CN105047953B - Base metal nitrogen carbon type oxygen reduction catalyst and preparation method thereof - Google Patents
Base metal nitrogen carbon type oxygen reduction catalyst and preparation method thereof Download PDFInfo
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
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- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
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Abstract
The present invention discloses a kind of M N C oxygen reduction catalysts and preparation method thereof.The raw material of the catalyst includes the polymer P (TPT) and base metal salt of tripyrrole [1,3,5] triazine (TPT)；Its preparation method comprises the following steps：(1) polymer P (TPT) of tripyrrole [1,3,5] triazine (TPT) is synthesized using Friedel Crafts；(2) P (TPT), base metal salt are added in ethanol, being placed in ultrasound in ultrasonic disperse instrument makes whole system be uniformly dispersed, then is evaporated ethanol, is placed in vacuum drying chamber and dries 4h in 80 DEG C；(3) it is heat-treated for the first time, obtains nitrogen-doped carbon material；(4) gained nitrogen-doped carbon material diluted acid is fully washed；(5) it is heat-treated for second, obtains final product M N C oxygen reduction catalysts.
Description
Technical field
It is a kind of M-N-C hydrogen reduction catalysis specifically the present invention relates to a kind of oxygen reduction catalyst and preparation method thereof
Agent and preparation method thereof, belongs to fuel cell science and technology field.
Background technology
Oxygen reduction reaction (oxygen reduction reaction, ORR) is one of most important electrocatalytic reaction, is
Very crucial process in the device such as fuel cell and metal-air battery.Platinum and platinum based catalyst are current catalysis activities
Highest and the most frequently used ORR catalyst, but its expensive, resource-constrained, and long-play stability is not good enough, it is serious to hinder
The development of the association areas such as fuel cell.Therefore, the non-precious metal catalyst of high activity and high stability is researched and developed, to drop
Low fuel battery cost, accelerate its commercialization process significant.
Using preserved on the earth abundant cheap metal element substitution platinum as ORR catalyst undoubtedly have it is considerable before
Scape.Therefore, it is also the focus of current fuel cell field research to the research of base metal ORR catalysis materials.Nitrogen-doped carbon-supported
Base metal (hereinafter referred to as M-N-C) catalyst is obtained generally by various transition metal, nitrogen source and carbon source presoma is heat-treated
Arrive.Nitrogen content and valence state structure in M-N-C catalyst have important influence to catalyst ORR activity and stability.It is logical
Normal nitrogen source persursor material has nitrogenous organic molecule (such as ethylenediamine, ammonia, acetonitrile), nitrogen-containing heterocycle compound (such as neighbour
Ferrosin, phthalocyanine, porphyrin etc.), nitrogenous organic polymer (such as polyaniline, polypyrrole).Carbon source presoma is urged improving M-N-C
Agent activity and stability aspect cut much ice, and content and valence state structure to nitrogen in catalyst suffers from different shadows
Ring.
Cote etc. under the conditions of 1000 DEG C, using different nitrogenous precursors such as polyacrylonitrile, phthalocyanine, 7,7,8,8- tetra- cyanogen
Base 1,4-benzoquinone bismethane, CH3CN、NH3, prepare Fe (OH)2- N-C catalyst, result of study shows, is nitrogen source forerunner with phthalocyanine
ORR activity preferably (the Journal of Catalysis, 2006,239 of the catalyst of body:83-86).Enrburger etc. is studied
It was found that, for same metal salt and nitrogen source presoma, the ORR of the M-N-C catalyst prepared using high-specific surface area carbon carrier is lived
Property (Journal of Colloid and Interface Science, 1983,91 higher:151-159).Chinese patent
CN101859906A disclose it is a kind of by cobalt chloride, nitrogen source (melamine or hexamethylenetetramine), carbon black (acetylene black or
Vulcan XC-72R) mechanical lapping mixing, under nitrogen protection high-temperature heat treatment M-N-C catalyst is obtained.Chinese patent
CN103170334A discloses a kind of carbon and carries cobalt oxide catalyst and its preparation and application, by solvent thermal reaction to carbon carrier
Surface is modified, at room temperature carbon-carried transition metal oxide, and the catalyst ORR activity for obtaining is high, low cost.
Above-mentioned method for preparing catalyst is mostly complex, and preparation process process conditions are difficult to control, and are unfavorable for catalyst
Industrialization.Therefore, cheap, preparation process is simple and the N doping ORR elctro-catalysts with high activity and stability are developed
System, development and industrialization process for promoting fuel cell are significant.
The content of the invention
For problem above, the present invention provides a kind of cheap, preparation process is simple and with high activity and stability
M-N-C oxygen reduction electro-catalysts and preparation method thereof, (P (TPT+Py)) used by the present invention is while before as nitrogen source and carbon source
Body is driven, the more excellent ORR elctro-catalysts of performance can be prepared by simple thermal treatment.
A kind of the first implementation method of the invention, there is provided base metal-nitrogen-carbon type (M-N-C) hydrogen reduction catalysis
Agent (abbreviation M-N-C oxygen reduction catalysts), it is by that will be comprising the polymer of (i) tripyrrole-[1,3,5]-triazine (TPT)
A kind of primary mix of P (TPT) and two kinds of components of (ii) base metal salt in an inert atmosphere 700-1000 DEG C, preferably
Heat treatment for the first time is carried out at a temperature of 750-950 DEG C, more preferably 800-900 DEG C and obtains nitrogen-doped carbon material, then mix nitrogen
Miscellaneous carbon material carries out pickling processes with dilute inorganic acid, finally by the material of pickling in an inert atmosphere 700-1000 DEG C,
It is preferred that carry out second heat treatment at a temperature of 750-950 DEG C, more preferably 800-900 DEG C and finally obtain.
