CN1630122A - Anode catalyst for direct methanol fuel battery and method for making same - Google Patents

Anode catalyst for direct methanol fuel battery and method for making same Download PDF

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CN1630122A
CN1630122A CNA2004100518750A CN200410051875A CN1630122A CN 1630122 A CN1630122 A CN 1630122A CN A2004100518750 A CNA2004100518750 A CN A2004100518750A CN 200410051875 A CN200410051875 A CN 200410051875A CN 1630122 A CN1630122 A CN 1630122A
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catalyst
solution
fuel cell
anode catalyst
methanol fuel
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CN1283016C (en
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周震涛
刘文杰
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South China University of Technology SCUT
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Abstract

This invention discloses anode catalyst Pt-Co-W/C for methanol fuel cell and preparation method, the liquid phase deposition reduction method, which contains (1), mixing deionized water and isopropyl alcohol according to definite mol ratio and adding carbon black and dispersion, (2), adding suitable chloroplatinic acid, cobalt chloride and sodium tungstate solution in mixed system and adjusting system pH by sodium bicarbonate solution, (3), washing, pumping filtering and drying.

Description

Direct methanol fuel cell anode catalyst and preparation method thereof
Technical field
The present invention relates to fuel cell field, more specifically relate to a kind of direct methanol fuel cell anode three-way catalyst.The invention still further relates to this Preparation of catalysts method.
Background technology
Fuel cell is a kind of Blast Furnace Top Gas Recovery Turbine Unit (TRT) that chemical energy is directly changed into electric energy by chemical reaction.Fuel cell can be divided into alkaline fuel cell, Solid Oxide Fuel Cell, molten carbonate fuel cell, phosphoric acid fuel cell and Proton Exchange Membrane Fuel Cells by the electrolytical difference of use.And Proton Exchange Membrane Fuel Cells (claiming polymer-membrane fuel battery) be after alkaline fuel cell, Solid Oxide Fuel Cell, molten carbonate fuel cell, phosphoric acid fuel cell, grow up the 5th generation fuel cell.Proton Exchange Membrane Fuel Cells (PEMFC) but have the restriction, high power density, high-energy conversion efficiency of the Carnot cycle of not being subjected to, pollution-free, high-energy-density, no burn into cold-starting, compact conformation and advantage such as easy to maintenance, promise to be the electrical source of power of motor vehicle, Move tool most.Now, because global energy crisis and environmental pollution are on the rise, caused people's extensive concern in recent years as Proton Exchange Membrane Fuel Cells novel, efficient, clear energy sources.
Proton Exchange Membrane Fuel Cells (PEMFC) can be divided into two classes according to the difference of fuel: a class is to be the fuel cell of fuel with hydrogen or reformation gas; Another kind of is to be the fuel cell of fuel with methyl alcohol directly, claims direct methanol fuel cell (DMFC) again.Originally, the fuel cell that with the hydrogen/oxygen is fuel is optimal chemical power source, but because the existing insecurity of preparation, transportation, storage and use of its fuel, thus in recent years people to have proposed be the notion of the direct methanol fuel cell (DMFC) of fuel with methyl alcohol directly.Direct methanol fuel cell (DMFC) does not need methyl alcohol is changed into hydrogen, utilizes methyl alcohol directly to react on electrode and makes chemical energy change electric energy into, uses for load.Because under energy density height in organic solvent of the fuel methanol of DMFC, the room temperature is that liquid, toxicity are not high, cheap, adds the simplicity of design of DMFC, thereby gets a good chance of the electrical source of power as Move tool, motor vehicle etc.Although DMFC has vast potential for future development and tempting application market, also exist some technical barriers restricting application and the development of DMFC so far.Alcohol-rejecting ability such as used perfluorinated sulfonic acid proton exchange membrane (Nafion film) is poor, can occur more serious saturating pure phenomenon, used Pt catalyst when being used for DMFC and easily be poisoned by the intermediate product CO that course of reaction produced and cost an arm and a leg etc.More particularly, mainly there are following three problems in DMFC with catalyst: the electro catalytic activity of catalyst is not high, catalyst is poisoned easily and the costing an arm and a leg of catalyst.Current, the anode catalyst of DMFC mainly is that the high carbon of bullion content carries binary platinum alloy.Wherein Pt-Ru/C is the anode catalyst that generally acknowledged at present DMFC uses preferably.But in above-mentioned catalyst, the intermediate products such as CO that the oxidized process of methyl alcohol is produced can be attracted on the surface of catalyst consumingly, in occupation of the reaction active site of catalyst surface and be difficult to be come out by desorption, cause the partition of getting in touch between catalyst and the reactant, thereby the catalytic efficiency of catalyst is reduced, the problem of catalyst poisoning occurs.In addition, be that Pt or Ru are rare metals, shortage of resources, cost an arm and a leg, be unfavorable for that DMFC realizes commercially producing on a large scale.Having the professional person to do statistics, is 0.5mg/cm according to the consumption of Pt in the present DMFC catalyst 2Calculate, even the explored Pt reserves in the whole world are all used, also only enough millions of DMFC electric automobiles use.
