CN110629248A - Fe-doped Ni (OH)2Preparation method of/Ni-BDC electrocatalyst - Google Patents
Fe-doped Ni (OH)2Preparation method of/Ni-BDC electrocatalyst Download PDFInfo
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- CN110629248A CN110629248A CN201910891098.7A CN201910891098A CN110629248A CN 110629248 A CN110629248 A CN 110629248A CN 201910891098 A CN201910891098 A CN 201910891098A CN 110629248 A CN110629248 A CN 110629248A
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- 238000000034 method Methods 0.000 title abstract description 10
- 239000010411 electrocatalyst Substances 0.000 title description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims abstract description 62
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 34
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 32
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 32
- 239000003054 catalyst Substances 0.000 claims abstract description 32
- 239000004744 fabric Substances 0.000 claims abstract description 30
- 239000002131 composite material Substances 0.000 claims abstract description 21
- 239000002135 nanosheet Substances 0.000 claims abstract description 21
- 238000002360 preparation method Methods 0.000 claims abstract description 16
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims abstract description 12
- VCJMYUPGQJHHFU-UHFFFAOYSA-N iron(3+);trinitrate Chemical compound [Fe+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O VCJMYUPGQJHHFU-UHFFFAOYSA-N 0.000 claims abstract description 12
- 239000012621 metal-organic framework Substances 0.000 claims abstract description 12
- DDFHBQSCUXNBSA-UHFFFAOYSA-N 5-(5-carboxythiophen-2-yl)thiophene-2-carboxylic acid Chemical compound S1C(C(=O)O)=CC=C1C1=CC=C(C(O)=O)S1 DDFHBQSCUXNBSA-UHFFFAOYSA-N 0.000 claims abstract description 6
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000004202 carbamide Substances 0.000 claims abstract description 6
- KBJMLQFLOWQJNF-UHFFFAOYSA-N nickel(ii) nitrate Chemical compound [Ni+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O KBJMLQFLOWQJNF-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000002243 precursor Substances 0.000 claims abstract description 6
- 239000007864 aqueous solution Substances 0.000 claims description 10
- 238000004729 solvothermal method Methods 0.000 claims 1
- 238000001027 hydrothermal synthesis Methods 0.000 abstract description 3
- 239000008204 material by function Substances 0.000 abstract description 2
- 239000000126 substance Substances 0.000 abstract 1
- 239000013099 nickel-based metal-organic framework Substances 0.000 description 19
- 238000006243 chemical reaction Methods 0.000 description 10
- 239000000463 material Substances 0.000 description 7
- 230000003197 catalytic effect Effects 0.000 description 5
- 238000001816 cooling Methods 0.000 description 5
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 4
- 238000005868 electrolysis reaction Methods 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 230000007547 defect Effects 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 230000002195 synergetic effect Effects 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229910021607 Silver chloride Inorganic materials 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 239000013122 aluminium-based metal-organic framework Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 238000004070 electrodeposition Methods 0.000 description 1
- 239000008151 electrolyte solution Substances 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000000707 layer-by-layer assembly Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 1
- 230000010287 polarization Effects 0.000 description 1
- 231100000719 pollutant Toxicity 0.000 description 1
- 230000027756 respiratory electron transport chain Effects 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000004506 ultrasonic cleaning Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/26—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24
- B01J31/28—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24 of the platinum group metals, iron group metals or copper
-
- B01J35/33—
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B1/00—Electrolytic production of inorganic compounds or non-metals
- C25B1/01—Products
- C25B1/02—Hydrogen or oxygen
- C25B1/04—Hydrogen or oxygen by electrolysis of water
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B11/00—Electrodes; Manufacture thereof not otherwise provided for
- C25B11/04—Electrodes; Manufacture thereof not otherwise provided for characterised by the material
- C25B11/051—Electrodes formed of electrocatalysts on a substrate or carrier
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B11/00—Electrodes; Manufacture thereof not otherwise provided for
- C25B11/04—Electrodes; Manufacture thereof not otherwise provided for characterised by the material
- C25B11/051—Electrodes formed of electrocatalysts on a substrate or carrier
- C25B11/073—Electrodes formed of electrocatalysts on a substrate or carrier characterised by the electrocatalyst material
- C25B11/091—Electrodes formed of electrocatalysts on a substrate or carrier characterised by the electrocatalyst material consisting of at least one catalytic element and at least one catalytic compound; consisting of two or more catalytic elements or catalytic compounds
- C25B11/095—Electrodes formed of electrocatalysts on a substrate or carrier characterised by the electrocatalyst material consisting of at least one catalytic element and at least one catalytic compound; consisting of two or more catalytic elements or catalytic compounds at least one of the compounds being organic