It is preferred that, it is the salt of transition metal as the base metal salt of component (ii)；The preferably nitrate of transition metal, vinegar
Hydrochlorate, sulfate or chloride；Be more preferably selected from Mn, Fe, Co, Ni, Cu one or two or more plant metal
Salt, be more preferably selected from Mn, Fe, Co, Ni, Cu one or two or more plant metal nitrate, acetate, sulfuric acid
Salt or chloride.
It is preferred that, P (TPT) and the mass ratio of the base metal salt as component (ii) as component (i) they are 1:0.06-1,
It is preferred that 1:0.08-0.9, more preferably 1:0.12-0.8, more preferably 1:0.15-0.7, more preferably 1:0.18-0.6, more preferably 1:
0.2-0.5。
It is preferred that, component (i), the polymer of tripyrrole-[1,3,5]-triazine (TPT), i.e. P (TPT), be by tripyrrole-[1,
3,5] alkylating reagent or acylting agent and Friedel-Crafts catalysts of-triazine (TPT) monomer in difunctionality
In the presence of react synthesized by Friedel-Crafts.
It is preferred that, the alkylating reagent of difunctionality described in step (1) is double halo C2-C6 alkanes, straight or branched C2-
C12 olefines, straight or branched C3-C10 dihydroxylic alcohols or with (such as dimethoxymethane of 3-18 bis ether of carbon atom altogether
CH3OCH2OCH3) in one or more.
It is preferred that, the acylting agent of difunctionality is have the 3-12 straight or branched of C carbon atoms pair carboxylic acid halides, altogether altogether
Straight or branched bisgallic acid acid anhydride with 4-8 C carbon atom has the 4-10 straight or branched of C carbon atoms pair carboxylic acids altogether
In one or more.
According to the second embodiment of the present invention, there is provided a kind of preparation method of M-N-C oxygen reduction catalysts or preparation
The method of above-mentioned catalyst, the method is comprised the following steps：
(1) preparation of polymer P (TPT)：By tripyrrole-[1,3,5]-triazine (TPT) monomer in a solvent in difunctionality
Alkylating reagent or acylting agent and Friedel-Crafts catalysts in the presence of by Friedel-Crafts it is anti-
The polymer P (TPT) of tripyrrole-[1,3,5]-triazine (TPT), i.e. component (i) should be prepared,
(2) formation of primary mix：Using the P (TPT) as component (i) of 1 weight portion with 0.06-1 weight portions (preferably
0.08-0.9, more preferably 0.12-0.8, more preferably 0.15-0.7, more preferably 0.18-0.6, more preferably 0.2-0.5 weight portions)
Base metal salt as component (ii) is dispersed in solvent (such as ethanol), dries, and obtains and includes component (i) and component
(ii) a kind of primary mix,
(3) it is heat-treated for the first time：The primary mix that will be obtained in step (2) in an inert atmosphere 700-1000 DEG C,
It is preferred that being once heat-treated at a temperature of 750-950 DEG C, more preferably 800-900 DEG C, nitrogen-doped carbon material is obtained.
(4) acid pickling step：Pickling is carried out to nitrogen-doped carbon material with dilute inorganic acid.
(5) it is heat-treated for second：By through the material after overpickling again in an inert atmosphere 700-1000 DEG C, preferably
Secondary heat treatment is carried out at a temperature of 750-950 DEG C, more preferably 800-900 DEG C, final products M-N-C hydrogen reduction catalysis is obtained
Agent.
More specifically, there is provided a kind of preparation method of M-N-C oxygen reduction catalysts, the method is comprised the following steps：
(1) preparation of polymer P (TPT)：The tripyrrole of 1 weight portion-[1,3,5]-triazine (TPT) is dissolved in solvent (example
Such as 5-50 weight portions, such as 8-40 weight portions, more preferably 10-30 weight portions) in, add 0.5-10 weight portions (preferred 1-4 weight
Part) difunctionality alkylating reagent or acylting agent, additions weight portion be 0.5-12 weight portions (preferably 1.2-6 weight portions)
Friedel-Crafts catalysts, under agitation reaction (for example, in 25-50 DEG C of stirring reaction 2-10 hours (preferably 3-
6 hours), then rise to 60-100 DEG C stirring reaction 15-25 hours)；Reaction is finished, and pours into methyl alcohol or ethanol (such as 60-400 weights
Amount part) in separate, filtering, washing, dry, obtain P (TPT)；
(2) formation of primary mix：Using the P (TPT) as component (i) of 1 weight portion with 0.06-1 weight portions (preferably
0.08-0.9, more preferably 0.12-0.8, more preferably 0.15-0.7, more preferably 0.18-0.6, more preferably 0.2-0.5 weight portions)
In ethanol or methyl alcohol (such as 50~200 parts) being added to as the base metal salt of component (ii), ultrasonication (such as 120
~300min) whole system is uniformly dispersed；Ethanol or methyl alcohol are evaporated, drying (is for example placed in vacuum drying chamber in 60-100
DEG C dry 2-10h), obtain the primary mix comprising copolymer and base metal salt；
(3) it is heat-treated for the first time：By step (2) gained mixture in inert gas at 700-1000 DEG C, preferably 750-
First time heat treatment is carried out at a temperature of 950 DEG C, more preferably 800-900 DEG C, nitrogen-doped carbon material is obtained；
(4) pickling：Gained nitrogen-doped carbon material (for example washs 5 with dilute inorganic acid with dilute inorganic acid in 50~80 DEG C
~10h), filtering dries (be for example placed in vacuum drying chamber and dry 2-10h in 60-100 DEG C) after being washed to neutrality；
(5) it is heat-treated for second：The nitrogen-doped carbon material that step (4) is obtained is again in inert gas in 700-1000
DEG C, carry out second heat treatment at a temperature of preferably 750-950 DEG C, more preferably 800-900 DEG C, obtain final product M-N-C hydrogen reduction catalysis
Agent.