Consider that metal Co and W have and stronger help that catalytic capability, resource are abundant, price is relative more cheap, so the present invention, substitute rare metal Ru among the background technology Pt-Ru/C with transition metal Co and W,, processing ease simple, power consumption with technology less, safety, and the structure of product is easy to control, the uniform liquid deposition reducing process of particle size prepares that resource is abundant, price is cheaper, catalytic activity is high and DMFC with strong resisting CO poison ability with anode three-way catalyst Pt-Co-W/C.
Summary of the invention
The objective of the invention is to shortcoming, the direct methanol fuel cell that a kind of raw material sources are abundant, cheap, electro catalytic activity is high and the resisting CO poison ability is strong anode catalyst is provided at the prior art existence.
Another object of the present invention provides a kind of simple for process, low, safety of power consumption of this catalyst, and the structure of product and the performance preparation method that can control.
Direct methanol fuel cell of the present invention is called the liquid deposition reducing process with the preparation method of anode catalyst, specifically comprises the steps:
(1) with the mixed of deionized water and isopropyl alcohol 1.0: 1.0 in molar ratio～4.0, add the carrier of carbon black as catalyst, under 40～90 ℃, disperse 20～60min with supersonic oscillations, present ink-like until mixed system;
(2) mixed system that step (1) is obtained stirs 0.5～2.5h with mixer under 40～90 ℃ constant temperature; Press Pt: Co: W=1.0 then: 0.2～0.6: 0.2～1.0 atomic molar is than the aqueous solution that adds chloroplatinic acid, cobalt chloride and sodium tungstate;
(3) under 40～90 ℃, be 8～13 with the pH value of sodium bicarbonate solution regulating step (2) gained solution, dropwise drip formaldehyde or sodium formate solution, be reduced fully to metallic element, the time of reduction reaction is 1～4h;
(4) product of usefulness deionized water cyclic washing step (3) gained, suction filtration, chloride ion-containing not in system, product is put into vacuum drying chamber at 80～140 ℃ of following vacuumize 1～24h, dried product cooling back is taken out, cross 400 mesh sieves, thereby prepare direct methanol fuel cell anode catalyst Pt-Co-W/C.
Preferred plan of the present invention comprises the steps:
(1) with the mixed of deionized water and isopropyl alcohol 1.0: 1.0 in molar ratio～2.5, add the carrier of carbon black as catalyst, under 55～75 ℃, disperse 30～50min with supersonic oscillations, present ink-like until mixed system;
(2) mixed system that step (1) is obtained stirs 0.5～2.5h with mixer under 55～75 ℃ constant temperature; Press Pt: Co: W=1.0 then: 0.2～0.4: 0.8～1.0 atomic molar is than the aqueous solution that adds chloroplatinic acid, cobalt chloride and sodium tungstate;
(3) under 45～75 ℃, the pH value that obtains solution with sour hydrogen sodium solution regulating step (2) is 9～12, dropwise drips formaldehyde or sodium formate solution, is reduced fully to metallic element, and the time of reduction reaction is 1～4h;
(4) product of usefulness deionized water cyclic washing step (3) gained, suction filtration, chloride ion-containing not in system, product is put into vacuum drying chamber at 90～130 ℃ of following vacuumize 5～18h, dried product cooling back is taken out, cross 400 mesh sieves, thereby prepare direct methanol fuel cell anode catalyst Pt-Co-W/C.
