JPH06256986A - Method for manufacturing hydrogen storage material - Google Patents

Method for manufacturing hydrogen storage material

Info

Publication number
JPH06256986A
JPH06256986A JP5072896A JP7289693A JPH06256986A JP H06256986 A JPH06256986 A JP H06256986A JP 5072896 A JP5072896 A JP 5072896A JP 7289693 A JP7289693 A JP 7289693A JP H06256986 A JPH06256986 A JP H06256986A
Authority
JP
Japan
Prior art keywords
hydrogen
deuterium
ions
cathode
hydrogen storage
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP5072896A
Other languages
Japanese (ja)
Inventor
Masato Mino
正人 三野
Toru Koyashiki
徹 小屋敷
Maki Ishizawa
真樹 石沢
Kazuhiko Takeno
和彦 竹野
Tetsuo Take
武  哲夫
Takahisa Masashiro
尊久 正代
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
NTT Inc
Original Assignee
Nippon Telegraph and Telephone Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Nippon Telegraph and Telephone Corp filed Critical Nippon Telegraph and Telephone Corp
Priority to JP5072896A priority Critical patent/JPH06256986A/en
Publication of JPH06256986A publication Critical patent/JPH06256986A/en
Pending legal-status Critical Current

Links

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E30/00Energy generation of nuclear origin
    • Y02E30/10Nuclear fusion reactors

Landscapes

  • Electrolytic Production Of Metals (AREA)

Abstract

(57)【要約】 (修正有) 【目的】 重水素あるいは水素の蓄積量を飛躍的に高め
た水素蓄積材料の製造方法を提供し、水素蓄積材料内で
の水素同位体同士の核融合を効率的に生ぜしめることを
実現するのを目的とする。 【構成】 水素イオンあるいは重水素イオンもしくはそ
の両方を含み、パラジウムイオンを含む溶液3を用い
て、陽極1および陰極2に水素発生電圧を印加すること
により、陰極1に水素あるいは重水素もしくはその両方
を吸蔵したパラジウムを析出させることを特徴とする。
(57) [Summary] (Modified) [Purpose] Providing a method for producing hydrogen storage materials that dramatically increases the amount of deuterium or hydrogen stored, and the fusion of hydrogen isotopes within the hydrogen storage materials. The purpose is to achieve efficient production. [Structure] A solution 3 containing hydrogen ions and / or deuterium ions and containing palladium ions is used to apply a hydrogen generation voltage to the anode 1 and the cathode 2, thereby producing hydrogen and / or deuterium at the cathode 1. It is characterized in that palladium occluding is deposited.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は水素蓄積材料の製造方
法、さらに詳細には水素同位体同士の核融合を生ぜしめ
るに有効な(重)水素蓄積材料の製造方法に関するもの
である。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing a hydrogen storage material, and more particularly to a method for producing a (deuterated) hydrogen storage material effective for causing nuclear fusion of hydrogen isotopes.

【0002】[0002]

【従来の技術】これまでに、1000℃以下の温度にお
いて、固体中で水素の関与した発熱反応を行わせる方法
として、電気分解法(例えば特願平1−90311号)
および真空法(例えば特願平1−322662号)が提
案されている。
2. Description of the Related Art Heretofore, as a method for causing an exothermic reaction involving hydrogen in a solid at a temperature of 1000 ° C. or lower, an electrolysis method (for example, Japanese Patent Application No. 1-90311).
And a vacuum method (for example, Japanese Patent Application No. 1-232262).

【0003】電気分解法は、重水(D2O)の電気分解
により発生した重水素をパラジウム(Pd)もしくはチ
タン(Ti)中に吸蔵させ重水素のPdあるいはTi中
濃度を上げることにより発熱にいたらしめる方法であ
り、真空法はPdあるいはTi中に重水素あるいは水素
ガスを吸蔵させた後、温度勾配、電位勾配、圧力勾配等
を与えることにより、吸蔵した重水素あるいは水素の蓄
積層を形成させ発熱にいたらしめる方法である。いずれ
の方法においても、重水素あるいは水素の十分な蓄積が
発熱反応を効率的に行わせるのに重要な要素となってい
る。
In the electrolysis method, deuterium generated by electrolysis of heavy water (D 2 O) is occluded in palladium (Pd) or titanium (Ti) to increase the concentration of deuterium in Pd or Ti to generate heat. The vacuum method is a method of occluding deuterium or hydrogen gas in Pd or Ti, and then applying a temperature gradient, a potential gradient, a pressure gradient, etc., to form an accumulated layer of deuterium or hydrogen stored therein. This is a method that causes heat generation. In either method, sufficient accumulation of deuterium or hydrogen is an important factor for efficient exothermic reaction.

