CN1913219A - Magnesium negative material and preparation method and application - Google Patents
Magnesium negative material and preparation method and application Download PDFInfo
- Publication number
- CN1913219A CN1913219A CNA2006100138676A CN200610013867A CN1913219A CN 1913219 A CN1913219 A CN 1913219A CN A2006100138676 A CNA2006100138676 A CN A2006100138676A CN 200610013867 A CN200610013867 A CN 200610013867A CN 1913219 A CN1913219 A CN 1913219A
- Authority
- CN
- China
- Prior art keywords
- magnesium
- stainless steel
- nanometer
- diameter
- micron
- 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
Links
Images
Classifications
-
- 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
- Y02E60/10—Energy storage using batteries
Landscapes
- Hybrid Cells (AREA)
- Inert Electrodes (AREA)
Abstract
This invention relates to a Mg negative electrode material and its preparation method and application, which applies a gas phase deposition method to prepare Mgnm/mum material in the shapes of nano-balls, nano-plates, nano-rods, nano-sea hedgehog balls, mum balls, mum plates, mum rods and mum sea hedgehog balls. Since the ratio surface area and chemical activation are high, the prepared air battery assembled by nano Mg is in good chemical performance, especially the Mg nano sea hedgehog balls of porous network structure has higher energy density (1200Wh/Kg) and excellent high rate discharge performance.
Description
Technical field
The present invention relates to magnesium negative material and preparation method and application.Adopt vapour deposition process to make magnesium nanometer and micro materials, comprise nanosphere, nanometer sheet, nanometer rods, nanometer Sea urchin ball etc.The magnesium nano material has high specific area and chemism, has excellent electrochemical properties in magnesium/air cell, and especially the magnesium nanometer Sea urchin ball of porous network structure has more high-energy-density (1200Wh/kg) and excellent high-rate discharge ability.
Technical background
Along with economy and development of science and technology, high-energy battery is widely used day by day in fields such as household electrical appliance, instrument and meter, mobile communication equipment, portable electric appts, defence equipments.In numerous applications, harsh more requirement has been proposed all for economy and durability, security reliability, ease of use and the environment friendly of battery.The metal/air battery is with metal (Zn, Mg, Fe, Al etc.) as negative electrode active material and air (oxygen) the high end cell of a class as positive active material, its main feature is big capacity, high power, low cost and of low pollution, get more and more people's extensive concerning, be called as " green energy resource geared to the 21st century ".And magnesium/air cell occupies a tiny space in field of batteries with its high advantage such as theoretical specific energy, becomes one of focus of development of new Green Chemistry power supply.
As everyone knows, magnesium is one of most important alkali earth metal, is widely used in organic synthesis, biochemistry and electrochemical field.At present, though the traditional preparation process method of magnesium is comparatively ripe, but domestic and international research to the magnesium nano material only limits to high-energy ball milling method and prepares magnesium nano particle and relevant nano composition (as: Y.K.Zhang thereof, S.J.Liao, Y.H.Fan, Chemical reactivities of magnesium nanopowders.J.Nanopart.Res.2001,3,23; J.L.Bobet, E.Grigorova, M.Khrussanova, M.Khristov, P.Stefanov, P.Peshev, D.Radev, Hydrogen sorption propertiesof graphite-modified magnesium nanocomposites prepared by ball-milling.J.Alloys Compd.2004,366,298).In addition, the magnesium nano wire has just carried out theoretical research (as: H.Li, F.Pederiva with computer simulation, G.H.Wang, B.L.Wang, Helical multishell structures of magnesium nanowires.J.Appl.Phys.2004,96,2214.).Up to now, only see the magnesium nano particle of ball milling preparation and calculate the nano wire of simulation, but yet there are no the controlled preparation of other pattern magnesium nano material of bibliographical information at home and abroad, more do not have document that the nanometer Mg material is applied to high-end chemical power source and study its comprehensive electrochemical.
Magnesium/air cell is the energy storage instrument, is again a kind of fuel cell.Compare with general battery, magnesium/air cell has advantages such as high theoretical voltage (3.09V), high theoretical energy density (3910Wh/kg), low-cost, pollution-free and lightweight.But because general magnesium electrode is a pellet electrode, under same apparent current density, its actual current density ratio porous zinc electrodes is much smaller, and electrode polarization is bigger, so the performance of magnesium/air cell is poorer than zinc/air cell.Because the design feature of magnesium/air cell is improved the magnesium electrode performance and will be improved magnesium/air cell whole synthesis performance to a great extent.
Summary of the invention
The purpose of this invention is to provide a kind of magnesium negative material and preparation method and application.By regulating experimental conditions such as heating-up temperature, gas flow rate, reaction time and depositing temperature, with the controlled preparation magnesium of vapour deposition process nanosphere, nanometer sheet, nanometer rods, nanometer Sea urchin ball, micron ball, micron bar, micron film and micron sea urchin etc., realized effective control preparation to its pattern.The present invention can obviously improve its physics and chemical property after being characterised in that magnesium/cathode of air battery critical material magnesium nanometer, particularly along with the nanometer of magnesium, the atomicity ratio on surface increases, make the electro-chemical activity of material increase the utilance that also improves magnesium electrode greatly, improved the energy density and the high-rate discharge ability of battery simultaneously.
