TW201225386A - Method for manufaturing battery - Google Patents

Abstract

Embodiments of the present invention provide a manufacturing method of a battery. The method includes the steps of S1: manufacturing high aggregation solution; step S2: manufacturing a cathode structure; step S3: manufacturing an isolation structure; step S4: assembling the negative electrode structure and the isolation structure into a housing; and step S5: inseting a mass flow body into the housing and filling the cathode material to the structure to form a positive electrode structure, wherein at least one of the cathode structure and the anode structure includes chlorophyll. In at least one of the embodiments of the present invented cell manufacturing method, a battery can be produced using the chlorophyll in the positive and the negative electrode structures to store hydrogen thereby achieving power supply. Because the battery using an environment-protecting material instead of the conventional battery contamination component, even if discarded after exhausted, it does not pollute the environment, which is more environmentally-friendly than conventional batteries.

Description

201225386 VI. Description of the invention: [Technical field to which the invention belongs]

The present application claims the prior benefit of U.S. Patent Application Serial No., filed on Dec. 24, and Taiwan Patent Application No. 97U8207, filed on May 16, the same. The entire contents of the above two patents are incorporated herein by reference. The present invention relates to a method of making a yarn by electrospinning, and relates to a battery using chlorophyll to generate electric energy and a method of manufacturing the same. [Prior Art] In recent years, there have been mobile phones, portable cameras, notebook computers, digital cameras, PDAs, CDplayers and other portable electronic devices, and they are seeking small and lightweight ones. Constipation batteries are also subject to _ note. The battery types include dry batteries, hydrogen batteries, and battery batteries. A brief description of common batteries is given below. • Most of the dry batteries used for the day are miscellaneous batteries, also called carbon-zinc batteries. Carbon word The outer casing of the battery is made of zinc. It can be used as a battery container or as a negative electrode. The stone anti-zinc battery was developed from a liquid Lec]anch battery. Traditional or general-type carbon batteries use gasification as an electrolyte; super or high-energy carbon-zinc batteries are usually carbon-zinc batteries using zinc-xide as an electrolyte, which is an improved version of a general-purpose battery. The positive electrode of the carbon! xin battery is mainly composed of powdered manganese dioxide and 201225386 carbon. The electrolyte is a paste solution formed by dissolving zinc chloride and ammonium chloride in water. Carbon-zinc batteries are the cheapest primary batteries, so they are the first choice of many manufacturers' because they often need to distribute batteries in the equipment sold by these manufacturers. Zinc-carbon batteries can be used in low-power equipment such as remote controls, flashlights, toys or transistor radios. 0 However, when the carbon-zinc battery is used for a period of time, the zinc casing will gradually become thinner due to the oxidation of metallic zinc to zinc ions. . Therefore, the gasification solution can often leak out of the battery. The leaked zinc oxide tends to make the surface of the battery sticky. Some old batteries have no leakage protection. The service life of zinc-carbon batteries is relatively short. The shelf life is generally - half a year. In addition, even if the battery is not used, the gasification in the battery is marked with a new property, which can react with zinc, and the zinc casing can also be thinned. Now the 3C industry often mentions that the battery is actually a bribe battery. The generalized charge and discharge tank refers to the anode of a graphite crucible, Na Na, the iron of the thief, and the electrolyte used to transport the clock ions. Composition. A miscellaneous battery can be used as a bungee. (4) The development of the pool industry is focused on the 3C industry in the past year. The market is small and the energy storage and power battery (the instantaneous current is large). This market covers pure electric vehicles and hybrid vehicles. , medium and large, solar, large energy storage batteries, electric hand tools, electric motorcycles, electric bicycles, aerospace equipment and aircraft batteries. The main reason is that the cathode material used in the past clock battery 201225386 material (LiCo〇2 ' is the most common lithium battery now) can not be applied to the need for high current, high voltage, high torque and withstand puncture, collision and high temperature, Special circumstances such as low temperatures, etc., more importantly, they have been criticized for failing to meet people's absolute requirements for safety. At the same time, 'lithium-cobalt batteries can't achieve the purpose of fast charging and completely avoiding secondary pollution. Moreover, it is necessary to design protection circuits to prevent overcharging or over-discharging. Otherwise, there will be dangers such as explosions, and even explosions such as Sony battery will cause the world. The brand NB industry casts the situation of the recovery of the moment. In addition, the starting price is getting higher and higher, the world's largest element of the country's largest production country, the war is more and more troublesome, resulting in the price of the element is rising. The powder of Zhongming battery has risen from the original price of 4 US dollars to 60 to 70 US dollars due to the rising price of cobalt. Dish acid bell powder is good or bad according to the quality, and the price per kilogram is 3〇~6〇. The recording of the battery & also counts from the recording battery. In 1982, the United States ovonic company requested the hydrogen storage alloy patent for electrode manufacturing, which made this material pay attention to. In 1985, Philips of the Netherlands broke through the problem of capacity decay of hydrogen storage alloy during charge and discharge, and finally made nickel-hydrogen battery. stand out. At present, there are more than 8 hydrogen batteries in Japan, and Germany, the United States, Hong Kong, and Taiwan also have hydrogen battery production, and the market has responded well. The pollution caused by (10) hydrogen batteries will be smaller than that of nickel-containing nickel pools. The current battery has been gradually replaced by nickel-hydrogen 201225386 batteries. Fuel cell is a device that uses Qin material to carry out chemical reaction to generate electricity. It was first invented by English _ Giwe. The most common 质 氢 氢 氢 氢 氢 氢 氢 氢 氢 氢 氢 氢 氢 氢 氢 氢 氢 氢 氢 氢 氢 氢 氢 氢 氢 氢 氢 氢 氢 氢 氢 氢 氢 氢 氢 氢 氢 氢 氢 氢 氢 氢

