US2008283413A1PendingUtilityA1

Method for manufacturing oxygen reduction electrode, oxygen reduction electrode and electrochemical element using same

Assignee: MATSUSHITA ELECTRIC INDUSTRIAL CO LTDPriority: Jun 11, 2003Filed: Dec 28, 2007Published: Nov 20, 2008
Est. expiryJun 11, 2023(expired)· nominal 20-yr term from priority
G01N 27/404H01M 4/96H01M 4/8885H01M 4/8605Y02E60/50
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Claims

Abstract

It is an object of the present invention to provide an oxygen reduction electrode which provides four-electron reduction reaction with high selectivity in the reaction of reducing oxygen. The present invention involves a method of manufacturing an electrode for reducing oxygen used for four-electron reduction of oxygen, having (1) a first step wherein a charcoal-based material is obtained by carbonization of a starting material comprising a nitrogen-containing synthetic polymer, and (2) a second step wherein the electrode for reducing oxygen is manufactured using an electrode material comprising the charcoal-based material.

Claims

exact text as granted — not AI-modified
1 - 19 . (canceled) 
     
     
         20 . A method for performing a four-electron reduction of oxygen in a generator cell;
 (1) the generator cell comprising a positive electrode, a negative electrode, and an electrolyte;   (2) the electrolyte being interposed between the positive electrode and the negative electrode;   (3) the four-electron reduction of oxygen being conducted on the positive electrode;   (4) the positive electrode being obtained by a process comprising:
 (a) a first step of obtaining a charcoal-based material by carbonizing a starting raw material comprising a nitrogen-containing synthetic polymer at a temperature from 500 to 1000° C. in an atmosphere of 10% or less oxygen concentration by volume, and subjecting the charcoal-based material to steam activation; and 
 (b) a second step of producing the positive electrode using an electrode material containing the steam-activated charcoal-based material; and 
   (5) said method comprising:   a step of supplying oxygen and water to the positive electrode.   
     
     
         21 . The method according to  claim 20 , wherein the nitrogen-containing synthetic polymer is made from at least one kind of monomer having one or more nitrogen atoms in the molecule. 
     
     
         22 . The method according to  claim 20 , wherein the nitrogen-containing synthetic polymer is at least one selected from the group consisting of a polyacrylonitrile, a polyimide, a polyamide, a polyurethane, a polyurea and a polyaniline. 
     
     
         23 . The method according to  claim 20 , wherein the atmosphere is an inert gas atmosphere. 
     
     
         24 . The method according to  claim 20 , wherein the positive electrode is produced in the second step by forming the electrode material into a specific shape to obtain a formed body, and laminating or pressure-bonding the formed body to an electrically conductive base. 
     
     
         25 . The method according to  claim 20 , wherein the positive electrode is produced in the second step by preparing a paste containing the electrode material, and coating the paste onto an electrically conductive base. 
     
     
         26 . The method according to  claim 20  wherein an inorganic component is added to at least one of the starting material, the charcoal-based material and the electrode material. 
     
     
         27 . The method according to  claim 26 , wherein the inorganic component comprises at least one selected from the group consisting of manganese, silicon, aluminum, phosphorus, calcium, potassium and magnesium. 
     
     
         28 . The method according to  claim 20 , wherein the charcoal-based material exhibits the infrared absorption in the range of from about 3000 to 3500 cm −1 . 
     
     
         29 . The method according to  claim 28 , wherein the infrared absorption is based on stretching of nitrogen (N)−hydrogen (H). 
     
     
         30 . The method according to  claim 20 , wherein the charcoal-based material exhibits the infrared absorption in the range of from about 2000 to 2300 cm −1 . 
     
     
         31 . The method according to  claim 30 , wherein the infrared absorption is based on stretching of carbon (C)=nitrogen (N) of nitrile. 
     
     
         32 . The method according to  claim 30 , wherein the infrared absorption is based on stretching of nitrogen (N)=carbon (C)=nitrogen (N) of carbodiimide. 
     
     
         33 . The method according to  claim 30 , wherein the infrared absorption is based on stretching of carbon (C)=nitrogen (N). 
     
     
         34 . The method according to  claim 20 , wherein the charcoal-based material exhibits the infrared absorption in the range of from about 1600 to 1800 cm −1 . 
     
     
         35 . The method according to  claim 34 , wherein the infrared absorption is based on stretching of nitrogen (N)−carbon (C)=oxygen (O) of amide or imide. 
     
     
         36 . The method according to  claim 20 , wherein the charcoal-based material exhibits 1) the infrared absorption in the range of from about 3000 to 3500 cm −1 , 2) the infrared absorption in the range of from about 2000 to 2300 cm −1  and 3) the infrared absorption in the range of from about 1600 to 1800 cm −1 . 
     
     
         37 . The method according to  claim 20 , wherein at least one type of metal and oxide thereof is added to at least one of the starting material, the charcoal-based material and the electrode material. 
     
     
         38 . The method according to  claim 37 , wherein the oxide is a lower oxide of manganese represented by the general formula MnO y , wherein y is a number of oxygen atoms determined by the valence of manganese (Mn), and is less than two. 
     
     
         39 . The method according to  claim 20 , wherein metal is added to at least one of the starting material, the charcoal-based material and the electrode material.

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