Reaction mechanism of the present invention: 1, methyl alcohol is adsorbed to the surperficial of electrode catalyst and progressively takes off proton and form the carbon containing intermediate product; 2, oxygenated species participates in reaction, and the carbon containing intermediate product is removed in oxidation.In the process of reaction, some reaction intermediate CO type objects are adsorbed on the surface of the effective ingredient Pt of catalyst consumingly, occupy the active sites of catalyst surface, stop the further absorption of first alcohol and water to be decomposed, cause catalyst poisoning, reduce the utilization ratio of catalyst.Metal W in the catalyst of the present invention is with oxidation state WO 3Form have WO 3Played a kind of effect of active carrier.Electrochemical reaction on the Pt can be transferred to WO like this 3Carry out on the carrier.This situation is called hydrogen meter face overflow effect (Hydrogen Spillorver Effect).By this effect, the dehydrogenation oxidation of methyl alcohol can be at WO 3On carry out WO 3With H xWO 3Form transmit proton, make methanol dehydrogenation form (CO) Ads, make water decomposition form (OH) simultaneously Ads, Pt also simultaneously can form (OH) Ads, make (CO) AdsOxidized under lower electromotive force, and WO 3Existence also make Pt to (CO) AdsAbsorption weaken.Because the atomic structure of metal Co has more d unoccupied orbital than the atomic structure of Pt, the d electronics can shift from the unoccupied orbital of Pt track to Co, the empty d track of Pt is the easier acceptor that becomes the oxygen lone pair electrons just, thereby strengthened the absorption affinity of Pt to oxygenated species, make between metal and the oxygen to interact byer force, oxygenated species is easier to be attracted on the surface of metallic atom.While, the overflow effect of hydrogen meter face strengthened owing to electronics flows, and had weakened the influence of poisonous middle CO class product to the catalytic active site of Pt.And the adding of Co also can promote the formation of Pt lattice defect.These all help the raising of catalyst electrocatalysis characteristic.
Compare with background technology, the present invention has following advantage:
1, three-way catalyst Pt-Co-W/C of the present invention is suitable to the electro catalytic activity of the electro catalytic activity of methyl alcohol and existing binary catalyst Pt-Ru/C, but has the resisting CO poison ability stronger than Pt-Ru/C catalyst;
2, Pt-Co-W/C three-way catalyst of the present invention is compared with the Pt-Ru/C binary catalyst of prior art, and transition metal W that is adopted and Co are abundanter than the resource of precious metal element Ru, cost is relatively low honest and clean;
3, simple, the processing ease of Preparation of catalysts method technology of the present invention, energy consumption is low, fail safe good, and controlled, the constant product quality of the structure of product.
Description of drawings
Fig. 1 is used for the current-voltage polarization curve of direct methanol fuel cell monomer for the commercially available Pt-Ru/C binary catalyst of the Pt-Co-W/C three-way catalyst of the present invention of embodiment 1 preparation and prior art;
Fig. 2 is the cyclic voltammetry curve of embodiment 1, embodiment 2 and the Pt-Co-W/C three-way catalyst of the of the present invention different atomic molar proportionings of embodiment 3 preparations, and sweep speed is 10mv/s;
Fig. 3 is the cyclic voltammetry curve of embodiment 1, embodiment 4 and the Pt-Co-W/C three-way catalyst product of the different preparation temperatures of the present invention of embodiment 5 preparations, and sweep speed is 10mv/s;
Fig. 4 is the cyclic voltammetry curve of the embodiment 1 and the Pt-Co-W/C three-way catalyst of the different carbon carriers of the present invention of embodiment 6 preparations, and sweep speed is 10mv/s;
Fig. 5 is the cyclic voltammetry curve of the present invention of embodiment 1 and embodiment 7 preparations with the Pt-Co-W/C three-way catalyst of different reducing agent preparations, and sweep speed is 10mv/s.