The daring age is in the US military, and after Yu Congnian should listen to the Mei Zizi constellation Gemini constellation No. 5 spacecraft. There are also some notes (four) that the brain began to study the battery. However, due to the small amount of electricity generated, it is not possible to provide a large amount of electricity. The fuel cell is a dynamic mechanism that combines a battery body and a fuel tank. The selectivity of the female is very high, including pure nitrogen, methanol, ethanol, natural gas, and even the most widely used gasoline, it can be used as fuel for fuel cells. Whether it is a new type of carbon-zinc battery, alkaline battery and secondary battery that emphasizes environmental protection, the slaves will be less than the thieves or other materials, raw materials and processes, which are harmful to the environment and the human body. .曰 赝 赝 赝 赝 赝 赝 赝 赝 赝 赝 赝 赝 赝 赝 赝 赝 赝 赝 赝 赝 赝 锂 锂 锂 锂 锂 锂 锂 锂 锂 锂 锂 锂 锂 锂 锂 锂 锂 锂 锂 锂 锂 锂 锂 锂 锂 锂 锂 锂 锂 锂 锂,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,, , to prevent the passage of ions, block the battery reaction, raise the internal p^2kn). (-{jn. Lii.xc〇〇2), (LixC) The clock mine is getting milk, making its price rise rapidly. • Performance and longevity begin to decrease rapidly in outdoor or ambient environments. Because of the memory effect, the mining battery or the money battery is very difficult (4) poor charge and discharge, resulting in reduced available capacity. SUMMARY OF THE INVENTION An object of the present invention is to provide a method of manufacturing a battery. In order to solve the above problems, an embodiment of the present invention provides a method for manufacturing a battery, comprising: step S1: preparing a polymer solution; step S2: fabricating a negative electrode structure; step S3: fabricating an isolation structure; and step S4: forming a negative electrode structure And assembling the isolation structure into the outer casing; and step 85: inserting a current collector into the outer casing and filling the positive electrode material to the above-described junction to form a positive electrode structure, wherein at least one of the negative electrode structure and the positive electrode structure includes chlorophyll. According to a preferred embodiment of the present invention, the step si includes the step of: slowly adding a polymer powder in a solvent having a temperature of 4 〇 Celsius; the step is: using a magnetizer at a speed of 500 to 700 RpM_the above solution; 201225386 S13: Using a conductivity meter to detect whether the conductivity of the solution reaches 50-250 ms/cm; when the above detection result is no, returning to the execution step, and when the above detection result is YES, executing step S14; Step SM: Finish. According to a preferred embodiment of the invention, the high polymer powder comprises a metal ion and a compound of various acid ions and a high polymer, wherein the concentration is between 0.1 and 10 m/l. According to a preferred embodiment of the invention, the high polymer powder further comprises a vitamin. According to a preferred embodiment of the invention the vitamin is vitamin D. According to a preferred embodiment of the invention the polymer is a polymer of glucose. According to a preferred embodiment of the present invention, the high polymer of glucose is one or more of potato starch, water chestnut starch, corn starch, sweet potato powder, lotus root starch, fennel powder and pueraria powder. According to a preferred embodiment of the invention, the compound of the metal ion and various acid ion ions is a carbonic acid mother. According to a preferred embodiment of the present invention, the metal ion and various acid ion compounds are natural phytochemical components including lignans, oligosaccharides, polysaccharides, flavonoids, and cyclic ethers. Terpenoids, fatty acids, East 201225386 Laughing vinegar, catechins, beta-sitosterol, sucralose and alkaloids. According to a preferred embodiment of the invention, the solvent is a solvent having a polarity and a pH greater than 3. Preferably, the solvent is one or more selected from the group consisting of water, sea water, tea, coffee, fruit juice, and wine. According to a preferred embodiment of the invention, the high polymer solution has a pH of 5.5-8. According to a preferred embodiment of the present invention, the step S2 includes the step S21: filtering the chlorophyll powder by filtering and meshing; step S22: pouring the polymer solution; and step 523. stirring by using a magnet mixer at a rotation speed of 500 to 700 RPM; 524. determining whether the uniform fluid is reached; when the determination result is no, then returning to step S22, when the determination result is YES, proceeding to step S25; step S25: applying the fluid to the conductive material layer; Step S26: The above structure is placed in an oven at 100 degrees Celsius, and baked until the water is evaporated to complete the fabrication of the negative electrode structure. According to a preferred embodiment of the invention, the layer of electrically conductive material is made of a conductive material. According to a preferred embodiment of the invention, the electrically conductive material is a metal. According to a preferred embodiment of the invention, the metal is selected from the group consisting of Ming and/or Gold. According to a preferred embodiment of the invention, the electrically conductive material is a metal compound. 9 201225386 According to a preferred embodiment of the invention, the metal compound is selected from one or more of the group consisting of oxidized, zinc oxide and magnesium oxide. According to a preferred embodiment of the invention, the electrically conductive material is a conductive polymeric material. According to a preferred embodiment of the invention, the electrically conductive polymeric material is selected from the group consisting of heterocyclic or aromatic heterocyclic compounds. According to a preferred embodiment of the present invention, the conductive polymer material is selected from one or more of the group consisting of polyacetylene, polyaryl hydrocarbon, polythiophene, & strepamine, polypyrrole, polypyrrole and the above compounds Derivatives. According to a preferred embodiment of the present invention, the chlorophyll is one or more of chlorophyll a, leaf, element b, chlorophyll cl and chlorophyll c2, chlorophyll d, and chlorophyll e. According to a preferred embodiment of the invention, the chlorophyll does not comprise a chlorophyll oxidase. According to a preferred embodiment of the present invention, the negative electrode structure is in the form of a diaphragm. According to a preferred embodiment of the invention, the negative electrode structure has a length of 111 ′ and a width of 50 mm. According to a preferred embodiment of the present invention, the step S3 comprises the step S31: cutting the separator; the step S32: soaking the cut separator in the polymer solution, step S33: taking out the separator and placing it on the membrane In a 1 degree Celsius oven 201225386, 'bake to moisture to evaporate to make a double-sided film; step: take out a separator and evenly spray the electrolyte material; and step S35: cover another separator. According to the invention, it is preferably made of high-fiber material. According to a preferred embodiment of the invention, the high fiber material is paper. According to a preferred embodiment of the invention, the paper comprises cellophane, cotton paper, rice paper and crepe paper. According to a preferred embodiment of the invention, the high fiber material has a pore size between Ο.ΟΙμιη~lcm. According to a preferred embodiment of the invention, the separator is in the form of a membrane. According to a preferred embodiment of the invention, the separator has a length of 55 mm' width of 5 mm and a thickness of 0.2 mm. According to a preferred embodiment of the invention, the electrolyte material is an aqueous solution of an organic or inorganic salt or an aqueous solution of an organic salt and chlorophyll. According to a preferred embodiment of the invention, the organic salt aqueous solution has a conductivity of from 10 ms/cm to 500 ms/cm. According to a preferred embodiment of the present invention, the organic salt is an organic salt other than lithium. The organic or inorganic salt according to a preferred embodiment of the present invention is one or more comprising 11 201225386 sodium telluride, gasified steel and hydrogen hydroxide.