It is preferred that, the alkylating reagent of difunctionality described in step (1) is double halo C2-C6 alkanes, straight or branched C2-
C12 olefines, straight or branched C3-C10 dihydroxylic alcohols or with (such as dimethoxymethane of 3-18 bis ether of carbon atom altogether
CH3OCH2OCH3) in one or more.
It is preferred that, the acylting agent of difunctionality is have the 3-12 straight or branched of C carbon atoms pair carboxylic acid halides, altogether altogether
Straight or branched bisgallic acid acid anhydride with 4-8 C carbon atom has the 4-10 straight or branched of C carbon atoms pair carboxylic acids altogether
In one or more.
It is preferred that, solvent described in step (1) is nitrobenzene, nitromethane, tetrachloroethanes, dichloroethanes, carbon tetrachloride, two
One or more in nitric sulfid.
It is preferred that, Friedel-Crafts catalysts described in step (1) are AlCl3、FeCl3、SnCl4、ZnCl2、
H2SO4、H3PO4、BF3, one or more in HF etc..
It is preferred that, the base metal salt as component (ii) described in step (2) is the salt of transition metal.More preferably cross
Cross nitrate, acetate, sulfate or the chloride of metal.One kind being more preferably selected from Mn, Fe, Co, Ni, Cu or two
Kind or more plants the salt of metal.Be more preferably selected from Mn, Fe, Co, Ni, Cu one or two or more plant metal nitre
Hydrochlorate, acetate, sulfate or chloride.
It is preferred that, the inert gas described in step (3) and (5) is：Ar、He、N2In one or more.
It is preferred that, the dilute inorganic acid described in step (4) is the nothings such as hydrochloric acid, sulfuric acid, nitric acid, phosphoric acid, perchloric acid, hydrofluoric acid
One kind in machine acid.Typically, the concentration of dilute inorganic acid be 0.05~5mol/L, preferably 0.1~3mol/L, more preferably
0.2~1mol/L.
It is preferred that, the halogen atom in above-mentioned pair of halogenated paraffin is one or more in fluorine, chlorine, bromine, iodine.
It is preferred that, heat treatment time described in step (3) and (5) is 30~120min.
The structural formula of tripyrrole-[1,3,5]-triazine (TPT) is in the present invention：
Because the copolymer that the application is obtained has cross-linked structure, therefore, it is difficult to represent that it is tied with accurate structural formula
Structure.
For example, work as using bis ether (such as dimethoxymethane CH3OCH2OCH3) or work as using double halo C2-C6 alkanes (i.e.
X- (CH2) n-X, wherein n is 2-6) as alkylating agent when, the part-structure of polymer P (TPT) is in the present invention：
The methylene (n=1) of wherein alkylidene-(CH2) n-be derived from dimethoxymethane, or from double halogen
For C2-C6 alkanes, such as 1,2- dichloroethanes (n=2), 1,3- dibromopropane (n=3).
The oxygen reduction catalyst that the present invention is provided has advantages below：
1st, it is cross-linked structure that the present invention uses the polymer P TPT that Friedel-Crafts is synthesized, by priority twice
The M-N-C oxygen reduction catalysts being thermally treated resulting in are loose structures, and with larger specific surface area, degree of graphitization is higher.It is many
Pore structure forms more catalytic active centers, is additionally favorable for the diffusion transmission of reactant and electrolyte, therefore gained catalyst
Not only there is good ORR catalysis activities, also with excellent stability and methanol tolerance performance.
2nd, being investigated using rotating disk electrode (r.d.e) and linear voltammetric scan method, electrochemical AC impedance method, chronoamperometry should
Catalyst oxygen reduction catalytic activity in the basic conditions.Result shows, the catalyst has ORR catalysis activities higher and excellent
Different stability and methanol tolerance performance：With Ag/AgCl as reference electrode, Pt be to electrode, be coated with a diameter of of catalyst
The glass-carbon electrode of 3mm is that working electrode constitutes three electrode test systems, with O2The 0.1mol/L KOH solutions of saturation are electrolyte
A series of electro-chemical tests are carried out, is as a result shown, oxygen reduction catalyst of the invention has good take-off potential (0.045V), excellent
In the take-off potential (0V) of business Pt/C；Meanwhile, the catalyst has excellent stability, by the test of 10000s, electric current
Density loss rate is 6%, and the current density loss late of business Pt/C is 29%.The catalyst has excellent methanol tolerance
Can, after 145s adds methyl alcohol, current density there is no the obvious decay of generation, and the current density of business Pt/C is rapid
Decay to the 70% of initial value.
