Bipyridine compound, synthetic method and symmetrical flow battery system thereof
阅读说明：本技术 联吡啶类化合物、合成方法及其对称性液流电池系统 (Bipyridine compound, synthetic method and symmetrical flow battery system thereof ) 是由 苏志俊 徐俊辉 武奕 韩俊甜 崔耀星 陈留平 李丹 于 2019-09-25 设计创作，主要内容包括：本发明公开了一种联吡啶类化合物、合成方法及其对称性液流电池系统,含TEMPO的联吡啶类化合物的合成方法,包括：在强碱条件下,化合物A与4-羟基-2,2,6,6-四甲基哌啶-1-氧自由基进行反应,得到产物为含TEMPO的联吡啶类化合物B,其化学反应式如式(1)所示：<Image he="304" wi="700" file="DDA0002214345550000011.GIF" imgContent="drawing" imgFormat="GIF" orientation="portrait" inline="no"></Image>该含TEMPO的联吡啶类化合物的合成方法操作方便,得到的含TEMPO的联吡啶类化合物能够作为液流电池的正极活性物质及负极活性物质。(The invention discloses a bipyridine compound, a synthetic method and a symmetrical flow battery system thereof, wherein the synthetic method of the bipyridine compound containing TEMPO comprises the following steps: under the strong alkaline condition, the compound A reacts with 4-hydroxy-2, 2,6, 6-tetramethyl piperidine-1-oxygen free radical to obtain a product, namely a bipyridine compound B containing TEMPO, wherein the chemical reaction formula is shown as the formula (1): the synthesis method of the bipyridyl compound containing TEMPO is convenient to operate, and the obtained bipyridyl compound containing TEMPO can be used as a positive electrode active material and a negative electrode active material of a flow battery.)
1. A synthetic method of a bipyridine compound containing TEMPO is characterized by comprising the following steps:
under the strong alkali condition, the compound A and 4-hydroxy-2, 2,6, 6-tetramethyl piperidine-1-oxygen free radical carry out nucleophilic substitution reaction to obtain a product, namely a bipyridine compound B containing TEMPO, wherein the chemical reaction formula is shown as the formula (1):
2. the synthetic method according to claim 1, wherein the preparation of compound B comprises the following steps:
mixing 4-hydroxy-2, 2,6, 6-tetramethylpiperidine-1-oxygen radical and sodium hydride, and then adding a reaction solvent for reaction to prepare a mixed solution;
adding a reaction solvent into the compound A, dropwise adding the mixed solution for reaction, removing unreacted sodium hydride and the solvent after the reaction is finished, extracting to obtain an organic phase, removing water in the organic phase, filtering, distilling under reduced pressure to remove the solvent in the filtrate, and carrying out aftertreatment on the precipitated product to obtain the bipyridine compound B containing TEMPO.
3. The synthesis method according to claim 1, wherein n in formula (1) is one of 3-7, and the compound B has a symmetrical structure.
4. The method of synthesis according to claim 1, further comprising the steps of:
adding a reaction solvent and an acid-binding agent into a compound C, dropwise adding p-methylbenzenesulfonyl chloride for reaction, wherein alcoholic hydroxyl in the compound C reacts with p-toluenesulfonic acid to form sulfonate, and removing part of the solvent after the reaction is finished to obtain a solid product compound A, wherein the chemical reaction formula is shown as a formula (2):
5. the synthesis method of claim 4, wherein the acid-binding agent is one of sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, triethylamine and potassium acetate.
6. The method of synthesis according to claim 4, further comprising the steps of:
mixing 4, 4' -bipyridyl and monohydric alcohol with the end group being halogen, adding a reaction solvent, carrying out Menschutkin reaction, and removing part of the solvent after the reaction is finished to obtain a solid product compound C, wherein the chemical reaction formula is shown as formula (3):
7. the synthesis method according to claim 6, wherein the halogen X is chlorine, and the molar ratio of the 4, 4' -bipyridyl to the chlorine-terminated monoalcohol is 1:5 to 1: 10.
