Method for preparing three-dimensional porous graphene material

Patent metadata

Field	Value
Publication number	US-2017267533-A1
Application number	US-201715614574-A
Country	US
Kind code	A1
Filing date	Jun 5, 2017
Priority date	Dec 25, 2014
Publication date	Sep 21, 2017
Grant date	—

Abstract

A method for preparing a three-dimensional porous graphene material, including: a) constructing a CAD model corresponding to a required three-dimensional porous structure, and designing an external shape and internal structure parameters of the model; b) based on the CAD model, preparing a three-dimensional porous metal structure using a metal powder as material; c) heating the three-dimensional porous metal structure and preparing a metal template of the required three-dimensional porous structure; d) placing the metal template in a tube furnace and heating the metal template to a temperature of between 800 and 1000° C.; standing for 0.5-1 hr, introducing a carbon source to the tube furnace for continued reaction, cooling resulting products to room temperature to yield a three-dimensional graphene grown on the metal template; and e) preparing a corrosive solution, and immersing the three-dimensional graphene in the corrosive solution.

First claim

The invention claimed is:

1 . A method for preparing a three-dimensional porous graphene material, the method comprising:
a) constructing a CAD model corresponding to a required three-dimensional porous structure, and designing an external shape and internal structure parameters of the model comprising a pore size, a porosity, and a pore shape, respectively; b) based on the CAD model constructed in a), preparing, by using additive manufacturing in the presence of an inert gas, a three-dimensional porous metal structure having a shape corresponding to that of the CAD model with a metal powder as material, wherein, the metal powder is nickel, copper, iron, or cobalt, an average particle size of the metal powder is 5-50 mm, and a particle shape of the metal powder is spherical or approximately spherical; c) heating the three-dimensional porous metal structure to a temperature of 900° C.-1500° C. for 4-24 hrs in the presence of the inert gas, cooling the three-dimensional porous metal structure to room temperature; performing sand blasting and ultrasonic cleaning on the three-dimensional porous metal structure, to acquire a metal template of the required three-dimensional porous structure; d) placing the metal template in a tube furnace in the presence of mixed gases of the inert gas and hydrogen and heating the metal template to 800-1000° C.; standing for 0.5-1 hr, introducing a carbon source to the tube furnace for continued reaction, cooling resulting products to room temperature in the presence of the inert gas, to yield a three-dimensional graphene grown on the metal template; and e) preparing a corrosive solution having a molar concentration of 1-3 mol/L; immersing the three-dimensional graphene prepared in d) in the corrosive solution, refluxing the corrosive solution at 60-90° C. until the metal template is completely melted; washing and drying the three-dimensional graphene to yield a three-dimensional porous graphene material, wherein, internal structure parameters comprising a pore size, a porosity, and a pore shape and external shape of the three-dimensional porous graphene material are the same as those of the CAD model constructed in a).

2 . The method of claim 1 , wherein in a), the CAD model is a periodic ordered porous structure or an interconnected disordered three-dimensional porous structure, a unit dimension thereof is between 0.5-10 mm, and a porosity is adjustable within a range of 20-90%.

3 . The method of claim 1 , wherein the additive manufacturing in b) comprises selective laser melting technique, direct metal laser sintering technique, or electron beam melting technique; and an average particle size of the metal powder is controlled within 10-30 μm.

4 . The method of claim 2 , wherein the additive manufacturing in b) comprises selective laser melting technique, direct metal laser sintering technique, or electron beam melting technique; and an average particle size of the metal powder is controlled within 10-30 μm.

5 . The method of claim 3 , wherein in c), the three-dimensional porous metal structure is heated to 1200-1370° C. in the presence of argon, maintained for 12 hrs, and then cooled to room temperature.

6 . The method of claim 4 , wherein in c), the three-dimensional porous metal structure is heated to 1200-1370° C. in the presence of argon, maintained for 12 hrs, and then cooled to room temperature.

7 . The method of claim 1 , wherein in d), the carbon source is selected from the group consisting of styrene, methane, and ethane; a flow rate of the carbon source is controlled at 0.2-200 mL/h; and a charging time of the carbon source lasts for 0.5-3 hrs.

8 . The method of claim 6 , wherein in d), the carbon source is selected from the group consisting of styrene, methane, and ethane; a flow rate of the carbon source is controlled at 0.2-200 mL/h; and a charging time of the carbon source lasts for 0.5-3 hrs.

9 . The method of claim 1 , wherein the inert gas is argon, a volume ratio of the argon to the hydrogen is between 1:1 and 3:1; in the mixed gases of the argon and the hydrogen, a flow rate of the argon is controlled at 100-200 mL/min, and a flow rate of the hydrogen is controlled at 180-250 mL/min.

10 . The method of claim 8 , wherein the inert gas is argon, a volume ratio of the argon to the hydrogen is between 1:1 and 3:1; in the mixed gases of the argon and the hydrogen, a flow rate of the argon is controlled at 100-200 mL/min, and a flow rate of the hydrogen is controlled at 180-250 mL/min.

11 . The method of claim 1 , wherein in e), the corrosive solution is selected from the group consisting of hydrochloric acid, sulfuric acid, nitric acid, iron chloride, and a mixture thereof.

12 . The method of claim 10 , wherein in e), the corrosive solution is selected from the group consisting of hydrochloric acid, sulfuric acid, nitric acid, iron chloride, and a mixture thereof.

Assignees

• Univ Huazhong Science Tech

Inventors

• Yan Chunze
• Shi Yusheng
• Zhu Wei

Classifications

• C01B32/194

  After-treatment · CPC title

• C01B32/184

  Preparation · CPC title

• C01B32/186

  by chemical vapour deposition [CVD] · CPC title

• C01P2006/12

  Surface area · CPC title

• C01B2204/32

  Size or surface area · CPC title