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/02—Compositional aspects of complexes used, e.g. polynuclearity
- B01J2531/0213—Complexes without C-metal linkages
- B01J2531/0216—Bi- or polynuclear complexes, i.e. comprising two or more metal coordination centres, without metal-metal bonds, e.g. Cp(Lx)Zr-imidazole-Zr(Lx)Cp
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/80—Complexes comprising metals of Group VIII as the central metal
- B01J2531/84—Metals of the iron group
- B01J2531/847—Nickel
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/30—Hydrogen technology
- Y02E60/36—Hydrogen production from non-carbon containing sources, e.g. by water electrolysis
Abstract
The invention relates to a carbon cloth loaded Fe doped Ni (OH)2A Ni-BDC composite electrolyzed water catalyst and a preparation method thereof, belonging to the technical field of preparation of novel inorganic nano functional materials. The invention uses Fe to dope Ni (OH)2The nanosheet array is a precursor, and part of the nanosheet array is converted into a metal organic framework through a hydrothermal method to form a carbon cloth-loaded Fe-doped Ni (OH)2the/Ni-BDC composite electrolytic water catalyst. The method comprises the following specific steps: firstly, nickel nitrate, ferric nitrate, ammonium fluoride, urea and other substances are utilized to prepare Fe-doped Ni (OH) loaded on carbon cloth under hydrothermal condition2Nanosheets; further doping Fe with Ni (OH)2The nano-sheet is a precursor and a template, and the nano-sheet reacts with terephthalic acid partially under the solvothermal condition to form a metal organic framework, and finally Fe-doped Ni (OH) is prepared2/Ni‑BDC is compounded with an electrolyzed water catalyst.
Description
Technical Field
Hair brushThe invention relates to a Fe-doped Ni (OH)2a/Ni-BDC composite electrolyzed water catalyst and a preparation method thereof, belonging to the technical field of novel inorganic nano functional materials.
Background
With the increasing prominence of the problem of energy shortage, the development and utilization technology of novel renewable energy sources is more and more paid attention by people. As a novel clean energy, the hydrogen has important significance for solving the problem of environmental pollution by overcoming the problem of energy shortage and realizing zero emission. The water electrolysis is a technology for conveniently and efficiently obtaining hydrogen, but the overpotential commonly existing in the reaction process causes excessive consumption of energy. The novel water electrolysis catalyst is designed, so that the overpotential in the water decomposition process is effectively reduced, and the novel water electrolysis catalyst has important practical value for reducing energy consumption and improving the water electrolysis efficiency.
The metal organic framework has the advantages of high specific surface area, open structural framework, more metal active sites, easy regulation and control of components and the like, and has important application value in the fields of gas adsorption, sensing, catalysis and the like. However, the application of the metal organic framework in the field of electrocatalysis is has been limited due to the disadvantages of poor conductivity, low electron transfer efficiency, etc. Recent studies have shown that metal organic framework materials with sheet structures can expose more catalytically active sites and thus have higher catalytic activity. However, the sheet metal organic framework is easy to stack in the preparation process, and the sheet structure still cannot solve the defect of poor conductivity. In addition, the preparation of the sheet metal organic framework material at present adopts a layer-by-layer assembly method, and the preparation process is complex, long in time consumption and difficult to control; the polymer cross-linking agent used in the process can also cover the active sites of the polymer cross-linking agent, and reduce the catalytic activity and stability of the material. Therefore, the development of the efficient and practical preparation method of the sheet metal organic framework material has important significance. Meanwhile, the inherent defect that poor conductivity is a metal organic framework material is considered, the catalyst is combined with a material with relatively better conductivity while the catalytic activity of the catalyst is not influenced, the synergistic effect between the catalyst and the material is fully exerted, and the catalyst has important significance for preparing a novel efficient electrolyzed water catalyst.
Disclosure of Invention
The invention aims to make up the defects of the prior art, and Fe prepared in advance is doped with Ni (OH) by a hydrothermal method2Partial conversion to a nickel-based metal organic framework (Ni-BDC) to form Fe-doped Ni (OH)2the/Ni-BDC composite electrolytic water catalyst. The invention provides a simple and easy Fe-doped Ni (OH) with low cost2A preparation method of a/Ni-BDC composite electrolyzed water catalyst. The preparation method provided by the invention has the advantages of simple process and low cost, and the prepared Fe-doped Ni (OH)2the/Ni-BDC has excellent electrolytic water catalytic performance and higher practical application value.
