Method of fabricating transition metal dichalcogenide

US9840764B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9840764-B2
Application numberUS-201514870014-A
CountryUS
Kind codeB2
Filing dateSep 30, 2015
Priority dateSep 30, 2015
Publication dateDec 12, 2017
Grant dateDec 12, 2017

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  1. Title

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  2. Abstract

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  5. First independent claim

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  7. Citations and related patents

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Abstract

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A method of fabricating transition metal dichalcogenides includes a preparing step, a steaming step and a depositing step. The preparing step is performed for providing a transition metal substrate, a reactive gas and a solid chalcogenide. The steaming step is performed for heating the solid chalcogenide to generate a chalcogenide gas in a steaming space. The depositing step is performed for introducing the reactive gas into the chalcogenide gas to ionize the chalcogenide gas so as to generate a chalcogenide plasma in a depositing space. The depositing step is performed under a process vacuum pressure from low vacuum pressure to atmospheric pressure. The reactive gas and the chalcogenide gas are flowed from top to bottom through a top of the transition metal substrate. The loading substrate is heated at a loading substrate temperature, and the steaming space is different from the depositing space.

First claim

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What is claimed is: 1. A method of fabricating transition metal dichalcogenides, comprising: performing a preparing step for providing a loading substrate, a solid transition metal, a reactive gas and a solid chalcogenide, wherein the solid chalcogenide is a chemical element selected from the group consisting of sulfur, selenium, and tellurium; performing a pre-plating step for heating the solid transition metal to generate a transition metal gas so as to deposit the transition metal gas on the loading substrate to form a transition metal oxide layer in a pre-plating space; performing a steaming step for heating the solid chalcogenide to generate a chalcogenide gas in a steaming space; performing a depositing step for introducing the reactive gas into the chalcogenide gas to ionize the chalcogenide gas so as to generate a chalcogenide plasma in a depositing space, wherein the chalcogenide plasma is reacted with a surface of the transition metal oxide layer to form a transition metal dichalcogenide layer by heating the loading substrate, and the depositing step is performed under a process vacuum pressure; performing a thickness controlling step for changing the thickness of the transition metal oxide layer thereby changing the number of atomic layers corresponding to the transition metal dichalcogenide layer; and performing a conversion controlling step for controlling a flow rate ratio of the reactive gas to change a conversion efficiency of the transition metal dichalcogenide layer during the process of the chalcogenide plasma reacting with the transition metal oxide layer; wherein the steps of the method of fabricating transition metal dichalcogenides are carried out in order of the preparing step, the pre-plating step, the steaming step, the depositing step, the thickness controlling step, and where the step of the conversion controlling step is performed during the depositing step; wherein in the depositing step, the reactive gas and the chalcogenide gas are flowed from top to bottom through a top of the transition metal oxide layer, the process vacuum pressure is performed from low vacuum pressure to atmospheric pressure, the loading substrate is heated at a loading substrate temperature from 150° C. to 500° C., and the depositing space is different from the steaming space and the pre-plating space; wherein the process vacuum pressure is greater than or equal to 2 Torr and is smaller than or equal to 760 Torr; wherein the depositing step is performed with a plasma power which is greater than or equal to 0 watt and smaller than or equal to 500 watts; wherein after performing the pre-plating step, a thickness of the transition metal oxide layer is greater than or equal to 1 nm and smaller than or equal to 10 nm; wherein the reactive gas comprises nitrogen and hydrogen. 2. The method of claim 1 , wherein the loading substrate is made of polyamide, stainless steel, glass, silicon nitride, silicon dioxide, aluminum oxide or hafnium oxide. 3. The method of claim 1 , wherein the solid transition metal is made of tungsten, molybdenum, nickel, copper, indium, germanium, tantalum, iron, cobalt or titanium. 4. The method of claim 1 , wherein the steaming step is for heating the solid chalcogenide at a steaming temperature from 90° C. to 150° C. when the solid chalcogenide is made from sulfur. 5. The method of claim 1 , wherein the steaming step is for heating the solid chalcogenide at a steaming temperature from 150° C. to 300° C. when the solid chalcogenide is made from selenium. 