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MnxIr1#x2212;xO2/C used as bifunctional electrocatalyst in alkaline medium

机译:Mn x Ir 1-x O 2 / C在碱性介质中用作双功能电催化剂

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There is a growing interest in oxygen electrochemistry as conversions between O2 and H2O play an important role in a variety of renewable energy technologies. In this paper, bifunctional electrocatalysts of the general formula MnxIr1−xO2/C were prepared using a pyrolysis method. Their physical characteristics were examined via transmission electron microscopy, and the electrochemical properties were examined via cyclic voltammetry and linear sweep voltammetry measurements in 1M KOH solution. Experimental results show that with the content of iridium increasing in MnxIr1−xO2/C, the oxygen reduction reaction (ORR) activity first increases and then decreases. Mn0.75Ir0.25O2/C has the highest ORR activity and its half-wave potential obtains −0.071V (relative to Hg/HgO electrode). It is worth noting that doping the MnO2/C nanoparticles with only a small amount of iridium can considerably improve the oxygen evolution reaction (OER) activity of MnO2 in the alkaline medium. The oxygen evolution current density at 0.75 V vs. Hg/HgO of Mn0.75Ir0.25O2/C was nearly 4.31 times as that of MnO2/C. The results offer an important direction for the development of bifunctional oxygen catalysts in alkaline medium.
机译:氧气电化学的兴趣与日俱增,因为O2和H2O之间的转化在各种可再生能源技术中发挥着重要作用。本文采用热解法制备了通式为MnxIr1-xO2 / C的双功能电催化剂。通过透射电子显微镜检查它们的物理特性,并通过在1M KOH溶液中的循环伏安法和线性扫描伏安法测量来检查其电化学性质。实验结果表明,随着MnxIr1-xO2 / C中铱含量的增加,氧还原反应(ORR)活性先升高后降低。 Mn0.75Ir0.25O2 / C具有最高的ORR活性,其半波电位为-0.071V(相对于Hg / HgO电极)。值得注意的是,仅用少量铱掺杂MnO2 / C纳米颗粒就可以显着改善碱性介质中MnO2的氧释放反应(OER)活性。 Mn0.75Ir0.25O2 / C在0.75 V相对于Hg / HgO的氧气析出电流密度是MnO2 / C的近4.31倍。研究结果为碱性介质中双功能氧催化剂的开发提供了重要的指导。

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