CN108767277A - A kind of Fe-Pd bases nano-porous materials and preparation method thereof - Google Patents

A kind of Fe-Pd bases nano-porous materials and preparation method thereof Download PDF

Info

Publication number
CN108767277A
CN108767277A CN201810560651.4A CN201810560651A CN108767277A CN 108767277 A CN108767277 A CN 108767277A CN 201810560651 A CN201810560651 A CN 201810560651A CN 108767277 A CN108767277 A CN 108767277A
Authority
CN
China
Prior art keywords
nano
porous materials
alloy
preparation
bases
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CN201810560651.4A
Other languages
Chinese (zh)
Other versions
CN108767277B (en
Inventor
李雪
卢公昊
郑继波
宁佳林
黎曦宁
刘瑜
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
University of Science and Technology Liaoning USTL
Original Assignee
University of Science and Technology Liaoning USTL
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by University of Science and Technology Liaoning USTL filed Critical University of Science and Technology Liaoning USTL
Priority to CN201810560651.4A priority Critical patent/CN108767277B/en
Publication of CN108767277A publication Critical patent/CN108767277A/en
Application granted granted Critical
Publication of CN108767277B publication Critical patent/CN108767277B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/86Inert electrodes with catalytic activity, e.g. for fuel cells
    • H01M4/90Selection of catalytic material
    • H01M4/9041Metals or alloys
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y30/00Nanotechnology for materials or surface science, e.g. nanocomposites
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/86Inert electrodes with catalytic activity, e.g. for fuel cells
    • H01M4/88Processes of manufacture
    • H01M4/8825Methods for deposition of the catalytic active composition
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/86Inert electrodes with catalytic activity, e.g. for fuel cells
    • H01M4/90Selection of catalytic material
    • H01M4/92Metals of platinum group
    • H01M4/921Alloys or mixtures with metallic elements
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/30Hydrogen technology
    • Y02E60/50Fuel cells

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nanotechnology (AREA)
  • Condensed Matter Physics & Semiconductors (AREA)
  • Composite Materials (AREA)
  • General Physics & Mathematics (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Manufacturing & Machinery (AREA)
  • Inert Electrodes (AREA)
  • Catalysts (AREA)
  • Fuel Cell (AREA)

Abstract

A kind of nano-porous materials and preparation method thereof, belong to new material technology field.The catalysis material is using Fe-Pd-P non-crystaline amorphous metals as presoma alloy, under room temperature acidic environment, using the de- alloying technology of chemistry, the nano-porous materials with uniform reticular structure are prepared, the Fe-Pd bases nano-porous materials of acquisition have excellent electrocatalysis characteristic to formic acid etc..The nano-porous materials of acquisition are made into electrode material, hence it is evident that improve the electrocatalysis characteristic to formic acid.For the present invention compared with traditional metal materials, the nano-porous materials structure of preparation is uniform, and specific surface area is high, and stability is good, and occurs to being poisoned without CO during formic acid electro-catalysis;Chemistry is de-, and alloyage is at low cost, is simple and efficient, easily realizes industrialized production;The nano-porous materials of preparation are widely used in the new energy electrode material such as fuel cell field.