3rd, catalyst of the invention is cheap, and preparation process is simple is prepared and is easily controlled, and is conducive to catalyst to produce
Industry.
Brief description of the drawings
The infrared spectrogram of Fig. 1, polymer as prepared by embodiment 1.
The transmission electron microscope photo of Fig. 2, catalyst as prepared by embodiment 1.
The nitrogen adsorption desorption isotherm figure of Fig. 3, catalyst as prepared by embodiment 1.
The pore size distribution figure of Fig. 4, catalyst as prepared by embodiment 1.
Fig. 5, the catalyst as prepared by embodiment 1, embodiment 2, embodiment 3, embodiment 4 and business Pt/C catalyst
Rotating disk electrode (r.d.e) polarization curve (the test condition of (Johnson Matthey) under rotating speed 1600rpm：Rotating disk electrode (r.d.e),
O2The 0.1M KOH solutions of saturation, sweep speed for 10mV/s).
The electric current of Fig. 6, the catalyst as prepared by embodiment 1 and business Pt/C catalyst (Johnson Matthey)~
The timing ampere curve of time.(test condition：Rotating disk electrode (r.d.e), O2The 0.1M KOH solutions of saturation, sweep speed for 10mV/s,
Operating voltage -0.25V, rotating speed 1600rpm).
The electric current of Fig. 7, the catalyst as prepared by embodiment 1 and business Pt/C catalyst (Johnson Matthey)~
The timing ampere curve of time.(test condition：Rotating disk electrode (r.d.e), O2The 0.1M KOH solutions of saturation, sweep speed for 10mV/s,
The time that operating voltage -0.25V, rotating speed 1600rpm, 10wt% methyl alcohol are added is about 145s).
Specific embodiment
The raw material used in embodiment
Pyrroles：Aladdin chemical reagents corporation, AR.
Nitrobenzene：Tianjin Fu Yu Fine Chemical Co., Ltd, AR..
Anaesthetie Ether：Aladdin chemical reagents corporation, AR.
Alchlor：Sa En chemical technologies Co., Ltd, AR.
Methyl alcohol：Tianjin Kermel Chemical Reagent Co., Ltd., AR.
Ferric nitrate：Aladdin chemical reagents corporation, AR.
Ethanol：Tianjin Fu Yu Fine Chemical Co., Ltd, AR.
Sulfuric acid：Tianjin great Mao chemical reagent factories, AR.
Nafion solution：U.S. DuPont, 5%.
Cobaltous sulfate：Aladdin chemical reagents corporation, AR.
Nickel acetate：Aladdin chemical reagents corporation, AR.
Tripyrrole-[1,3,5]-triazine：Reference literature Electrochim.Acta 38 (1993) 2481-2484. synthesizes.
The equipment used in embodiment：Rotating disk electrode (r.d.e)：ATA-1B, Jiangsu river point.Fourier transform infrared spectroscopy
(FTIR)：Thermo Nieolet 6700, Thermo Fischer Scient Inc..Transmission electron microscope TEM：JEOL-2010, day
This.Specific surface area and Porosimetry：Tristar II 3020, Micromeritics companies of the U.S..
Preparation example
The synthesis of tripyrrole-[1,3,5]-triazine (TPT)：
By 6.78g (0.10mol) pyrroles, 80mL anhydrous tetrahydro furans are added into the single necked round bottom flask of 250mL, in ice
Under bath, during KOH (8.86g, 0.15mol) added into above-mentioned system, reaction 3h is warmed to room temperature, then be dividedly in some parts 5.59g
(0.03mol) cyanuric trichloride, continues to stir 18h at room temperature.Reaction is finished, during reaction system poured into 250mL ice-water baths
Sedimentation, filtering, then be washed with deionized three times (200mL × 3), it is subsequently placed in 80 DEG C of vacuum drying chambers and dries 24h.Gained is thick
Product 15mL acetone and alcohol mixed solvent (acetone：Ethanol is 4:1) recrystallize, filtering, ethanol washing, by gained canescence
Solid room temperature is dried under vacuum to constant weight, 4.64g, yield 56%, fusing point：210℃.
Embodiment 1
(1) synthesis P (TPT)：110g (0.4mol) tripyrrole-[1,3,5]-triazine (TPT) is dissolved in 2000mL nitrobenzene
In, 18.26g (0.24mol) dimethoxymethane and 32.28g (0.24mol) aluminum trichloride (anhydrous) are added, in 45 DEG C of stirrings
5h, then rise to 80 DEG C of stirring 19h；Reaction is finished, and is poured into 10L methyl alcohol and is settled, filters, washing (1000mL × 2), and drying is standby
With；The infrared spectrogram of polymer P (TPT) is as shown in Figure 1；
The part-structure (i.e. repeat unit) of polymer is as follows：
N=1 in formula；
(2) 2.5g P (TPT), 0.7g ferric nitrates (or ferric trichloride) are added in 300mL ethanol, ultrasonic 180min makes
Whole system is uniformly dispersed, then is evaporated ethanol, is placed in vacuum drying chamber and dries 4h in 80 DEG C；
(3) gained 3.2g pulverulent solids are in N21h is heat-treated in 800 DEG C in atmosphere, 0.97g nitrogen-doped carbon materials are obtained；
(4) gained nitrogen-doped carbon material washs 8h with 2000mL 0.5M dilute sulfuric acids in 80 DEG C, after filtering, being washed to neutrality
It is placed in vacuum drying chamber and dries 4h in 80 DEG C；
(5) the dried nitrogen-doped carbon material 0.5g of pickling is again in N21h is heat-treated in 800 DEG C in atmosphere, 0.44g is obtained final product
M-N-C oxygen reduction catalysts, are designated as Fe-N-C-800.
