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Oxygen Reduction Electrode Properties of the Ba(Ce,Gd,Ru)O{sub}(3-δ) Oxides in Alkaline Aqueous Solution

机译:碱性水溶液中Ba(Ce,Gd,Ru)O {um}(3-δ)氧化物的氧还原电极性质

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Two series of compositions, BaCe{sub}(0.8-x)Gd{sub}0.2Ru{sub}xO{sub}(3-δ)(BCGR{sub}x, x=0-0.8) and BaGd{sub}(1-y)Ru{sub}yO{sub}(3-δ)(BGR{sub}y, y=0.5-1.0), were synthesized and their crystal phases were examined. The BCGR{sub}0.15 and BGR{sub}0.5 oxides were a single phase of perovskite solid solution, while BCGR{sub}0.67 and BGR{sub}0.67 were a perovskite-related superstructure phase. The onset voltage (V{sub}o) of the reduction current and the efficiency (E{sub}4) of the 4-electron reduction of oxygen were evaluated by semi-steady state voltammetry with rotating ring-disk electrodes. In the BCGR{sub}x series, the activities for electrochemical oxygen reduction (EOR) increased with increasing Ru content. In the BGR{sub}y series, the BGR{sub}0.67 superstructure phase showed a higher EOR activity than the perovskite BGR{sub}0.5 and the hexagonal (4H) BaRuO{sub}3. This indicates that the EOR activity depends on the crystal phase. The BGR{sub}0.67 exhibited the best EOR activity of all the samples. The V{sub}o value was 0.80 V vs. reversible hydrogen electrode and the E{sub}4 value was almost 100%.
机译:两个系列组成,BACE {sub}(0.8-x)gd {sub} 0.2ru {sub} xo}(3-Δ)(bcgr {sub} x,x = 0-0.8)和bagd {sub} (1-y)ru {sub} yo {sub}(3-δ)(bgr {sub} y,y = 0.5-1.0),并检查它们的晶相。 BCGR {Sub} 0.15和BGR {亚} 0.5氧化物是钙钛矿固溶体的单相,而BCGR {Sub} 0.67和BGR {Sub} 0.67是钙钛矿相关的上层建平相。通过具有旋转环形盘电极的半稳态伏安法评估氧的4-电子减少的降低电流和效率(e {sub} 4)的开始电压(v {sub} 4)。在BCGR {Sub} X系列中,电化学氧还原(EOR)的活动随着RU含量的增加而增加。在BGR {Sub} Y系列中,BGR {Sub} 0.67上层结构阶段显示比Perovskite BGR {Sub} 0.5和六边形(4H)Baruo {Sub} 3更高的EOR活性。这表明EOR活性取决于晶相。 BGR {sub} 0.67表现出所有样本的最佳EOR活动。 V {Sub} O值为0.80V与可逆氢电极,E {Sub} 4值几乎为100%。

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