Description

A kind of Fe-Pd bases nano-porous materials and preparation method thereof
Technical field
The invention belongs to field of new materials, more particularly to a kind of Fe-Pd base noncrystal alloys prepare nano-porous materials and its Preparation method.
Background technology
Nano-porous materials are field of new materials research hotspots, and compared to traditional metal materials, nano porous metal material has High-specific surface area and special surface criticality, are widely used in the fields such as fuel cell, capacitor, sensor, catalysis.
The method for preparing nano-porous materials has de- alloyage, template, sintering process, layer-by-layer etc..Wherein, The de- alloyage of chemistry is chemical corrosion process, and in the solution, corrosion dissolution occurs for more active element in alloy, and inert element expands Bulk weight group forms nano-porous structure.De- alloyage is at low cost, be simple and efficient, easily realizes industrialized production, therefore, takes off alloyage Show one's talent in numerous preparation methods.
The key that de- alloyage prepares nano porous metal material is that the selection of presoma alloy, presoma will meet conjunction The feature that golden ingredient is uniform and monophase field ingredient is wide, which has limited the multicomponent alloy system ranges that de- alloyage is applicable in.Currently, selection Presoma alloy system be concentrated mainly on Ni bases, Cu bases, Mn bases, Mg bases, Zn bases, Al based alloys etc., to Fe based alloys, system grinds Study carefully less.Compared to the amorphous alloy material that conventional crystal material, rapid cooling are formed, have chemical composition uniform, nodeless mesh, The advantages such as the defects of dislocation occurs, and component adjustability is larger, and component range of choice is wider.Therefore, non-crystaline amorphous metal is to prepare The excellent persursor material of polynary nanometer porous metals expands the applicable alloy system range of de- alloyage.
Currently, global energy and environment challenge getting worse, it is further urgent to the exploitation of new energy.It is led in fuel cell Domain, mainly using Pt base catalysis materials, Pt is expensive and low memory, limits the development and application of fuel cell, The research and development of cause rather than Pt base catalysis materials are very necessary.However the price of Pd is the half of Pt, and it is straight during Catalyzed by Formic Acid It connects dehydration and generates CO2, no CO poisonings appearance;Transition-metal Fe element contains vacant electron orbit and not pairs of electronics, with After Pd forms alloy, the electronic structure of Pd is improved, Pd can be improved to formic acid electrocatalysis characteristic;The addition of nonmetallic P can be improved Precious metals pd is to the electro catalytic activity and stability of formic acid, in consideration of it, by Fe-Pd-P non-crystaline amorphous metals by the de- alloy treatment of chemistry It can get efficient nano-porous materials.Research efficiently prepares the Fe-Pd base nano-porous materials with excellent electrocatalysis characteristic The development of new energy field is of great significance to.
Invention content
The technical problem to be solved in the present invention:De- alloyage is overcome to be applicable in the limitation of alloy system and be difficult to efficiently make The problems such as standby nano-porous materials with excellent electrocatalysis characteristic, it is more to provide a kind of Fe-Pd base noncrystal alloys preparation nanometer The method of Porous materials.Using the de- alloyage of chemistry, using principle of oxidation and reduction, Fe elements are rotten in Fe-Pd-P non-crystaline amorphous metals Erosion dissolving, the recombination of Pd elements diffusions, form the nano-porous materials with three-dimensional uniformly reticular structure, and have studied Fe-Pd bases Electrocatalysis characteristic of the nano-porous materials in formic acid solution provides new method and think of for the electrode catalytic materials of fuel cell Road.
The present invention adopts the following technical scheme that:
A kind of nano-porous materials, using Fe-Pd-P non-crystaline amorphous metals as presoma alloy, under room temperature acidic environment, using change It learns and takes off alloying technology, prepare the nano-porous materials with uniform reticular structure, the Fe-Pd base nano-porous materials of acquisition are to first Acid etc. have excellent electrocatalysis characteristic.Wherein, transition-metal Fe element can improve the electrocatalysis characteristic of Pd.Fe-Pd bases are non- Peritectic alloy ingredient is uniform, and zero defect occurs, and is excellent persursor material.
The nano-porous materials are that the three-dimensional that aperture size is 40 ~ 180nm, hole wall size is 15 ~ 30nm is uniformly netted Structure.
A kind of method that Fe-Pd base noncrystal alloys prepare nano-porous materials, specifically includes following steps:
Step 1, amorphous alloy component is determined:Using the Fe of high-purity(99.9mass%),Fe3P(99.5mass%),Pd (99.9mass%)Element and compound press FeaPdbPcComposition of alloy is at assignment system, wherein and 50≤a≤70,0 < b≤ 30,0 c≤30 <, and+c=100 a+b;The atomic percent of Fe is bigger in Fe-Pd-P alloy systems, easier formation Nano-porous structure.