The invention provides magnesium/air cell that magnesium negative material nanosphere, nanometer sheet, nanometer rods and the nanometer Sea urchin ball of preparation be assembled into and have excellent electrochemical properties, especially have the magnesium nanometer Sea urchin ball of porous network structure, have high energy density (1200Wh/kg) and good high-rate discharge ability.Therefore, the application of exploitation nanometer Mg in air cell has far-reaching practical significance for the novel magnesium/air cell of development and other magnesium base battery.
Magnesium negative material provided by the invention comprises nanosphere, nanometer sheet, nanometer rods or nanometer Sea urchin ball, and wherein, magnesium nanosphere diameter is 200-500nm; Magnesium nanometer sheet diameter is 150-160nm, and thickness is 30-50nm, has smooth surface and regular shape; Magnesium nanometer rods diameter is 70-100nm only, and length reaches 200-500nm; The diameter of magnesium nanometer Sea urchin ball is 500nm, and the surface is made of the ultra-fine beard shape of several 10-100 nanometers fiber.Also comprise: magnesium micron ball, magnesium micron film, magnesium micron bar or magnesium micron Sea urchin ball.Magnesium micron bulb diameter: 3-5 μ m, magnesium micron film diameter: 1-1.5 μ m, magnesium micron bar diameter 0.15-0.50 μ m, length is 5-20 μ m, and magnesium micron Sea urchin ball diameter is 1.0-5.0 μ m, and the diameter of surperficial beard shape fiber only is the 10-100 nanometer.
The preparation method of magnesium negative material of the present invention may further comprise the steps:
1) the tungsten boat with producing high purity metal magnesium (99.9%) is placed in the stainless steel tube; in the tubular type burner hearth; earlier with logical 1 hour of 200ml/min flow velocity high-purity Ar (99.95%) with oxygen in the system of removing; at flow velocity is under the Ar gas shiled of 400-800ml/min; 850-950 ℃ is incubated 1-2 hour; stainless steel or copper substrate lie in stainless steel tube downstream colling end and collect product, naturally cool to room temperature, obtain magnesium negative material at substrate surface.
2) stainless steel tube soaks with 0.5mol/L HCl that 30min, washing, alcohol wash, drying.
Described magnesium metal use amount is the 0.1-5.0 gram.
The isolated plant that the invention provides magnesium Nano/micron electrode material preparation method comprises: Ar gas cylinder, gas-drying apparatus, gas flowmeter, stainless steel reactor, tube furnace, temperature programmed control device, substrate and cooling and dedusting device; Ar gas cylinder, gas-drying apparatus, gas flowmeter, stainless steel reactor, cooling and dedusting device connect successively, stainless steel reactor passes the tube furnace of band thermocouple temperature programmed control device, substrate is placed on the stainless steel reactor colling end, and stainless steel reactor is connected with Pressure gauge, valve, cooling and dedusting device in turn.
The high-purity Ar gas cylinder closely is connected with gas drier by the stainless steel pipeline, then passes through gas flowmeter; Dried gas stream enters stainless steel reactor through tube furnace left side valve; After the temperature of tube furnace rises to high temperature, gas will transmit metal vapors in the reactor to the colling end substrate.In the described device, the length of stainless steel tube reactor is 80.0cm, Φ
Internal diameterBe 1.2cm; Tube furnace is the main body of whole heating systems, and heating-up temperature is controlled by thermocouple by programmed temperature control instrument; The cooling and dedusting device is the superfine magnesium powder that utilizes water-cooled to remove in the reaction end gas to be contained, and reduces solid dust and pollutes.
The characteristics of the present invention aspect preparation are: 1) adopt the high-purity magnesium powder of heating evaporation, vapour deposition process makes multiple ultrapure magnesium nano material, and is raw materials used cheap and easy to get, whole system non-environmental-pollution; 2) novel magnesium Nano/micron material can effectively be controlled by regulating experimental conditions such as heating-up temperature, gas flow rate, heating time, and simple to operate, process controllability is strong.
Magnesium/air cell is made up of magnesium negative electrode gel, cellulose barrier film and air electrode among the present invention.Wherein the magnesium gel is made up of 90wt% nanometer Mg, 5wt% carbon black, 2wt% sodium carboxymethylcellulose (CMC) gel and 3wt% additive (transition metal Ni, Co and oxide thereof).Air electrode mainly is made of waterproof ventilative layer and catalysis conductive layer, and order from outside to inside is followed successively by waterproof ventilative layer, currect collecting net (nickel foam) and catalysis conductive layer; Wherein, waterproof ventilative layer is with acetylene black, PTFE emulsion, Na
2SO
4Mix, ultrasonic to the pasty state roll-forming get catalytic membrane, thickness is 200-400 μ m; Close electrolyte one side Catalytic Layer is by perovskite La
0.6Ca
0.4CoO
3Nanotube, acetylene black, PTFE emulsion, Na
2SO
4Mix ultrasonic to the pasty state the catalytic membrane of roll-forming, thickness is 100-400 μ m; La
0.6Ca
0.4CoO
3Nanotube eelctro-catalyst comprehensive utilization sol-gel process and alumina formwork method make, and diameter is 200nm, the consistency of thickness of length and template (50-60 μ m), wall thickness 15nm.Electrolyte is selected for use and has been added 2.6M Mg (NO
3)
23.6M NaNO
2Neutral electrolyte.The discharge curve of battery under different current densities measured by Arbin 2000 charge-discharge test instrument.