8. A TEMPO-containing bipyridine compound characterized in that it is prepared by the method for synthesizing a TEMPO-containing bipyridine compound according to any one of claims 1 to 7.
9. A symmetrical flow battery system, comprising:
the electrolyte comprises two electrolyte liquid storages, wherein the two electrolyte liquid storages are arranged at intervals, each electrolyte liquid storage is a liquid storage tank for storing electrolyte or a salt cave which is formed after salt mines are mined and is provided with a physical dissolution cavity, the electrolyte in one electrolyte liquid storage comprises a positive electrode active substance and a supporting electrolyte, the electrolyte in the other electrolyte liquid storage comprises a negative electrode active substance and a supporting electrolyte, and the positive electrode active substance and the negative electrode active substance are respectively directly dissolved or dispersed in a system which takes water as a solvent in a body form;
a flow cell stack comprising a cell membrane dividing the flow cell stack into an anode region and a cathode region distributed at intervals, the anode region communicating with one electrolyte reservoir and the cathode region communicating with another electrolyte reservoir, the positive and negative active materials being the TEMPO-containing bipyridine-like compound according to claim 8.
10. The symmetric flow battery system of claim 9, wherein the positive active material and the negative active material are the same organic material.
11. The symmetric flow battery system of claim 10, wherein the positive active material and the negative active material are both at a concentration of 0.1 mol-L-1～3.0mol·L-1。
12. The symmetric flow battery system of claim 9, wherein the electrolyte reservoir is a pressurized sealed container with a pressure of 0.1MPa to 0.5 MPa.
13. The symmetric flow battery system of claim 9, wherein an inert gas is introduced into the electrolyte reservoir to purge and maintain pressure.
14. The symmetric flow battery system of claim 13, wherein the inert gas is nitrogen or argon.
15. The symmetric flow battery system of claim 9, wherein the battery diaphragm is an anion exchange membrane, a cation exchange membrane or a polymer porous membrane with a pore size of 10nm to 300 nm.
16. The symmetric flow battery system of claim 9, wherein the supporting electrolyte is a NaCl salt solution, a KCl salt solution, Na2SO4Salt solution, K2SO4Salt solution, MgCl2Salt solution, MgSO4Salt solution, CaCl2Salt solution, NH4At least one of a Cl salt solution.
17. The symmetric flow battery system of claim 16, wherein the supporting electrolyte has a molar concentration of 0.1 mol-L-1～8.0mol·L-1。
18. The symmetrical flow battery system of claim 9, wherein the anode region and the cathode region each have an electrode disposed therein, and the positive and negative electrodes are carbon material electrodes.
19. The symmetric flow battery system according to claim 18, wherein the carbon material electrode is one or more of carbon felt, carbon paper, carbon cloth, carbon black, activated carbon fiber, activated carbon particles, graphene, graphite felt, and glass carbon material.
20. The symmetric flow battery system of claim 18, wherein the electrodes are formed as electrode plates having a thickness of 2mm to 8 mm.
21. The symmetric flow battery system of claim 9, further comprising:
and the current collectors are respectively arranged on two sides of the flow battery stack and can collect and conduct current generated by active substances of the flow battery stack to an external lead.
22. The symmetric flow battery system of claim 21, wherein the current collector is one of a conductive metal plate, a graphite plate, or a carbon-plastic composite plate.
23. The symmetric flow battery system of claim 22, wherein the conductive metal plate comprises at least one metal of copper, nickel, and aluminum.
Technical Field
The invention belongs to the field of flow batteries, and particularly relates to a synthetic method of a bipyridyl compound containing TEMPO.
Background
With the rapid development of human economy, the problems of environmental pollution, energy shortage and the like are increasingly aggravated, and the world countries are promoted to widely develop and utilize renewable energy sources such as wind energy, solar energy, tidal energy and the like. However, the renewable energy sources have the characteristics of discontinuity, instability, limitation by regional environment and difficult grid connection, so that the utilization rate is low, the wind and light abandoning rate is high, and resources are wasted. There is a need for a robust development of efficient, inexpensive, safe and reliable energy storage technology that can be used in conjunction therewith.
Among various electrochemical energy storage strategies, Flow Batteries (RFBs) have several particular technical advantages over static Batteries such as lithium ion Batteries and lead acid Batteries, and are most suitable for large-scale (megawatt/megawatt hour) electrochemical energy storage, such as relatively independent energy and power control, high-current and high-power operation (fast response), high safety performance (mainly, non-flammability and non-explosion), and the like. The redox active material is a carrier for energy conversion of the flow battery and is also the most core part in the flow battery. Conventional flow batteries utilize inorganic materials as active materials (e.g., vanadium-based flow batteries), however, the disadvantages of high inorganic material cost, toxicity, limited resources, dendrite formation, and low electrochemical activity limit the large-scale application of flow batteries. The organic active substance has the advantages of low cost, green color, rich resources, easy adjustment of molecular energy level, quick electrochemical reaction and the like, and has attracted wide attention at home and abroad. The electrolyte of the water-based organic flow battery has the advantage of incombustibility and is safer to operate. In addition, in the water-based organic flow battery, the conductivity of the electrolyte is high, the electrochemical reaction rate is high, and the output power is high. Therefore, the water-based organic flow battery is an ideal large-scale energy storage technology.
Most of aqueous phase organic flow batteries use different electrochemical active substances at the cathode and the anode, and cross contamination of electrolyte is easily caused in the charging and discharging processes, so that the service life of the battery is shortened. At the same time, the solubility of the active material (organic matter), low operating current density, side reactions of water electrolysis, etc. also affect the lifetime of the aqueous phase organic flow battery. Therefore, the development and use of highly water-soluble and stable organic active materials are of great significance for expanding the chemical space (e.g., open circuit voltage, energy density, stability, etc.) of organic flow batteries.
Disclosure of Invention
The present invention is directed to solving at least one of the problems of the prior art.
Therefore, the invention provides a synthetic method of a bipyridine compound containing TEMPO, which is simple to operate and can prepare the bipyridine compound simultaneously having two redox active groups of 4-Hydroxy-2, 2,6, 6-tetramethylpiperidine-1-oxygen radical (4-Hydroxy-TEMPO) and 4, 4' -bipyridine.
The invention also provides a bipyridyl compound containing TEMPO, which can be applied to flow batteries.
The invention also provides a symmetrical flow battery system, which comprises the bipyridyl compound containing TEMPO, wherein the bipyridyl compound containing TEMPO can be used as a negative electrode active substance and a positive electrode active substance, and the cross contamination of the electrolyte can not be caused in the charging and discharging process.
According to the first aspect of the invention, the synthesis method of the TEMPO-containing bipyridine compound comprises the following steps: under the strong alkali condition, the compound A and 4-hydroxy-2, 2,6, 6-tetramethyl piperidine-1-oxygen free radical carry out nucleophilic substitution reaction to obtain a product, namely a bipyridine compound B containing TEMPO, wherein the chemical reaction formula is shown as the formula (1):
according to one embodiment of the invention, the preparation of compound B comprises the following steps: mixing 4-hydroxy-2, 2,6, 6-tetramethylpiperidine-1-oxygen radical and sodium hydride, and then adding a reaction solvent for reaction to prepare a mixed solution; adding a reaction solvent into the compound A, dropwise adding the mixed solution for reaction, removing unreacted sodium hydride and the solvent after the reaction is finished, extracting to obtain an organic phase, removing water in the organic phase, filtering, distilling under reduced pressure to remove the solvent in the filtrate, and carrying out aftertreatment on the precipitated product to obtain the bipyridine compound B containing TEMPO.
According to an embodiment of the invention, n in the formula (1) is one of 3-7, and the compound B has a symmetrical structure.
According to an embodiment of the present invention, the synthesis method further comprises the steps of: adding a reaction solvent and an acid-binding agent into a compound C, dropwise adding p-methylbenzenesulfonyl chloride for reaction, wherein alcoholic hydroxyl in the compound C reacts with p-toluenesulfonic acid to form sulfonate, and removing part of the solvent after the reaction is finished to obtain a solid product compound A, wherein the chemical reaction formula is shown as a formula (2):
according to an embodiment of the present invention, the acid-binding agent is one of sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, triethylamine, and potassium acetate.
According to an embodiment of the present invention, the synthesis method further comprises the steps of: mixing 4, 4' -bipyridyl and monohydric alcohol with the end group being halogen, adding a reaction solvent, carrying out Menschutkin reaction, and removing part of the solvent after the reaction is finished to obtain a solid product compound C, wherein the chemical reaction formula is shown as formula (3):
according to one embodiment of the invention, the halogen X is chlorine, the molar ratio of the 4, 4' -bipyridine to the chlorine-terminated monoalcohol is 1:5 to 1: 10.
The TEMPO-containing bipyridine compounds according to the second aspect of the embodiment of the invention are prepared by the method for synthesizing TEMPO-containing bipyridine compounds according to any of the embodiments described above.
A symmetrical flow battery system according to an embodiment of a third aspect of the present invention includes: the electrolyte comprises two electrolyte liquid storages, wherein the two electrolyte liquid storages are arranged at intervals, each electrolyte liquid storage is a liquid storage tank for storing electrolyte or a salt cave which is formed after salt mines are mined and is provided with a physical dissolution cavity, the electrolyte in one electrolyte liquid storage comprises a positive electrode active substance and a supporting electrolyte, the electrolyte in the other electrolyte liquid storage comprises a negative electrode active substance and the supporting electrolyte, the positive electrode active substance and the negative electrode active substance are respectively directly dissolved or dispersed in a system which takes water as a solvent in a body form, and the supporting electrolyte is dissolved in the system; the redox flow battery stack comprises a battery diaphragm, the battery diaphragm divides the redox flow battery stack into an anode region and a cathode region which are distributed at intervals, the anode region is communicated with one electrolyte liquid storage tank, the cathode region is communicated with the other electrolyte liquid storage tank, and the positive active material and the negative active material are bipyridine compounds containing TEMPO according to any embodiment of the invention.
According to one embodiment of the present invention, the positive electrode active material and the negative electrode active material are the same organic material.
According to one embodiment of the present invention, the concentrations of the positive electrode active material and the negative electrode active material are both 0.1mol · L-1～3.0mol·L-1。
According to one embodiment of the present invention, the electrolyte reservoir is a pressurized and sealed container having a pressure of 0.1 to 0.5 MPa.
According to one embodiment of the invention, an inert gas is introduced into the electrolyte reservoir to purge and maintain pressure.
According to one embodiment of the invention, the inert gas is nitrogen or argon.
According to one embodiment of the invention, the battery diaphragm is an anion exchange membrane, a cation exchange membrane or a polymer porous membrane with a pore size of 10nm to 300 nm.
According to one embodiment of the invention, the supporting electrolyte is a NaCl salt solution, a KCl salt solution, Na2SO4Salt solution, K2SO4Salt solution, MgCl2Salt solution, MgSO4Salt solution, CaCl2Salt solution, NH4At least one of a Cl salt solution.
According to one embodiment of the invention, the supporting electrolyte has a molar concentration of 0.1mol · L-1～8.0mol·L-1。
According to one embodiment of the invention, the anode region and the cathode region are respectively provided with electrodes, and the positive electrode and the negative electrode are carbon material electrodes.
According to one embodiment of the invention, the carbon material electrode is one or a composite of several of carbon felt, carbon paper, carbon cloth, carbon black, activated carbon fiber, activated carbon particles, graphene, graphite felt and glass carbon material.
According to one embodiment of the invention, the electrodes are formed as electrode plates, the thickness of the electrode plates being 2mm to 8 mm.
According to an embodiment of the present invention, the symmetrical flow battery system further includes: and the current collectors are respectively arranged on two sides of the flow battery stack and can collect and conduct current generated by active substances of the flow battery stack to an external lead.
According to an embodiment of the invention, the current collector is one of a conductive metal plate, a graphite plate or a carbon-plastic composite plate.
According to one embodiment of the present invention, the conductive metal plate includes at least one metal of copper, nickel, and aluminum.
Additional aspects and advantages of the invention will be set forth in part in the description which follows and, in part, will be obvious from the description, or may be learned by practice of the invention.
Drawings
The above and/or additional aspects and advantages of the present invention will become apparent and readily appreciated from the following description of the embodiments, taken in conjunction with the accompanying drawings of which:
fig. 1 is a schematic structural diagram of a symmetrical flow battery system according to an embodiment of the invention;
FIG. 2 is a CV diagram of a solution of Compound C according to example 1 of the present invention at a concentration of 2mM in aqueous sodium chloride solution at pH 7 at a scan rate of 20 mV/s;
FIG. 3 is a CV diagram of a solution of Compound A according to example 1 of the present invention at a concentration of 2mM in aqueous sodium chloride solution at pH 7 at a scan rate of 20 mV/s;
FIG. 4 is a CV diagram of a solution of Compound B according to example 1 of the present invention at a concentration of 2mM in aqueous sodium chloride solution at pH 7 at a scan rate of 20 mV/s;
fig. 5 shows coulombic efficiency, voltage efficiency and energy efficiency of a symmetric flow battery with compound B as positive and negative electrode compositions according to example 1 of the present invention under different charging and discharging currents;
FIG. 6 shows a flow cell with a positive electrode and a negative electrode of a symmetrical flow cell at 200mA/cm for the compound B of example 12Cycling performance under charge and discharge current.
Reference numerals:
a symmetric
an
a
Detailed Description
Reference will now be made in detail to embodiments of the present invention, examples of which are illustrated in the accompanying drawings, wherein like or similar reference numerals refer to the same or similar elements or elements having the same or similar function throughout. The embodiments described below with reference to the accompanying drawings are illustrative only for the purpose of explaining the present invention, and are not to be construed as limiting the present invention.
In the description of the present invention, it is to be understood that the terms "central," "longitudinal," "lateral," "length," "width," "thickness," "upper," "lower," "front," "rear," "left," "right," "vertical," "horizontal," "top," "bottom," "inner," "outer," "clockwise," "counterclockwise," "axial," "radial," "circumferential," and the like are used in the orientations and positional relationships indicated in the drawings for convenience in describing the invention and to simplify the description, and are not intended to indicate or imply that the referenced devices or elements must have a particular orientation, be constructed and operated in a particular orientation, and are therefore not to be considered limiting of the invention. Furthermore, a feature defined as "first" or "second" may explicitly or implicitly include one or more of that feature. In the description of the present invention, "a plurality" means two or more unless otherwise specified.
In the description of the present invention, it should be noted that, unless otherwise explicitly specified or limited, the terms "mounted," "connected," and "connected" are to be construed broadly, e.g., as meaning either a fixed connection, a removable connection, or an integral connection; can be mechanically or electrically connected; they may be connected directly or indirectly through intervening media, or they may be interconnected between two elements. The specific meanings of the above terms in the present invention can be understood in specific cases to those skilled in the art.
The following describes in detail the synthesis of TEMPO-containing bipyridine compounds according to embodiments of the invention with reference to the accompanying drawings.
The synthetic method of the TEMPO-containing bipyridine compound according to the embodiment of the invention comprises the following steps: under the strong alkali condition, the compound A and 4-hydroxy-2, 2,6, 6-tetramethyl piperidine-1-oxygen free radical carry out nucleophilic substitution reaction to obtain a product, namely a bipyridine compound B containing TEMPO, wherein the chemical reaction formula is shown as the formula (1):
in other words, in the preparation of the product, the compound a and 4-hydroxy-2, 2,6, 6-tetramethylpiperidine-1-oxyl can be subjected to nucleophilic substitution reaction under certain conditions to obtain the product B. The product B is a bipolar organic matter, and the product B has two redox active groups, namely 4-Hydroxy-2, 2,6, 6-tetramethylpiperidine-1-oxygen free radical (4-Hydroxy-TEMPO) and 4, 4' -bipyridyl, and the two redox active groups are connected by using an oxygen-containing ether bond.
According to an embodiment of the present invention, in preparing the compound B, the 4-hydroxy-2, 2,6, 6-tetramethylpiperidine-1-oxyl and the sodium hydride may be mixed first, and then the mixture may be added to a reaction solvent to react to obtain a mixed solution; adding a reaction solvent into the compound A, dropwise adding the mixed solution for reaction, removing unreacted sodium hydride and the solvent after the reaction is finished, extracting to obtain an organic phase, removing water in the organic phase, filtering, distilling under reduced pressure to remove the solvent in the filtrate, and carrying out aftertreatment on a precipitated product to obtain a product of the bipyridine compound B containing TEMPO.
According to one embodiment of the invention, n in the formula (1) is one of 3-7, and the compound B has a symmetrical structure.
According to an embodiment of the present invention, the dropping speed of the mixed solution during the preparation of the compound B is controlled to be 1d/s to 2 d/s.
In some embodiments of the present invention, the synthesis method further comprises synthesizing a compound a, when synthesizing the compound a, adding a reaction solvent and an acid-binding agent into a compound C, then dropwise adding p-toluenesulfonyl chloride to react, wherein an alcoholic hydroxyl group in the compound C reacts with p-toluenesulfonic acid to form a sulfonate, and removing a part of the solvent after the reaction is finished to obtain a solid product compound a, wherein the chemical reaction formula of the compound a is as shown in formula (2):
optionally, the acid-binding agent is one of sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, triethylamine, and potassium acetate.
According to an embodiment of the present invention, the dropping speed of the p-toluenesulfonyl chloride is 1d/s to 2 d/s.
In some embodiments of the present invention, the synthesis method further comprises synthesizing compound C, in the synthesis of compound C, first mixing 4, 4' -bipyridine and monohydric alcohol with end group being halogen, then adding reaction solvent, performing Menschutkin reaction, and removing part of solvent after the reaction is finished to obtain solid product compound C, whose chemical reaction formula is shown as formula (3):
further, the halogen X is chlorine, and the molar ratio of the 4, 4' -bipyridyl to the monohydric alcohol with the end group being chlorine is 1: 5-1: 10.
According to one embodiment of the invention, the reaction time is 24h to 48 h.
In some embodiments of the invention, the method for synthesizing the TEMPO-containing bipyridine compound comprises the following steps:
(1) mixing 4, 4' -bipyridyl and monohydric alcohol (n represents the length of an alkyl chain) with chlorine as an end group, putting the mixture into a reactor, adding acetonitrile serving as a reaction solvent, heating to reflux reaction, distilling under reduced pressure after the reaction is finished to remove part of the solvent to precipitate a solid, and filtering, washing, recrystallizing and drying the precipitated product to obtain the compound C.
The reaction formula is as follows:
(2) putting the compound C prepared in the step (1) into a reactor, adding absolute ethyl alcohol as a reaction solvent, then adding a proper amount of an acid-binding agent, dropwise adding an absolute ethyl alcohol solution of p-toluenesulfonyl chloride (TsCl) at 0-5 ℃, heating to 30-40 ℃ after dropwise adding for reaction, removing part of the solvent by reduced pressure distillation after the reaction is finished, separating out a solid, filtering, washing, recrystallizing and drying the separated product to obtain the compound A.
The reaction formula is as follows:
(3) firstly, mixing 4-Hydroxy-2, 2,6, 6-tetramethylpiperidine-1-oxygen free radical (4-Hydroxy-TEMPO) and sodium hydride (NaH) and putting into a reactor, then adding N, N' -Dimethylformamide (DMF) as a reaction solvent, heating to 60-70 ℃ under the protection of nitrogen for reaction, and after the reaction is finished, putting the mixed solution into a constant-pressure dropping funnel; and (3) putting the compound A prepared in the step (2) into a reactor, adding N, N' -Dimethylformamide (DMF) as a reaction solvent, heating to 60-70 ℃ under the protection of nitrogen, dropwise adding the mixed solution, continuing the reaction at 60-70 ℃ after the dropwise adding is finished, adding a proper amount of water to remove unreacted sodium hydride (NaH) after the reaction is finished, distilling under reduced pressure to remove all solvents, extracting with a mixed solution of ethyl acetate and water, taking an organic phase, adding anhydrous magnesium sulfate to remove water in the organic phase, filtering, distilling under reduced pressure to remove the solvent in the filtrate, precipitating solids, filtering, washing, recrystallizing and drying the precipitated product to obtain a final product B.
The reaction formula is as follows:
therefore, the method for synthesizing the TEMPO-containing bipyridyl compound according to the embodiment of the invention can obtain the TEMPO-containing bipyridyl compound, and the final product TEMPO-containing bipyridyl compound can be synthesized through multiple steps.
According to the TEMPO-containing bipyridine compound of the embodiment of the invention, the TEMPO-containing bipyridine compound is prepared by the synthesis method of any one of the TEMPO-containing bipyridine compounds of the embodiment, and the final product has two redox active groups, namely 4-Hydroxy-2, 2,6, 6-tetramethylpiperidine-1-oxyl (4-Hydroxy-TEMPO) and 4, 4' -bipyridine, and is a bipolar organic matter by using an oxygen-containing ether bond as a connection.
As shown in fig. 1, a symmetrical
Specifically, two
According to one embodiment of the present invention, the positive electrode active material and the negative electrode active material are the same organic material, and molecules of the organic material are bonded by covalent bonds between two redox active molecules. By adopting the same electrochemical active substance, the cross contamination of the electrolyte can be avoided in the charging and discharging process, and the service life of the battery is prolonged. Specifically, the same electrochemically active material is used in the cathode portion and the anode portion of the symmetric flow battery system, respectively, after charging, the cathode active portion in the active material molecules is oxidized in the catholyte, and simultaneously, the anode portion is reduced in the anolyte to balance the charge, the composition of the catholyte and the anolyte are identical, and the battery is easily rebalanced during charge and discharge cycles without any adverse effects.
Alternatively, the concentrations of the positive electrode active material and the negative electrode active material are both 0.1mol · L-1～3.0mol·L-1。
According to one embodiment of the present invention, the electrolyte reservoir is a pressurized sealed container having a pressure of 0.1MPa to 0.5 MPa.
In some embodiments of the present invention, an inert gas is introduced into the electrolyte reservoir to purge and maintain the pressure, and the inert gas can be used to protect the electrolyte during the charging and discharging processes.
Preferably, the inert gas is nitrogen or argon.
According to one embodiment of the present invention, the battery separator is an anion exchange membrane, a cation exchange membrane, or a polymer porous membrane having a pore size of 10nm to 300 nm.
Optionally, the supporting electrolyte is NaCl salt solution, KCl salt solution, Na2SO4Salt solution, K2SO4Salt solution, MgCl2Salt solution, MgSO4Salt solution, CaCl2Salt solution, NH4At least one of Cl salt solution, supporting electrolyte can be dissolved in the system, and the battery diaphragm can be penetrated by the supporting electrolyte and prevent the positive electrode active material and the negative electrode active material from penetrating.
Further, the molar concentration of the supporting electrolyte was 0.1mol · L-1～8.0mol·L-1。
In some embodiments of the invention, electrodes are disposed in the anode region and the cathode region, respectively, and the positive and negative electrodes are carbon material electrodes.
Further, the carbon material electrode is one or a composite of several of carbon felt, carbon paper, carbon cloth, carbon black, activated carbon fiber, activated carbon particles, graphene, graphite felt and a glassy carbon material.
Alternatively, the electrode is formed as an electrode plate having a thickness of 2mm to 8 mm.
According to an embodiment of the present invention, the symmetric
Optionally,
Preferably, the conductive metal plate includes at least one metal of copper, nickel, and aluminum.
Therefore, the symmetrical
The symmetrical aqueous redox
In the cyclic voltammetry test of the galvanic couple, a CS series electrochemical workstation of Wuhan Cornst is adopted, a three-electrode system is adopted to test the electrochemical performance of the organic galvanic couple, a working electrode is a glassy carbon electrode (Tianjin Adamantang Hengcheng), a reference electrode is an Ag/AgCl electrode, a counter electrode is a platinum electrode, the scanning ranges of the positive and negative galvanic couples are-1.0V respectively, and the scanning speed is 20mV s-1。
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