Step 2, non-crystaline amorphous metal master alloy ingot is prepared:Above-mentioned alloy raw material is positioned in induction melting device, is vacuumized To 8 × 10-3 Pa is hereinafter, and in high-purity argon gas(Purity is 99.99%)Master alloy ingot is made in abundant melting 0.5h under protection;
Step 3, it gets rid of band method using chilling and prepares amorphous alloy ribbon:In chilling gets rid of carrying device, suction less than 2.0 × 10-3Pa hereinafter, and be filled with high-purity argon gas protection(Purity is 99.99%), master alloy is added using electromagnetic induction effect Heat sprays master alloy melt to high-speed rotating water-cooled copper roller to after 2000 DEG C, and the rotating speed of copper roller is 2000 revs/min, It is quickly cooled down obtained amorphous alloy ribbon;
Step 4, nano-porous materials are prepared using the de- alloyage of chemistry:In salpeter solution environment, amorphous alloy ribbon is taken off Alloy treatment 1 ~ 5h, Fe element corrosion dissolution, Pd elements build up recombination, obtain nano-porous materials, fully clear with deionized water After washing dry to get.
The non-alloyed strip width of the step 3 is 1 ~ 2mm, thickness is 15 ~ 40 μm.
The salpeter solution of the step 4 is the solution of mass fraction 40 ~ 65%.
Compared with prior art, the present invention advantage is:
The present invention expands the application field of Fe base noncrystal alloys using Fe-Pd base noncrystal alloys as presoma, has also widened de- The applicable multi-element alloy system range of alloyage;
The present invention prepares nano-porous materials with the de- alloyage of chemistry, and preparation process is simple and efficient, with short production cycle, material cost Low, applicability is extensive, is easy to industrialized production;
The uniform netted nano-porous materials of three-dimensional prepared by the present invention, aperture size is 40 ~ 180nm, hole wall size be 15 ~ 30nm, stable structure, ingredient are adjustable with pattern;
Fe-Pd bases nano-porous materials prepared by the present invention have excellent electrocatalysis characteristic to formic acid etc., can be used as electrode and urge Change application of the material in electro-catalysis field.
Description of the drawings
Fig. 1 is Fe in the embodiment of the present invention 170Pd20P10The stereoscan photograph figure of amorphous alloy ribbon sample surfaces.
Fig. 2 is the nano-porous materials surface scan electromicroscopic photograph figure that in the embodiment of the present invention 1 prepared by the de- alloy of chemistry.
Fig. 3 be in the embodiment of the present invention 1 amorphous original strip and nano-porous materials to the cyclic voltammetry curve figure of formic acid.
Fig. 4 is the nano-porous materials surface scan electromicroscopic photograph figure that in the embodiment of the present invention 2 prepared by the de- alloy of chemistry.
Fig. 5 is the nano-porous materials surface scan electromicroscopic photograph figure that in the embodiment of the present invention 3 prepared by the de- alloy of chemistry.
Specific implementation mode
Below with reference to accompanying drawings and embodiments, the present invention is described in further detail.
Embodiment 1:Fe70Pd20P10Non-crystaline amorphous metal chemistry takes off alloy treatment and prepares nano-porous materials.
Step 1:Dispensing
According to Fe70Pd20P10The atomic percent of alloying component is converted into weight percent, using the Fe of high-purity (99.9mass%),Fe3P(99.5mass%),Pd(99.9mass%)Element and compound are weighed by composition of alloy ingredient.
Step 2:Master alloy melting ingot.
The raw metal of preparation is positioned over new skill of Japanese day to grind in NEV-SM04 type vacuum induction melting devices, is vacuumized It spends to 8 × 10-3 Pa is hereinafter, and in high-purity argon gas(Purity is 99.99%)Abundant melting obtains master alloy ingot under protection.
Step 3:Amorphous alloy ribbon prepares and characterization.
NEV-SM04 type vacuum chillings are ground using new skill of Japanese day and get rid of band device, and suction is less than 2.0 × 10-3Pa with Under, and it is filled with the argon gas protection of high-purity(Purity is 99.99%), master alloy is positioned over to the quartz of fast cooling device after broken After master alloy is heated to 2000 DEG C using electromagnetic induction effect, master alloy melt is sprayed to high-speed rotating water cooling by Guan Zhong On copper roller, the rotating speed of copper roller is 2000 revs/min, is quickly cooled down the amorphous alloy thin that obtained width is 2mm, thickness is 25 μm Band;Amorphous alloy ribbon material phase analysis, Cu are carried out using the Xpert powder type X-ray diffractometers of Dutch Panaco company K α radiation, λ 0.15406nm, 2 θ of scanning range are 30 ° ~ 90 °, can test to obtain Fe70Pd20P10Alloy sample is without apparent crystallization Peak occurs, and has non crystalline structure;Using the Zeiss- Σ IGMA HD type field emission scanning electron microscopes of Zeiss, Germany company to preparation Amorphous alloy ribbon carries out sample topography observation, and Fe is observed that in stereoscan photograph70Pd20P10Alloy sample ingredient is equal It is even, the defects of nodeless mesh, dislocation, as shown in Fig. 1.