The present invention is by regulating experimental conditions such as heating-up temperature, gas flow rate and reaction time, with the controlled preparation magnesium of vapour deposition process nanosphere, nanometer sheet, nanometer rods, nanometer Sea urchin ball, micron ball, micron film, micron bar and micron sea urchin etc., realized effective control preparation to its pattern.The present invention can obviously improve its physics and chemical property after being characterised in that magnesium/cathode of air battery critical material magnesium nanometer, particularly along with the nanometer of magnesium, the atomicity ratio on surface increases, make the electro-chemical activity of material increase the utilance that also improves magnesium electrode greatly, improve the energy density and the high-rate discharge ability of battery simultaneously.Magnesium/air cell that nanosphere, nanometer sheet, nanometer rods, nanometer Sea urchin ball are assembled into has excellent electrochemical properties, especially have the magnesium nanometer Sea urchin ball of porous network structure, have high energy density (1200Wh/kg) and good high-rate discharge ability.Therefore, the application of exploitation nanometer Mg in air cell has far-reaching practical significance for the novel magnesium/air cell of development and other magnesium base battery.The nanometer Mg material not only will greatly promote developing rapidly of magnesium/air cell, but also can be at Mg-MnO
2, Mg-Ag
2There is bright application prospect in other magnesium base battery fields such as O, Mg-seawater battery.
Description of drawings:
Fig. 1 is the experimental provision schematic diagram of preparation magnesium nano material.
Fig. 2 is the SEM figure of different-shape magnesium nano material.
Fig. 3 is the XRD figure of different-shape magnesium nano material.
Fig. 4 is the SEM figure of magnesium micron ball.
Fig. 5 is the SEM figure of magnesium micron film.
Fig. 6 is the SEM figure of magnesium nano wire.
Fig. 7 is the SEM figure of magnesium nano wire.
Fig. 8 is the polarization curve of the magnesium/air cell of different-shape nano material.
Embodiment
The preparation of magnesium nanosphere
Fig. 1 utilizes vapour deposition process to prepare the experimental provision schematic diagram of multiple magnesium nano material.1-high-purity Ar protection gas, the dry system of 2-gas, control of 3-flow velocity and display device, 4-stainless steel reactor, 5-heating and temperature-controlling system, 6-substrate, 7-cooling and dedusting device.
Ar gas cylinder, gas-drying apparatus, gas flowmeter, stainless steel reactor, cooling and dedusting device connect successively, stainless steel reactor passes the tube furnace of band thermocouple temperature programmed control device, substrate is placed on the stainless steel reactor colling end, and stainless steel reactor is connected with Pressure gauge, valve, cooling and dedusting device in turn.
The high-purity Ar gas cylinder closely is connected with gas drier by the stainless steel pipeline, then passes through gas flowmeter; Dried gas stream enters stainless steel reactor through tube furnace left side valve; After the temperature of tube furnace rises to high temperature, gas will transmit metal vapors in the reactor to the colling end substrate.Wherein, tube furnace is the main body of whole heating systems, and heating-up temperature is controlled by thermocouple by programmed temperature control instrument, and the tube furnace heating-up temperature is by the thermocouple control of artificial intelligence temperature controller and body of heater central authorities, and actual furnace temperature and design temperature error are less than 2 ℃.The cooling and dedusting device is the superfine magnesium powder that utilizes water-cooled to remove in the reaction end gas to be contained, and reduces solid dust and pollutes.
With length is 80.0cm, Φ
Internal diameterFor the stainless steel tube of 1.2cm is placed in the tubular type burner hearth of said apparatus, the tungsten boat that fills the high-purity magnesium of 0.5 gram is placed in the stainless steel tube, stainless steel or copper substrate lie in stainless steel tube downstream colling end.Led to high-purity Ar (99.95%) 1 hour with the 200ml/mjn flow velocity, with oxygen in the system of removing; Under the Ar of 400ml/min protection, 850 ℃ of insulations 1 hour, after reaction finished, system naturally cooled to room temperature, can obtain silver gray magnesium film at substrate surface, collected samples and put into vacuum desiccator and preserve by different crystallizing fields; Stainless steel tube soaks 30min with 0.5mol/L HCl, and washing, alcohol are washed, drying, reusable edible.
Fig. 2 is the SEM figure of different-shape magnesium nano material: (a) magnesium nanosphere, (b) nanometer sheet, (c) nanometer rods (d) nanometer Sea urchin ball; And the TEM of nanometer rods figure: (e) low power TEM figure, (f) HRTEM for white square frame district in (e) schemes (illustration is a Fourier transformation).The ESEM of the magnesium nanosphere of described method preparation is shown in Fig. 2 a: diameter is that the magnesium nano particle of 200-500nm has regular hexagonal structure, and the corner angle of the accumulation horizon of six side's sheets are high-visible.
The preparation of magnesium nanometer sheet
Experimental rig is 80.0cm as described in the embodiment 1 with length, Φ
Internal diameterFor the 1.2cm stainless steel tube is placed in the tubular type burner hearth, the tungsten boat that fills the high-purity magnesium of 1.5 grams is placed in the stainless steel tube, and stainless steel or copper substrate lie in stainless steel tube downstream colling end.Led to high-purity Ar (99.95%) 1 hour with the 200ml/min flow velocity, with oxygen in the system of removing; Under Buchholz protection, 850 ℃ are incubated 1 hour, and the high-purity Ar carrier gas is controlled at 800ml/min in heating process, after reaction finishes, system naturally cools to room temperature, can obtain silver gray magnesium film at substrate surface, collects samples and puts into vacuum desiccator and preserve by different crystallizing fields; Stainless steel tube soaks 30min with 0.5mol/L HCl, and washing, alcohol are washed, drying, reusable edible.