Embodiment
The invention will be further described below in conjunction with Figure of description and specific embodiment.The test system of the electrocatalysis characteristic of catalyst of the present invention and resisting CO poison ability thereof is as follows:
(1) catalytic performance of utilization cyclic voltammetry test catalyst of the present invention: with catalyst and solid content is that 5% polytetrafluoroethylene (PTFE) emulsion is mixed, be coated on the glass-carbon electrode as the research electrode, to electrode, saturated calomel electrode (SCE) is as reference electrode, at 0.5M H with pure platinized platinum conduct 2SO 4With 0.5M CH 3In the mixed solution of OH, with the sweep speed of 10mv/s, the current-voltage polarization curve of this catalyst oxidation methyl alcohol of test under 80 ℃ of conditions.
(2) by homemade apparatus, be assembled into the direct methanol fuel cell monocell, the catalysis that detects Pt-Co-W/C ternary anode catalyst of the present invention is qualitative, the ability of resisting CO poison.Monocell is to be anode catalyst with Pt-Co-W/C, and Pt/C is a cathod catalyst, and working temperature is 80 ℃, and methanol in water concentration is 2M, adopts the feeding manner of direct liquid, and the feed rate of methanol solution is 6ml/min.Cathode oxidant is an atmospheric air.
Embodiment 1
Get 100mg Vulcan XC-72 carbon black, the isopropyl alcohol of putting into the 200ml mol ratio and being 1.0: 1.0 mixes with the solution of deionized water, disperses 30min with supersonic oscillations under 70 ℃, is ink-like to system.Then, according to prepared catalyst Pt: Co: W metallic atom mol ratio is Pt: Co: W=1.0: 0.2: 1.0 ratio adds the platinum acid chloride solution 5.070g that concentration is 1wt%, the CoCl of 5wt% successively 2The Na of solution 0.0932g, 5wt% 2WO 4Solution 646mg continues to stir 1.5h with blender under 70 ℃ condition.PH with the sodium bicarbonate solution regulation system is 10.Dropwise drip formalin then, be reduced fully to metallic element, the reduction reaction time is 2.5 hours, with deionized water rinsing, suction filtration, does not contain chloride ion in system, puts into vacuum drying chamber then in 120 ℃ of following vacuumize 8h.The cooling of dried product is taken out, cross 400 mesh sieves, and be Pt: Co: W=1.0: 0.2: 1.0 direct methanol fuel cell anode catalyst from preparing metallic atom mole atomic ratio.
Adopt make among this embodiment of self-control Pt-Co-W/C three-way catalyst and Pt percentage by weight be that 20% Pt/C (E-TEK) catalyst is respectively as anode and cathod catalyst.Negative electrode, anode Pt content are 0.5mg/cm 2With a certain amount of catalyst and 5wt%Nafion solution, solid content is after the PTFE of 5wt% mixes, disperse 30min with supersonic oscillations, be applied to after fully mixing is uniformly dispersed on the carbon paper that the PTFE emulsion that former content is 30wt% was handled, then under 110 ℃ of conditions, vacuumize 1h is again to Catalytic Layer surface spray one deck Nafion solution (0.8mg/cm 2).Negative electrode, anode-catalyzed aspect are placed on the two sides of treated Nafion115 film, under 120 ℃ and 10Mpa condition, carry out hot pressing, make three in one membreane electrode, cool off stand-by.Three in one membreane electrode is fastened on the side that bipolar plates has runner with sealing ring, is assembled into monocell, the anode methanol concentration is 2M, and flow velocity is 6ml/min.The cathode terminal oxidant is an air, normal pressure.Test result as shown in Figure 1.As can be seen from Figure 1, the prepared catalyst activity with Pt-Ru/C on the methanol oxidation catalytic activity of patent of the present invention is suitable substantially.
Take by weighing a certain amount of Pt-Co-W/C eelctro-catalyst of the present invention, add an amount of absolute ethyl alcohol and solid content and be 5% PTFE emulsion.After sonic oscillation is uniformly dispersed, drip several surfaces that drop in the platinum carbon electrode, after the vacuumize.Be that research electrode, calomel electrode are that reference electrode, platinum electrode carry out the cyclic voltammetric test in to the three-electrode system of electrode with the glass-carbon electrode of handling, test is at 0.5MH 2SO 4And 0.5MCH 3Carry out in the mixed solution of OH, sweep speed is 10mv/s.Cyclic voltammetry curve under the normal temperature condition as shown in Figure 2.As can be seen from Figure 2, total metal content atomic molar ratio is Pt: Co: W=1.0: 0.2: 1.0 catalyst methanol oxidation current density reaches 35mA/cm 2, have best catalytic activity.
