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Niobium-based catalysts prepared by reactive radio-frequency magnetron sputtering and arc plasma methods as non-noble metal cathode catalysts for polymer electrolyte fuel cells

机译:通过反应性射频磁控溅射和电弧等离子体方法制备的铌基催化剂,作为聚合物电解质燃料电池的非贵金属阴极催化剂

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摘要

Two vacuum methods, reactive radio-frequency (RF) magnetron sputtering and arc plasma deposition, were used to prepare niobium-based catalysts for an oxygen reduction reaction (ORR) as non-noble metal cathodes for polymer electrode fuel cells (PEFCs). Thin films with various N and O contents, denoted as NbO_x and Nb-O-N, were prepared on glassy carbon plates by RF magnetron sputtering with controlled partial pressures of oxygen and nitrogen. Electrochemical measurements indicated that the introduction of the nitrogen species into the thin film resulted in improved ORR activity compared to the oxide-only film. Using an arc plasma method, niobium was deposited on highly oriented pyrolytic graphite (HOPG) substrates, and the sub-nanoscale surface morphology of the deposited particles was investigated using scanning tunneling microscopy (STM). To prepare practical cathode catalysts, niobium was deposited on carbon black (CB) powders by arc plasma method. STM and transmission electron microscopy observations of samples on HOPG and CB indicated that the prepared catalysts were highly dispersed at the atomic level. The onset potential of oxygen reduction on Nb-O-N/CB was 0.86 V vs. a reversible hydrogen electrode, and the apparent current density was drastically improved by the introduction of nitrogen.
机译:两种真空方法分别是反应性射频(RF)磁控管溅射和电弧等离子体沉积,用于制备用于氧还原反应(ORR)的铌基催化剂,作为聚合物电极燃料电池(PEFC)的非贵金属阴极。在控制碳氧和氮分压的条件下,通过射频磁控溅射在玻璃碳板上制备具有不同N和O含量的薄膜,分别表示为NbO_x和Nb-O-N。电化学测量表明,与仅使用氧化物的薄膜相比,将氮物种引入薄膜可提高ORR活性。使用电弧等离子体方法,将铌沉积在高度定向的热解石墨(HOPG)衬底上,并使用扫描隧道显微镜(STM)研究沉积颗粒的亚纳米级表面形态。为了制备实用的阴极催化剂,通过电弧等离子体方法将铌沉积在炭黑(CB)粉末上。 STM和HOPG和CB样品的透射电子显微镜观察表明,所制备的催化剂在原子水平上高度分散。与可逆氢电极相比,Nb-O-N / CB上氧还原的起始电位为0.86 V,并且通过引入氮,表观电流密度大大提高。

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