The ESEM of the magnesium nanometer sheet of described method preparation is shown in Fig. 2 b: ganoid nanometer sheet has single-size (50-460nm), and its laminated structure has six fixing side's geometries and thickness only to be 30-50nm.
The preparation of magnesium nanometer rods
In device as Fig. 1, be 80.0cm with length, Φ
Internal diameterFor the 1.2cm stainless steel tube is placed in the tubular type burner hearth, the tungsten boat that fills the high-purity magnesium of 3.0 grams is placed in the stainless steel tube, and stainless steel or copper substrate lie in stainless steel tube downstream colling end.Led to high-purity Ar (99.95%) 1 hour with the 200ml/min flow velocity, with oxygen in the system of removing; Under Buchholz protection, 950 ℃ are incubated 1 hour, and the high-purity Ar carrier gas is controlled at 400ml/min in heating process, after reaction finishes, system naturally cools to room temperature, can obtain silver gray magnesium film at substrate surface, collects samples and puts into vacuum desiccator and preserve by different crystallizing fields; Stainless steel tube soaks 30min with 0.5mol/L HCl, and washing, alcohol are washed, drying, reusable edible.
The ESEM of the magnesium nanometer rods of described method preparation is shown in Fig. 2 c: the length of nanometer rods is 200-500nm, the diameter dimension homogeneous.The fine structure of magnesium nanometer rods can pass through projection electron microscope (TEM), and (Fig. 2 e f) observes, and its diameter only is 70-100nm, and the oxide-film on surface is very thin, illustrates and utilizes embodiment 1 described experimental provision can prepare ultrapure light metal nano material; The interplanar distance of the high resolution diffraction striped of nanometer rods only is 0.26nm, and is identical with (002) character spacing, thereby infers the magnesium nanometer rods along the growth of [001] direction, and this is consistent with Fourier transformation (FFT) analysis result among Fig. 2 f.
The preparation of magnesium nanometer Sea urchin ball
Device is 80.0cm as described in the embodiment 1 with length, Φ
Internal diameterFor the 1.2cm stainless steel tube is placed in the tubular type burner hearth, the tungsten boat that fills the high-purity magnesium of 4.0 grams is placed in the stainless steel tube, and stainless steel or copper substrate lie in stainless steel tube downstream colling end.Led to high-purity Ar (99.95%) 1 hour with the 200ml/min flow velocity, with oxygen in the system of removing; Under Buchholz protection, 950 ℃ are incubated 1 hour, and the high-purity Ar carrier gas is controlled at 800ml/min in heating process, after reaction finishes, system naturally cools to room temperature, can obtain silver gray magnesium film at substrate surface, collects samples and puts into vacuum desiccator and preserve by different crystallizing fields; Stainless steel tube soaks 30min with 0.5mol/L HCl, and washing, alcohol are washed, drying, reusable edible.
The ESEM of the magnesium nanometer Sea urchin ball of described method preparation is shown in Fig. 2 d: the nanometer Sea urchin ball is the spherical pattern of thorniness, and the surface is the ultra-fine beard shape of a 10-100 nanometer fiber, and the nanometer beard is cross-linked to form the network configuration of porous each other.
Fig. 3 is the XRD figure of different-shape magnesium nano material: (a) nanosphere, (b) nanometer sheet, (c) nanometer rods, (d) nanometer Sea urchin ball.The XRD spectrum of 4 kinds of nanometer Mg of described embodiment 1-4 condition preparation shows as Fig. 3: (Fig. 3 a), the XRD spectra characteristic peak positions of nanometer sheet (Fig. 3 b), nanometer rods (Fig. 3 c), nanometer Sea urchin ball (Fig. 3 d) is similar, is peak difference to some extent by force for the magnesium nanosphere.Because the advantages of good crystallization of nanosphere and nanometer sheet makes characteristic peak stronger; And the small-size effect of nanometer rods and nanometer Sea urchin ball and Geng Duo defective cause the broadening at peak.But the position of all diffraction maximums all with JCDPS standard card (No.35-0821) data consistent of pure magnesium.Do not have the dephasign diffraction maximum in the drawings, show that making sample is pure magnesium, further specifies the reasonability of design of test.
The preparation of magnesium micron ball
Used temperature retention time is 1 hour among the above embodiments 1-4, when prolonging temperature retention time to 2 hour, because of the nucleus growth time increases, has obtained corresponding micron deposition morphology.
Device is 80.0cm as described in the embodiment 1 with length, and the Φ internal diameter is for the 1.2cm stainless steel tube is placed in the tubular type burner hearth, and the tungsten boats that fill the high-purity magnesium of 5.0 grams are placed in the stainless steel tube, and stainless steel or copper substrate lie in stainless steel tube downstream colling end.Led to high-purity Ar (99.95%) 1 hour with the 200ml/min flow velocity, with oxygen in the system of removing; Under Buchholz protection, 850 ℃ are incubated 2 hours, and the high-purity Ar carrier gas is controlled at 400ml/min in heating process, after reaction finishes, system naturally cools to room temperature, can obtain silver gray magnesium film at substrate surface, collects samples and puts into vacuum desiccator and preserve by different crystallizing fields; Stainless steel tube soaks 30min with 0.5mol/L HCl, and washing, alcohol are washed, drying, reusable edible.