Embodiment 2
Get 100mgVulcan XC-72 carbon black, the isopropyl alcohol of putting into the 200ml mol ratio and being 1.0: 2.5 mixes with the solution of deionized water, disperses 40min to be ink-like to system with supersonic oscillations under 70 ℃.Then, be Pt: Co: W=1.0 according to metallic atom mol ratio in the prepared catalyst: 0.6: 0.2 standard adds the platinum acid chloride solution 2.9600g that concentration is 1wt%, the CoCl of 5wt% successively 2The Na of solution 0.1632g, 5wt% 2WO 4Solution 75.4mg continues to stir 0.5h with blender under 70 ℃ condition.PH with the sodium bicarbonate solution regulation system is 11.Dropwise drip formalin then, be reduced fully to metallic element, the reduction reaction time is 1 hour, with deionized water rinsing, suction filtration, does not contain chloride ion in system, puts into vacuum drying chamber then in 80 ℃ of following vacuumize 24h.The cooling of dried product is taken out, cross 400 mesh sieves, and be Pt: Co: W=1.0: 0.6: 0.2 direct methanol fuel cell anode catalyst from preparing the metallic atom mol ratio.
Take by weighing a certain amount of Pt-Co-W/C eelctro-catalyst of the present invention, add an amount of absolute ethyl alcohol and solid content and be 5% PTFE emulsion.After sonic oscillation is uniformly dispersed, drip several surfaces that drop in the platinum carbon electrode, after the vacuumize.Be that research electrode, calomel electrode are that reference electrode, platinum electrode carry out the cyclic voltammetric test in to the three-electrode system of electrode with the glass-carbon electrode of handling, test is at 0.5MH 2SO 4And 0.5MCH 3Carry out in the mixed solution of OH, sweep speed is 10mv/s.Cyclic voltammetry curve under the normal temperature condition as shown in Figure 2.As can be seen from Figure 2, the metallic atom mol ratio is that 1.0: 0.6: 0.2 catalyst has methanol oxidation catalytic activity preferably.
Embodiment 3
Get 100mg Vulcan XC-72 carbon black, the isopropyl alcohol of putting into the 200ml mol ratio and being 1.0: 4.0 mixes with the solution of deionized water, disperses 50min with supersonic oscillations under 70 ℃, is ink-like to system.Then, be Pt: Co: W=1.0 according to metallic atom ratio in the prepared catalyst: 0.5: 0.5 standard adds the platinum acid chloride solution 9.68g that concentration is 1wt%, the CoCl of 5wt% successively 20.4550g the Na of solution, 5wt% 2WO 4Solution 616.5mg continues to stir 2.5h with blender under 70 ℃ condition.PH with the sodium bicarbonate solution regulation system is 10.Dropwise drip formalin then, be reduced fully to metallic element, the reduction reaction time is 3 hours, with a large amount of deionized water rinsings, suction filtration, does not contain chloride ion in system, puts into vacuum drying chamber then in 140 ℃ of following vacuumize 1h.The cooling of dried product is taken out, cross 400 mesh sieves, and be Pt: Co: W=1.0: 0.5: 0.5 direct methanol fuel cell anode catalyst from preparing the metallic atom mol ratio.
Take by weighing a certain amount of Pt-Co-W/C eelctro-catalyst of the present invention, add an amount of absolute ethyl alcohol and solid content and be 5% PTFE emulsion.After sonic oscillation is uniformly dispersed, drip several surfaces that drop in the platinum carbon electrode, after the vacuumize.Be that research electrode, calomel electrode are that reference electrode, platinum electrode carry out the cyclic voltammetric test in to the three-electrode system of electrode with the glass-carbon electrode of handling, test is at 0.5MH 2SO 4And 0.5MCH 3Carry out in the mixed solution of OH, sweep speed is 10mv/s.Cyclic voltammetry curve under the normal temperature condition as shown in Figure 2.As can be seen from Figure 2, metallic atom mol ratio Pt: Co: W=is that 1.0: 0.5: 0.5 catalyst has methanol oxidation catalytic activity preferably.