【0004】[0004]

【発明が解決しようとする課題】しかしながら、例えば
電気分解法においては、陰極中への重水素あるいは水素
の蓄積は、陰極表面に発生する重水素の陰極内部への拡
散のみによるため、重水素の拡散速度が律速となり、吸
蔵量が少ない、吸蔵に時間がかかる、発熱量が少ない等
の問題点があった。また、真空法においても、(重)水
素雰囲気中で加熱冷却等によりPdあるいはTi等に
(重)水素を吸蔵させているが、電気分解法と同じく
(重)水素の蓄積は試料表面からの拡散のみを利用して
いるため、拡散速度が律速となり、吸蔵量が少ない、吸
蔵に時間がかかる、発熱量が少ない等の問題があった。
However, for example, in the electrolysis method, the accumulation of deuterium or hydrogen in the cathode is due to the diffusion of deuterium generated on the surface of the cathode into the inside of the cathode. There are problems that the diffusion rate is rate-determining, the amount of occlusion is small, the time required for occlusion is long, and the amount of heat generated is small. Also in the vacuum method, (deuterium) hydrogen is occluded in Pd, Ti, etc. by heating and cooling in a (deuterium) hydrogen atmosphere, but the accumulation of (heavy) hydrogen from the sample surface is the same as in the electrolysis method. Since only diffusion is used, there are problems that the rate of diffusion is rate-determining, the amount of occlusion is small, the time required for occlusion is long, the amount of heat generated is small, etc.

【0005】本発明は上述の課題に鑑みなされたもので
あり、重水素あるいは水素の蓄積量を飛躍的に高めた水
素蓄積材料を提供し、水素蓄積材料内での水素同位体同
士の核融合を効率的に生ぜしめることを実現するのを目
的とする。
The present invention has been made in view of the above problems, and provides a hydrogen storage material in which the amount of deuterium or hydrogen accumulated is dramatically increased, and nuclear fusion of hydrogen isotopes in the hydrogen storage material is provided. The purpose is to realize to efficiently generate.

【0006】[0006]

【課題を解決するための手段】上述した目的を達成する
ため、本発明は水素イオンあるいは重水素イオンもしく
はその両方を含み、パラジウムイオンを含む溶液を用い
て、陽極および陰極に水素発生電圧を印加することによ
り、陰極に水素あるいは重水素もしくはその両方を吸蔵
したパラジウムを析出させることを特徴とする。
In order to achieve the above object, the present invention applies a hydrogen generating voltage to an anode and a cathode using a solution containing hydrogen ions and / or deuterium ions or both and containing palladium ions. By doing so, palladium having hydrogen or deuterium or both stored therein is deposited on the cathode.

【0007】本発明をさらに詳しく説明する。The present invention will be described in more detail.

【0008】本発明による溶液は、水素イオンあるいは
重水素イオンもしくはその両方を含み、パラジウムイオ
ンを含むものであればいかなるものでもよい。たとえ
ば、水素イオンあるいは重水素イオンもしくはその両方
を含むパラジウム塩化物溶液、陽極がパラジウムを含む
ものであるときには、水素イオンあるいは重水素イオン
もしくはその両方を含むジアミノ亜硝酸塩溶液などを有
効に使用することができる。
The solution according to the present invention may be any as long as it contains hydrogen ions and / or deuterium ions and palladium ions. For example, a palladium chloride solution containing hydrogen ions or deuterium ions or both, and when the anode contains palladium, a diaminonitrite solution containing hydrogen ions or deuterium ions or both can be effectively used. .

【0009】陽極は本発明で基本的に限定されるもので
はなく、たとえば白金などの不溶性陽極、パラジウムで
あることができる。
The anode is not fundamentally limited in the present invention and may be, for example, an insoluble anode such as platinum or palladium.

【0010】陰極も基本的に限定されるものではなく、
パラジウム、水素吸蔵合金などを使用することができ
る。
The cathode is not basically limited, either.
Palladium, hydrogen storage alloy, etc. can be used.