According to a preferred embodiment of the present invention, the step s4 includes a step S41 of: attaching the negative electrode structure to the outer casing; step s42: using the first hollow rod to isolate, "close the structure; step S43: rolling up The first hollow rod of the isolation structure is inserted into the outer casing having the negative electrode structure in the direction of the visitor; step S44: taking the first hollow rod in a counterclockwise direction to retain the isolation structure in the outer portion having the negative electrode structure, the steps S45. Detecting whether the isolation structure is attached to the negative electrode structure in the outer casing; when the upper miscellaneous result is the section, the occupation step S46; when the above inspection result is YES, then step s46 is performed: the isolation structure is extracted and the isolation is determined Whether the structure is damaged; when the above judgment result is no, returning to him, when the above judgment result is YES, executing the step coffee; step S46a, replacing the isolation check to return to execute the spicy (10); and _π: completing the assembly. According to the present invention Preferably, the first hollow rod has an inner diameter of 4.5_' outer diameter of 6.36_ and a length of 47.2 mm. According to a preferred embodiment of the invention, the outer casing has an outer diameter of 14.5 mm. A paper tube having an inner diameter of 12 5 legs and a length of 48 4 coffee. "In accordance with a preferred embodiment of the present invention, the step S5 includes steps such as a negative filling material with a negative __ and an isolation structure. · Step loose: insert the current collector into the shell; Step S53: Use the first 1 rod and the vise _ and _ fill in the positive material; Step (5): View the cathode material: 12 201225386 Whether the required weight I is reached - Large step w, A, if no, return to the execution step. If the result of the above-mentioned inspection is YES, then S55 is executed: the first milk is executed, and the step is made. _ positive _, its towel from the ridge red pole structure. According to a preferred embodiment of the present invention, the inner diameter of the second hollow rod is