Embodiment 4
Get 100mg Vulcan XC-72 carbon black, the isopropyl alcohol of putting into the 200ml mol ratio and being 1.0: 2.0 mixes with the solution of deionized water, disperses 40min with supersonic oscillations under 40 ℃, is ink-like to system.Then, be Pt: Co: W=1.0 according to metallic atom mol ratio in the prepared catalyst: 0.2: 1.0 standard adds the platinum acid chloride solution 5.070g that concentration is 1wt%, the CoCl of 5wt% successively 2The Na of solution 0.0932g, 5wt% 2WO 4Solution 646mg continues to stir 1h with blender under 40 ℃ condition.PH with the sodium bicarbonate solution regulation system is 12.Dropwise drip formalin then, be reduced fully to metallic element, the reduction reaction time is 4 hours, with a large amount of deionized water rinsings, suction filtration, does not contain chloride ion in system, puts into vacuum drying chamber then in 90 ℃ of following vacuumize 12h.The cooling of dried product is taken out, cross 400 mesh sieves, and be Pt: Co: W=1.0: the direct methanol fuel cell anode catalyst that is at 0.2: 1.0 from preparing the metallic atom mol ratio.
Take by weighing a certain amount of Pt-Co-W/C eelctro-catalyst of the present invention, add an amount of absolute ethyl alcohol and solid content and be 5% PTFE emulsion.After supersonic oscillations are uniformly dispersed, drip several surfaces that drop in the platinum carbon electrode, after the vacuumize.Be that research electrode, calomel electrode are that reference electrode, platinum electrode carry out the cyclic voltammetric test in to the three-electrode system of electrode with the glass-carbon electrode of handling, test is at 0.5MH 2SO 4And 0.5MCH 3Carry out in the mixed solution of OH, sweep speed is 10mv/s.Cyclic voltammetry curve under the normal temperature condition as shown in Figure 3.As can be seen from Figure 3, the catalyst of present embodiment preparation has methanol oxidation catalytic activity preferably.
Embodiment 5
Get 100mgVulcan XC-72 carbon black, the isopropyl alcohol of putting into the 200ml mol ratio and being 1.0: 1.5 mixes with deionized water solution, disperses 45min with supersonic oscillations under 90 ℃, is ink-like to system.Then, be Pt: Co: W=1.0 according to metallic atom mol ratio in the prepared catalyst: 0.2: 1.0 standard adds the platinum acid chloride solution 5.070g that concentration is 1wt%, the CoCl of 5wt% successively 2The Na of solution 0.0932g, 5wt% 2WO 4Solution 646mg continues to stir 2.5h with blender under 90 ℃ condition.PH with the sodium bicarbonate solution regulation system is 13.Dropwise drip formalin then, be reduced fully to metallic element, the reduction reaction time is 3 hours, with a large amount of deionized water rinsings, suction filtration, does not contain chloride ion in system, puts into vacuum drying chamber then in 130 ℃ of following vacuumize 7h.The cooling of dried product is taken out, cross 400 mesh sieves, and be Pt: Co: W=1.0: 0.2: 1.0 direct methanol fuel cell anode catalyst from preparing the metallic atom mol ratio.
Take by weighing a certain amount of Pt-Co-W/C eelctro-catalyst of the present invention, add an amount of absolute ethyl alcohol and solid content and be 5% PTFE emulsion.After supersonic oscillations are uniformly dispersed, drip several surfaces that drop in the platinum carbon electrode, after the vacuumize.Be that research electrode, calomel electrode are that reference electrode, platinum electrode carry out the cyclic voltammetric test in to the three-electrode system of electrode with the glass-carbon electrode of handling, test is at 0.5MH 2SO 4And 0.5MCH 3Carry out in the mixed solution of OH, sweep speed is 10mv/s.Cyclic voltammetry curve under the normal temperature condition as shown in Figure 3.As can be seen from Figure 3, the catalyst of present embodiment preparation has methanol oxidation catalytic activity preferably.
