Catalysts for Carbon Dioxide Conversion

US2016145752A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2016145752-A1
Application numberUS-201414392120-A
CountryUS
Kind codeA1
Filing dateJun 27, 2014
Priority dateJun 27, 2013
Publication dateMay 26, 2016
Grant date

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

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The disclosure relates generally to improved methods for the reduction of carbon dioxide. The disclosure relates more specifically to catalytic methods for electrochemical reduction of carbon dioxide that can be operated at commercially viable voltages and at low overpotentials. The disclosure uses a transition metal dichalcogenide and helper catalyst in contact within the cell.

First claim

Opening claim text (preview).

1 . A method of electrochemically reducing carbon dioxide in an electrochemical cell having a cathode comprising at least one transition metal dichalcogenide, an electrolyte in contact with the cathode, and an anode, the method comprising contacting the carbon dioxide with the at least one transition metal dichalcogenide of the cathode of the electrochemical cell, the electrolyte comprising at least one helper catalyst, each helper catalyst comprising at least one positively charged nitrogen, sulfur, or phosphorus group and applying a potential to the electrochemical cell sufficient to reduce the carbon dioxide. 2 - 4 . (canceled) 5 . A method of claim 1 , wherein the transition metal dichalcogenide is selected from the group consisting of TiX 2 , VX 2 , CrX 2 , ZrX 2 , NbX 2 , MoX 2 , HfX 2 , WX 2 , TaX 2 , TcX 2 , and ReX 2 , wherein X is independently S, Se, or Te. 6 - 8 . (canceled) 9 . A method of claim 1 , wherein the transition metal dichalcogenide is MoS 2 or MoSe 2 . 10 - 11 . (canceled) 12 . A method of claim 1 , wherein the transition metal dichalcogenide is in nanoparticle form. 13 . A method of claim 12 , wherein the transition metal dichalcogenide nanoparticles have an average size between about 1 nm and 400 nm. 14 . A method of claim 1 , wherein the transition metal dichalcogenide is in nanoflake, nanosheet, or nanoribbon form. 15 . A method of claim 14 , wherein the transition metal dichalcogenide nanoflakes, nanosheets, or nanoribbons have an average size between about 1 nm and 400 nm. 16 . (canceled) 17 . A method of claim 1 , wherein the helper catalyst is an imidazolium, pyridinium, pyrrolidinium, phosphonium, ammonium, choline, sulfonium, prolinate, or methioninate salt. 18 . (canceled) 19 . A method of claim 18 , wherein the imdazolium is of the formula: wherein R 1 , R 2 , and R 3 are independently selected from the group consisting of hydrogen, linear aliphatic C 1 -C 6 group, branched aliphatic C 1 -C 6 group and cyclic aliphatic C 1 -C 6 group. 20 . (canceled) 21 . (canceled) 22 . A method of claim 1 , wherein the helper catalyst is ethyl-3-methylimidazolium tetrafluoroborate. 23 . A method of claim 1 , wherein the electrolyte is an aqueous solution. 24 . A method of claim 23 , wherein the helper catalyst is present in the aqueous solution within the range from about 2 mol % to about 10 mol %. 25 - 26 . (canceled) 27 . A method of claim 1 of, wherein the carbon dioxide is reduced to CO or a mixture of CO and H 2 . 28 . A method of claim 1 , wherein the applied potential is about −2 to about +2 V vs. reversible hydrogen electrode. 29 . (canceled) 30 . A method of claim 1 , wherein the reduction of carbon dioxide is initiated at overpotential of less than about 100 mV. 31 . (canceled) 32 . A method of claim 1 , wherein the reduction of carbon dioxide is at least of about 90% Faradaic efficiency. 33 . (canceled) 34 . An electrochemical cell having a cathode comprising least one transition metal dichalcogenide, and an electrolyte comprising at least one helper catalyst comprising at least one positively charged nitrogen, sulfur, or phosphorus group in contact with the transition metal dichalcogenide. 35 . An electrochemical cell according to claim 34 , wherein the transition metal dichalcogenide is MoS 2 . 36 . (canceled) 37 . An electrochemical cell according to claim 34 , wherein the helper catalyst is present in an amount of about 4 mol % to about 10 mol %. 38 . An electrochemical cell according to claim 34 , wherein the helper catalyst is ethyl-3-methylimidazolium salt tetrafluoroborate. 39 . (canceled) 40 . A composition comprising at least one transition metal dichalcogenide in contact with at least one helper catalyst comprising at least one positively charged nitrogen, sulfur, or phosphorus group. 41 - 45 . (canceled) 46 . An electrochemical cell of claim 34 , wherein the helper catalyst is an imidazolium, pyridinium, pyrrolidinium, phosphonium, ammonium, choline, sulfonium, prolinate, or methioninate salt.

Assignees

Inventors

Classifications

  • Chemistry & Metallurgy · mapped topic

  • Electrolytic production of inorganic compounds or non-metals · CPC title

  • Reduction · CPC title

  • C25B1/02Primary

    Hydrogen or oxygen · CPC title

  • C25B11/075Primary

    consisting of a single catalytic element or catalytic compound · CPC title

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Frequently asked questions

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What does patent US2016145752A1 cover?
The disclosure relates generally to improved methods for the reduction of carbon dioxide. The disclosure relates more specifically to catalytic methods for electrochemical reduction of carbon dioxide that can be operated at commercially viable voltages and at low overpotentials. The disclosure uses a transition metal dichalcogenide and helper catalyst in contact within the cell.
Who is the assignee on this patent?
Univ Illinois
What technology area does this patent fall under?
Primary CPC classification C25B11/0447. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu May 26 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).