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The effect of morphological difference and hydride incorporation on the activity of Pd/C catalysts in direct alkaline formate fuel cell

机译:形态学差异和氢化物掺入对直接碱性甲酸盐燃料电池中Pd / C催化剂活性的影响

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摘要

Palladium (Pd) on carbon support, electron-enriched by hydrogen incorporation (Pd-H/C), is synthesized via dimethylamine borane complex at multiple temperatures and used for the oxidation of formate (HCOO-). The electronic effect of H is confirmed by physicochemical and electrochemical analysis. Physicochemical analysis revealed no significant changes in the Pd-H/C structures, with changes only in the particle size and dispersion. Pd-H/C 0 degrees C showed the best catalytic activity for the oxidation of HCOO-, even though it possesses the less electrochemical surface area than commercial Pd/C. Its remarkable power density of 272 mW cm(-2) at the nominal cell voltage of 0.5 V is recorded in single cell operation. The observed performance is attributed to the electronic effect brought by the incorporation of H in the Pd lattice. Still the electronic effect of H does not always compensate for the small ECSA caused by large particle size and severe agglomeration.
机译:碳载体上的钯(Pd)是通过二甲胺硼烷络合物在多个温度下合成的,通过氢掺入(Pd-H/C)富集电子,用于甲酸盐(HCOO-)的氧化。物理化学和电化学分析证实了H的电子效应。物理化学分析显示,Pd-H/C结构没有显著变化,仅在粒径和分散度上发生变化。Pd-H/C 0°C对HCOO-的氧化表现出最好的催化活性,尽管它的电化学表面积比市售Pd/C小。在单电池运行中,其标称电池电压为0.5 V时的显著功率密度为272 mW cm(-2)。所观察到的性能归因于氢在钯晶格中的掺入所带来的电子效应。然而,H的电子效应并不总是能够补偿大颗粒尺寸和严重团聚造成的小ECSA。

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