The outer diameter is 9.94 mm and the length is 47.2 mm. According to a preferred embodiment of the invention, the current collector is a cylinder. According to the present invention, the current collector has four sides and has a length of 47.2 mm. According to a preferred embodiment of the invention, the positive electrode material is in the form of a powder. The positive electrode (four) according to the present invention - a preferred embodiment, comprises chlorophyll powder. According to the present invention, preferably, the positive electrode material comprises carbon cloth, carbon powder or nano conductive polymer powder. "In accordance with a preferred embodiment of the present invention, the carbon cloth or carbon is white carbon or stone black, stone anti-smoke, glassy carbon or glassy carbon, carbon nanotube, activated carbon, iron diamond, amorphous One or more of carbonaceous, graphite, fullerene, graphite, carbyne, diatomic cesium, C3, atomic carbon, graphitized carbon, thermal decomposition carbon, and coke. According to a preferred embodiment of the present invention, the material of the conductive polymer is selected from the group consisting of 13 201225386 heterocyclic or aromatic heterocyclic compounds. The battery manufactured by the battery manufacturing method of the embodiment of the present invention can utilize the chlorophyll in the positive and negative electrode structures to perform hydrogen storage to achieve the purpose of power supply. That is, in the redox reaction of the battery, when chlorophyll is decomposed from magnesium ions to form pheophytin, the magnesium-depleted portion can combine two hydrogen ions to store hydrogen. Moreover, since the battery manufactured by the battery manufacturing method of the embodiment of the present invention uses a natural environmentally-friendly material to replace the pollution component in the conventional battery, even if it is discarded, it does not pollute the environment, and the environmental protection degree is far superior to the conventional battery. [Embodiment] Hereinafter, embodiments of the present invention will be described in detail with reference to the accompanying drawings and embodiments. 1 is a schematic diagram showing the structure of a battery according to an embodiment of the invention.

Figure. As shown in FIG. 1, an embodiment of the present invention provides a battery 1A including a current collector 110' positive electrode structure 120, an isolation structure 130, a negative electrode structure 14A, and a casing 150. The positive electrode structure 120, the isolation structure 13A, the negative electrode structure_, and the outer casing 150 are circumferentially disposed around the current collector 110. Fig. 2 is a view showing the structure of a negative electrode structure disclosed in the embodiment of the present invention. As shown in FIG. 2, the negative electrode structure disclosed in the embodiment of the present invention includes a conductive material layer (4) and a negative electrode material layer 142, wherein the negative electrode material layer (4) may be formed on the conductive material layer 141.曰 14 201225386 wherein the conductive material layer 141 is made of a conductive material. The conductive material may be a metal, a metal compound or a conductive polymer material. The metal can be selected from the group and / or gold. The metal compound may be selected from one or more of a oxidized, oxidized, and oxidized town. The conductive polymer material is selected from a heterocyclic ring or an aromatic heterocyclic compound. According to the preferred embodiment of the present invention, the conductive polymer material is selected from the group of compounds.