6. The method of claim 1 , wherein the steaming step is for heating the solid chalcogenide at a steam temperature from 400° C. to 650° C. when the solid chalcogenide is made from tellurium. 7. The method of claim 1 , wherein when the thickness is smaller than 7 nm and the loading substrate temperature is equal to 500° C., the plasma power is 0 watt. 8. The method of claim 1 , wherein the thickness controlling step is for generating one atomic layer corresponding to the transition metal dichalcogenide layer when the thickness is equal to 1 nm. 9. The method of claim 1 , wherein the flow rate ratio between nitrogen and hydrogen is 1:2 or 2:1. 10. The method of claim 1 , wherein the pre-plating step is for forming a transition metal oxide layer by an atomic layer epitaxy process, a sputtering process or an evaporation process. 11. The method of claim 1 , further comprising: performing a transferring step for transferring the loading substrate out of the depositing space after the depositing step, wherein the loading substrate is made of flexible material; and performing a mass production step for sequentially repeating the preparing step, the pre-plating step, the steaming step, the depositing step and the transferring step. 12. A method of fabricating transition metal dichalcogenides, comprising: performing a preparing step for providing a loading substrate, a solid transition metal, a reactive gas and a solid chalcogenide, wherein the solid chalcogenide is a chemical element selected from the group consisting of sulfur, selenium, and tellurium; performing a pre-plating step for heating the solid transition metal to generate a transition metal gas so as to deposit the transition metal gas on the loading substrate to form a transition metal layer in a pre-plating space; performing a steaming step for heating the solid chalcogenide to generate a chalcogenide gas in a steaming space; performing a depositing step for introducing the reactive gas into the chalcogenide gas to ionize the chalcogenide gas so as to generate a chalcogenide plasma in a depositing space, wherein the chalcogenide plasma is reacted with a surface of the transition metal layer to form a transition metal dichalcogenide layer by heating the loading substrate, and the depositing step is performed under a process vacuum pressure; performing a thickness controlling step for changing the thickness of the transition metal layer thereby changing the number of atomic layers corresponding to the transition metal dichalcogenide layer; and performing a conversion controlling step for controlling a flow rate ratio of the reactive gas to change a conversion efficiency of the transition metal dichalcogenide layer during the process of the chalcogenide plasma reacting with the transition metal layer; wherein the steps of the method of fabricating transition metal dichalcogenides are carried out in order of the preparing step, the pre-plating step, the steaming step, the depositing step, the thickness controlling step, and where the step of the conversion controlling step is performed during the depositing step; wherein in the depositing step, the reactive gas and the chalcogenide gas are flowed from top to bottom through a top of the transition metal layer, the process vacuum pressure is performed from low vacuum pressure to atmospheric pressure, the loading substrate is heated at a loading substrate temperature from 150° C. to 500° C., and the depositing space is different from the steaming space and the pre-plating space; wherein the process vacuum pressure is greater than or equal to 2 Torr and is smaller than or equal to 760 Torr, wherein the depositing step is performed with a plasma power which is greater than or equal to 0 watt and smaller than or equal to 500 watts; wherein after performing the pre-plating step, a thickness of the transition metal layer is greater than or equal to 1 nm and smaller than or equal to 50 nm; wherein the reactive gas comprises nitrogen and hydrogen. 13. The method of claim 12 , wherein the loading substrate is made of polyamide, stainless steel, glass, silicon nitride, silico

Assignees

Inventors

Classifications

  • Generic processes or apparatus for manufacture or treatments not covered by the other groups of this subclass · CPC title

  • C23C14/08Primary

    Oxides (C23C14/10 takes precedence) · CPC title

  • Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes (reactive sputtering or vacuum evaporation C23C14/00) · CPC title

  • Electricity · mapped topic

  • Treatment with charged particles (C23C14/582 takes precedence) · CPC title

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What does patent US9840764B2 cover?
A method of fabricating transition metal dichalcogenides includes a preparing step, a steaming step and a depositing step. The preparing step is performed for providing a transition metal substrate, a reactive gas and a solid chalcogenide. The steaming step is performed for heating the solid chalcogenide to generate a chalcogenide gas in a steaming space. The depositing step is performed for in…
Who is the assignee on this patent?
Univ Nat Tsing Hua
What technology area does this patent fall under?
Primary CPC classification C23C14/08. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Dec 12 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).