(following embodiment obtains catalyst and the business Pt/C (Johnson for contrasting to catalyst performance method of testing
Matthey) tested with the method)
(1) catalyst 2mg is weighed, is added in 1mL Nafion- ethanol (1.5/98.5vol/vol) solution, ultrasound point
30min is dissipated, the μ L of above-mentioned catalyst suspension 20 are pipetted, is added drop-wise to by several times on the rotating circular disk glass-carbon electrode of a diameter of 3mm, it is natural
Dry.
(2) electro-chemical test instrument is CHI760D electrochemical workstations (Shanghai Chen Hua).Using above-mentioned electrode as work
O is placed in as electrode2In the 0.1M KOH solutions of saturation, with Ag/AgCl as reference electrode, Pt be to electrode, with 10mV/s's
Speed is swept, polarization curve of the test rotating disk electrode (r.d.e) under 1600rpm rotating speeds, the reaction for investigating the catalyst oxygen reduction process is moved
Mechanics.
(3) in above-mentioned system, under voltage -0.25V, with the prepared catalyst of rotating speed 1600rpm tests and business
The timing ampere curve of the electric current~time of Pt/C catalyst (Johnson Matthey).
(4) in above-mentioned system, under voltage -0.25V, with the prepared catalyst of rotating speed 1600rpm tests and business
(time that 10wt% methyl alcohol is added is about for the timing ampere curve of the electric current~time of Pt/C catalyst (Johnson Matthey)
It is 145s).
The properties of the product of the present embodiment are listed in accompanying drawing 1-6.
Embodiment 2
(1) synthesis P (TPT)：110g (0.4mol) tripyrrole-[1,3,5]-triazine (TPT) is dissolved in 2000mL nitrobenzene
In, 24g (0.24mol) dichloroethanes and 32.28g (0.24mol) aluminum trichloride (anhydrous) are added, 5h is stirred in 45 DEG C, then rise
To 80 DEG C of stirring 19h；Reaction is finished, and is poured into 10L methyl alcohol and is settled, filters, washing (1000mL × 2), drying for standby；Polymer
The infrared spectrogram of P (TPT) is as shown in Figure 1；
(2) 2.5g P (TPT), 0.7g ferric trichlorides are added in 300mL ethanol, ultrasonic 180min makes whole system point
Dissipate uniform, then be evaporated ethanol, be placed in vacuum drying chamber and 4h is dried in 80 DEG C, obtain primary mix；
(3) gained 3.2g pulverulent solids are in N21h is heat-treated in 800 DEG C in atmosphere, 0.98g nitrogen-doped carbon materials are obtained；
(4) gained nitrogen-doped carbon material washs 8h with 2000mL 0.5M dilute sulfuric acids in 80 DEG C, after filtering, being washed to neutrality
It is placed in vacuum drying chamber and dries 4h in 80 DEG C；
(5) the dried nitrogen-doped carbon material 0.5g of pickling is again in N21h is heat-treated in 800 DEG C in atmosphere, 0.45g is obtained final product
M-N-C oxygen reduction catalysts, are designated as Fe-N-C-800.
(following embodiment obtains catalyst and the business Pt/C (Johnson for contrasting to catalyst performance method of testing
Matthey) tested with the method)
(1) catalyst 2mg is weighed, is added in 1mL Nafion- ethanol (1.5/98.5vol/vol) solution, ultrasound point
30min is dissipated, the μ L of above-mentioned catalyst suspension 20 are pipetted, is added drop-wise to by several times on the rotating circular disk glass-carbon electrode of a diameter of 3mm, it is natural
Dry.
(2) electro-chemical test instrument is CHI760D electrochemical workstations (Shanghai Chen Hua).Using above-mentioned electrode as work
O is placed in as electrode2In the 0.1M KOH solutions of saturation, with Ag/AgCl as reference electrode, Pt be to electrode, with 10mV/s's
Speed is swept, polarization curve of the test rotating disk electrode (r.d.e) under 1600rpm rotating speeds, the reaction for investigating the catalyst oxygen reduction process is moved
Mechanics.
(3) in above-mentioned system, under voltage -0.25V, with the prepared catalyst of rotating speed 1600rpm tests and business
The timing ampere curve of the electric current~time of Pt/C catalyst (Johnson Matthey).
(4) in above-mentioned system, under voltage -0.25V, with the prepared catalyst of rotating speed 1600rpm tests and business
(time that 10wt% methyl alcohol is added is about for the timing ampere curve of the electric current~time of Pt/C catalyst (Johnson Matthey)
It is 145s).