Embodiment 6
Get 100mg acetylene black, the isopropyl alcohol of putting into the 200ml mol ratio and being 1.0: 4.0 mixes with deionized water solution, disperses 60min with supersonic oscillations under 70 ℃, is ink-like to system.Then, be Pt: Co: W=1.0 according to metallic atom mol ratio in the prepared catalyst: 0.2: 1.0 standard adds the platinum acid chloride solution 5.07g that concentration is 1wt%, the CoCl of 5wt% successively 2The Na of solution 0.0932g, 5wt% 2WO 4Solution 646mg continues to stir 1.5h with blender under 70 ℃ condition.The pH that regulates with sodium bicarbonate solution is 11.Dropwise drip formalin then, be reduced fully to metallic element, the reduction reaction time is 2 hours, with a large amount of deionized water rinsings, suction filtration, does not contain chloride ion in system, puts into vacuum drying chamber then in 140 ℃ of following vacuumize 5h.The cooling of dried product is taken out, cross 400 mesh sieves, and be Pt: Co: W=1.0: 0.2: 1.0 direct methanol fuel cell anode catalyst from preparing the metallic atom mol ratio.
Take by weighing a certain amount of Pt-Co-W/C eelctro-catalyst of the present invention, add an amount of absolute ethyl alcohol and solid content and be 5% PTFE emulsion.After supersonic oscillations are uniformly dispersed, drip several surfaces that drop in the platinum carbon electrode, after the vacuumize.Be that research electrode, calomel electrode are that reference electrode, platinum electrode carry out the cyclic voltammetric test in to the three-electrode system of electrode with the glass-carbon electrode of handling, test is at 0.5MH 2SO 4And 0.5MCH 3Carry out in the mixed solution of OH, sweep speed is 10mv/s.Cyclic voltammetry curve under the normal temperature condition as shown in Figure 4.As can be seen from Figure 4, the catalyst of present embodiment preparation has methanol oxidation catalytic activity preferably.
Embodiment 7
Get 100mgVulcan XC-72 carbon black, the isopropyl alcohol of putting into the 200ml mol ratio and being 1.0: 2.0 mixes with deionized water solution, disperses 30min with supersonic oscillations under 70 ℃, is ink-like to system.Then, be Pt: Co: W=1.0 according to metallic atom mol ratio in the prepared catalyst: 0.2: 1.0 standard adds the CoCl that concentration is 1wt% platinum acid chloride solution 5.07g, 5wt% successively 2The Na of solution 0.0932g, 5wt% 2WO 4Solution 646mg continues to stir 2h with blender under 70 ℃ condition.PH with the sodium bicarbonate solution regulation system is 7.Dropwise drip sodium formate solution then, sustained response 4 hours with a large amount of deionized water rinsings, suction filtration, does not contain chloride ion in system, puts into vacuum drying chamber then in 110 ℃ of following vacuumize 12h.The cooling of dried product is taken out, cross 400 mesh sieves, and be Pt: Co: W=1.0: 0.2: 1.0 direct methanol fuel anode catalyst from preparing the metallic atom mol ratio.
Take by weighing a certain amount of Pt-Co-W/C eelctro-catalyst of the present invention, add an amount of absolute ethyl alcohol and solid content and be 5% PTFE emulsion.After supersonic oscillations are uniformly dispersed, drip several surfaces that drop in the platinum carbon electrode, after the vacuumize.Be that research electrode, calomel electrode are that reference electrode, platinum electrode carry out the cyclic voltammetric test in to the three-electrode system of electrode with the glass-carbon electrode of handling, test is at 0.5MH 2SO 4And 0.5MCH 3Carry out in the mixed solution of OH, sweep speed is 10mv/s.Cyclic voltammetry curve under the normal temperature condition as shown in Figure 5.As can be seen from Figure 5, the catalyst of present embodiment preparation has methanol oxidation catalytic activity preferably.

