical vapour deposition [CVD] · CPC title
being chalcogenide semiconductor materials not being oxides, e.g. ternary compounds · CPC title
characterised by the method used for heating the substrate (C23C16/48, C23C16/50 take precedence) · CPC title
Sulfides, selenides, or tellurides · CPC title
by evaporation using carrier gas in contact with the source material (C23C16/4486 takes precedence) · CPC title
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