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Tailor-made preparation of Co–C, Co–B, and Co catalytic thin films using magnetron sputtering: insights into structure–composition and activation effects for catalyzed NaBH4 hydrolysis

机译:使用磁控溅射量身定制的Co–C,Co–B和Co催化薄膜的制备:洞察催化NaBH4水解的结构组成和活化效应

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摘要

The magnetron sputtering (MS) methodology is a powerful tool for tailor-made fabrication of Co-based thin\udfilm catalysts with controlled microstructures and compositions for sodium borohydride (SBH) hydrolysis. In\udparticular, Co–C catalysts were tested in this reaction and compared to Co–B and Co catalyst coatings. The\udmicrostructural and chemical analyses by X-ray diffraction (XRD), scanning and transmission electron\udmicroscopy (SEM and TEM), Rutherford back scattering (RBS) and X-ray photoelectron spectroscopy\ud(XPS) were used to characterize a complete library of thin film catalysts. Pure Co materials were\udcharacterized by their nanocrystalline microstructure, and grain refinement was achieved via an increase\udin the deposition pressure. The incorporation of boron or carbon via co-deposition results in\udamorphization and dispersion of the active metallic Co phase. The composition can be tuned while\udkeeping a controlled microstructure, and a comparison of activity at 25 C was performed on catalysts\uddeposited on Ni foam substrates. A comparison of the initial activities showed that the Co–B samples\udwere more active than the Co–C samples because of electronic effects. However, a strong activation\udwas found for the Co–C catalysts after the first use. This effect was dependent upon the incorporation\udof cobalt boride (CoxB) species on the catalysts' surface, as shown by XPS. After the first several uses, the\udactivity of the Co–C samples (values up to 2495 mL min 1 gcatalyst\ud 1) were as high as that of fresh Co–B,\udand the surface composition of both the catalysts was similar. This activation was not observed for the\udpure Co and was very weak for the Co–B catalysts. The use of polymeric (PTFE) substrates (flexible\udmembranes) illustrated the versatility of the methodology to obtain catalytic membranes and allowed for\uda TEM microstructural analysis at the nanoscale. Catalytic activities at 60 C were as high as 16.7 and\ud20 L min 1 gCo\ud 1 for the Co–C and Co–B membranes, respectively. We determined the optimized\udconditions to increase the catalytic activity of Co-based coatings prepared via magnetron sputtering.
机译:磁控溅射(MS)方法学是用于定制制造具有受控的微结构和组成的硼氢化钠(SBH)水解的Co基薄膜/ udud催化剂的强大工具。特别是,在该反应中测试了Co–C催化剂,并将其与Co–B和Co催化剂涂层进行了比较。通过X射线衍射(XRD),扫描和透射电子显微镜(SEM和TEM),卢瑟福背散射(RBS)和X射线光电子能谱\ ud(XPS)对\ ud的微观结构和化学分析进行了表征。薄膜催化剂库。纯Co材料通过其纳米晶体的微观结构表征,并通过增加沉积压力实现晶粒细化。通过共沉积结合硼或碳会导致活性金属Co相的变质和分散。可以在维持可控的微观结构的同时调节组成,并且对在25℃下沉积在Ni泡沫基材上的催化剂进行活性比较。初始活动的比较表明,由于电子效应,Co-B样品比Co-C样品更具活性。但是,首次使用后发现Co-C催化剂具有很强的活化性。如XPS所示,这种效果取决于在催化剂表面上掺入的硼化钴(CoxB)种类。经过前几次使用后,Co–C样品的活度(值高达2495 mL min 1 g催化剂\ ud 1)与新鲜Co–B的活度一样高,\ ud,两种催化剂的表面组成相似。对于\ udpure Co,未观察到这种活化作用,对于Co-B催化剂,这种活化作用非常弱。聚合(PTFE)基材(柔性\双膜)的使用说明了获得催化膜的方法的多功能性,并允许在纳米级进行TEM显微结构分析。对于Co–C和Co–B膜,在60 C时的催化活性分别高达16.7和\ ud20 L min 1 gCo \ ud 1。我们确定了优化的条件,以提高通过磁控溅射制备的Co基涂层的催化活性。

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