【0011】水素イオンあるいは重水素イオンもしくは
その両方を含み、パラジウムイオンを含む溶液および上
述の陽極および陰極を用いて、水素発生電圧を両極に印
加することにより、陰極で水素あるいは重水素を発生さ
せ、水素を多量に吸蔵した過飽和状態のPdを析出させ
る。なお、Pd中に効率良く(重)水素を吸蔵させるた
めに、溶液中の(重)水素イオン濃度を高めるためのp
Hの調整、溶液組成の調整ならびに(重)水素発生リッ
チとなるように両極に電圧を印加している。
Hydrogen or deuterium is generated at the cathode by applying a hydrogen generation voltage to both electrodes by using a solution containing hydrogen ions and / or deuterium ions or both and containing palladium ions and the above-mentioned anode and cathode. , Pd in a supersaturated state in which a large amount of hydrogen is stored is deposited. In order to efficiently store (deuterium) hydrogen in Pd, p for increasing the concentration of (heavy) hydrogen ion in the solution
Voltage is applied to both electrodes so that H is adjusted, the composition of the solution is adjusted, and (heavy) hydrogen generation is rich.

【0012】[0012]

【作用】本発明水素蓄積材料の製造方法においては、陰
極部分には電界により(重)水素イオンが誘引され、イ
オン、原子あるいはガスの状態で多量に存在している。
この陰極でPdを析出させるため、Pdの析出成長過程
で(重)水素の取り込みが連続的に行われ、過飽和状態
の水素吸蔵Pdを形成することが可能となる。こうして
作製した本発明水素蓄積材料を常温核融合の原料として
使用することにより、水素蓄積材料内での水素同位体同
士の核融合の発生確率が高まり、これまでの電気分解法
あるいは真空法等に比べて、反応発熱量を飛躍的に高め
ることが可能となる。
In the method for producing a hydrogen storage material of the present invention, (deuterium) hydrogen ions are attracted to the cathode portion by the electric field, and a large amount of ions (ions), atoms or gases are present.
Since Pd is deposited at this cathode, (heavy) hydrogen is continuously taken in during the Pd deposition growth process, and it becomes possible to form hydrogen-storing Pd in a supersaturated state. By using the hydrogen storage material of the present invention thus prepared as a raw material for cold fusion, the probability of nuclear fusion of hydrogen isotopes in the hydrogen storage material is increased, and the conventional electrolysis method or vacuum method can be used. In comparison, it is possible to dramatically increase the reaction heat value.

【0013】[0013]

【実施例1】以下、本発明の一実施例を、図面を参照し
て詳細に説明する。
Embodiment 1 An embodiment of the present invention will be described in detail below with reference to the drawings.

【0014】図1に示すように、本発明第1の実施例に
おける水素蓄積材料の製造方法は、陽極1を白金(P
t)、陰極2をPdとし、溶液3としてPd塩化物を用
いたもので、具体的には重水中に塩化第一パラジウム
(3.7g/l)、第二リン酸ナトリウム(100g/
l)、第二リン酸アンモニウム(20g/l)および安
息香酸(2.5g/l)を加えた溶液3を調整し、陰陽
極間に1〜10Vの直流電圧を印加し、陰極で(重)水
素が盛んに発生する条件で電着を行った。電着過程にお
いてPd陰極では、(重)水素の発生が観察されるとと
もに陰極にはPdが析出した。析出したPdの表面には
多数の微細なクラックが見られ、この析出したPdが多
量の(重)水素を吸蔵し、部分的に水素化物を形成して
いることがわかる。こうして作製した水素蓄積材料(1
0mm×10mm×1mm)を用いて発熱反応の実験を
行った。はじめに、作製した水素蓄積材料の片面に酸化
膜を形成し、他面に金薄膜を形成して内部の重水素を封
止した。その後、試料を真空容器に移して、真空中で試
料を電気ヒータにより加熱して温度勾配を与えた結果、
試料温度は1000℃を越え試料治具が熱により変形し
た。また、発熱反応と同時に真空容器中にヘリウム4が
検出された。発熱量は従来の電気分解法や真空法で報告
されている例に比べて著しく増加していた。
As shown in FIG. 1, in the method of manufacturing a hydrogen storage material according to the first embodiment of the present invention, the anode 1 is made of platinum (P).
t), using Pd as the cathode 2 and using Pd chloride as the solution 3, specifically, in heavy water, palladium (I) chloride (3.7 g / l) and dibasic sodium phosphate (100 g / l).
1), diammonium phosphate (20 g / l) and benzoic acid (2.5 g / l) were added to the solution 3 to apply a DC voltage of 1 to 10 V between the negative and positive electrodes, ) Electrodeposition was carried out under the condition that hydrogen was actively generated. During the electrodeposition process, generation of (heavy) hydrogen was observed at the Pd cathode, and Pd was deposited at the cathode. Many fine cracks are seen on the surface of the deposited Pd, and it is understood that the deposited Pd occludes a large amount of (heavy) hydrogen and partially forms a hydride. The hydrogen storage material (1
(0 mm × 10 mm × 1 mm) was used to perform an exothermic reaction experiment. First, an oxide film was formed on one surface of the produced hydrogen storage material, and a gold thin film was formed on the other surface to seal the deuterium inside. After that, the sample was transferred to a vacuum container, and the sample was heated by an electric heater in a vacuum to give a temperature gradient.
The sample temperature exceeded 1000 ° C and the sample jig was deformed by heat. In addition, helium 4 was detected in the vacuum container simultaneously with the exothermic reaction. The calorific value was significantly increased as compared with the cases reported by the conventional electrolysis method and vacuum method.