Step 4:The de- alloy of chemistry prepares nano-porous materials and characterization.
Using the supersonic wave cleaning machine of model JP-020 type bench-top laboratories, by 25 μm of wide 2mm × thickness Fe70Pd20P10Amorphous alloy ribbon is placed in alcoholic solution after ultrasonic cleaning 5min, using the non-crystaline amorphous metal after cleaning as The persursor material of the de- alloy of chemistry, be placed on 25 DEG C, the mass fraction of 0.1L be 65% concentrated nitric acid solution in take off at alloy 3h Reason, salpeter solution are Sinopharm Chemical Reagent Co., Ltd.'s production, are fully cleaned with deionized water after the de- alloy 3h of chemistry It is spontaneously dried after sample and obtains nano-porous materials;It is scanned using the Zeiss- Σ IGMA HD type Flied emissions of Zeiss, Germany company Electronic Speculum carries out sample topography observation to the nano-porous materials of preparation, is observed that aperture size is 40 in stereoscan photograph The uniform netted nano-porous materials of three-dimensional that ~ 80nm, hole wall size are 15 ~ 30nm, as shown in Fig. 2.
Step 5:Nano-porous materials electrocatalysis characteristic is tested.
Cyclic voltammetry curve test, work are carried out using the CHI660 electrochemical workstations of Shanghai Hua Chen Instrument Ltd. Battery is glass-carbon electrode, with nafion solution by the nano-porous materials and Fe of width 2mm70Pd20P10Amorphous alloy ribbon is distinguished It is adhered to electrode surface, reference electrode is mereurous sulfate, is platinum filament to electrode.In 25 DEG C, the 0.5mol/L H of 0.01L2SO4+ Nano-porous materials are tested in 0.5mol/L HCOOH electrolyte to formic acid electrocatalysis characteristic;The sweep speed of cyclic voltammetry curve For 0.1V/s, scanning range is -0.8V ~ 0.8V, as shown in Fig. 3;Through electro-chemical test, Fe70Pd20P10Amorphous alloy ribbon The oxidation spike potential of formation is 0.1V, and oxidation peak current density is 640 A/m2, the chemical nano-porous materials taken off after alloy 3h It is -0.09V to form oxidation spike potential, and oxidation peak current density is 1200 A/m2, compared with former strip, oxidation spike potential is negative to be moved 0.19V, oxidation peak current density improve 560A/m2, show Fe70Pd20P10Amorphous alloy ribbon takes off through chemistry at alloy The nano-porous materials that reason 3h is obtained can improve the electrocatalysis characteristic to formic acid.
Embodiment 2:Fe70Pd20P10Non-crystaline amorphous metal increases the chemistry de- alloy time and prepares nano-porous materials to 5h
With embodiment 1, difference is method:
(1)By 25 μm of Fe of wide 2mm × thickness70Pd20P10Amorphous alloy ribbon be placed on 25 DEG C, the mass fraction of 0.1L be 65% Alloy 5h processing is taken off in concentrated nitric acid solution prepares nano-porous materials.
(2)It is uniform it to be prepared for the three-dimensional that aperture size is 55 ~ 90nm, hole wall size is 10 ~ 30nm after the de- alloy 5h of chemistry The nano-porous materials of reticular structure;As shown in Fig. 4.
(3)Increase the chemistry de- alloy time to 5h, promotes Fe70Pd20P10Amorphous alloy ribbon chemistry take off alloying into Corrosion dissolution persistently occurs for row, Fe elements, and the aperture size of nano-porous materials, which is persistently corroded, to become larger.Illustrate in acid solution In, increase the chemistry de- alloy time, promotes Fe element etchant solutions, be conducive to the state of tending towards stability.
Embodiment 3:Fe60Pd20P20Non-crystaline amorphous metal chemistry takes off alloy treatment 5h and prepares nano-porous materials
With embodiment 1, difference is method:
(1)By Fe60Pd20P20The melting of nominal composition dispensing and vacuum chilling are got rid of is prepared into 30 μm of wide 2mm × thickness with alloy Fe60Pd20P20Amorphous alloy ribbon;
(2)By 30 μm of Fe of wide 2mm × thickness60Pd20P20The dense nitre that amorphous alloy ribbon is 65% in the mass fraction of 25 DEG C, 0.1L In acid solution after the de- alloy 5h of chemistry, sample forms the corrosion cracking structure that a large amount of width are 50 ~ 180nm, as shown in Fig. 5.
(3)Fe60Pd20P20Amorphous alloy ribbon and Fe70Pd20P10Non-crystaline amorphous metal is compared, due to the reduction of Fe elements, 25 DEG C, in the concentrated nitric acid solution that the mass fraction of 0.1L is 65%, Fe70Pd20P10It is molten that non-crystaline amorphous metal is easier generation Fe elements corrosion Solution, Pd elements diffusions recombinate to form three-dimensional uniform netted nano-porous structure.Illustrate the atom hundred of Fe in Fe-Pd-P alloy systems Divide ratio bigger, it is easier to form nano-porous structure.
The foregoing is only a preferred embodiment of the present invention, is not intended to restrict the invention, for the skill of this field For art personnel, the invention may be variously modified and varied.All within the spirits and principles of the present invention, any made by repair Change, equivalent replacement, improvement etc., should all be included in the protection scope of the present invention.

