ぺロブスカイト型酸化物La<sub>1-</sub><i><sub>x</sub></i>A<i><sub>x</sub></i>MnO<sub>3</sub>(A = Na, K, Rb)の濃アルカリ水溶液中での電気化学的酸素還元特性
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- Electrochemical Oxygen Reduction Properties of Perovskite-type Oxides La<sub>1−</sub><i><sub>x</sub></i>A<i><sub>x</sub></i>MnO<sub>3</sub>(A = Na, K, Rb) in Concentrated Alkaline Solution
- ペロブスカイト型酸化物La1-xAxMnO3(A=Na,K,Rb)の濃アルカリ水溶液中での電気化学的酸素還元特性
- ペロブスカイトガタ サンカブツ La1-xAxMnO3 A Na K Rb ノ ノウアルカリ スイヨウエキ チュウ デ ノ デンキ カガクテキ サンソ カンゲン トクセイ
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<p>Oxygen reduction properties of gas diffusion-type oxygen electrodes loaded by 50 wt% with perovskite-type oxides, La1−xAxMnO3(A = Na, K, Rb, 0.0 ≦ x ≦ 0.2), were investigated in 8 mol dm−3 KOH aqueous solution at 60°C under air flow. Among these oxides, La0.8Rb0.2MnO3 gave the highest electrode performance, i.e., current density of 341 mA cm−2 at −150 mV vs. Hg/HgO. This oxide was found to be highly active for the direct 4-electron reduction of oxygen as revealed by a rotating ring-disk electrode (RRDE) analysis. Electrode performances changed with a change in A or x over the oxides, and tended to be higher with the oxide which exhibited a smaller amount of oxygen desorption in temperature-programmed desorption (TPD) experiments. On the basis of the iodometry and electron spin resonance (ESR) analysis, the 4-electron reduction was suggested to take place most favorably at the sites composed of a pair of Mn3+ and Mn4+ on the oxide surface. The electrode loaded with La0.8Rb0.2MnO3 was confirmed to be fairly stable over a continuous operation for 100 h under a galvanostatic condition of 300 mA cm−2. The same electrode allowed to construct a zinc-air battery with a maximum power density as large as 293 mW cm−2 at a cell voltage of 0.7 V.</p>
収録刊行物
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- Electrochemistry
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Electrochemistry 68 (2), 112-118, 2000-02-05
公益社団法人 電気化学会
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詳細情報 詳細情報について
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- CRID
- 1390001277391070080
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- NII論文ID
- 10004454824
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- NII書誌ID
- AN00151637
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- ISSN
- 21862451
- 13443542
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- NDL書誌ID
- 4981059
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- 本文言語コード
- ja
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- データソース種別
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- JaLC
- NDL
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