【0015】[0015]

【実施例2】以下、本発明の一実施例を、図面を参照し
て詳細に説明する。
Embodiment 2 An embodiment of the present invention will be described in detail below with reference to the drawings.

【0016】図2に示すように、本発明第2の実施例に
おける水素蓄積材料の製造方法は、陽極11をPd、陰
極12をPdとし、溶液としてジアミノ亜硝酸塩を用い
たもので、具体的には重水中にジアミノ亜硝酸パラジウ
ム(4g/l)、硝酸アンモニウム(100g/l)、
亜硝酸ナトリウム(10g/l)を加えた溶液13を調
整し、陰陽極間に1〜10Vの直流電圧を印加し、陰極
で(重)水素が盛んに発生する条件で電着を行った。電
着過程においてPd陰極では、(重)水素の発生が観察
されるとともに陰極にはPdが析出した。析出したPd
の表面には多数の微細なクラックが見られ、この析出し
たPdが多量の(重)水素を吸蔵し部分的に水素化物を
形成していることがわかる。こうして作製した水素蓄積
材料(10mm×10mm×1mm)を用いて実施例1
と同様に発熱反応の実験を行った。その結果、実施例1
と同様に多量の過剰熱とヘリウム4が検出され、その発
熱量は従来の電気分解法や真空法で報告されている例に
比べて著しく増加していた。なお、4、14の多孔質膜
は陰極、陽極で発生するガスの混合を防止するものであ
る。図中、符号5、15は槽、6、16は電源、7、1
7は配線を示す。
As shown in FIG. 2, the method for producing a hydrogen storage material according to the second embodiment of the present invention uses Pd for the anode 11 and Pd for the cathode 12 and uses diaminonitrite as a solution. Diaminopalladium nitrite (4 g / l), ammonium nitrate (100 g / l),
A solution 13 to which sodium nitrite (10 g / l) was added was prepared, a direct current voltage of 1 to 10 V was applied between the negative and positive electrodes, and electrodeposition was performed under the condition that (deuterium) hydrogen was actively generated at the cathode. During the electrodeposition process, generation of (heavy) hydrogen was observed at the Pd cathode, and Pd was deposited at the cathode. Precipitated Pd
A large number of fine cracks were observed on the surface of Pd, and it can be seen that the precipitated Pd occludes a large amount of (heavy) hydrogen and partially forms a hydride. Example 1 using the hydrogen storage material (10 mm × 10 mm × 1 mm) thus produced
An exothermic reaction experiment was conducted in the same manner as in. As a result, Example 1
Similarly, a large amount of excess heat and helium 4 were detected, and the amount of generated heat was remarkably increased as compared with the cases reported by the conventional electrolysis method and vacuum method. The porous membranes 4 and 14 prevent mixing of gases generated at the cathode and the anode. In the figure, reference numerals 5 and 15 are tanks, 6 and 16 are power supplies, 7 and 1
Reference numeral 7 indicates wiring.

