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Sulfur-doped molybdenum compound self-supporting electrode, preparation method and water catalytic decomposition method

A self-supporting electrode and molybdenum compound technology, applied in the field of electrocatalysis, can solve the problems of unfavorable hydrogen energy development, hydrogen economy development, limited hydrogen production on the cathode, slow kinetics, etc., achieve good catalytic hydrogen evolution performance and stability, and reduce energy consumption. The effect of consumption and cost saving

Active Publication Date: 2022-03-04
STATE GRID JIANGXI ELECTRIC POWER CO LTD RES INST +2
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  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

The hydrogen production efficiency of water electrolysis hydrogen production is 75%-85%, and the process is simple, which can be said to be pollution-free, but the disadvantage is that the power consumption is relatively large
Studies have shown that the kinetics of the oxygen evolution reaction (OER) at the anode is slow, which severely limits the production of hydrogen at the cathode, which is not conducive to the development of hydrogen energy and the development of hydrogen economy

Method used

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  • Sulfur-doped molybdenum compound self-supporting electrode, preparation method and water catalytic decomposition method
  • Sulfur-doped molybdenum compound self-supporting electrode, preparation method and water catalytic decomposition method

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preparation example Construction

[0031] A method for preparing a sulfur-doped molybdenum compound self-supporting electrode, comprising the following steps:

[0032] Soak molybdenum wire in 1.5% H 2 o 2 The solution is 1.5-2.5 hours, preferably soaked for 2 hours, taken out and dried; then placed in an etching solution containing a sulfur source for 10-14 hours, preferably, reacted for 12 hours, taken out and dried; then placed in an autoclave at 170-190 Heating reaction at ℃ for 22~26h, preferably at 180℃ for 24h; take out and dry in oven at 75~85℃ for 8~12h, then dry in oven at 110~130℃ for 20~22h, preferably at 80℃ Dry for 10 hours, and then dry in an oven at 120°C for 21 hours to obtain a sulfur-doped molybdenum compound self-supporting electrode.

[0033] Wherein, the etching solution containing sulfur source includes sulfur source, polyethylene glycol, acetic acid, formic acid, water, and the sulfur source includes one or more of potassium thiocyanate, carbon disulfide, sulfur powder and thiourea.

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Embodiment 1

[0044] Take 5 molybdenum wires of the same specification, respectively numbered 1#, 2#, 3#, 4#, 5#. Among them, the 1# molybdenum wire was not treated as a control group; the 2#, 3#, 4#, and 5# molybdenum wires were treated according to the following methods:

[0045] Use 2#, 3#, 4#, 5# molybdenum wire with a volume fraction of 1.5% H 2 o 2 Soak for 2 hours, take out and dry for later use;

[0046] Prepare four etching solutions containing different sulfur sources, as follows:

[0047] ①Measure 1.2g potassium thiocyanate, 50mL H 2 0. Put 10mL polyethylene glycol, 2mL formic acid and 2mL acetic acid in a beaker to prepare an etching solution containing potassium thiocyanate; ② Measure 10mL carbon disulfide, 50mL H 2 0, 10mL Polyethylene Glycol, 2mL formic acid and 2mL acetic acid are in beaker, make the etchant containing carbon disulfide;

[0048] ③ Measure 0.5g sulfur powder, 50mL H 2 0, 10mL Polyethylene Glycol, 2mL formic acid and 2mL acetic acid are in beaker, make t...

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Abstract

The invention discloses a sulfur-doped molybdenum compound self-supporting electrode and a preparation method, and relates to the field of electrode preparation, and the preparation method comprises the following steps: soaking a molybdenum wire in a 1.5% H2O2 solution for 1.5-2.5 h, taking out and drying the molybdenum wire, then placing the molybdenum wire in a sulfur source-containing etching solution for reaction for 10-14 h, taking out and drying the molybdenum wire, then placing the molybdenum wire in a high-pressure kettle for heating reaction, and taking out and drying the molybdenum wire to obtain the sulfur-doped molybdenum compound self-supporting electrode. The invention also provides a method for catalytically decomposing water by using the sulfur-doped molybdenum compound self-supporting electrode, and relates to the technical field of electro-catalysis, the sulfur-doped molybdenum compound self-supporting electrode is used as a working electrode, a silver chloride electrode is used as a reference electrode, a carbon rod is used as an auxiliary electrode, and an alkaline solution is used as an electrolyte to catalytically decompose water to release hydrogen. The sulfur-doped molybdenum compound self-supporting electrode has the beneficial effects that the electrode preparation method is simple, the electrode shows excellent electrochemical performance and stability, and the energy consumption and the cost can be reduced by utilizing the sulfur-doped molybdenum compound self-supporting electrode prepared by the invention to decompose water.

Description

technical field [0001] The invention belongs to the technical field of electrocatalysis, and in particular relates to a sulfur-doped molybdenum compound self-supporting electrode, a preparation method thereof and a method for catalytically decomposing water. Background technique [0002] With the successful development of power plants using hydrogen as fuel, the application range of hydrogen energy is gradually expanding, and people's demand for hydrogen energy is increasing day by day. Currently, various hydrogen production methods have been researched and developed. The most important method of producing hydrogen is to produce hydrogen from coal, oil and natural gas. But exchanging fossil fuels for hydrogen fuels is not a long-term solution and is contrary to the concept of sustainable development. According to literature reports, under normal temperature and pressure conditions, hydrogen can also be produced by using microorganisms to carry out acid-catalyzed reactions....

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C25B11/091C25B11/052C25B11/061C25B1/04
CPCC25B11/091C25B11/052C25B11/061C25B1/04Y02E60/36
Inventor 裴锋李志美刘欣田旭贾蕗路李财芳邓辰星徐碧川曾祥
Owner STATE GRID JIANGXI ELECTRIC POWER CO LTD RES INST