Fig. 4 is at 850 ℃, flow velocity 400ml/min, 300 ℃ of SEM figure that deposit preparation magnesium micron ball under 2 hours: (a) low power enlarged drawing, (b) high magnification map.The ESEM of the magnesium micron ball of described method preparation is as shown in Figure 4: magnesium micron ball is evenly (3-5 μ m), a ganoid chondritic of diameter.
The preparation of magnesium micron film
Device is 80.0cm as described in the embodiment 1 with length, Φ
Internal diameterFor the 1.2cm stainless steel tube is placed in the tubular type burner hearth, the tungsten boat that fills the high-purity magnesium of 5.0 grams is placed in the stainless steel tube, and stainless steel or copper substrate lie in stainless steel tube downstream colling end.Led to high-purity Ar (99.95%) 1 hour with the 200ml/min flow velocity, with oxygen in the system of removing; Under Buchholz protection, 850 ℃ are incubated 2 hours, and the high-purity Ar carrier gas is controlled at 800ml/min in heating process, after reaction finishes, system naturally cools to room temperature, can obtain silver gray magnesium film at substrate surface, collects samples and puts into vacuum desiccator and preserve by different crystallizing fields; Stainless steel tube soaks 30min with 0.5mol/L HCl, and washing, alcohol are washed, drying, reusable edible.
Fig. 5 is at 850 ℃, flow velocity 800ml/min, 300 ℃ of SEM figure that deposit 2 hours magnesium micron films: (a) low power enlarged drawing, (b) high magnification map.The ESEM of the magnesium micron film of described method preparation is as shown in Figure 5: the diameter of magnesium micron film is the hexagonal structure micron film of 1.0-1.5 μ m, and comparatively regular reunion together.
The preparation of magnesium micron bar
Device is 80.0cm as described in the embodiment 1 with length, Φ
Internal diameterFor the 1.2cm stainless steel tube is placed in the tubular type burner hearth, the tungsten boat that fills the high-purity magnesium of 5.0 grams is placed in the stainless steel tube, and stainless steel or copper substrate lie in stainless steel tube downstream colling end.Led to high-purity Ar (99.95%) 1 hour with the 200ml/min flow velocity, with oxygen in the system of removing; Under Buchholz protection, 950 ℃ are incubated 2 hours, and the high-purity Ar carrier gas is controlled at 400ml/min in heating process, after reaction finishes, system naturally cools to room temperature, can obtain silver gray magnesium film at substrate surface, collects samples and puts into vacuum desiccator and preserve by different crystallizing fields; Stainless steel tube soaks 30min with 0.5mol/L HCl, and washing, alcohol are washed, drying, reusable edible.
Fig. 6 is at 950 ℃, flow velocity 400ml/min, 300 ℃ of SEM figure that deposit 2 hours magnesium nano wires: (a) low power enlarged drawing, (b) high magnification map.The ESEM of the magnesium micron bar of described method preparation is as shown in Figure 6: described magnesium micron bar is characterized in that length is that 5-20 μ m and diameter are 0.15-0.50 μ m; Along with the increase of sedimentation time, the length of micron bar increases, and at the some nano particles of the even distribution in the surface of micron bar.
Embodiment 8
The preparation of magnesium micron Sea urchin ball
Device is 80.0cm as described in the embodiment 1 with length, Φ
Internal diameterFor the 1.2cm stainless steel tube is placed in the tubular type burner hearth, the tungsten boat that fills the high-purity magnesium of 5.0 grams is placed in the stainless steel tube, and stainless steel or copper substrate lie in stainless steel tube downstream colling end.Led to high-purity Ar (99.95%) 1 hour with the 200ml/min flow velocity, with oxygen in the system of removing; Under Buchholz protection, 950 ℃ are incubated 2 hours, and the high-purity Ar carrier gas is controlled at 800ml/min in heating process, after reaction finishes, system naturally cools to room temperature, can obtain silver gray magnesium film at substrate surface, collects samples and puts into vacuum desiccator and preserve by different crystallizing fields; Stainless steel tube soaks 30min with 0.5mol/L HCl, and washing, alcohol are washed, drying, reusable edible.
Fig. 7 is at 950 ℃, the SEM figure of flow velocity 800ml/min, 2 hours magnesium nano wires of 300 ℃ of depositions: (a) low power enlarged drawing, (b) high magnification map.The ESEM of the magnesium micron Sea urchin ball of described method preparation is as shown in Figure 7: described magnesium micron Sea urchin ball it is characterized in that the surface still is nanometer beard formation network configuration, but the increasing diameter of sea urchin is added to 1.0-5.0 μ m, and the part agglomeration is arranged.
Embodiment 9
The Electrochemical Properties of typical case's magnesium nano material
Be to investigate the application characteristic of magnesium nano material in magnesium/air cell, the chemical property of several typical magnesium nanotopographies that the invention is characterized in system research.
