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Carbon nanofiber layers on metal and carbon substrates : PEM fuel cell and microreactor applications

机译:金属和碳基材上的碳纳米纤维层:PEM燃料电池和微反应器应用

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摘要

This thesis describes the preparation of CNF layers on flat and porous substrates and their application as catalyst supports for chemical and electrochemical gas‐liquidsolid (G‐L‐S) catalytic reactions. Metal nanoparticles growing CNFs on flat metal substrates at 600°C are easily formed from NiO, in contrast to Fe and Co oxides, leading to higher carbon deposition rates. However, high activity towards total carbon deposition is generally detrimental for obtaining well‐attached and homogenously distributed CNFs. Dense carbon (C) and entangled CNF layers are deposited on Ni foils at 450°C after either oxidation or oxidation‐reduction pretreatments. The preparation of stable and thick CNF layers involves a compromise between the deposition of a thick C layer and the amount of weakly attached CNFs. The addition of 5% H2 produces thicker, rougher and more porous CNF layers than when 1% H2 is used. The water wetting properties of the samples are more significantly influenced by the CNF layer thickness than both surface roughness and porosity. A CNF layer is also grown on a porous stainless steel substrate. Pd nanoparticles deposition on the CNFs is performed for the catalytic reduction of nitrite with H2 in an aqueous solution. The presence of the CNFs on the stainless steel surface had a significant effect on the reactor performance. Even without the presence of H2 and Pd, the NO2‐ ions were successfully reduced. A CNF layer and subsequent Pt nanoparticles deposition is performed on a carbon paper substrate for the electrocatalytic oxygen reduction reaction (ORR). The Pt electrochemical surface area, when deposited on CNFs, is much higher than that obtained for commercial Pt/Vulcan. The external oxygen diffusion is higher for Pt/CNFs, as compared to Pt/Vulcan, due to the intrinsic morphology of the CNFs that allow a better accessibility to oxygen diffusion.
机译:本文描述了在平坦和多孔基材上的CNF层的制备及其作为化学和电化学气体 - 液体溶剂(G-L-S)催化反应的催化剂载体。与Fe和Co氧化物形成较高的碳沉积速率,从NIO容易地形成在600℃的扁平金属衬底上生长在扁平金属基材上的金属纳米粒子。然而,朝向总碳沉积的高活性通常是有害的,用于获得良好连接和均匀分布的CNF。在氧化或氧化还原预处理后,在450℃下沉积致密的碳(C)和缠绕的CNF层。稳定和厚的CNF层的制备涉及厚C层的沉积与弱附着的CNF的量之间的折衷。添加5%H 2的加厚,比使用1%H 2的较厚,更粗糙和更多孔的CNF层。样品的水润湿性能比表面粗糙度和孔隙率更显着地受CNF层厚度的影响。 CNF层也在多孔不锈钢基板上生长。对CNF的PD纳米粒子沉积在水溶液中具有H 2的亚硝酸盐的催化还原。在不锈钢表面上的CNFS对反应器性能的显着影响。即使没有H2和Pd的存在,也成功降低了NO 2.在用于电催化氧还原反应(ORR)的碳纸基材上进行CNF层和随后的Pt纳米颗粒沉积。在CNF上沉积时Pt电化学表面积远高于商业Pt / vulcan的高得多。与Pt / Vulcan相比,Pt / CNFS的外部氧扩散较高,由于允许更好地可达氧气扩散的CNF的内在形态。

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    Sergio Pacheco Benito;

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  • 年度 -1
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