Claims (4)

1, a kind of direct methanol fuel cell becomes the liquid deposition reducing process with the preparation method of anode catalyst, specifically comprises the steps:
(1) with the mixed of deionized water and isopropyl alcohol 1.0: 1.0 in molar ratio～4.0, add the carrier of carbon black as catalyst, under 40～90 ℃, disperse 20～60min with supersonic oscillations, present ink-like until mixed system;
(2) mixed system that step (1) is obtained stirs 0.5～2.5h with mixer under 40～90 ℃ constant temperature; Press Pt: Co: W=1.0 then: 0.2～0.6: 0.2～1.0 atomic molar is than the aqueous solution that adds chloroplatinic acid, cobalt chloride and sodium tungstate;
(3) under 40～90 ℃, the pH value of regulating step (2) gained solution is 7～13, dropwise drips formaldehyde or sodium formate solution, is reduced fully to metallic element, and the time of reduction reaction is 1～4h;
(4) product of usefulness deionized water cyclic washing step (3) gained, suction filtration, chloride ion-containing not in system, product is put into vacuum drying chamber at 80～140 ℃ of following vacuumize 1～24h, dried product cooling back is taken out, cross 400 mesh sieves, thereby prepare direct methanol fuel cell anode catalyst Pt-Co-W/C.
2, direct methanol fuel cell according to claim 1 is characterized in that comprising the steps: with the preparation method of anode catalyst
(1) with the mixed of deionized water and isopropyl alcohol 1.0: 1.0 in molar ratio～2.5, add the carrier of carbon black as catalyst, under 55～75 ℃, disperse 30～50min with supersonic oscillations, present ink-like until mixed system;
(2) mixed system that step (1) is obtained stirs 1.0～2.5h with mixer under 55～75 ℃ constant temperature; Press Pt: Co: W=1.0 then: 0.2～0.4: 0.8～1.0 atomic molar is than the aqueous solution that adds chloroplatinic acid, cobalt chloride and sodium tungstate;
(3) under 45～75 ℃, with sodium bicarbonate solution regulating step (2) the pH value of solution is 9～12, dropwise drip formaldehyde or sodium formate solution, be reduced fully to metallic element, the time of reduction reaction is 1～4h;
(4) product of usefulness deionized water cyclic washing step (3) gained, suction filtration, chloride ion-containing not in system, product is put into vacuum drying chamber at 90～140 ℃ of following vacuumize 5～18h, product cooling back is after drying taken out, cross 400 mesh sieves, just prepare direct methanol fuel cell anode catalyst Pt-Co-W/C.
3, the anode catalyst Pt-Co-W/C for preparing with the preparation method of anode catalyst of the described direct methanol fuel cell of claim 1.
4, anode catalyst Pt-Co-W/C according to claim 3 is characterized in that the metallic atom mol ratio is Pt: Co: W=1.0: 0.2～0.6: 0.2～1.0.
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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100462142C (en) * 2007-01-15 2009-02-18 厦门大学 Method for preparing anode catalyst of direct methanol fuel cell
CN104393312A (en) * 2014-11-19 2015-03-04 中国科学院长春应用化学研究所 Preparation method of ultralow platinum-loading capacity Pt-CoP/C anode electrocatalyst for high-activity high-stability direct methanol fuel cell
CN110931808A (en) * 2019-11-11 2020-03-27 中国科学院上海硅酸盐研究所 Pd-WO3Anode electrocatalyst of/C proton exchange membrane fuel cell and its preparing method and use
CN112186204A (en) * 2020-09-30 2021-01-05 华中科技大学 Carbon-supported multi-metal multi-stage material and preparation method and application thereof
CN112599797A (en) * 2020-12-16 2021-04-02 上海电力大学 Bimetallic PtSn/C catalyst for high-activity fuel cell and preparation and application thereof

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100462142C (en) * 2007-01-15 2009-02-18 厦门大学 Method for preparing anode catalyst of direct methanol fuel cell
CN104393312A (en) * 2014-11-19 2015-03-04 中国科学院长春应用化学研究所 Preparation method of ultralow platinum-loading capacity Pt-CoP/C anode electrocatalyst for high-activity high-stability direct methanol fuel cell
CN110931808A (en) * 2019-11-11 2020-03-27 中国科学院上海硅酸盐研究所 Pd-WO3Anode electrocatalyst of/C proton exchange membrane fuel cell and its preparing method and use
CN112186204A (en) * 2020-09-30 2021-01-05 华中科技大学 Carbon-supported multi-metal multi-stage material and preparation method and application thereof
CN112599797A (en) * 2020-12-16 2021-04-02 上海电力大学 Bimetallic PtSn/C catalyst for high-activity fuel cell and preparation and application thereof

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