Electrode for electrolysis and preparation method thereof

US11396709B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11396709-B2
Application numberUS-201816328224-A
CountryUS
Kind codeB2
Filing dateJul 30, 2018
Priority dateAug 11, 2017
Publication dateJul 26, 2022
Grant dateJul 26, 2022

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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

Official abstract text for this publication.

Provided is an electrode for electrolysis and a preparation method of the same. The electrode for electrolysis has an improved needle-like structure of a rare earth metal compared to conventional electrodes, and thus detachment of catalytic materials is reduced, so that the electrode is excellent in durability such as exhibiting stable performance even in a reverse current flow. Further, since the electrode for electrolysis has a low overvoltage value, an overvoltage required amount of the electrolytic cell can be remarkably reduced. In addition, an electrode for electrolysis having the above effect can be prepared without introducing additional precursors or changing manufacturing facilities.

First claim

Opening claim text (preview).

The invention claimed is: 1. A preparation method of an electrode for electrolysis, comprising the steps of: preparing a coating solution for preparing an electrode by: dissolving a platinum group metal precursor and a rare earth metal precursor in an organic solvent that is a mixed solvent comprising a C1 to C6 alcohol and a C5 to C8 glycol ether in a volume ratio of from 2:1 to 1:1 to yield a precursor solution; mixing the precursor solution and an amine-based solvent comprising a C6 to C30 unsaturated aliphatic amine to yield the coating solution; applying the coating solution on a metal substrate to form a catalyst layer; drying the catalyst layer; and heat-treating the catalyst layer, wherein the catalyst layer comprises a needle-like structure of the rare earth element. 2. The method of claim 1 , wherein the platinum group metal precursor is at least one selected from the group consisting of ruthenium chloride hydrate (RuCl 3 .nH 2 O), tetraamine platinum(II) chloride hydrate (Pt(NH 3 ) 4 Cl 2 .H 2 O), rhodium chloride (RhCl 3 ), rhodium nitrate hydrate (Rh(NO 3 ) 3 .nH 2 O), iridium chloride hydrate (IrCl 3 . nH 2 O), and palladium nitrate (Pd(NO 3 ) 2 ). 3. The method of claim 1 , wherein the rare earth metal precursor is at least one selected from the group consisting of cerium(III) nitrate (Ce(NO 3 ) 3 ), cerium(III) carbonate (Ce 2 (CO 3 ) 3 ), cerium(III) chloride (CeCl 3 ), yttrium oxide (Y 2 O 3 ), and yttrium carbonate (Y 2 (CO 3 ) 3 ). 4. The method of claim 1 , wherein the amine-based solvent is oleylamine. 5. The method of claim 1 , wherein the platinum group metal precursor and the rare earth metal precursor are present in a molar ratio of 1:1 to 10:1. 6. The method of claim 1 , wherein the amine-based solvent is present in an amount of 3 to 40 vol % based on 100 vol % of the coating solution. 7. The method of claim 1 , wherein a total concentration of the platinum group metal precursor and the rare earth metal precursor in the coating solution is 50 to 150 g/L. 8. The method of claim 1 , wherein the drying step is carried out at a temperature of 70 to 200° C. 9. The method of claim 1 , wherein the heat-treating step is carried out at a temperature of 300 to 600° C. 10. The method of claim 1 , wherein the drying step is carried out at a temperature of 200° C. for 5 to 15 minutes. 11. The method of claim 1 , wherein: the platinum group metal precursor that is at least one selected from the group consisting of ruthenium chloride hydrate (RuCl 3 .nH 2 O), rhodium chloride (RhCl 3 ), rhodium nitrate hydrate (Rh(NO 3 ) 3 .nH 2 O), iridium chloride hydrate (IrCl 3 .nH 2 O), and palladium nitrate (Pd(NO 3 ) 2 ); the rare earth metal precursor is at least one selected from the group consisting of cerium(III) nitrate (Ce(NO 3 ) 3 ), cerium(III) carbonate (Ce 2 (CO 3 ) 3 ), cerium(III) chloride (CeCl 3 ), yttrium oxide (Y 2 O 3 ), and yttrium carbonate (Y 2 (CO 3 ) 3 ); and the platinum group metal precursor and the rare earth metal precursor are present in a molar ratio of 3:1 to 10:1.

Assignees

Inventors

Classifications

  • C25B11/02Primary

    characterised by shape or form · CPC title

  • characterised by the deposition of metallic material · CPC title

  • in diaphragm cells · CPC title

  • consisting of a single element or compound · CPC title

  • C25B11/095Primary

    at least one of the compounds being organic · CPC title

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Frequently asked questions

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What does patent US11396709B2 cover?
Provided is an electrode for electrolysis and a preparation method of the same. The electrode for electrolysis has an improved needle-like structure of a rare earth metal compared to conventional electrodes, and thus detachment of catalytic materials is reduced, so that the electrode is excellent in durability such as exhibiting stable performance even in a reverse current flow. Further, since …
Who is the assignee on this patent?
Lg Chemical Ltd
What technology area does this patent fall under?
Primary CPC classification C25B11/02. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jul 26 2022 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 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).