Preparation method for ni and mn bimetallic electrocatalyst and its application in small molecule electrooxidation

Patent metadata

Field	Value
Publication number	US-2025091040-A1
Application number	US-202418829233-A
Country	US
Kind code	A1
Filing date	Sep 9, 2024
Priority date	May 31, 2023
Publication date	Mar 20, 2025
Grant date	—

Abstract

A preparation method for Ni and Mn bimetallic electrocatalyst and its application in small molecule electrooxidation are provided. The method includes the following steps: cleaning a matrix to remove a surface oxide layer; dissolving nickel salt, manganese salt, terephthalic acid, salicylic acid, and urea into a mixed solution of ethanol, DMF, and water and transferring to a hydrothermal reaction kettle together with the treated matrix for a hydrothermal reaction; then, obtaining a NiMn-MOF/NF precursor by cooling, cleaning, and drying. Dissolving and stirring sodium borohydride and selenium powder and transferring the above solution to the hydrothermal reaction kettle for hydrothermal selenization reaction with NiMn-MOF/NF; then, obtaining a self-supporting NiMn-MOF-Se catalyst with uniform nanosheet structure by cooling and cleaning. The catalyst synthesis method is simple and controllable, with low cost, uniform catalyst morphology, and good conductivity, it can be directly used as an electrode.

First claim

What is claimed is:

1 . A preparation method for a Ni and Mn bimetallic electrocatalyst, comprising the following steps:
(1) cleaning a matrix to remove a surface oxide layer, and obtaining a treated matrix; (2) dissolving nickel salt, manganese salt, terephthalic acid, salicylic acid, and urea into a mixed solution and transferring to a high-pressure hydrothermal reaction kettle together with the treated matrix for a hydrothermal reaction, then, obtaining a NiMn-MOF precursor by cooling, cleaning, and drying; a molar ratio of the nickel salt to the manganese salt is (0.5:1)-(2:1), and a molar ratio of the terephthalic acid to the nickel salt and the manganese salt is (1:8)-(1:2); the mixed solution is a mixture of ethanol, N, N-dimethylformamide, and water; and (3) dissolving sodium borohydride and selenium powder into deionized water, and stirring continuously for 0.5-2 h in a nitrogen atmosphere to obtain a resulting solution; then transferring the resulting solution to the high-pressure hydrothermal reaction kettle, meanwhile adding the NiMn-MOF precursor to carry out a hydrothermal selenization reaction; then, obtaining a self-supporting NiMn-MOF-Se catalyst with a uniform nanosheet structure by cooling and cleaning; a mass ratio of the sodium borohydride and the selenium powder is (1:1)-(1:4).

2 . The preparation method for the Ni and Mn bimetallic electrocatalyst according to claim 1 , wherein the matrix is a nickel foam, a copper foam, or a carbon fiber paper.

3 . The preparation method for the Ni and Mn bimetallic electrocatalyst according to claim 2 , wherein the matrix is preferably a nickel foam matrix.

4 . The preparation method for the Ni and Mn bimetallic electrocatalyst according to claim 1 , wherein the step (1) comprises cleaning the matrix with hydrochloric acid, the ethanol, and the water in turn.

5 . The preparation method for the Ni and Mn bimetallic electrocatalyst according to claim 1 , a volume ratio of the ethanol, the N, N-dimethylformamide, and the water in the mixture is 1:3:2.

6 . The preparation method for the Ni and Mn bimetallic electrocatalyst according to claim 1 , wherein in the step (2), a temperature of the hydrothermal reaction is 120-160° C. and a reaction time is 6-24 h.

7 . The preparation method for the Ni and Mn bimetallic electrocatalyst according to claim 1 , wherein in step (3), a temperature of the hydrothermal selenization reaction is 120-160° C. and a reaction time is 6-24 h.

8 . The preparation method for the Ni and Mn bimetallic electrocatalyst according to claim 1 , wherein the nickel salt is nickel nitrate, nickel acetate, nickel chloride, or nickel sulfate; the manganese salt is manganese sulfate, manganese nitrate, or manganese chloride.

9 . A method of using the self-supporting NiMn-MOF-Se catalyst prepared by the preparation method for the Ni and Mn bimetallic electrocatalyst according to claim 1 , wherein the self-supporting NiMn-MOF-Se catalyst is applied to electrochemical oxidation of small molecule alcohol chemicals.

10 . The method according to claim 9 , wherein the small molecule alcohol chemicals are methanol, ethylene glycol, or glycerol.

11 . The method according to claim 9 , wherein in the preparation method, the matrix is a nickel foam, a copper foam, or a carbon fiber paper.

12 . The method according to claim 11 , wherein in the preparation method, the matrix is preferably a nickel foam matrix.

13 . The method according to claim 9 , wherein in the preparation method, the step (1) comprises cleaning the matrix with hydrochloric acid, the ethanol, and the water in turn.

14 . The method according to claim 9 , wherein in the preparation method, a volume ratio of the ethanol, the N, N-dimethylformamide, and the water in the mixture is 1:3:2.

15 . The method according to claim 9 , wherein in the step (2) of the preparation method, a temperature of the hydrothermal reaction is 120-160° C. and a reaction time is 6-24 h.

16 . The method according to claim 9 , wherein in the step (3) of the preparation method, a temperature of the hydrothermal selenization reaction is 120-160° C. and a reaction time is 6-24 h.

17 . The method according to claim 9 , wherein in the preparation method, the nickel salt is nickel nitrate, nickel acetate, nickel chloride, or nickel sulfate; the manganese salt is manganese sulfate, manganese nitrate, or manganese chloride.

Assignees

• Univ Beijing Chem Tech

Inventors

• Qiu Jieshan
• Qi Jun
• Yang Qi

Classifications

• B01J31/1691 Primary

  Coordination polymers, e.g. metal-organic frameworks [MOF] (preparation of metal complexes containing carboxylic acid moieties C07C51/418; MOF's per se C07F) · CPC title

• C25B11/054

  Electrodes comprising electrocatalysts supported on a carrier · CPC title

• C25B11/065

  Carbon · CPC title

• C25B11/052

  Electrodes comprising one or more electrocatalytic coatings on a substrate · CPC title

• C25B11/061

  Metal or alloy · CPC title