Fig. 8 is the polarization curve of the magnesium/air cell of different-shape nano material: (a) nanosphere, (b) nanometer sheet, (c) nanometer rods, (d) nanometer Sea urchin ball.Polarization curve such as Fig. 8 of being assembled into magnesium/air cell according to 4 kinds of nanometer Mg that prepare under the embodiment 1-4 condition show: (Fig. 8 a), the operating voltage of the magnesium/air cell of nanometer sheet (Fig. 8 b), nanometer rods (Fig. 8 c), nanometer Sea urchin ball (Fig. 8 d) assembling increases with discharge current density and reduce for the magnesium nanosphere; And the amplitude that reduces is followed successively by: a＞b＞c＞d; Especially, the change in voltage of the magnesium/air cell of nanometer Sea urchin ball assembling is steady and have high operating voltage, shows that it has high energy density and high-rate discharge ability.
Under the described embodiment 1-4 condition 4 kinds of nanometer Mg of preparation to make the energy density of magnesium/air cell under different discharge current densities as shown in table 1: it is the energy density the best (950-1200mA/cm of battery under different discharging currents of negative pole that magnesium/air cell that various magnesium nano materials are assembled into has excellent chemical property, especially magnesium nanometer Sea urchin ball
2).The magnesium nano material in battery, have particular performances main because: 1) key reaction in magnesium/air cell is:
(+)
Φ°＝0.40V (1)
(-)
Φ°＝-2.69V (2)
Net reaction: 2Mg+O
2+ 2H
2O → 2Mg (OH)
2E °=3.09V (3)
The electric energy of magnesium/air cell is to generate Mg (OH) by Mg
2The chemical energy of reaction is transformed, and the gross energy that this means magnesium/air cell is mainly by the negative pole decision, so its electrochemical kinetics is main relevant with surface area and battery structure.The subject matter of magnesium/air cell is magnesium sheet is lower in discharge process coulombic efficiency and higher electrode polarization.2) chemical property by the nanometer rods of magnesium shown in the table 1 and nanometer Sea urchin ball ratio nano ball and nanometer sheet is good, may be because the size of nanometer rods and nanometer Sea urchin ball is smaller.As everyone knows, will change its physics and chemical property to a great extent after the material nanoization.Along with reducing of granularity, the atomicity ratio on surface increases, and makes the electro-chemical activity of material increase the utilance that also improves magnesium electrode greatly.3) in these four kinds of nanotopographies, the air cell of nanometer Sea urchin ball assembling not only has the highest energy density (1200Wh/kg), but also shows best high-rate discharge ability; This may have direct relation with the high-specific surface area of sea urchin structure and unique porous network structure.As shown in Figure 8, along with discharge current density increases, the polarization of magnesium electrode increases, thereby causes operating voltage to descend.The high-specific surface area of magnesium nanometer Sea urchin ball can reduce the current density of magnesium electrode in discharge process, make the polarization of magnesium electrode less relatively, this small-size effect increased battery current density, improved high-rate discharge capacity.4) high specific area increase active material contacts with the effective of electrolyte, helps to reduce the resistance of electrode reaction, has improved discharge voltage simultaneously to a certain extent.
The energy density of magnesium/air cell under different discharge current densities of table 1 different-shape magnesium nanometer assembling
| The magnesium nano material of different-shape | Different current density (mA/cm
2) under, the actual energy density (Wh/kg) of magnesium/ | |||
| 5 | 25 | 50 | 100 | |
| The a nano particle | 650 | 575 | 532 | 450 |
| The b nanometer sheet | 760 | 680 | 623 | 560 |
| The c nanometer rods | 920 | 830 | 770 | 705 |
| D nanometer Sea urchin ball | 1200 | 1100 | 1010 | 950 |
Claims (7)
1, a kind of magnesium negative material is characterized in that it comprises: nanosphere, nanometer sheet, nanometer rods or nanometer Sea urchin ball, and wherein, magnesium nanosphere diameter is 200-500nm; Magnesium nanometer sheet diameter is 150-160nm, and thickness is 30-50nm, has smooth surface and regular shape; Magnesium nanometer rods diameter is 70-100nm only, and length reaches 200-500nm; The diameter of magnesium nanometer Sea urchin ball is 500nm, and the surface is made of the ultra-fine beard shape of several 10-100 nanometers fiber;
Also comprise: magnesium micron ball, magnesium micron film, magnesium micron bar and magnesium micron Sea urchin ball; Magnesium micron bulb diameter: 3-5 μ m, magnesium micron film diameter: 1-1.5 μ m, magnesium micron bar diameter: 0.15-0.50 μ m, length is 5-20 μ m, magnesium micron Sea urchin ball diameter is 1.0-5.0 μ m.
2, the preparation method of the described magnesium negative material of claim 1 is characterized in that it may further comprise the steps:
1) the tungsten boat with magnesium metal is placed in the stainless steel tube, in the tubular type burner hearth, lead to 1 hour Ar gas to remove oxygen in the system with the 200ml/min flow velocity earlier, at flow velocity is under the Ar gas shiled of 400-800ml/min, 850-950 ℃ is incubated 1-2 hour, stainless steel or copper substrate lie in stainless steel tube downstream colling end and collect product, naturally cool to room temperature, obtain magnesium negative material at substrate surface;
2) stainless steel tube soaks with 0.5mol/L HCl that 30min, washing, alcohol wash, drying.
3,, it is characterized in that described magnesium metal use amount is the 0.1-5.0 gram according to the preparation method of the described magnesium negative material of claim 2.