Claims (6)

1. a kind of Fe-Pd bases nano-porous materials, which is characterized in that using Fe-Pd-P non-crystaline amorphous metals as presoma alloy, in room Under warm acidic environment, using the de- alloying technology of chemistry, the nano-porous materials with uniform reticular structure are prepared.
2. a kind of Fe-Pd bases nano-porous materials according to claim 1, which is characterized in that the nano-porous materials It is 40 ~ 180nm for aperture size, the uniform reticular structure of three-dimensional that hole wall size is 15 ~ 30nm.
3. a kind of Fe-Pd bases nano-porous materials according to claim 1, which is characterized in that the nano-porous materials With excellent electrocatalysis characteristic.
4. a kind of a kind of preparation method of Fe-Pd bases nano-porous materials as described in claim 1, which is characterized in that the system Preparation Method specifically includes following steps:
Step 1, amorphous alloy component is determined:Using the Fe of high-purity(99.9mass%),Fe3P(99.5mass%),Pd (99.9mass%)Element and compound press FeaPdbPcComposition of alloy is at assignment system, wherein and 50≤a≤70,0 < b≤ 30,0 c≤30 <, and+c=100 a+b;The atomic percent of Fe is bigger in Fe-Pd-P alloy systems, easier formation Nano-porous structure;
Step 2, non-crystaline amorphous metal master alloy ingot is prepared:Above-mentioned alloy raw material is positioned in induction melting device, it is evacuated to 8 × 10-3 Pa is hereinafter, and in high-purity argon gas(Purity is 99.99%)Master alloy ingot is made in abundant melting 0.5h under protection;
Step 3, it gets rid of band method using chilling and prepares amorphous alloy ribbon:In chilling gets rid of carrying device, suction is less than 2.0 × 10-3Pa hereinafter, and be filled with high-purity argon gas protection(Purity is 99.99%), master alloy is heated using electromagnetic induction effect To after 2000 DEG C, master alloy melt is sprayed to high-speed rotating water-cooled copper roller, the rotating speed of copper roller is 2000 revs/min, soon Amorphous alloy ribbon is but made in quickly cooling;
Step 4, nano-porous materials are prepared using the de- alloyage of chemistry:In salpeter solution environment, amorphous alloy ribbon is taken off Alloy treatment 1 ~ 5h, Fe element corrosion dissolution, Pd elements build up recombination, obtain nano-porous materials, fully clear with deionized water After washing dry to get.
5. a kind of preparation method of Fe-Pd bases nano-porous materials according to claim 4, which is characterized in that the step Rapid 3 non-alloyed strip width is 1 ~ 2mm, thickness is 15 ~ 40 μm.
6. a kind of preparation method of Fe-Pd bases nano-porous materials according to claim 4, which is characterized in that the step Rapid 4 salpeter solution is the solution of mass fraction 40 ~ 65%.
CN201810560651.4A 2018-05-25 2018-05-25 Fe-Pd-based nano-porous material and preparation method thereof Active CN108767277B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201810560651.4A CN108767277B (en) 2018-05-25 2018-05-25 Fe-Pd-based nano-porous material and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201810560651.4A CN108767277B (en) 2018-05-25 2018-05-25 Fe-Pd-based nano-porous material and preparation method thereof