One or more of: a poly(block), a poly(tetra)hydrocarbyl ethylene, a phenol, a polyaniline, a polypyrrole, a polypyrrole, and a derivative of the above compound. The negative electrode material layer M2 includes chlorophyll and a high polymer solution, and the negative electrode material layer 142 may be formed on the conductive material layer (4) by coating or the like. The chlorophyll may be one or more of chlorophyll a, chlorophyll b, chlorophyll el and chlorophyll & phytochemical d, and chlorophyll e. _ can be a fan or liquid. The chlorophyll used has removed chlorophyll oxidase. The high polymer solution has a bond, which is attached to the physical and chemical layers of the conductive material layer, so that the negative electrode layer 142 is more adhesive to the conductive material layer (4). In addition, the conductivity of the high polymer solution is suppressed by the mail/coffee. The high polymer solution may include boron, L35, or zinc. The high polymer solution also secretly adjusts the work function of the layer of electrically conductive material 141 such that the potential difference between the positive and negative electrodes can reach a desired volt, such as 15V. The high polymer solution can be prepared by blending (4) gold, a compound, a polymer, and a solvent of each ion. The filaments can be mixed with high polymer. 201225386 The high polymer of glucose can be plant gall, such as one or more of Ma Lingya Dian powder, Lingjiaodian powder, corn house powder, sweet potato powder, lotus root starch, fennel powder and kudzu root powder. The compound of metal ions and various acid ions can be a carbonic acid mother. The metal ion and the compound of each mirror can be called the chemical composition of the city. Natural phytochemical ages include lignan····················································································· The solvent may be a solvent having a polarity and a enthalpy value greater than 3, for example: X sea X, coffee, wine or wine. The enthalpy of the high polymer solution is preferably 5.5-8. The high polymer solution may also include a vitamin such as vitamin D. The negative electrode structure 140 can be formed into a diaphragm shape, thereby increasing the amount of chlorophyll used, and increasing the contact Φ product to increase the reaction area of the battery. Further, it will be understood by those skilled in the art that the present invention can also increase the amount of chlorophyll used, increase the contact area to increase the reaction area of the battery, and the like by any known technique. Preferably, in the present embodiment, the length of the 贞 贞 structure 14 〇 is 6 Gmm, and the screaming degree is . Please continue to refer to the drawings. The remaining structure of the battery 100 disclosed in the present invention will be further described below. The current collector 110 is a cylinder, and preferably, the current collector n〇 has a diameter of 4 mm and a length of 47.2 mm. The positive electrode structure 120 is composed of a powdery positive electrode material. Preferably, the powdery positive electrode material in the positive electrode structure 120 contains chlorophyll powder. In addition, the powdery positive electrode material may further include carbon cloth, carbon powder or nano conductive polymer powder 201225386. Carbon cloth or carbon powder includes white carbon or waxite (Chaoite), carbon black, carbon black, glass barrier or glassy carbon, carbon nanotube, activated carbon ), Diamond, Diamond, Amorphous carbon, Graphene, Fulerene, Graphite, Carbyne, Diatomic carbon , C3 (Tricarbon), Atomic carbon, graphitized carbon, thermal decomposition of carbon, coke and other carbon allotropes. The material of the electron-conducting molecule is selected from a heterocyclic ring or an aromatic heterocyclic compound. Preferably, the electrically conductive material is selected from one or more of the group consisting of polyacetylene, polyaramid ethylene, polythiophene, polyaniline, polyπ-pyrrole, polypyrrole, and derivatives of the above compounds. The isolation structure 130 includes a first isolation film 131, a second isolation film 132, and an electrolyte material 133 interposed between the two isolation films. The first isolation film 131 and the second isolation film 132 are respectively made of high fiber material, wherein the high fiber material can be paper, the paper type includes cellophane, cotton paper, rice paper and crepe paper, and the high fiber material preferably has a pore size. For 〇.0_~lem. Further, in the present embodiment, the first-isolation film 131 and the second separator 132 are each in the form of a diaphragm, and have a length of 55 mm, a width of 50 mm, and a film thickness of 〇 2 mm. Electrolyte material Π3 can be used as a water solution for money or money surface. The 'organic salt aqueous solution has a conductivity of 1 〇ms/cm 5 〇〇ms/cm. 201225386 Organic salts are organically based on non-clocks. The organic or inorganic bribe is selected from the group consisting of: - or a variety of sodium, sodium hydride and sodium oxynitride. The outer cymbal is 150 疋, an outer diameter of 14 5 _, an inner diameter of 12 5 _, and a length of 48, 4 mm, which is coated with a hard surface, a positive electrode structure U0, an isolation structure 130, and a negative electrode structure 14 〇. ▲ In the present embodiment, both the negative electrode structure 14A and the positive electrode structure 12A contain a leaf '., a halogen', and thus, when the battery is in operation, the chlorophyll in the negative electrode structure (10)