Embodiment 3
(1) synthesis P (TPT)：110g (0.4mol) tripyrrole-[1,3,5]-triazine (TPT) is dissolved in 2000mL nitrobenzene
In, 24g (0.24mol) dichloroethanes and 32.28g (0.24mol) aluminum trichloride (anhydrous) are added, 5h is stirred in 45 DEG C, then rise
To 80 DEG C of stirring 19h；Reaction is finished, and is poured into 10L methyl alcohol and is settled, filters, washing (1000mL × 2), drying for standby；
(2) 2.5g P (TPT), 0.7g cobaltous sulfates are added in 300mL ethanol, ultrasonic 180min disperses whole system
Uniformly, then ethanol is evaporated, is placed in vacuum drying chamber and dries 4h in 80 DEG C；
(3) gained 3.2g pulverulent solids are in N21h is heat-treated in 800 DEG C in atmosphere, 1.1g nitrogen-doped carbon materials are obtained；
(4) gained nitrogen-doped carbon material washs 8h with 2000mL 0.5M dilute sulfuric acids in 80 DEG C, after filtering, being washed to neutrality
It is placed in vacuum drying chamber and dries 4h in 80 DEG C；
(5) the dried nitrogen-doped carbon material 0.6g of pickling is again in N21h is heat-treated in 800 DEG C in atmosphere, 0.5g is obtained final product
M-N-C oxygen reduction catalysts, are designated as Co-N-C-800.
Embodiment 4
(1) synthesis P (TPT)：110g (0.4mol) tripyrrole-[1,3,5]-triazine (TPT) is dissolved in 2000mL nitrobenzene
In, 24g (0.24mol) dichloroethanes and 32.28g (0.24mol) aluminum trichloride (anhydrous) are added, 5h is stirred in 45 DEG C, then rise
To 80 DEG C of stirring 19h；Reaction is finished, and is poured into 10L methyl alcohol and is settled, filters, washing (1000mL × 2), drying for standby；
(2) 2.5g P (TPT), 0.7g nickel acetates are added in 300mL ethanol, ultrasonic 180min disperses whole system
Uniformly, then ethanol is evaporated, is placed in vacuum drying chamber and dries 4h in 80 DEG C；
(3) gained 3.2g pulverulent solids are in N21h is heat-treated in 800 DEG C in atmosphere, 1.02g nitrogen-doped carbon materials are obtained；
(4) gained nitrogen-doped carbon material washs 8h with 2000mL 0.5M dilute sulfuric acids in 80 DEG C, after filtering, being washed to neutrality
It is placed in vacuum drying chamber and dries 4h in 80 DEG C；
(5) the dried nitrogen-doped carbon material 0.7g of pickling is again in N21h is heat-treated in 800 DEG C in atmosphere, 0.501g is obtained final product
M-N-C oxygen reduction catalysts, are designated as Ni-N-C-800.
Embodiment 5
(1) synthesis P (TPT)：110g (0.4mol) tripyrrole-[1,3,5]-triazine (TPT) is dissolved in 2000mL nitrobenzene
In, 24g (0.24mol) dichloroethanes and 32.28g (0.24mol) aluminum trichloride (anhydrous) are added, 5h is stirred in 45 DEG C, then rise
To 80 DEG C of stirring 19h；Reaction is finished, and is poured into 10L methyl alcohol and is settled, filters, washing (1000mL × 2), drying for standby；
(2) 2.5g P (TPT), 0.7g ferric trichlorides are added in 300mL ethanol, ultrasonic 180min makes whole system point
Dissipate uniform, then be evaporated ethanol, be placed in vacuum drying chamber and dry 4h in 80 DEG C；
(3) gained 3.2g pulverulent solids are in N21h is heat-treated in 1000 DEG C in atmosphere, 0.7g nitrogen-doped carbon materials are obtained；
(4) gained nitrogen-doped carbon material washs 8h with 2000mL 0.5M dilute sulfuric acids in 80 DEG C, after filtering, being washed to neutrality
It is placed in vacuum drying chamber and dries 4h in 80 DEG C；
(5) the dried nitrogen-doped carbon material 0.5g of pickling is again in N21h is heat-treated in 1000 DEG C in atmosphere, 0.3g is obtained final product
M-N-C oxygen reduction catalysts, are designated as Fe-N-C-1000.
Claims (25)
1. a kind of M-N-C oxygen reduction catalysts, it is by will be comprising the polymer of (i) tripyrrole-[1,3,5]-triazine (TPT)
That is a kind of primary mix of P (TPT) and two kinds of components of (ii) base metal salt is in an inert atmosphere in 700-1000 DEG C of temperature
Heat treatment for the first time is carried out under degree and obtains nitrogen-doped carbon material, then nitrogen-doped carbon material is carried out at pickling with dilute inorganic acid
Reason, finally carries out second heat treatment and finally obtains at a temperature of 700-1000 DEG C in an inert atmosphere by the material of pickling
.
2. catalyst according to claim 1, wherein the temperature of heat treatment is 750-950 DEG C for the first time, at second heat
The temperature of reason is 750-950 DEG C.
3. catalyst according to claim 2, wherein the temperature of heat treatment is 800-900 DEG C for the first time, at second heat
The temperature of reason is 800-900 DEG C.
4. catalyst according to claim 1, wherein being the salt of transition metal as the base metal salt of component (ii).
5. catalyst according to claim 4, wherein being the nitric acid of transition metal as the base metal salt of component (ii)
Salt, acetate, sulfate or chloride.