4, the preparation method's of the described magnesium negative material of a kind of claim 2 special equipment is characterized in that it comprises Ar gas cylinder, gas-drying apparatus, gas flowmeter, stainless steel reactor, tube furnace, temperature programmed control device, substrate and cooling and dedusting device; Ar gas cylinder, gas-drying apparatus, gas flowmeter, stainless steel reactor, cooling and dedusting device connect successively, stainless steel reactor passes the tube furnace of band thermocouple temperature programmed control device, substrate is placed on the stainless steel reactor colling end, and stainless steel reactor is connected with Pressure gauge, valve and cooling and dedusting device in turn.
5,, it is characterized in that described reactor stainless steel tube length is 80.0cm, Φ according to the described special equipment of claim 4
Internal diameterBe 1.2cm.
6, the application of the described magnesium negative material of claim 1 is characterized in that it is applied to magnesium/air cell, Mg-MnO
2, Mg-Ag
2The magnesium base battery of O or Mg-seawater battery.
7, according to the application of the described magnesium negative material of claim 6, it is characterized in that described magnesium/air cell is made up of magnesium negative electrode gel, cellulose barrier film and air electrode, wherein 90wt% nanometer Mg, 5wt% carbon black, 2wt% sodium carboxymethylcellulose gel and 3wt% additive transition metal Ni, Co and oxide thereof are formed; Air electrode mainly is made of waterproof ventilative layer and catalysis conductive layer, and order from outside to inside is followed successively by waterproof ventilative layer, currect collecting net or nickel foam and catalysis conductive layer; Wherein, waterproof ventilative layer is with acetylene black, PTFE emulsion, Na
2SO
4Mix, ultrasonic to the pasty state roll-forming get catalytic membrane, thickness is 200-400 μ m; Close electrolyte one side Catalytic Layer is by perovskite La
0.6Ca
0.4CoO
3Nanotube, acetylene black, PTFE emulsion, Na
2SO
4Mix ultrasonic to the pasty state roll-forming get catalytic membrane, thickness is 100-400 μ m; La
0.6Ca
0.4CoO
3Nanotube eelctro-catalyst comprehensive utilization sol-gel process and alumina formwork method make, and diameter is 200nm, and the consistency of thickness of length and template is 50-60 μ m, and wall thickness 15nm, electrolyte select for use and added 2.6M Mg (NO
3)
23.6M NaNO
2Neutral electrolyte.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2006100138676A CN100459279C (en) | 2006-05-26 | 2006-05-26 | Magnesium negative material and preparation method and application |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2006100138676A CN100459279C (en) | 2006-05-26 | 2006-05-26 | Magnesium negative material and preparation method and application |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1913219A true CN1913219A (en) | 2007-02-14 |
| CN100459279C CN100459279C (en) | 2009-02-04 |
Family
ID=37722064
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB2006100138676A Expired - Fee Related CN100459279C (en) | 2006-05-26 | 2006-05-26 | Magnesium negative material and preparation method and application |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN100459279C (en) |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102024996A (en) * | 2010-11-26 | 2011-04-20 | 南开大学 | High-performance rechargeable magnesium battery and manufacturing method thereof |
| CN102482788A (en) * | 2009-07-08 | 2012-05-30 | 尚塔尔·查普尔 | System For Converting Energy With An Enhanced Electric Field |
| CN101997107B (en) * | 2009-08-11 | 2012-12-26 | 中国电子科技集团公司第十八研究所 | Magnesium electrode for magnesium battery and preparation method thereof |
| CN103028734A (en) * | 2013-01-14 | 2013-04-10 | 北京科技大学 | Method for preparing nanometer magnesium |
| CN104846433A (en) * | 2015-04-23 | 2015-08-19 | 北京科技大学 | Method for high vacuum preparation of magnesium nano-wires |
| CN109638221A (en) * | 2018-12-19 | 2019-04-16 | 深圳先进技术研究院 | Negative electrode material, cathode and preparation method thereof and negative electrode slurry, secondary cell and electrical equipment |
| CN111933954A (en) * | 2020-08-07 | 2020-11-13 | 中科院过程工程研究所南京绿色制造产业创新研究院 | Air electrode, preparation method thereof and air battery |
| CN114951635A (en) * | 2022-06-17 | 2022-08-30 | 福州市微纳新创医疗科技有限公司 | Magnesium nanoparticle with controllable size and shape, preparation method, regulation method and application thereof |
| CN115188955A (en) * | 2022-06-28 | 2022-10-14 | 中国科学院青岛生物能源与过程研究所 | Composite magnesium metal negative electrode active material with multiphase material and application thereof |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH11345610A (en) * | 1998-06-02 | 1999-12-14 | Matsushita Electric Ind Co Ltd | Negative electrode for battery and manufacture thereof |
| CN1252311C (en) * | 2002-07-17 | 2006-04-19 | 清华大学 | Process for preparing large-area zinc oxide film with nano lines by physical gas-phase deposition |
-
2006
- 2006-05-26 CN CNB2006100138676A patent/CN100459279C/en not_active Expired - Fee Related
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102482788A (en) * | 2009-07-08 | 2012-05-30 | 尚塔尔·查普尔 | System For Converting Energy With An Enhanced Electric Field |
| CN101997107B (en) * | 2009-08-11 | 2012-12-26 | 中国电子科技集团公司第十八研究所 | Magnesium electrode for magnesium battery and preparation method thereof |