The chlorophyll phase in the positive electrode structure 120 receives light or encounters a solution to generate electrons or holes, thereby forming a potential difference between the positive electrode structure 12G of the battery (10) and the negative electrode structure 14A to provide continuity. That is, the battery of the present invention Qing provides electrical energy using the negative electrode structure 14G and the chlorophyll in the positive electrode structure m as a source of energy. Preferably, the chlorophyll in the negative electrode structure (10) has a different work function from the chlorophyll in the positive electrode structure 120 (in the case of the present embodiment, the negative electrode structure v ... the hole ''this yang> (containing chlorophyll, however, it is understood by those skilled in the art that the battery disclosed by the present invention can also be provided with chlorophyll only in the negative electrode structure (10), or chlorophyll in the fine positive electrode structure 120, and the battery provides Wei. (4) * The diagram is shown as a machine diagram of the method for manufacturing the battery. As shown in Fig. 3, the method for manufacturing the above-mentioned Wei includes the following steps: 18 201225386 Step S1: Making a high_solution; Step S2: Making a negative electrode structure; step S3 • making an isolation structure; step S4: assembling the drain structure and the isolation structure into the outer casing; and step S5. inserting the current collector into the outer casing and filling the positive electrode material into the above-mentioned structure to open The positive electrode structure is completed to complete the fabrication of the entire battery. Figure 4 is a detailed flow chart of the step S1 shown in Figure 3. As shown in Figure 4, the preparation of the high polymer solution of the step S1 comprises the following steps: Step S11: slowly adding the polymer powder in a solvent having a temperature of 40 degrees Celsius; Step S12. Mixing the solution at a rotation speed of 500 to 700 RPM using a magnet dialing machine; • Step S13: detecting the conductivity of the solution using a conductivity meter Up to 5〇-250ms/cm; when the above detection result is no, then return to step §11, and when the above detection result is YES, then step S14 is performed; and step S14: is completed. In this embodiment, The solvent is a solvent having a polarity and a pH of more than 3. Preferably, the solvent is selected from one or more of water, sea water, tea, coffee, fruit juice, wine, etc. Figure 5 is a step S2 of Figure 3 The specific flow chart is as shown in Fig. 5, 201225386. The negative electrode structure of the step S2 includes the following steps: Step S21: filtering the chlorophyll powder with a sieve; Step S22: pouring the polymer solution; Step S23: using a magnet mixer at a rotation speed 5〇〇~7〇〇RpM is given to the drop; Step S24··determine whether the uniform fluid is reached; when the above judgment result is No, the process returns to step S22, and when the above judgment result is YES, the execution is performed. Step S25: Step S25: applying the above fluid onto the conductive material layer; Step S26: placing the above structure in an oven just after Celsius for baking until the water is evaporated to complete the fabrication of the negative electrode structure. - Figure 6 is a diagram A specific flow chart of the steps shown in Fig. 3. As shown in Fig. 6, the fabrication of the isolation structure of the step S3 comprises the following steps: • Step S31 ··Removing the isolation film; Step S32: Soaking the cut isolation film in the high concentration In the body solution; Step S33: taking out the separator and placing it in the excitation 'baking until the water is evaporated to make two separators; baking step S34: taking out a separator, spraying the electrolyte material; and steps S35H is another side-side _ complete _ structure production. The edge of Fig. 7 is shown as a specific flow chart of step S4 shown in Fig. 3. As shown in Figure 7, the negative electrode structure and the isolation structure are assembled into the outer casing as shown in step S4. ♦ include the steps of 20 201225386: Step S41: attaching the negative electrode structure to the outer casing; step S42: using the first hollow rod to close the isolation structure Rolled up, wherein the first hollow rod has an inner diameter of 4.5 mm, an outer diameter of 6 36 mm, and a length of 47.2 mm. » Step S43: screwing the first hollow rod of the winding structure into the outer casing with a negative electrode structure in a clockwise direction Step S44: retaining the first hollow rod take-out isolation structure in a counterclockwise direction in the outer casing having the negative electrode structure; step S45: checking whether the isolation structure is attached to the negative electrode structure in the outer casing; when the above inspection result is no If the result of the above-mentioned inspection is YES, step S47 is performed; step S46: whether the isolated structure is broken or not; if the result of the determination is no, the process returns to step S42; Knot: If yes, then step S46a is performed; step S46a. The isolation structure is replaced and the process returns to step S42; and step 47 is completed. Figure 8 is not a specific flow chart of the step % shown in Figure 3. The step of inserting the current collector into the foreign material and filling the positive electrode material to form the positive electrode structure as shown in step S5 of FIG. 2 includes the following steps: 201225386 Step S51: slowly filling the positive electrode material in the outer casing having the negative electrode structure and the isolation structure; vStep S52: Insert the current collector into the center of the outer casing; Step S53. Fill the pressure material with the first hollow rod and the vise and continue to fill the positive electrode material; • Step S54 • Examine whether the positive electrode material reaches the required weight; ,. If the result is no, then go back to step S53, when the above-mentioned inspection result is YES, then step S55 is performed; and v is step S55. The positive structure is modified by the second hollow rod, wherein the inner diameter of the second hollow rod is 4.5 mm. The outer balance is 9.94 mm and the length is 47 2 mm to complete the fabrication of the positive electrode structure. The battery disclosed in the present invention can utilize the chlorophyll in its positive and negative structures to store hydrogen to achieve the purpose of power supply. Preferably, the positive and negative structures all comprise chlorophyll, but have different work functions. That is, in the oxidation of the battery, the chlorophyll is formed by the detachment of the magnesium ions of the towel to form chlorophyll (Phe〇Phytln), and the magnesium-deficient portion can combine two hydrogen ions, so that hydrogen can be stored. . In addition, since the battery of the present invention replaces the dyeing component of the conventional battery with a natural environmentally-friendly substance, it does not pollute the environment even if it is discarded, and the degree of environmental protection is much better than that of the conventional battery. It should be noted that in the embodiment of the present invention, the words "first", 22 201225386 second, and the like are only used as needed, and are not limited to this in practice, and the characters can be used interchangeably. . The subject matter disclosed above is considered to be illustrative and not restrictive, and the scope of the appended claims are intended to cover all modifications and other embodiments of the invention. Therefore, the maximum range allowed by law can be improved by riding and equalizing

The most discriminating of the substance is to determine the material of this (4) and is not limited or limited by the detailed description of the foregoing embodiments. BRIEF DESCRIPTION OF THE DRAWINGS [0009] A further understanding of the present invention is incorporated in and constitutes an exemplary embodiment of the present disclosure. In the drawings: FIG. 1 is a schematic structural view of a battery disclosed in an embodiment of the present invention. 2 is a schematic view showing the structure of a (four) pole structure disclosed in the present invention. Fig. 3 is a flow chart showing a method of fabricating a battery according to the present invention. FIG. 4 is a detailed flowchart of step S1 shown in FIG. 3. 5 is a specific flow chart of step S2 shown in FIG. 3, FIG. 6 is a specific flowchart of step S3 shown in FIG. 3, and FIG. 7 is a specific diagram of step S4 shown in FIG. 8 is illustrated as a specific spear of step S5 shown in FIG. Figure [Main component symbol description] 23 201225386 100 Battery 110 Current collector 120 Positive structure 130 Isolation structure 131 First isolation film 132 Second isolation film 133 Electrolyte material 140 Negative electrode structure 141 Conductive material layer 142 Anode material layer 150 Case