【0017】[0017]

【発明の効果】以上の説明で明らかなように、本発明の
水素蓄積材料製造方法によれば、(重)水素イオンが多
量に存在する溶液中においてPdを析出させるため、P
dの析出成長過程で(重)水素吸蔵が行われ効率的に
(重)水素吸蔵Pdが形成される。そのため、(重)水
素拡散が表面からのみ行われる従来の水素吸蔵方法に比
べて、吸蔵量と吸蔵速度を飛躍的に高めることが可能と
なる。さらに、こうして作製された水素蓄積材料を用い
て、常温核融合反応を生ぜしめる場合、従来の試料に比
べて多量の(重)水素を含んでいるために、試料の単位
体積当たりの発熱量を高くすることができる。
As is apparent from the above description, according to the method for producing a hydrogen storage material of the present invention, since Pd is precipitated in a solution containing a large amount of (deuterium) hydrogen ions, Pd
In the precipitation growth process of d, (deuterium) hydrogen storage is performed and the (heavy) hydrogen storage Pd is efficiently formed. Therefore, compared to the conventional hydrogen storage method in which (heavy) hydrogen diffusion is performed only from the surface, it becomes possible to dramatically increase the storage amount and storage rate. Furthermore, when a cold fusion reaction is generated using the hydrogen storage material produced in this way, it contains a larger amount of (deuterium) than the conventional sample, so the calorific value per unit volume of the sample is increased. Can be higher.

【図面の簡単な説明】[Brief description of drawings]

【図1】本発明の実施例1を実施するための装置の概略
図。
FIG. 1 is a schematic diagram of an apparatus for carrying out Example 1 of the present invention.

【図2】本発明の実施例2を実施するための装置の概略
図。
FIG. 2 is a schematic diagram of an apparatus for carrying out Example 2 of the present invention.

【符号の説明】[Explanation of symbols]

1 Pt電極(陽極) 2 Pd電極(陰極) 3 溶液 4 多孔質膜 5 槽 6 電源 7 配線 11 Pd電極(陽極) 12 Pd電極(陰極) 13 溶液 14 多孔質膜 15 槽 16 電源 17 配線 1 Pt electrode (anode) 2 Pd electrode (cathode) 3 solution 4 porous film 5 tank 6 power supply 7 wiring 11 Pd electrode (anode) 12 Pd electrode (cathode) 13 solution 14 porous film 15 tank 16 power supply 17 wiring

───────────────────────────────────────────────────── フロントページの続き (72)発明者 竹野 和彦 東京都千代田区内幸町1丁目1番6号 日 本電信電話株式会社内 (72)発明者 武 哲夫 東京都千代田区内幸町1丁目1番6号 日 本電信電話株式会社内 (72)発明者 正代 尊久 東京都千代田区内幸町1丁目1番6号 日 本電信電話株式会社内 ─────────────────────────────────────────────────── ─── Continuation of front page (72) Inventor Kazuhiko Takeno 1-1-6 Uchisaiwaicho, Chiyoda-ku, Tokyo Nihon Telegraph and Telephone Corporation (72) Inventor Tetsuo Take 1-16-6 Uchisaiwaicho, Chiyoda-ku, Tokyo Nihon Telegraph and Telephone Corp. (72) Inventor Masahisa Masahiro 1-1-6 Uchisaiwaicho, Chiyoda-ku, Tokyo Nihon Telegraph and Telephone Corp.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】水素イオンあるいは重水素イオンもしくは
その両方を含み、パラジウムイオンを含む溶液を用い
て、陽極および陰極に水素発生電圧を印加することによ
り、陰極に水素あるいは重水素もしくはその両方を吸蔵
したパラジウムを析出させることを特徴とする水素蓄積
材料の製造方法。
1. A solution containing hydrogen ions and / or deuterium ions, and a solution containing palladium ions is used to apply a hydrogen generation voltage to the anode and the cathode to occlude hydrogen or deuterium or both into the cathode. A method for producing a hydrogen storage material, characterized by depositing palladium.
JP5072896A 1993-03-08 1993-03-08 Method for manufacturing hydrogen storage material Pending JPH06256986A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5072896A JPH06256986A (en) 1993-03-08 1993-03-08 Method for manufacturing hydrogen storage material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5072896A JPH06256986A (en) 1993-03-08 1993-03-08 Method for manufacturing hydrogen storage material

Publications (1)

Publication Number Publication Date
JPH06256986A true JPH06256986A (en) 1994-09-13

Family

ID=13502581

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5072896A Pending JPH06256986A (en) 1993-03-08 1993-03-08 Method for manufacturing hydrogen storage material

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