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Pt–Ru decorated self-assembled TiO2–carbon hybrid nanostructure for enhanced methanol electrooxidation

机译:Pt-Ru装饰的自组装TiO2-碳杂化纳米结构用于增强甲醇电氧化

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摘要

Porous titanium oxide–carbon hybrid nanostructure (TiO2–C) with a specific surface area of 350 m2/g and an average pore-radius of 21 · 8 Å is synthesized via supramolecular self-assembly with an in situ crystallization process. Subsequently, TiO2–C supported Pt–Ru electro-catalyst (Pt–Ru/TiO2–C) is obtained and investigated as an anode catalyst for direct methanol fuel cells (DMFCs). X-ray diffraction, Raman spectroscopy and transmission electron microscopy (TEM) have been employed to evaluate the crystalline nature and the structural properties of TiO2–C. TEM images reveal uniform distribution of Pt–Ru nanoparticles (d Pt − Ru  = 1·5–3·5 nm) on TiO2–C. Methanol oxidation and accelerated durability studies on Pt–Ru/TiO2–C exhibit enhanced catalytic activity and durability compared to carbon-supported Pt–Ru. DMFC employing Pt–Ru/TiO2–C as an anode catalyst delivers a peak-power density of 91 mW/cm2 at 65 °C as compared to the peak-power density of 60 mW/cm2 obtained for the DMFC with carbon-supported Pt–Ru anode catalyst operating under similar conditions.
机译:通过超分子自组装和原位结晶过程合成了比表面积为350m2 / g,平均孔半径为21·8Å的多孔氧化钛-碳杂化纳米结构(TiO2-C)。随后,获得了TiO2-C负载的Pt-Ru电催化剂(Pt-Ru / TiO2-C),并作为直接甲醇燃料电池(DMFC)的阳极催化剂进行了研究。 X射线衍射,拉曼光谱和透射电子显微镜(TEM)已用于评估TiO2-C的晶体性质和结构性质。 TEM图像显示了TiO2-C上Pt-Ru纳米粒子的均匀分布(d Pt-Ru = 1·5–3·5nm)。与碳载Pt-Ru相比,Pt-Ru / TiO2-C的甲醇氧化和加速耐久性研究显示出增强的催化活性和耐久性。使用Pt-Ru / TiO2-C作为阳极催化剂的DMFC在65°C时提供91mW / cm2的峰值功率密度,而碳载Pt的DMFC的峰值功率密度为60mW / cm2 -Ru阳极催化剂在类似条件下运行。

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