Sb S2, S3, S4, S5, S11, S12, S13, S14, S2, S22, S23, S24, S25, S26, S31, S32, S33, S34, S35, S4, S42, S43, S44, S45, S46, S46a, S47, S51, S52, S53, S54, S55: Steps

twenty four

Claims (1)

201225386 VII. Patent application scope: 1. A method for manufacturing an electric phase, characterized in that the steps are as follows: Step S1: preparing a polymer solution; Step S2: fabricating a negative structure; Step S3: fabricating an isolation structure; S4: assembling the negative electrode structure and the isolation structure into the outer casing; and step S5: inserting the current collector into the outer casing and filling the positive electrode material into the above structure to form a positive electrode structure; wherein at least the negative electrode structure and the positive electrode structure One includes chlorophyll. 2. The method of manufacturing a battery according to claim 1, wherein the step S1 comprises the following steps: • Step SU: slowly adding a polymer powder in a solvent having a temperature of 40 degrees Celsius; Step S12: The solution is stirred by a magnet mixer at a rotation speed of 5 〇〇 to 7 Torr RpM; Step S13. Using a conductivity meter to detect whether the conductivity of the solution reaches 50-250 ms/cm; when the above detection result is no, return to the execution step. Su, and when the above detection result is YES, step S14 is performed; and step S14: is completed. 25 201225386 3. According to the method for manufacturing a battery according to claim 2, the feature of the battery is that the compound powder and the high polymer are in a concentration of 0. U10. Moor / liter. The method for producing a battery according to the third aspect of the invention, wherein the polymer powder further comprises a vitamin. The method for producing a battery according to the fourth aspect of the invention, wherein the vitamin is vitamin D. 6. The method according to claim 3, wherein the polymer is a polymer of glucose. 7. According to the method for preparing the battery according to Item 6 of the application, the high polymer of the glucose is potato starch, water chestnut powder, corn starch 'sweet potato powder' lotus root lotus powder, mustard powder And one or more of the puerarin powders. 8. The method for producing a battery according to the third aspect of the application, which is characterized in that the compound of the lining metal ion and each nucleus ion is about carbonic acid. 9. The method according to claim 8, wherein the metal ion and the compound of the various acid ions are natural phytochemical components, and the natural phytochemical comprises lignans. Classes, oligosaccharides, polysaccharides, flavonoids, cycloolefins (tetra), fatty acids, sorghum, catechins, steroids, succulents and bioassays. 10. The method according to claim 2, wherein the solvent is a solvent having a polarity and a pH greater than 3. 11. The method of producing a battery according to claim 10, wherein the solvent is one or more selected from the group consisting of water, sea water, tea, coffee, fruit juice, and west. 12. The method of producing a battery according to claim 1, wherein the polymer solution has a pH of 5.5-8. The method for manufacturing a battery according to claim 2, wherein the step S2 comprises the following steps: Step S21: filtering the chlorophyll powder according to the net; step S22: pouring the polymer solution; S23: using a magnet scrambler to perform the scrambling at a rotation speed of ~7〇〇RpM; step S24: determining whether a uniform fluid is reached; when the determination result is no, then returning to step S22, when the determination result is yes, , step S25, and step S25: applying the above fluid to the conductive material layer; Step S%: placing the above structure in an oven of a degree Celsius, and evaporating the water to complete the fabrication of the negative electrode structure. The method for fabricating the battery according to claim 13 is characterized in that the conductive material layer is made of a conductive material. The method for fabricating the battery of claim 14, wherein the conductive material is a metal. 16. A method of fabricating a battery according to claim 5, characterized in that the metal is selected from the group consisting of aluminum and/or gold. The battery according to claim 14 is characterized in that the conductive material is a metal compound. 18. The method of producing a battery according to the invention, wherein the metal compound is selected from one or more of the group consisting of manganese monoxide, zinc oxide and magnesium oxide. 19. The method of manufacturing a battery according to claim 14, wherein the conductive material is a conductive polymer material. The battery according to claim 19, wherein the conductive polymer material is selected from a heterocyclic or aromatic heterocyclic human. The method for fabricating a battery according to claim 20, wherein the conductive polymer material is selected from the group consisting of polyacetylene, polyarylene, polythiophene, poly A strepamine, a polypyrrole, a poly(R) and a derivative of the above compound. 