Publications (2)

Publication Number Publication Date
CN108767277A true CN108767277A (en) 2018-11-06
CN108767277B CN108767277B (en) 2020-10-30

Family

ID=64002135

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201810560651.4A Active CN108767277B (en) 2018-05-25 2018-05-25 Fe-Pd-based nano-porous material and preparation method thereof

Country Status (1)

Country Link
CN (1) CN108767277B (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109518215A (en) * 2018-11-16 2019-03-26 佛山科学技术学院 A kind of nano-meter porous amorphous state electro catalytic electrode and its preparation method and application
CN110224148A (en) * 2019-05-24 2019-09-10 华中科技大学 The porous PdFe intermetallic compound and the preparation method and application thereof of Pt or Au modification
CN111068647A (en) * 2020-01-02 2020-04-28 南京工程学院 Nano TiO (titanium dioxide)2-SnO2Preparation method of solid solution photocatalytic material
CN111118523A (en) * 2020-01-16 2020-05-08 暨南大学 Method for improving catalytic activity of Fe-based amorphous alloy for hydrogen evolution by electrolysis water through dealloying treatment
CN114192132A (en) * 2021-12-15 2022-03-18 合肥工业大学 Method for simultaneously obtaining nano-porous strip and nano-fiber powder
CN114724861A (en) * 2022-04-18 2022-07-08 东南大学 Method for preparing flexible sandwich type amorphous alloy composite electrode
CN115537622A (en) * 2022-06-08 2022-12-30 湖南大学 Transition metal atom modified nanoporous ReSe 2 Material and method for the production thereof

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105648478A (en) * 2016-01-13 2016-06-08 大连理工大学 Preparation method of magnetic nano porous Fe-Pt alloy with electro-oxidation catalytic performance

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105648478A (en) * 2016-01-13 2016-06-08 大连理工大学 Preparation method of magnetic nano porous Fe-Pt alloy with electro-oxidation catalytic performance

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
杨改秀等: "炭载Pd-P催化剂对甲酸氧化的电催化性能", 《燃料化学学报》 *
王宝林: "Al-Pd-M(M=Mn,Fe,Cr,Mg)二十面体准晶的电化学脱合金化研究", 《中国优秀硕士学位论文全文数据库 工程科技1辑》 *