The purpose of the invention is realized by the following technical scheme that Fe is doped with Ni (OH)2The preparation method of the/Ni-BDC composite electrolyzed water catalyst comprises the following steps:
1) cutting the carbon cloth (2X 1 cm)2) Ultrasonic cleaning with 5% hydrochloric acid, acetone and deionized water for 15 min to remove surface pollutant;
2) adding aqueous solution of nickel nitrate, ferric nitrate, ammonium fluoride and urea with certain concentration into a reaction kettle, immersing the carbon cloth obtained in the step 1 into the aqueous solution, and heating and reacting in an oven;
3) adding a certain mass of terephthalic acid into another reaction kettle, adding N, N' -dimethylformamide and a water solvent in a certain volume ratio, stirring and dissolving, and then doping the carbon cloth loaded with Fe and Ni (OH) into the carbon cloth obtained in the step 22Immersing in it, heating in oven to obtain Fe-doped Ni (OH) carried by carbon cloth2the/Ni-BDC composite electrolytic water catalyst.
The invention has the beneficial effects that:
(1) the invention provides a novel Fe-doped Ni (OH)2The preparation method of the/Ni-BDC composite electrolyzed water catalyst comprises the steps of firstly preparing Fe-doped Ni (OH) loaded on carbon cloth through simple electrodeposition2Nanosheets, and continuing to load Fe doped Ni (OH) with carbon cloth2The nano sheet is a precursor, and Fe-doped Ni (OH) is prepared by a hydrothermal method2The Ni-BDC. The preparation method is simpleThe method is easy to operate, does not need special equipment, has low cost, is suitable for large-scale preparation, and can meet the requirements of practical application;
(2) the product prepared by the invention is carbon cloth loaded Fe doped Ni (OH)2Ni-BDC, the metal-organic framework is formed by doping Fe with Ni (OH)2The nano sheet is a precursor, the product is regular in shape and uniform in size, and carbon cloth is used as a carrier to load the catalyst, so that the practical application is facilitated;
(3) fe doped Ni (OH) prepared by the invention2The existence of the heteroatom Fe in the/Ni-BDC composite electrolyzed water catalyst can effectively optimize the electronic structure of the catalyst, and meanwhile, the synergistic effect between the hydroxide and the metal organic framework can effectively improve the stability of the activator of the catalyst.
Drawings
FIG. 1 shows Fe-doped Ni (OH) prepared by the method of the present invention2Scanning Electron Microscope (SEM) picture of the/Ni-BDC composite electrolyzed water catalyst taken after being observed by using a scanning electron microscope of FEI QUANTA FEG250 of America;
FIG. 2 shows Fe-doped Ni (OH) prepared by the method of the present invention2X-ray diffraction (XRD) pattern of the/Ni-BDC composite electrolyzed water catalyst;
Detailed Description
The present invention will be described in further detail with reference to the following embodiments, which are not intended to limit the scope of the present invention.
Example 1
Adding a total volume of 15mL of aqueous solution of nickel nitrate (45 mM), ferric nitrate (5 mM), ammonium fluoride (100 mM) and urea (250 mM) into a reaction kettle with a volume of 20mL, immersing the carbon cloth treated in advance into the aqueous solution, placing the carbon cloth into an oven, reacting at 120 ℃ for 6 hours, and naturally cooling to obtain the carbon cloth-loaded Fe-doped Ni (OH)2Nanosheets. Then, 20 mg of terephthalic acid, 10.8 mL of water and 1.2 mL of N, N' -dimethylformamide were added to another reaction vessel having a capacity of 20mL, and Fe prepared previously was doped with Ni (OH) after dissolving by stirring2Immersing the nano-sheets in the solution, putting the nano-sheets into an oven to react for 2 hours at 120 ℃, and then naturally reactingCooling to obtain carbon cloth loaded Fe doped Ni (OH)2the/Ni-BDC composite electrolytic water catalyst.
Example 2
Adding a total volume of 15mL of aqueous solution of nickel nitrate (40 mM), ferric nitrate (10 mM), ammonium fluoride (100 mM) and urea (250 mM) into a reaction kettle with a volume of 20mL, immersing the carbon cloth treated in advance into the aqueous solution, placing the carbon cloth into an oven, reacting at 110 ℃ for 10 hours, and naturally cooling to obtain the carbon cloth-loaded Fe-doped Ni (OH)2Nanosheets. Then, 20 mg of terephthalic acid, 10.0 mL of water and 2.0 mL of N, N' -dimethylformamide were added to another reaction vessel having a capacity of 20mL, and Fe prepared previously was doped with Ni (OH) after dissolving by stirring2Immersing the nano-sheets in the solution, putting the nano-sheets into an oven to react for 4 hours at 110 ℃, and naturally cooling to obtain the carbon cloth loaded Fe doped Ni (OH)2the/Ni-BDC composite electrolytic water catalyst.