| CN102024996A (en) * | 2010-11-26 | 2011-04-20 | 南开大学 | High-performance rechargeable magnesium battery and manufacturing method thereof |
| CN102024996B (en) * | 2010-11-26 | 2012-12-19 | 南开大学 | High-performance rechargeable magnesium battery and manufacturing method thereof |
| CN103028734A (en) * | 2013-01-14 | 2013-04-10 | 北京科技大学 | Method for preparing nanometer magnesium |
| CN103028734B (en) * | 2013-01-14 | 2015-02-11 | 北京科技大学 | Method for preparing nanometer magnesium |
| CN104846433A (en) * | 2015-04-23 | 2015-08-19 | 北京科技大学 | Method for high vacuum preparation of magnesium nano-wires |
| CN104846433B (en) * | 2015-04-23 | 2017-05-10 | 北京科技大学 | Method for high vacuum preparation of magnesium nano-wires |
| CN109638221A (en) * | 2018-12-19 | 2019-04-16 | 深圳先进技术研究院 | Negative electrode material, cathode and preparation method thereof and negative electrode slurry, secondary cell and electrical equipment |
| CN111933954A (en) * | 2020-08-07 | 2020-11-13 | 中科院过程工程研究所南京绿色制造产业创新研究院 | Air electrode, preparation method thereof and air battery |
| CN114951635A (en) * | 2022-06-17 | 2022-08-30 | 福州市微纳新创医疗科技有限公司 | Magnesium nanoparticle with controllable size and shape, preparation method, regulation method and application thereof |
| CN115188955A (en) * | 2022-06-28 | 2022-10-14 | 中国科学院青岛生物能源与过程研究所 | Composite magnesium metal negative electrode active material with multiphase material and application thereof |
| CN115188955B (en) * | 2022-06-28 | 2024-05-14 | 中国科学院青岛生物能源与过程研究所 | Composite magnesium metal anode active material with multiphase material and application thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| CN100459279C (en) | 2009-02-04 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Wu et al. | A review of performance optimization of MOF‐derived metal oxide as electrode materials for supercapacitors | |
| CN107946560B (en) | Carbon-limited domain metal or metal oxide composite nano-structure material and preparation method and application thereof | |
| Ye et al. | Application of different carbon-based transition metal oxide composite materials in lithium-ion batteries | |
| CN1913219A (en) | Magnesium negative material and preparation method and application | |
| Zhang et al. | Metal–organic framework derived porous CuO/Cu 2 O composite hollow octahedrons as high performance anode materials for sodium ion batteries | |
| Xu et al. | Carbon-encapsulated Co3O4@ CoO@ Co nanocomposites for multifunctional applications in enhanced long-life lithium storage, supercapacitor and oxygen evolution reaction | |
| CN108390014B (en) | Preparation method of foam nickel loaded cobalt monoxide nano material with different morphologies | |
| Chu et al. | NiO nanocrystals encapsulated into a nitrogen-doped porous carbon matrix as highly stable Li-ion battery anodes | |
| Zhao et al. | Intercalating petroleum asphalt into electrospun ZnO/Carbon nanofibers as enhanced free-standing anode for lithium-ion batteries | |
| CN108711611B (en) | Three-dimensional high-density metal nanoparticle/graphene porous composite material and preparation method and application thereof | |
| Wang et al. | Hydrothermal synthesis and electrochemical performance of NiO microspheres with different nanoscale building blocks | |
| Jiang et al. | A novel CoO hierarchical morphologies on carbon nanofiber for improved reversibility as binder-free anodes in lithium/sodium ion batteries | |
| CN108962632B (en) | Preparation method of graphene/nitrogen-doped carbon/nickel oxide composite material | |
| CN108773859B (en) | Vulcanized nano material and preparation method and application thereof | |
| CN109748282B (en) | Method for preparing nano silicon carbide at low temperature | |
| Yang et al. | Nanoengineering of ZnCo2O4@ CoMoO4 heterogeneous structures for supercapacitor and water splitting applications | |
| Wei et al. | Inherently porous Co3O4@ NiO core–shell hierarchical material for excellent electrochemical performance of supercapacitors | |
| Liu et al. | A simple hydrothermal method for the preparation of 3D petal-like Ni (OH) 2/g-C3N4/RGO composite with good supercapacitor performance | |
| Zhao et al. | Metal-organic framework derived nickel‑cobalt layered double hydroxide nanosheets cleverly constructed on interconnected nano-porous carbon for high-performance supercapacitors | |
| CN110350170A (en) | A kind of preparation method of lithium titanate/graphene composite material | |
| Wang et al. | Natural cellulose derived nanofibrous Ag-nanoparticle/SnO2/carbon ternary composite as an anodic material for lithium-ion batteries | |
| CN103840176A (en) | Three-dimensional graphene-based combined electrode with Au nanoparticle-loaded surface, and preparation method and applications thereof | |
| CN103078120A (en) | Ferrous silicate lithium ion battery cathode material with hierarchical structure and preparation method | |
| Liu et al. | Hexadecyl trimethyl ammonium bromide assisted growth of NiCo 2 O 4@ reduced graphene oxide/nickel foam nanoneedle arrays with enhanced performance for supercapacitor electrodes | |
| CN1895993A (en) | Nano-silicone wire/carbon composite material, its preparation and use |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| C17 | Cessation of patent right | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20090204 Termination date: 20120526 |