6. catalyst according to claim 5, wherein as the base metal salt of component (ii) be selected from Mn, Fe, Co,
In Ni, Cu one or two or more plant the nitrate of metal, acetate, sulfate or chloride.
7. the catalyst according to any one of claim 1-6, wherein as component (i) P (TPT) with as component
(ii) mass ratio of base metal salt is 1:0.06-1.
8. catalyst according to claim 7, wherein the P (TPT) as component (i) and the non-noble gold as component (ii)
The mass ratio for belonging to salt is 1:0.08-0.9.
9. catalyst according to claim 8, wherein the P (TPT) as component (i) and the non-noble gold as component (ii)
The mass ratio for belonging to salt is 1:0.12-0.8.
10. the catalyst according to any one of claim 1-6,8 or 9, wherein component (i), tripyrrole-[1,3,5]-
The polymer of triazine (TPT), i.e. P (TPT) is that the alkylation by tripyrrole-[1,3,5]-triazine (TPT) monomer in difunctionality is tried
React synthesized by Friedel-Crafts in the presence of agent or acylting agent and Friedel-Crafts catalysts.
11. catalyst according to claim 7, wherein component (i), the polymerization of tripyrrole-[1,3,5]-triazine (TPT)
Thing, i.e. P (TPT), be by tripyrrole-[1,3,5]-triazine (TPT) monomer difunctionality alkylating reagent or acylting agent
React synthesized by Friedel-Crafts with the presence of Friedel-Crafts catalysts.
12. catalyst according to claim 10, wherein the alkylating reagent of the difunctionality is double halo C2-C6 alkanes
Hydrocarbon, straight or branched C2-C12 olefines, straight or branched C3-C10 dihydroxylic alcohols or with the double of 3-18 carbon atom altogether
One or more in ether；And/or
The acylting agent of difunctionality is have the 3-12 double carboxylic acid halides of the straight or branched of C carbon atoms altogether, have 4-8 altogether
The straight or branched bisgallic acid acid anhydride of C carbon atoms has one kind in the straight or branched pair carboxylic acids of 4-10 C carbon atom altogether
Or it is various.
13. catalyst according to claim 11, wherein the alkylating reagent of the difunctionality is double halo C2-C6 alkanes
Hydrocarbon, straight or branched C2-C12 olefines, straight or branched C3-C10 dihydroxylic alcohols or with the double of 3-18 carbon atom altogether
One or more in ether；And/or
The acylting agent of difunctionality is have the 3-12 double carboxylic acid halides of the straight or branched of C carbon atoms altogether, have 4-8 altogether
The straight or branched bisgallic acid acid anhydride of C carbon atoms has one kind in the straight or branched pair carboxylic acids of 4-10 C carbon atom altogether
Or it is various.
The catalyst of any one in the preparation method or preparation claim 1-13 of a kind of 14. M-N-C oxygen reduction catalysts
Method, the method is comprised the following steps：
(1) preparation of polymer P (TPT)：By tripyrrole-[1,3,5]-triazine (TPT) monomer in a solvent in the alkane of difunctionality
Reacted by Friedel-Crafts in the presence of base reagent or acylting agent and Friedel-Crafts catalysts and made
The polymer P (TPT) of standby tripyrrole-[1,3,5]-triazine (TPT), i.e. component (i),
(2) formation of primary mix：Using the P (TPT) and 0.06-1 weight portions as group as component (i) of 1 weight portion
Divide the base metal salt of (ii) dispersed in a solvent, dry, obtain a kind of primary mixed with component (ii) comprising component (i)
Compound,
(3) it is heat-treated for the first time：The primary mix that will be obtained in step (2) is in an inert atmosphere in 700-1000 DEG C of temperature
Under be once heat-treated, obtain nitrogen-doped carbon material,
(4) acid pickling step：Pickling is carried out to nitrogen-doped carbon material with dilute inorganic acid,
(5) it is heat-treated for second：To enter at a temperature of 700-1000 DEG C in an inert atmosphere again through the material after overpickling
Row secondary heat treatment, obtains final products M-N-C oxygen reduction catalysts.
15. methods according to claim 14, it is characterised in that：In step (2)：Using 1 weight portion as component (i)
P (TPT) is dispersed in a solvent with the base metal salt as component (ii) of 0.08-0.9 weight portions；
The temperature of heat treatment is 750-950 DEG C for the first time in step (3)；
Second temperature of heat treatment is 750-950 DEG C in step (5).
16. methods according to claim 15, it is characterised in that：In step (2)：Using 1 weight portion as component (i)
P (TPT) is dispersed in a solvent with the base metal salt as component (ii) of 0.12-0.8 weight portions；
The temperature of heat treatment is 800-900 DEG C for the first time in step (3)；
Second temperature of heat treatment is 800-900 DEG C in step (5).
