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Sodium Borohydride Oxidation on Pt and/or Pd-based Electrodes in Hydrogen Peroxide Direct Borohydride Fuel Cells (H_2O_2-DBFCs)

机译:硼氢化钠氧化在过氧化氢直接硼氢化物燃料电池中的Pt和/或Pd基电极(H_2O_2-DBFC)

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The direct electrooxidation of sodium borohydride (NaBH_4) provides a path to release the high energy of the 8-electron, multi-step borohydride oxidation reaction (BOR). In practice, no single electrocatalyst is known to effectively oxidize all steps of the reaction. We investigate whether more complete BOR is achieved using an anode with a mixed electrocatalyst of nanoparticulate Pt and/or Pd supported on carbon (noted Pt/C and Pd/C). Electrocatalysts are compared in a liquid flow-through hydrogen peroxide direct borohydride fuel cell (H_2O_2-DBFC) having single Pt/C or Pd/C electrocatalyst, a mixture, or a gradient of the two along the anode flow channel. The best performance and lowest impedance over a broad range of potentials comes from a graded catalyst in which the composition varies from Pd/C at the channel inlet to Pt/C at the outlet, suggesting that catalyst gradients might provide a path to more efficient fuel cells for flow-type reactant systems.
机译:硼氢化钠(NaBH_4)的直接电氧化提供了一种释放8-电子,多步硼氢化物氧化反应(BOR)的高能量的路径。在实践中,已知没有单一电催化剂可以有效地氧化反应的所有步骤。我们研究了是否使用阳极使用具有纳米颗粒Pt和/或Pd上的PD的混合电催化剂的阳极来实现更完整的BOR(注意到PT / C和PD / C)。将电催化剂在液体流过过氧化氢直接硼氢化氢氟化氢电池(H_2O_2-DBFC)进行比较,具有单个Pt / C或Pd / C电催化剂,混合物或沿阳极流动通道的两个梯度。在广泛的电位上的最佳性能和最低阻抗来自分级催化剂,其中组合物在出口处的通道入口处的PD / C处变化,表明催化剂梯度可以提供更有效的燃料的路径流动式反应物系统的细胞。

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