Cobalt molybdenum disulfide synthesized using alkyl-containing thiomolybdate precursors

Patent metadata

Field	Value
Publication number	US-2018171493-A1
Application number	US-201715846830-A
Country	US
Kind code	A1
Filing date	Dec 19, 2017
Priority date	Dec 20, 2016
Publication date	Jun 21, 2018
Grant date	—

Abstract

Embodiments of the invention are directed to CoMoS2 catlaysts, methods of making and using, as well as electrodes and systems incorporating such. Synthesis of CoMoS2 catalysts using ATM treated with different amines and ammonium bromide salts including 1-dodecylamine, diethylenetriamine, tetradecyltrimethylammonium bromide and cetyltrimethylammonium bromide, to form different alky containing ATM precursors. These materials are amorphous with porous surfaces that show reasonably big surfaces area due to the number of exposed edge sites, and increased catalytic activity as electrocatalysts for hydrogen generation.

First claim

What is claimed is:

1 . A hydrogen evolution catalyst comprising:
cobalt-promoted molybdenum disulfide (CoMoS 2 ) having a surface area greater than about 35 square meters per gram (m 2 /g).

2 . The hydrogen evolution catalyst of claim 1 , wherein the CoMoS 2 has a surface area of from about 35 m 2 /g to about 100 m 2 /g, preferably from about 38 m 2 /g to about 90 m 2 /g, more preferably from about 41 m 2 /g to about 80 m 2 /g, and most preferably from about 43 m 2 /g to about 69 m 2 /g.

3 . The hydrogen evolution catalyst of claim 1 , wherein the CoMoS 2 is synthesized from an alkylated thiosalt precursor.

4 . The hydrogen evolution catalyst of claim 3 , wherein the alkylated thiosalt precursor is ammonium thiomolybdate (ATM) alkylated by a reaction with one of the group consisting of C4 to C16 amines, C4 to C16 ammonium salts, and combinations thereof.

5 . The hydrogen evolution catalyst of claim 4 , wherein the amine is diethylenetriamine (DETA) or 1-dodecylamine (DDA).

6 . The hydrogen evolution catalyst of claim 4 , wherein the ammonium salt is tetradecyltrimethylammonium (TDTA) bromide or cetyltrimethylammonium (CTA) bromide.

7 . An electrolytic cell comprising:
an electrode at which a hydrogen evolution reaction occurs, the electrode comprising:
a metallic base; and
cobalt-promoted molybdenum disulfide (CoMoS 2 ), wherein the CoMoS 2 has a surface area greater than about 35 square meters per gram (m 2 /g).

8 . The electrolytic cell of claim 7 , wherein the CoMoS 2 has a surface area of from about 35 m 2 /g to about 100 m 2 /g, preferably from about 38 m 2 /g to about 90 m 2 /g, more preferably from about 41 m 2 /g to about 80 m 2 /g, and most preferably from about 43 m 2 /g to about 69 m 2 /g.

9 . The electrolytic cell of claim 7 , wherein:
the metallic base is selected from the group consisting of a metal base, a metal oxide base, a mixed metal oxide base, and combinations thereof; and the CoMoS 2 forms a coating on the metallic base.

10 . The electrolytic cell of claim 9 , wherein the metal oxide base is a tin oxide base.

11 . The electrolytic cell of claim 9 , wherein the metal base is platinum base.

12 . The electrolytic cell of claim 7 , wherein the CoMoS 2 is synthesized from an alkylated thiosalt precursor.

13 . The electrolytic cell of claim 12 , wherein the alkylated thiosalt precursor is ammonium thiomolybdate (ATM) alkylated by a reaction with one of the group consisting of C4 to C16 amines, C4 to C16 ammonium salts, and combinations thereof.

14 . The electrolytic cell of claim 13 , wherein the amine is diethylenetriamine (DETA) or 1-dodecylamine (DDA).

15 . The electrolytic cell of claim 13 , wherein the ammonium salt is tetradecyltrimethylammonium (TDTA) bromide or cetyltrimethylammonium (CTA) bromide.

16 . A method of generating hydrogen comprising:
forming an electrolytic cell, the electrolytic cell having an electrode at which a hydrogen evolution reaction occurs; and applying a current to the cell facilitating disassociation of water and the production of hydrogen; wherein the electrode comprises cobalt-promoted molybdenum sulfide (CoMoS 2 ) having a surface area greater than about 35 square meters per gram (m 2 /g).

17 . The method of claim 16 , wherein the CoMoS 2 has a surface area of from about 35 m 2 /g to about 100 m 2 /g, preferably from about 38 m 2 /g to about 90 m 2 /g, more preferably from about 41 m 2 /g to about 80 m 2 /g, and most preferably from about 43 m 2 /g to about 69 m 2 /g.

18 . The method of claim 16 , wherein the CoMoS 2 is synthesized from an alkylated thiosalt precursor.

19 . The method of claim 18 , wherein the alkylated thiosalt precursor is ammonium thiomolybdate (ATM) alkylated by a reaction with one of the group consisting of C4 to C16 amines, C4 to C16 ammonium salts, and combinations thereof.

20 . The method of claim 19 , wherein the amine is diethylenetriamine (DETA) or 1-dodecylamine (DDA).

21 . The method of claim 20 , wherein the ammonium salt is tetradecyltrimethylammonium (TDTA) bromide or cetyltrimethylammonium (CTA) bromide.

22 . A method for producing cobalt-promoted molybdenum disulfide (CoMoS 2 ), comprising:
alkylating ammonium thiomolybdate (ATM) with one the group consisting of C4 to C16 amines, C4 to C16 ammonium salts, and combinations thereof, to form an alkylated thiosalt precursor; and synthesizing the CoMoS 2 from the alkylated thiosalt precursor, wherein the CoMoS 2 has a surface area greater than about 35 square meters per gram (m 2 /g).

23 . The method of claim 22 , wherein the alkylating and synthesizing steps further comprise:
contacting an aqueous solution of ammonium thiomolybdate (ATM) with a second aqueous solution of the of C4 to C16 amines, C4 to C16 ammonium salts, and combinations thereof, forming a reaction mixture; adding a cobalt chloride solution to the reaction mixture; and reacting the reaction mixture at constant heat and pressure to form the CoMoS 2 .

24 . The method of claim 23 , wherein reacting the reaction mixture further comprises:
decomposing the C4 to C16 amines from the alkylated thiosalt precursor to form the CoMoS 2 having a surface area greater than about 35 square meters per gram (m 2 /g); and evaporating the C4 to C16 amines from the reaction mixture under constant pressure.

25 . The method of claim 22 , wherein the alkylated thiosalt precursor is ammonium thiomolybdate (ATM) alkylated by a reaction with one of the group consisting of C4 to C16 amines, C4 to C16 ammonium salts, and combinations thereof.

26 . The method of claim 25 , wherein the amine is diethylenetriamine (DETA) or 1-dodecylamine (DDA).

27 . The method of claim 25 , wherein the ammonium salt is tetradecyltrimethylammonium (TDTA) bromide or cetyltrimethylammonium (CTA) bromide.

Assignees

• Univ Texas

Inventors

• Villagran Dino
• Chianelli Russell R
• Wu Yanyu
• Torres Brenda
• Zarei-Chaleshtori Maryam

Classifications

• B01J27/0515 Primary

  with iron group metals or platinum group metals · CPC title

• C25B11/0405

  Chemistry & Metallurgy · mapped topic

• C25B11/0415

  Chemistry & Metallurgy · mapped topic

• C25B1/04

  by electrolysis of water · CPC title

• B01J35/1014

  Operations & Transport · mapped topic