22. The method of producing a battery according to claim 13, wherein the chlorophyll is one or more of chlorophyll a, chlorophyll b, chlorophyll cl and chlorophyll c2, chlorophyll d, and chlorophyll e. The production of the battery according to claim 22 is characterized in that the chlorophyll does not include chlorophyll oxidase. The method for producing a battery according to claim 13 is characterized in that the negative electrode structure is in the form of a diaphragm. '25. According to the method of manufacturing the battery according to claim 24, the negative electrode structure has a length of 6 mm and a width of 5 〇. 26. According to the scope of the patent application The method for manufacturing the battery according to claim 13 is characterized in that the step S3 comprises the following steps: Step S31: cutting off the separator; Step S32: immersing the cut separator in the polymer solution; S33: taking out the separator and placing it in an oven at a temperature of Celsius, baking until the water is evaporated to make two separators; Lu (4) S34: taking out a separator film to uniformly spray the electrolyte material; in step S35: covering Another barrier film. 27. The method of manufacturing a battery according to claim 26, wherein the separator is made of a high fiber material. According to the manufacturer of the battery described in the πth patent application scope, the feature is that the high-fiber material is paper. The method for producing a battery according to claim 28, characterized in that the paper comprises a glass paper, a cotton paper, a rice paper, and a paper or paper. , 29 201225386 30. The method for manufacturing a battery according to the item _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ < 31. The battery according to claim 27, wherein the separator is in the form of a sheet. 32. The battery according to claim 31, wherein the said ship has a length of 55 mm and a width of 5 Qmm and a thickness of 0.2 mm. The manufacturing method of the battery according to item % of the patent application scope is characterized by the fact that the water is produced by the salt and leaf of the water. μ organic 3: According to the method for manufacturing the battery according to the illusion of the patent application scope, the dragon is in that the conductivity of the aqueous solution of the organic salt is “10 ms/cm-500 ms/cm. 35. The lion is invited to patent _ The battery is characterized by 'the touched-containing_organic_. The method' is 36. The battery according to claim 100, characterized in that the right-handed method, the juice-side organic or inorganic salt The method of manufacturing a battery according to claim 26 of the invention, wherein the step S4 comprises the following steps: S41 · attaching the negative electrode structure to the outer casing; step S42: using the first hollow rod to tightly wind up the isolation structure; step S43: screwing the first hollow rod of the winding isolation structure into the negative electrode structure in a clockwise direction Step S44: taking the first intermediate rotation in a counterclockwise direction to retain the isolation knot in the outer casing having the negative electrode structure; 4S45. Whether the inspection structure is perpendicular to the negative electrode structure of the outer casing; If no Then, step tearing is performed; when the above-mentioned viewing result is 疋, then step S47 is performed; step S46: extracting the isolation structure and judging whether the isolation node is damaged or not; when the upper part is broken, the _ execution step is fine; #上_结:疋, then step S46a is performed; step S46a. The isolation structure is replaced and the process returns to step S42; and step S47: the assembly is completed. 38. The method of making the battery according to the item 37 is described in the The inner diameter of the hollow rod is 45 coffee, and the outer straight diameter is 636 mm 'the length is 47, 2 mm. 39. According to the method for manufacturing the battery according to claim 37, the dragon is characterized in that the outer shell is - outer A paper tube having a diameter of R5_, an inner diameter of 12 5_31 201225386 and a length of 48.4 mm. The method of manufacturing the battery according to the invention of claim 37, wherein the step S5 comprises the following steps: Step S51, filling the positive electrode material; slowly filling in the outer casing having the negative electrode structure and the isolation structure Step S52: inserting the current collector into the ten cores of the outer casing; Step S53. Filling with the first hollow rod and the vise and continuing to fill the positive electrode material ^S54. Check whether the positive electrode material reaches the required weight. If no, return to the execution step. When the above-mentioned inspection result is YES, step S55 is performed; and the second hollow rod is used to modify the positive electrode structure, thereby completing the fabrication of the pole structure. The battery according to the application (10) is characterized in that the inner diameter of the second hollow rod is 45_static'9·9-' and the length is 47.2 coffee. The method for producing a battery according to the fourth aspect of the invention, wherein the current collector is integrated. The method of manufacturing a battery according to claim 42, wherein the current collector has a diameter of 4 mm and a length of 47.2 mm. 32 201225386 44. According to the patent application model 4 4, the method of extracting the battery is 粉末, and the escaping cathode material is powdery. Its special = secretive at 44, as a method, ,;; depending on the cathode material contains chlorophyll powder. The method of manufacturing the battery according to claim 45, wherein the polymer powder/positive electrode material further comprises a carbon cloth, a carbon powder or a nanometer conductivity meter according to claim 46 of the patent application scope. The manufacturing method of the battery is characterized in that 'the carbon cloth or carbon powder is self-selling, carbon black, soot, glass carbon or glassy carbon, carbon nanotube, activated carbon, diamond, diamond, bismuth One or more of carbon, graphite thin, fullerene, graphite, carbyne, diatomic carbon, C3, original: graphitized carbon, thermal decomposition carbon type 'coke' 48. According to the scope of patent application 46 The battery described in the item is characterized in that the material of the conductive polymer is selected from a heterocyclic ring or an aromatic noisy @>. 33