Example 3
Adding a total volume of 12mL of aqueous solution of nickel nitrate (45 mM), ferric nitrate (5 mM), ammonium fluoride (90 mM) and urea (240 mM) into a reaction kettle with a volume of 20mL, immersing the carbon cloth treated in advance into the aqueous solution, placing the carbon cloth into an oven, reacting at 110 ℃ for 8 hours, and naturally cooling to obtain the carbon cloth-loaded Fe-doped Ni (OH)2Nanosheets. Then, 25 mg of terephthalic acid, 12mL of water and 1.0 mL of N, N' -dimethylformamide were added to another 20mL reaction vessel, and Fe prepared previously was doped with Ni (OH) after stirring and dissolving2Immersing the nano-sheets in the solution, putting the nano-sheets into an oven to react for 3 hours at 120 ℃, and naturally cooling to obtain the carbon cloth loaded Fe doped Ni (OH)2the/Ni-BDC composite electrolytic water catalyst.
Example 4
Fe doped Ni (OH) loaded on carbon cloth using Chenghua 660D electrochemical workstation2And testing the catalytic activity and stability of the/Ni-BDC composite electrolyzed water catalyst in electrolyzed water. Taking a platinum wire as a counter electrode, silver/silver chloride as a reference electrode and Fe doped Ni (OH) loaded by carbon cloth2the/Ni-BDC is the working electrode and 1.0 mol/L KOH aqueous solution is the electrolyte solution. Linear voltammetric scanning at a scan rate of 2 milliamps per second over a voltage range of 1.0 to 2.0VSo as to obtain the polarization curve of catalyzing the electrolyzed water to produce oxygen.
Claims (3)
1. Carbon cloth loaded Fe doped Ni (OH)2The preparation method of the/Ni-BDC composite electrolyzed water catalyst is characterized by comprising the following steps:
1) preparing Fe-doped Ni (OH) loaded on carbon cloth from mixed aqueous solution of nickel nitrate, ferric nitrate, ammonium fluoride and urea under hydrothermal condition2Nanosheets;
2) fe doped Ni (OH) loaded on the carbon cloth obtained in the step 12Nanosheet is a precursor, and then the nanosheet is partially converted into Ni-BDC through a solvothermal method to prepare Fe-doped Ni (OH)2the/Ni-BDC composite electrolytic water catalyst.
2. The carbon cloth-supported Fe-doped Ni (OH) of claim 12The preparation method of the/Ni-BDC composite electrolyzed water catalyst is characterized in that the composite catalyst is Fe doped Ni (OH) loaded by carbon cloth2The nano sheet is a precursor.
3. The carbon cloth-supported Fe-doped Ni (OH) of claim 12The preparation method of the/Ni-BDC composite electrolyzed water catalyst is characterized in that the metal organic framework in the composite catalyst is Fe-doped Ni (OH)2And terephthalic acid under solvothermal conditions.
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Cited By (3)
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CN112391649A (en) * | 2020-11-23 | 2021-02-23 | 西北师范大学 | Preparation and application of NiFe-LDH composite material |
CN113862694A (en) * | 2021-10-27 | 2021-12-31 | 电子科技大学 | Iron-doped nickel phosphide nano-particles and preparation method thereof |
CN115744841A (en) * | 2022-11-15 | 2023-03-07 | 西安近代化学研究所 | Nickel-based nitride nano combustion catalyst and preparation method thereof |
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CN107012473A (en) * | 2017-04-24 | 2017-08-04 | 北京化工大学 | A kind of double metallic composite material and its preparation method and application |
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Title |
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112391649A (en) * | 2020-11-23 | 2021-02-23 | 西北师范大学 | Preparation and application of NiFe-LDH composite material |
CN113862694A (en) * | 2021-10-27 | 2021-12-31 | 电子科技大学 | Iron-doped nickel phosphide nano-particles and preparation method thereof |
CN113862694B (en) * | 2021-10-27 | 2023-08-08 | 电子科技大学 | Iron-doped nickel phosphide nano-particle and preparation method thereof |
CN115744841A (en) * | 2022-11-15 | 2023-03-07 | 西安近代化学研究所 | Nickel-based nitride nano combustion catalyst and preparation method thereof |
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