Mo-doped transition metal hydroxide electrocatalyst constructed through deep self-reconstruction as well as preparation method and application of Mo-doped transition metal hydroxide electrocatalyst

A technology of hydroxide electricity and transition metals, applied in the direction of electrodes, electrolysis processes, electrolysis components, etc., can solve the problems of insufficient utilization of the internal components of the catalyst, limited depth, etc., and achieve low raw material prices, low production costs, and applicable wide-ranging effect

Active Publication Date: 2021-08-10
SOUTH CHINA UNIV OF TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

However, the depth of this surface self-reconstruction layer is limited, only ~10 nm, forming a core-shell structure, which leads to the underutilization of

Method used

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  • Mo-doped transition metal hydroxide electrocatalyst constructed through deep self-reconstruction as well as preparation method and application of Mo-doped transition metal hydroxide electrocatalyst
  • Mo-doped transition metal hydroxide electrocatalyst constructed through deep self-reconstruction as well as preparation method and application of Mo-doped transition metal hydroxide electrocatalyst
  • Mo-doped transition metal hydroxide electrocatalyst constructed through deep self-reconstruction as well as preparation method and application of Mo-doped transition metal hydroxide electrocatalyst

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Experimental program
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Effect test

Embodiment 1

[0060] (1) Molybdenum disulfide nanosheet arrays were prepared by hydrothermal synthesis on a carbon cloth substrate;

[0061] (2) Wash the molybdenum disulfide nanosheet array grown on the carbon cloth obtained in step (1) several times with pure water, and dry it in vacuum at 50° C. for 5 hours to obtain the dried molybdenum disulfide nanosheet array;

[0062] (3) activating the dried molybdenum disulfide nanosheet array obtained in step (2) at -0.6V (vs.RHE) overpotential for 300s to obtain activated molybdenum disulfide nanosheets;

[0063] (4) Soak molybdenum disulfide nanosheets after the activation of step (3) gained concentration in the nickel acetate solution of 30mM, the time of immersion is 5min, with molybdenum disulfide nanosheets as template 2+ Carry out adsorption to obtain molybdenum disulfide / hydroxide composite material;

[0064] (5) Soak the molybdenum disulfide / hydroxide composite material obtained in step (4) in KOH solution (concentration is 0.1M), then ...

Embodiment 2

[0068] (1) Molybdenum disulfide nanosheet arrays were prepared by hydrothermal synthesis on a carbon cloth substrate;

[0069] (2) The molybdenum disulfide nanosheet array grown on the carbon cloth obtained in step (1) is washed several times with pure water, and dried in vacuum at 60° C. for 3 hours to obtain the dried molybdenum disulfide nanosheet array;

[0070] (3) activating the dried molybdenum disulfide nanosheet array obtained in step (2) at -0.6V (vs.RHE) overpotential for 100s to obtain activated molybdenum disulfide nanosheets;

[0071] (4) Soak molybdenum disulfide nanosheets after the activation of the gained step (3) in a ferrous sulfate solution with a concentration of 50mM for 10min, and use molybdenum disulfide nanosheets as a template for Fe 2+ Carry out adsorption to obtain molybdenum disulfide / hydroxide composite material;

[0072] (5) Soak the molybdenum disulfide / hydroxide composite material obtained in step (4) in KOH solution (concentration is 0.5M), ...

Embodiment 3

[0076] (1) Molybdenum disulfide nanosheet arrays were prepared by hydrothermal synthesis on a carbon cloth substrate;

[0077] (2) Wash the molybdenum disulfide nanosheet array grown on the carbon cloth obtained in step (1) several times with pure water, and dry it in vacuum at 60° C. for 5 hours to obtain the dried molybdenum disulfide nanosheet array;

[0078] (3) activating the dried molybdenum disulfide nanosheet array obtained in step (2) at -0.6V (vs.RHE) overpotential for 500s to obtain activated molybdenum disulfide nanosheets;

[0079] (4) Soak molybdenum disulfide nanosheets after the activation of the gained step (3) in the mixed solution of nickel acetate solution and ferrous sulfate solution (according to the volume ratio of 3:1 by the nickel acetate solution of 50mM and the ferrous sulfate solution of 50mM prepared), the soaking time was 20min, and the Ni 2+ and Fe 2+ Adsorption is carried out to obtain molybdenum disulfide / hydroxide composite material.

[008...

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Abstract

The invention discloses a Mo-doped transition metal hydroxide electrocatalyst constructed through deep self-reconstruction and a preparation method and application of the Mo-doped transition metal hydroxide electrocatalyst. The method comprises the following steps: activating a MoS2 nanosheet array under an overpotential condition, soaking the MoS2 nanosheet array in a transition metal salt solution for ion adsorption, and performing deep self-reconstruction by a cyclic voltammetry scanning method to obtain the catalyst. According to the method, raw materials are low in price, high-temperature sintering is not needed, energy consumption in the production process is low, and the production cost is low; and according to the method, a transition metal ion adsorption strategy and an electrochemical self-reconstruction strategy are adopted, the preparation process is simple, and the method is suitable for large-scale production. The deep self-reconstruction Mo-doped transition metal hydroxide electrocatalyst provided by the invention has excellent oxygen evolution reaction intrinsic activity, the overpotential under the current density of 10mA/cm<2> is 242mV, and the mass activity current density under the overpotential of 300mV is 1910A/g.

Description

technical field [0001] The invention belongs to the technical field of electrocatalytic materials, and in particular relates to a Mo-doped transition metal hydroxide electrocatalyst constructed by deep self-reconfiguration and its preparation method and application. Background technique [0002] At present, hydrogen, as the energy carrier with the highest energy density, has attracted much attention among many new energy raw materials. Hydrogen energy not only has high energy density, clean and zero pollution, but also has a wide range of sources, which has broad prospects in the field of new energy development. At present, a major source of hydrogen is the cracking of fossil fuels such as petroleum. Its main disadvantages include scarcity and limited raw materials, serious energy consumption in the preparation process, and low purity of the hydrogen produced. The biggest disadvantage is that the hydrogen obtained through fossil fuel cracking still contains impurities such ...

Claims

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Application Information

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IPC IPC(8): C25B11/04C25B1/04
CPCC25B11/04C25B1/04Y02E60/36
Inventor 陈燕何祖韵宫志恒刘秋宇
Owner SOUTH CHINA UNIV OF TECH
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