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109518215A (en) * 2018-11-16 2019-03-26 佛山科学技术学院 A kind of nano-meter porous amorphous state electro catalytic electrode and its preparation method and application
CN109518215B (en) * 2018-11-16 2021-06-15 佛山科学技术学院 Nano porous amorphous electrocatalytic electrode and preparation method and application thereof
CN110224148A (en) * 2019-05-24 2019-09-10 华中科技大学 The porous PdFe intermetallic compound and the preparation method and application thereof of Pt or Au modification
CN111068647A (en) * 2020-01-02 2020-04-28 南京工程学院 Nano TiO (titanium dioxide)2-SnO2Preparation method of solid solution photocatalytic material
CN111068647B (en) * 2020-01-02 2022-12-09 南京工程学院 Nano TiO (titanium dioxide) 2 -SnO 2 Method for preparing solid solution photocatalytic material
CN111118523A (en) * 2020-01-16 2020-05-08 暨南大学 Method for improving catalytic activity of Fe-based amorphous alloy for hydrogen evolution by electrolysis water through dealloying treatment
CN114192132A (en) * 2021-12-15 2022-03-18 合肥工业大学 Method for simultaneously obtaining nano-porous strip and nano-fiber powder
CN114192132B (en) * 2021-12-15 2024-03-05 合肥工业大学 Method for simultaneously obtaining nano porous strip and nano fiber powder
CN114724861A (en) * 2022-04-18 2022-07-08 东南大学 Method for preparing flexible sandwich type amorphous alloy composite electrode
CN115537622A (en) * 2022-06-08 2022-12-30 湖南大学 Transition metal atom modified nanoporous ReSe 2 Material and method for the production thereof
CN115537622B (en) * 2022-06-08 2023-09-26 湖南大学 Transition metal atom modified nanoporous ReSe 2 Material and preparation method thereof

Also Published As

Publication number Publication date
CN108767277B (en) 2020-10-30

Similar Documents

Publication Publication Date Title
CN108767277A (en) A kind of Fe-Pd bases nano-porous materials and preparation method thereof
CN107051559B (en) A kind of hydrogen reduction and analysis oxygen phosphatization cobalt@NPC dual-function composite catalyst and its preparation method and application
Huang et al. Synthesis and application of platinum-based hollow nanoframes for direct alcohol fuel cells
CN105648478A (en) Preparation method of magnetic nano porous Fe-Pt alloy with electro-oxidation catalytic performance
CN104894595B (en) A kind of amorphous metal oxide hydrogen-precipitating electrode of high catalytic activity and preparation method thereof
CN110146531B (en) Large-size bicontinuous porous foam bismuth and preparation method thereof
CN106711419B (en) The porous composite lithium ion battery cathode material of the NiO/C of core-shell structure copolymer shape
CN106222584A (en) A kind of nanoporous Fe base noncrystal alloy and preparation method and the application on analysis oxygen catalysis electrode
CN104269278B (en) A kind of self-supporting nanoporous nickel nickel compound electric pole piece and preparation method thereof
CN104911639B (en) A kind of supported silver nano net and its preparation method and application
CN105603469B (en) A kind of CuO/Ni core-shell nanos line and preparation method thereof
CN104084216B (en) A kind of silver-copper nano alloy eelctro-catalyst and laser Gaseous deposition process thereof
CN115852390A (en) FeCoNiBPt high-entropy amorphous alloy electrolytic water catalytic material and preparation method thereof
CN108993511A (en) A kind of preparation method of the porous iron-doped nickel oxide elctro-catalyst of superfine nano
CN106207090B (en) Three-D nano-porous copper/one-dimensional nano cuprous oxide wire network-type negative electrode of lithium ion battery and one one-step preparation method
CN110339850A (en) A kind of Fe-Co-Ni-P-C system high-entropy alloy elctro-catalyst and preparation method thereof for evolving hydrogen reaction
Nkhaili et al. A simple method to control the growth of copper oxide nanowires for solar cells and catalytic applications
CN103695959A (en) Hierarchical porous Ni(OH)2/NiCu hydrogen evolution electrode and preparation method thereof
CN105256165A (en) Method for preparing nano-porous copper through Cu-Al alloy slightly doped with Ni/Ti
CN110923746A (en) Nano-porous Fe-P-C material, preparation method thereof and application thereof in hydrogen production by water electrolysis
CN107221637B (en) A kind of laser ablation oxidation in-situ preparation method of lithium ion battery integration cathode
Scaglione et al. Amorphous molybdenum sulphide@ nanoporous gold as catalyst for hydrogen evolution reaction in acidic environment
CN114045505B (en) High-activity large-size electrolysis water hydrogen evolution electrode and pulse laser preparation method thereof
CN113862722B (en) High-entropy amorphous anode oxygen evolution electrode material and preparation method thereof
Ng et al. Fabrication of nanometer-to-micron sized Cu2O single crystals by electrodeposition

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant