LU102451B1 - Aluminum (al) anode plate material for al-air battery and preparation method thereof, al anode plate for al-air battery and preparation method and use thereof - Google Patents
Aluminum (al) anode plate material for al-air battery and preparation method thereof, al anode plate for al-air battery and preparation method and use thereof Download PDFInfo
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- LU102451B1 LU102451B1 LU102451A LU102451A LU102451B1 LU 102451 B1 LU102451 B1 LU 102451B1 LU 102451 A LU102451 A LU 102451A LU 102451 A LU102451 A LU 102451A LU 102451 B1 LU102451 B1 LU 102451B1
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- air battery
- anode plate
- plate material
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- 239000000463 material Substances 0.000 title claims abstract description 55
- 229910052782 aluminium Inorganic materials 0.000 title claims abstract description 8
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title claims abstract description 8
- 238000002360 preparation method Methods 0.000 title abstract description 13
- 239000011777 magnesium Substances 0.000 claims abstract description 35
- 229910052749 magnesium Inorganic materials 0.000 claims abstract description 7
- 229910052738 indium Inorganic materials 0.000 claims abstract description 6
- 229910052718 tin Inorganic materials 0.000 claims abstract description 6
- 229910052684 Cerium Inorganic materials 0.000 claims abstract description 5
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims abstract description 3
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims abstract description 3
- GWXLDORMOJMVQZ-UHFFFAOYSA-N cerium Chemical compound [Ce] GWXLDORMOJMVQZ-UHFFFAOYSA-N 0.000 claims abstract description 3
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 claims abstract description 3
- 229910052751 metal Inorganic materials 0.000 claims description 43
- 239000002184 metal Substances 0.000 claims description 43
- 238000000034 method Methods 0.000 claims description 26
- 229910000636 Ce alloy Inorganic materials 0.000 claims description 16
- 238000000137 annealing Methods 0.000 claims description 15
- 238000005096 rolling process Methods 0.000 claims description 13
- 239000011888 foil Substances 0.000 claims description 12
- 238000002844 melting Methods 0.000 claims description 9
- 230000008018 melting Effects 0.000 claims description 9
- 238000005266 casting Methods 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract description 15
- 238000005260 corrosion Methods 0.000 abstract description 8
- 230000000694 effects Effects 0.000 abstract description 7
- 239000003792 electrolyte Substances 0.000 abstract description 7
- 229910045601 alloy Inorganic materials 0.000 abstract description 5
- 239000000956 alloy Substances 0.000 abstract description 5
- 230000010287 polarization Effects 0.000 abstract description 5
- 230000007797 corrosion Effects 0.000 abstract description 4
- 230000002195 synergetic effect Effects 0.000 abstract description 3
- 239000000243 solution Substances 0.000 description 17
- 230000000052 comparative effect Effects 0.000 description 7
- 230000008569 process Effects 0.000 description 7
- 229910052761 rare earth metal Inorganic materials 0.000 description 5
- 230000003647 oxidation Effects 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 3
- 150000002910 rare earth metals Chemical class 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- 230000008901 benefit Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000005097 cold rolling Methods 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 229910001092 metal group alloy Inorganic materials 0.000 description 2
- 239000002923 metal particle Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000005275 alloying Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C1/00—Making non-ferrous alloys
- C22C1/02—Making non-ferrous alloys by melting
- C22C1/026—Alloys based on aluminium
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C1/00—Making non-ferrous alloys
- C22C1/02—Making non-ferrous alloys by melting
- C22C1/03—Making non-ferrous alloys by melting using master alloys
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C21/00—Alloys based on aluminium
- C22C21/06—Alloys based on aluminium with magnesium as the next major constituent
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22F—CHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
- C22F1/00—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
- C22F1/04—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of aluminium or alloys based thereon
- C22F1/047—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of aluminium or alloys based thereon of alloys with magnesium as the next major constituent
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M12/00—Hybrid cells; Manufacture thereof
- H01M12/04—Hybrid cells; Manufacture thereof composed of a half-cell of the fuel-cell type and of a half-cell of the primary-cell type
- H01M12/06—Hybrid cells; Manufacture thereof composed of a half-cell of the fuel-cell type and of a half-cell of the primary-cell type with one metallic and one gaseous electrode
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/04—Processes of manufacture in general
- H01M4/043—Processes of manufacture in general involving compressing or compaction
- H01M4/0435—Rolling or calendering
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/04—Processes of manufacture in general
- H01M4/0471—Processes of manufacture in general involving thermal treatment, e.g. firing, sintering, backing particulate active material, thermal decomposition, pyrolysis
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/04—Processes of manufacture in general
- H01M4/0483—Processes of manufacture in general by methods including the handling of a melt
- H01M4/0485—Casting
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/04—Processes of manufacture in general
- H01M4/0483—Processes of manufacture in general by methods including the handling of a melt
- H01M4/0488—Alloying
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/06—Electrodes for primary cells
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/06—Electrodes for primary cells
- H01M4/08—Processes of manufacture
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/36—Selection of substances as active materials, active masses, active liquids
- H01M4/38—Selection of substances as active materials, active masses, active liquids of elements or alloys
- H01M4/46—Alloys based on magnesium or aluminium
- H01M4/463—Aluminium based
Abstract
The disclosure relates to the technical field of aluminum (Al)-air batteries, in particular to an Al anode plate material for an Al-air battery and a preparation method thereof, and an Al anode plate for an Al-air battery, a preparation method and use thereof. The disclosure provides an Al anode plate material for an Al-air battery, which includes the following elements by mass percentage: 0.02-0.2% of cerium (Ce), 0.02-0.2% of indium (In), 0.02-0.2% of tin (Sn), 0.3-0.7% of magnesium (Mg), and the balance being Al. The disclosure includes appropriate amounts of Ce, In, Sn and Mg in the Al anode plate material. The Ce in combination with the In, the Sn and the Mg shows a synergistic effect, so that alloy grains are refined, polarization is weakened, and electrochemical activity of an electrode plate is improved while relatively high corrosion resistance is ensured, which greatly improves discharge voltage and energy density of the Al anode plate. The disclosure is suitable for a high power alkaline Al-air battery with NaOH as an electrolyte.
Description
ALUMINUM (AL) ANODE PLATE MATERIAL FOR AL-AIR BATTERY AND 10102451 PREPARATION METHOD THEREOF, AL ANODE PLATE FOR AL-AIR BATTERY
TECHNICAL FIELD The disclosure relates to the technical field of aluminum (Al)-air batteries, in particular to an Al anode plate material for an Al-air battery and a preparation method thereof. and an Al anode plate for an Al-air battery, a preparation method and use thereof.
BACKGROUND Al-air batteries have advantages such as low cost, high specific volumetric capacity (8,200 Wh-kg') and low toxicity, and thus have extremely high potential. An alkaline system uses a NaOH or KOH solution with extremely high conductivity as an electrolyte. An oxide film on a surface of an Al anode in the system can be dissolved by the electrolyte and activity of Al is high, so an output of a large current density and power can be achieved. Waste electrolyte produced after discharge of the Al-air battery can be used to recover aluminum oxide therein with an industrial Bayer method. Therefore, the alkaline system has higher application value. However, polarization of the Al anode of the Al-air battery of this system is serious during use, resulting in a discharge voltage and an energy density of the Al-air battery much lower than theoretical values, which hinders application of the Al-air battery.
SUMMARY The disclosure aims to provide an Al anode plate material for an Al-air battery and a preparation method thereof, and an Al anode plate for an Al-air battery, a preparation method and use thereof. The disclosure can improve discharge voltage and energy density of the Al anode plate, and is suitable for a high power alkaline Al-air battery with NaOH as an electrolyte.
To achieve the above objective of the disclosure, the disclosure provides the following technical solutions: The disclosure provides an Al anode plate material for an Al-air battery, which includes the following elements by mass percentage: 0.02-0.2% of cerium (Ce), 0.02-0.2% of indium (In).
0.02-0.2% of tin (Sn), 0.3-0.7% of magnesium (Mg), and the balance being Al.
Preferably. the Al has a content of above 99%.
The disclosure provides a method for preparing the Al anode plate material for an Al-air battery of the above solution, which includes the following steps: melting pure Al to obtain molten Al; adding Al-Ce alloy, metal In, metal Sn and metal Mg which are wrapped by Al foil to the molten Al to obtain a mixed melt; casting the mixed melt to form an Al anode plate material for an Al-air battery:
where amounts of the pure Al, the Al-Ce alloy, the metal In, the metal Sn, the metal Mg anid 102451 the Al foil correspond to element composition of the Al anode plate material for the Al-air battery in the above solution.
Preferably, a mass percentage of the Ce in the Al-Ce alloy 1s 5-20%.
The disclosure provides an Al anode plate for an Al-air battery. which is prepared from the Al anode plate material for an Al-air battery of the above solution or an Al anode plate material for an Al-air battery prepared by the method of the above solution.
The disclosure provides a method for preparing an Al anode plate for an Al-air battery, which includes the following steps: rolling and annealing an Al anode plate material for an Al-air battery in sequence to obtain an Al anode plate for an Al-air battery: where the Al anode plate material for an Al-air battery is the one of the above solution or prepared by the method of the above solution.
Preferably, the annealing is carried out at 300-400°C for 3-15 h.
Preferably, the rolling is cold rolling.
The disclosure provides use of the Al anode plate for an Al-air battery of the above solution or an Al anode plate for an Al-air battery prepared by the method of the above solution as an anode in an Al-air battery.
The disclosure provides an Al anode plate material for an Al-air battery, which includes the following elements by mass percentage: 0.02-0.2% of Ce, 0.02-0.2% of In, 0.02-0.2% of Sn.
0.3-0.7% of Mg, and the balance being Al. The disclosure includes appropriate amounts of Ce, In, Sn and Mg in the Al anode plate material. The Ce in combination with the In, the Sn and the Mg shows a synergistic effect, so that alloy grains are refined, polarization is weakened, and electrochemical activity of an electrode plate is improved while relatively high corrosion resistance is ensured, which greatly improves discharge voltage and encrgy density of the Al anode plate. At the same time, the Ce can protect the In, the Sn and the Mg from oxidation during an Al anode plate production process, promote an overall reaction of the battery, and improve electrochemical performance of an electrode.
Results of examples show that, compared with the pure Al plate, the anode plate for an Al-air battery prepared by the Al anode plate material for an Al-air battery of the disclosure has a discharge voltage increased by 0.048-0.194 V and an energy density increased by 2-6.5 times at a low current density of 40 mAscm™. The disclosure can achieve discharge at a high current density of 100 mA+cm™, where a discharge voltage can reach 1 V, and an energy density can reach 3000 Wh-kg".
2
BRIEF DESCRIPTION OF DRAWINGS FIG. 1 shows metallographic phase images of the Al anode plates for an Al-air battery prepared in Comparative Example, Example 2 and Example 10.
DETAILED DESCRIPTION The disclosure provides an Al anode plate material for an Al-air battery, which includes the following elements by mass percentage: 0.02-0.2% of Ce. 0.02-0.2% of In, 0.02-0.2% of Sn,
0.3-0.7% of Mg, and the balance being Al.
Based on mass percentage, the Al anode plate material for an Al-air battery provided by the disclosure includes the Ce in an amount of 0.02-0.2%, preferably 0.06-0.10%, more preferably
0.08%. In examples of the disclosure, a content of the Ce is specifically 0.02%, 0.04%, 0.06%,
0.08%, 0.10%, 0.14% or 0.18%. In the disclosure, the Ce can ensure that grains of the Al anode plate material for an Al-air battery are refined, polarization is weakened, and self-corrosion rate is reduced. At the same time, the Ce can protect the In, the Sn and the Mg from oxidation during an Al anode plate production process, promote an overall reaction of the battery, and improve electrochemical performance of an electrode.
Based on mass percentage, the Al anode plate material for an Al-air battery provided by the disclosure includes the In in an amount of 0.02-0.2%, preferably 0.025-0.125%, more preferably
0.05%. In examples of the disclosure, a content of the In is specifically 0.025%, 0.05%, 0.075%,
0.100% or 0.125%.
Bascd on mass percentage, the Al anode plate material for an Al-air battery provided by the disclosure includes the Sn in an amount of 0.02-0.2%. preferably 0.04-0.15%, more preferably
0.06-0.08%. In examples of the disclosure, a content of the Sn is specifically 0.02%, 0.04%,
0.06% or 0.08%.
Based on mass percentage, the Al anode plate material for an Al-air battery provided by the disclosure includes the Mg in an amount of 0.3-0.7%, preferably 0.4-0.6%. In examples of the disclosure, a content of the Mg is specifically 0.3%, 0.4%. 0.5%, 0.6% or 0.7%. In the disclosure, the Mg can change a microstructure of an Al anode. reduce adverse effects of impurity elements, and reduce hydrogen evolution corrosion, In the disclosure, the Ce in combination with the In, the Sn and the Mg shows a synergistic effect. so that alloy grains are refined, polarization is weakened, and electrochemical activity of an electrode plate is improved while a relatively high corrosion resistance is ensured, which greatly improves discharge voltage and energy density of the Al anode plate.
Based on mass percentage, the Al anode plate material for an Al-air battery provided by the disclosure includes the Al as balance, preferably in an amount of 99% or more.
3
The Al anode plate material for an Al-air battery provided by the disclosure also includes” 102401 inevitable impurities.
The disclosure provides a method for preparing the Al anode plate material for an Al-air battery of the above technical solution, which includes the following steps: melting pure Al to obtain molten Al; adding Al-Ce metal alloy. metal In, metal Sn and metal Mg which are wrapped by Al foil to the molten Al to obtain a mixed melt; casting the mixed melt to form an Al anode plate material for an Al-air battery; where amounts of the pure Al, the Al-Ce alloy, the metal In, the metal Sn, the metal Mg and the Al foil correspond to clement composition of the Al anode plate material for an Al-air battery.
In the disclosure, raw materials used are all commercially available products well known in the art, unless otherwise specified.
The disclosure includes melting pure Al to obtain molten Al. In the disclosure, the pure Al preferably has a purity of 99.9% or more. The disclosure has no special requirement on a process of the melting, and a process of melting well known in the art can be used.
After the molten Al is obtained, the disclosure includes adding Al-Ce alloy, metal In, metal Sn, metal Mg and Al foil to the molten Al to obtain a mixed melt.
In the disclosure, a mass percentage of the Ce in the Al-Ce alloy is preferably 5-20%. more preferably 8-17%, and still more preferably 10-15%. A rare earth element (Ce) is used in the form of an Al-based master alloy, which greatly reduces cost of purchasing the rare earth metal while maintaining excellent properties of the rare earth element (Ce). At the same time, since a melting point of an Al-based Al-Ce alloy is much lower than that of the rare earth metal, difficulty of manufacturing the Al anode plate material is reduced. Moreover, compared with use of a pure rare earth metal, the Al-based Al-Ce alloy also has an advantage of high utilization rate of alloying elements.
In the disclosure, the metal In, the metal Sn and the metal Mg are preferably used in the form of metal particles. The disclosure has no special requirement on particle sizes of the metal particles, and particle sizes well known to those skilled in the art can be used. In the disclosure, the metal In, the metal Sn and the metal Mg preferably have a purity of more than 99.9%. In the disclosure, the In and the Sn are enriched in alloy grain boundaries in the form of segregated phases. and activate the Al anode plate in the form of "dissolution-redeposition” and "low solid solution".
In the disclosure, the Al-Ce alloy, the metal In, the metal Sn and the metal Mg are preferably wrapped by the Al foil. The disclosure has no special requirement on a thickness of the Al foil, and a thickness sufficient to completely wrap the Al-Ce alloy, the metal In, the metal Sn and the 4
ES metal Mg can be used. In the disclosure, the Al foil is used to wrap the Al-Ce alloy, the metal Irl,U102451 the metal Sn and the metal Mg to reduce oxidation of the In, the Sn and the Mg. At the same time, the Ce can also inhibit the oxidation of the In, the Sn and the Mg.
In the disclosure, amounts of the pure Al, the Al-Ce alloy, the metal In, the metal Sn, the metal Mg and the Al foil correspond to element composition of the Al anode plate material for an Al-air battery.
In the disclosure, during the melting pure Al and the adding Al-Ce metal alloy, metal In, metal Sn and metal Mg which are wrapped by Al {oil for melting, refining and slag removal and the like can be carried out according to actual needs.
After the mixed melt is obtained, the disclosure includes casting the mixed melt to form an Al anode plate material for an Al-air battery. In the disclosure, the casting is preferably carried out in a mold. The disclosure has no special requirements on a casting forming process, and a casting forming process well known in the art can be used. After casting forming, the obtained Al anode plate material for an Al-air battery is preferably a plate material. The disclosure has no special requirements on thickness of the plate material. Those skilled in the art can choose the thickness according to actual needs. In examples of the disclosure, the thickness is specifically 1 cm.
The disclosure provides an Al anode plate for an Al-air battery, which is prepared from the Al anode plate material for an Al-air battery of the above solution or an Al anode plate material for an Al-air battery prepared by the method of the above solution, The disclosure provides a method for preparing an Al anode plate for an Al-air battery. which includes the following steps: rolling and annealing an Al anode plate material for an Al-air battery in sequence to obtain an Al anode plate for an Al-air battery: where the Al anode plate material for an Al-air battery is the one of the above solution or prepared by the method of the above solution.
The disclosure includes rolling an Al anode plate material for an Al-air battery to obtain a rolled plate. In the disclosure, the rolling is preferably cold rolling. The rolling is preferably multi-pass rolling. The disclosure has no special requirements on reduction of each rolling pass, as long as cracking of the rolled plate can be prevented. In examples of the disclosure. a thickness of the Al anode plate material for an Al-air battery is 1 cm, total reduction of the rolling is 80%. reduction of each pass is 20%, and a thickness of an obtained rolled plate is 0.2 cm. In the disclosure, the rolling is carried out, so that the Al anode plate can obtain a thickness for actual use. At the same time, the grains of the Al anode plate material are secondarily refined by the rolling and the annealing.
After the rolled plate is obtained, the disclosure includes annealing the rolled plate to obtair-V102451 an Al anode plate for an Al-air battery. In the disclosure, the annealing is carried out at preferably 300-400°C, more preferably 320-380°C, most preferably 350°C for preferably 3-15 h, more preferably 5-10 h, and most preferably 6 h. The disclosure uses annealing to grow a fiber structure of the rolled Al anode plate into subgrains with more uniform chemical composition in crystals, thereby improving electrochemical performance of the Al anode plate.
The disclosure provides use of the Al anode plate for an Al-air battery of the above solution or an Al anode plate for an Al-air battery prepared by the method of the above solution as an anode in an Al-air battery. The Al anode plate for an Al-air battery of the disclosure is suitable for a high power alkaline Al-air battery with NaOH as an electrolyte.
The Al anode plate material of an Al-air battery and a preparation method thereof, and the Al anode plate for an Al-air battery, a preparation method and use thereof provided by the disclosure will be described in detail in connection with the following examples, but the examples should not be construed as limiting the claimed scope of the disclosure.
Example 1 Step 1: high pure Al was melt to obtain molten Al Step 2: Al-based Al-Ce alloy and metals In, Sn and Mg which were wrapped by Al foil were added to the molten Al obtained in step 1 (a total mass of each sample was 200 g, and addition by mass percentage was shown in Table 1), thoroughly mixing the five components to obtain a mixed melt.
Step 3: the mixed melt obtained in step 2 was casted in a mold to form a plate-shaped material for preparation of an Al electrode plate for an Al-air battery. A casted plate had a thickness of 1 cm.
Step 4: a plate material prepared in step 3 was rolled by a rolling mill (a rolled anode had a thickness of 0.2 cm, and a reduced thickness of cach pass was 0.2 cm), and then annealed (heat treatment process was shown in Table 1) to obtain an Al anode plate for an Al-air battery.
Examples 2-11 and Comparative Example Specific compositions and annealing processes were shown in Table 1, and the rest were the same as in Example 1.
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Table 1 Compositions and annealing parameters of anode plates for an Al-air battery in LU102451 Examples 1-11 and Comparative Example Structural characterization and performance test
1. Metallographic structures of the Al anode plates prepared in Comparative Example, Example 2 and Example 10 were observed and results were shown in FIG. 1 (specifically, in FIG. 1, (a) corresponded to Comparative Example, (b) corresponded to Example 2, and (©) corresponded to Example 10). It can be scen from FIG. 1 that, the Al anode plate prepared by the disclosure had finer grains compared with the pure Al plate and had a uniform size. Morcover, it can be seen from (b) and (c) in FIG. 1 that, effects were most significant when the annealing was carried out at 350°C-6h.
2. The Al anode plates prepared in the above Examples and Comparative Example were applied to Al-air batteries. À 4 mol/l. NaOH aqueous solution was added as an electrolyte. Performance of each Al anode plate was measured with results in Table 2.
7
A Table 2 Performance of the Al-air batteries associated with Examples and ComparativeUT02451 Example 40 mA cm’ 100 mA em” Open Self-corrosion circuit Discharge Energy Discharge Energy rate No. potential voltage density voltage density (mg cmb) (V) (Wh-kg") (V9 (Wh-kg”) Comparative
1.59 1.17 771.28 0.006 103.02 4.268 Example Example 1 1.364 1837.04 0.990 3000.00 10.12 Example 2 1.351 2953.01 1.022 2945.24 8.90 Example 3 1.357 2329.61 1.113 3117.65 11.89 Example 4 1.335 2567.31 ross 3269.94 15.66 Example 5 1.349 3270.30 1.039 2886.11 me Example 6 1.218 2298.11 0.856 2734.82 14.64 Example 7 1.292 2118.03 1.108 2682.81 14.21 Example 8 1.259 2289.09 0.812 2224.66 14.03 Example 9 1.277 2935.53 0.982 3116.65 12.332 Example 10 1.270 4837.64 0.985 3283.62 10.264 Example 11 1.267 1656.55 1.085 3021.65 11.284 It can be seen from results in Table 2 that, the pure Al had an open circuit potential of 1.59 V; a discharge voltage of 1.17 V and an energy density of 771.28 Wh-kg™! at a low current density of 40 mA cm; a discharge voltage too low for discharge at a high current density of 100 mA-em”; and a self-corrosion rate of 4.268 mg-em”-h". Compared with the pure Al plate. the Al anode plate prepared by the disclosure had a wider selection range of the open circuit potential between
1.47-1.74 V; a discharge voltage increased by about 0.048-0.194 V and an energy density 8 increased by 2-6.5 times at a low current density of 40 mA-em”. The disclosure can achiev! 102451 discharge at a high current density of 100 mA-cm?, where the discharge voltage can reach 1 V, and the energy density can reach 3000 Wh-kg". The disclosure had an increased self-corrosion rate, but the anode performance was still far better than that of the pure Al.
At the same time, comparison of Example 8-11 proved that the annealing process for the anode of the disclosure can increase the energy density of the anode, and effects were most significant at 350°C-6h.
The above descriptions are merely preferred implementations of the disclosure. It should be noted that a person of ordinary skill in the art may further make several improvements and modifications without departing from the principle of the disclosure, but such improvements and modifications should be deemed as falling within the protection scope of the disclosure.
9
Claims (9)
1. An aluminum (Al) anode plate material for an Al-air battery, comprising the following elements by mass percentage: 0.02-0.2% of cerium (Ce), 0.02-0.2% of indium (In), 0.02-0.2% of tin (Sn), 0.3-0.7% of magnesium (Mg), and the balance being Al.
2. The Al anode plate material for an Al-air battery according to claim 1, wherein the Al has a content of above 99%.
3. A method for preparing the Al anode plate material for an Al-air battery according to claim 1 or claim 2, comprising the following steps: melting pure Al to obtain molten Al; adding Al-Ce alloy, metal In, metal Sn and metal Mg which are wrapped by Al foil to the molten Al to obtain a mixed melt; casting the mixed melt to form an Al anode plate material for an Al-air battery; wherein amounts of the pure Al, the Al-Ce alloy, the metal In, the metal Sn, the metal Mg and the Al foil correspond to element composition of the Al anode plate material for an Al-air battery according to claim 1 or claim 2.
4. The method according to claim 3, wherein, a mass percentage of the Ce in the Al-Ce alloy is 5-20%.
5. An Al anode plate for an Al-air battery, wherein the Al anode plate for an Al-air battery is prepared from the Al anode plate material for an Al-air battery according to claim 1 or claim 2 or an Al anode plate material for an Al-air battery prepared by the method according to claim 3 or claim 4.
6. A method for preparing an Al anode plate for an Al-air battery, comprising the following steps: rolling and annealing an Al anode plate material for an Al-air battery in sequence to obtain an Al anode plate for an Al-air battery; wherein the Al anode plate material for an Al-air battery is the Al anode plate material for an Al-air battery according to claim 1 or claim 2 or prepared by the method according to claim 3 or claim 4.
7. The method according to claim 6, wherein the annealing is carried out at 300-400°C for 3-15 h.
8. The method according to claim 6, wherein the annealing is cold annealing.
9. Use of the Al anode plate for an Al-air battery according to claim 5 or an Al anode plate for an Al-air battery prepared by the method according to any of claims 6-8 as an anode in an Al-air battery.
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