Preparation method and application of carbon-loaded NiO/NiFe2O4 spinel type solid solution electrolysis water oxygen evolution catalyst

A spinel-type, solid solution technology, applied in the field of electrochemical catalysis, can solve the problems of poor stability, high activity, unfavorable industrial application, etc., and achieve good stability, high catalytic activity, and increase the chemically active surface area. Effect

Pending Publication Date: 2021-11-30
JILIN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

For example, Chinese patent CN111420663 A invented a copper-aluminum spinel solid solution structure, but copper-aluminum metal oxides are not as active as nickel-iron in the oxygen evolution reaction, and the OER overpotential still needs to be further reduced
Studies have shown that layered double metal hydroxides have excellent OER performance. For example, Chinese patent CN111686736A discloses a preparation method of NiFe LDH / NF electrolytic water catalyst containing highly active and high-valence iron, which has excellent catalytic performance, but its The stability is not as good as spinel, which is not conducive to industrial applications. If spinel can be directly obtained by calcining LDH, higher performance may be obtained

Method used

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  • Preparation method and application of carbon-loaded NiO/NiFe2O4 spinel type solid solution electrolysis water oxygen evolution catalyst
  • Preparation method and application of carbon-loaded NiO/NiFe2O4 spinel type solid solution electrolysis water oxygen evolution catalyst
  • Preparation method and application of carbon-loaded NiO/NiFe2O4 spinel type solid solution electrolysis water oxygen evolution catalyst

Examples

Experimental program
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Effect test

Embodiment 1

[0027] (1) Mixing of precursor solution: Weigh 0.0036mM nickel nitrate, 0.0012mM iron nitrate, 0.126M urea and 0.02mol NH 4 F in a beaker, add 100mL deionized water, stir for 20min to obtain a clear and transparent solution.

[0028] (2) Hydrothermal reaction: Transfer the solution obtained in (1) to a 100mL reaction kettle, conduct a hydrothermal reaction at 100°C for 12 hours, centrifuge and wash for 3 to 5 times, dry in vacuum for 12 hours, and grind into a fine powder.

[0029] (3) Stripping: Weigh 0.2g of the solid obtained in step (2), put it in 150mL of deionized water, use high-speed shear stirring to make it uniformly dispersed in the water, 800W intermittent ultrasonic crushing for 1h, and the finally obtained stripped NiFe-LDH suspension Cloudy liquid. Weigh 50 mg of GO and ultrasonicate at 450 W for 30 min in 150 mL of deionized water to obtain a transparent colloid of single-layer GO.

[0030] (4) Compounding: the NiFe-LDH suspension obtained in (3) was added dr...

Embodiment 2

[0036] Take the same preparation process as in Example 1, and change the amount of graphene to 30 mg. The half-cell test procedure used is as described in Example 1. The NiFe-LDH / rGO prepared by this method is 10mA / cm in 1M KOH electrolyte solution 2 The overpotential under the electrolytic current density is 213mV. After continuous water electrolysis for 20 h, it exhibits excellent electrochemical durability.

Embodiment 3

[0038] Take the same preparation process as in Example 1, and change the graphene consumption to 80 mg. The half-cell test procedure used is as described in Example 1. The NiFe-LDH / rGO prepared by this method is 10mA / cm in 1M KOH electrolyte solution 2 The overpotential under the electrolytic current density is 220mV. After continuous water electrolysis for 20 h, it exhibits excellent electrochemical durability.

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Abstract

The invention discloses a preparation method and application of a carbon-loaded NiO/NiFe2O4 spinel type solid solution electrolysis water oxygen evolution catalyst. The preparation method comprises the following steps: preparing flower-ball-shaped nickel/iron bimetal hydroxide (NiFe-LDH) through a hydrothermal reaction, stripping nanosheets through high-speed shearing and a cavitation effect of ultrasonic waves, then assembling the product with single-layer graphene oxide (GO), and performing reducing to obtain LDH-rGO; fully impregnating the LDH-rGO in low-concentration Fe (OH)3 colloid, introducing iron ions to the surface of the LDH-rGO, so that more catalytic active sites are formed; after high-temperature calcination, forming the rGO-loaded spinel type NiO/NiFe2O4 heterogeneous composite catalyst, NiO mainly existing in NiFe2O4 crystal lattices in a solid solution form. The prepared composite nano oxygen evolution electrocatalyst is large in specific surface area, has abundant catalytic active sites, and also has good conductivity. Compared with commercial RuO2, the oxygen evolution catalyst has the advantages of low cost, high catalytic activity, good stability and the like, and has wide utilization value in alkaline water electrolysis.

Description

technical field [0001] The invention belongs to the field of new energy material technology and electrochemical catalysis, and in particular relates to a rGO loaded NiO / NiFe 2 o 4 A spinel-type solid solution electrolysis oxygen evolution catalyst material and a preparation method thereof. Background technique [0002] At present, the vast majority of hydrogen production still relies on reactions involving fossil energy such as natural gas reforming. Hydrogen production by water electrolysis provides a zero-carbon hydrogen production method. It only needs to provide electricity and water to easily obtain hydrogen energy. . Alkaline water electrolysis is currently the most mature electrolytic water hydrogen production technology, and the efficiency of water splitting hydrogen production is mainly restricted by the slow kinetic process of oxygen evolution reaction. At present, the main precious metal catalysts on the market are RuO 2 , IrO 2 , while their scarcity and high...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C25B1/04C25B11/091
CPCC25B1/04C25B11/091Y02E60/36
Inventor 李芳菲杨杨薛兵刘静茹夏茂盛雒锋
Owner JILIN UNIV
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