A kind of 17. preparation methods of M-N-C oxygen reduction catalysts, the method is comprised the following steps：
(1) preparation of polymer P (TPT)：The tripyrrole of 1 weight portion-[1,3,5]-triazine (TPT) is dissolved in solvent, then is added
Enter the alkylating reagent or acylting agent of the difunctionality of 0.5-10 weight portions, it is 0.5-12 weight portions to add weight portion
Friedel-Crafts catalysts, react under agitation；Reaction is finished, and pours into separation in methyl alcohol or ethanol, filtering, water
Wash, dry, obtain P (TPT)；
(2) formation of primary mix：Using the P (TPT) and 0.06-1 weight portions as group as component (i) of 1 weight portion
The base metal salt of (ii) is divided to be added in ethanol or methyl alcohol, ultrasonication makes whole system be uniformly dispersed；Be evaporated ethanol or
Methyl alcohol, dries, and obtains the primary mix comprising copolymer and base metal salt；
(3) it is heat-treated for the first time：Step (2) gained mixture is carried out at a temperature of 700-1000 DEG C the in inert gas
Once it is heat-treated, obtains nitrogen-doped carbon material；
(4) pickling：Gained nitrogen-doped carbon material is dried with dilute inorganic acid, filtering after being washed to neutrality；
(5) it is heat-treated for second：The nitrogen-doped carbon material that step (4) is obtained is again in 700-1000 DEG C of temperature in inert gas
Second heat treatment is carried out under degree, M-N-C oxygen reduction catalysts are obtained final product.
18. methods according to claim 17, it is characterised in that：
Step (1) is specially：The tripyrrole of 1 weight portion-[1,3,5]-triazine (TPT) is dissolved in 5-50 parts by weight solvent, then
The alkylating reagent or acylting agent of the difunctionality of 1-4 weight portions are added, it is 1.2-6 weight portions to add weight portion
Friedel-Crafts catalysts, in 25-50 DEG C stirring reaction 2-10 hours, then rise to 60-100 DEG C of stirring reaction 15-
25 hours；Reaction is finished, and is poured into 60-400 parts by weight Methanol or ethanol and is separated, filters, washing, drying, and obtains P (TPT)；
Step (2) is specially：Using the P (TPT) and 0.08-0.9 weight portions as component as component (i) of 1 weight portion
(ii) base metal salt is added in 50~200 parts by weight of ethanol or methyl alcohol, 120~300min of ultrasonication, is made whole
System is uniformly dispersed；Ethanol or methyl alcohol are evaporated, are placed in vacuum drying chamber and are dried 2-10h in 60-100 DEG C, obtained comprising copolymerization
The primary mix of thing and base metal salt；
Step (3) is specially：Step (2) gained mixture is carried out first in inert gas at a temperature of 750-950 DEG C
Secondary heat treatment, obtains nitrogen-doped carbon material；
Step (4) is specially：Gained nitrogen-doped carbon material washs 5~10h, filtering, washing in 50~80 DEG C with dilute inorganic acid
It is placed in vacuum drying chamber after to neutrality and dries 2-10h in 60-100 DEG C；
Step (5) is specially：The nitrogen-doped carbon material that step (4) is obtained is again in 750-950 DEG C of temperature in inert gas
Under carry out second heat treatment, obtain final product M-N-C oxygen reduction catalysts.
19. method according to any one of claim 14-18, wherein, the alkylation examination of difunctionality described in step (1)
Agent is double halo C2-C6 alkanes, straight or branched C2-C12 olefines, straight or branched C3-C10 dihydroxylic alcohols or with total
One or more in the bis ether of common 3-18 carbon atom；And/or
The acylting agent of difunctionality is have the 3-12 double carboxylic acid halides of the straight or branched of C carbon atoms altogether, have 4-8 altogether
The straight or branched bisgallic acid acid anhydride of C carbon atoms has one kind in the straight or branched pair carboxylic acids of 4-10 C carbon atom altogether
Or it is various.
20. method according to any one of claim 14-18, solvent is nitrobenzene, nitro wherein described in step (1)
One or more in methane, tetrachloroethanes, dichloroethanes, carbon tetrachloride, carbon disulfide, and/or
Friedel-Crafts catalysts described in step (1) are AlCl3、FeCl3、SnCl4、ZnCl2、H2SO4、H3PO4、
BF3, one or more in HF.
21. method according to any one of claim 14-18, it is characterised in that：Conduct group described in step (2)
The base metal salt for dividing (ii) is the salt of transition metal.
22. methods according to claim 19, it is characterised in that：The non-noble as component (ii) described in step (2)
Slaine is the salt of transition metal.
23. methods according to claim 20, it is characterised in that：The non-noble as component (ii) described in step (2)
Slaine is the salt of transition metal.
24. methods according to claim 21, it is characterised in that：The non-noble as component (ii) described in step (2)
Slaine is nitrate, acetate, sulfate or the chloride of transition metal.
25. method according to any one of claim 22-24, it is characterised in that：Described in step (2) as component
(ii) base metal salt be selected from Mn, Fe, Co, Ni, Cu one or two or more plant nitrate, the acetic acid of metal
Salt, sulfate or chloride.
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| CN109192997B (en) * | 2018-08-13 | 2020-07-14 | 湘潭大学 | Nitrogen-sulfur co-doped carbon-supported non-noble metal oxygen reduction catalyst and preparation method thereof |
| CN109346735A (en) * | 2018-09-28 | 2019-02-15 | 东华大学 | Nano carbon balls oxygen reduction catalyst and its preparation and application derived from porous polymer |
| CN110061251B (en) * | 2019-05-22 | 2020-10-16 | 湘潭大学 | Pyridyl triazine derivative polymer-based nitrogen-doped carbon catalyst and preparation method and application thereof |
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