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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:随着O2和H2O之间的转化在各种可再生能源技术中起重要作用,对氧电化学的兴趣日益增长。本文使用热解法制备通式Mnxir1-XO2 / C的双官能电催化剂。通过透射电子显微镜检查它们的物理特性,通过循环伏安法和1M KOH溶液中的线性扫描伏安法测量来检查电化学性质。实验结果表明,随着Mnxir1-XO2 / C中铱的含量增加,氧还原反应(ORR)活性首先增加,然后降低。 MN0.75IR0.25O2 / c具有最高的ORR活动,其半波电位获得-0.071V(相对于HG / HGO电极)。值得注意的是,用少量铱掺杂掺杂MnO2 / C纳米粒子可以大大改善MnO 2在碱性介质中的氧气进化反应(Oer)活性。 Mn0.7510.2502 / c的0.75V与Hg / hgo的氧气进化电流密度为MnO 2 / C的近4.31倍。结果为碱性介质中的双官能氧催化剂进行了重要方向。

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