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Palladium and Palladium Gold Catalysts Supported on MWCNTs for Electrooxidation of Formic Acid

机译:MWCNTs上负载的钯和钯金催化剂用于甲酸的电氧化

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Novel multi-wall carbon nanotubes (MWCNTs) supported Pd-Au catalyst for electrooxidation of formic acid was prepared and compared with a similarly prepared Pd/ MWCNTs and with a commercial Pt-Ru/Vulcan catalyst. The catalysts were prepared by a two-stage polyol method, followed by H_2-Ar annealing and were characterised by using X-ray diffraction, FE-TEM and EDX. Cyclic voltammetry (CV) was used to test their catalytic activity towards formic acid electrooxidation and accessible metal surface in the catalyst layer. In the case of the precursor of Pd-Au/ MWCNTs catalyst (before H_2-Ar annealing), subsequent deposition of Pd and Au led to a material of the core-shell structure, catalytically inactive. Annealing of the core shell Pd-Au/MWCNTs precursor in H_2-Ar resulted in the formation of the novel Pd-Au/MWCNTs catalyst. A highly dispersed Pd-Au solid solution (average XRD particle size 4.8 nm) is formed, and the novel catalyst is more active than the Pd/MWCNTs one. Both the Pd-Au/MWCNTs and the Pd/MWCNTs catalysts turned out to be more active than a commercial, highly dispersed Pt-Ru/Vulcan catalyst.
机译:制备了新型的多壁碳纳米管(MWCNTs)负载的Pd-Au催化剂,用于甲酸的电氧化,并与类似制备的Pd / MWCNTs和市售Pt-Ru / Vulcan催化剂进行了比较。通过两步多元醇法,然后通过H_2-Ar退火制备催化剂,并通过X射线衍射,FE-TEM和EDX对其进行表征。循环伏安法(CV)用于测试它们对甲酸电氧化和催化剂层中可及金属表面的催化活性。对于Pd-Au / MWCNTs催化剂的前体(在H_2-Ar退火之前),Pd和Au的后续沉积会导致核-壳结构的材料失去催化活性。核壳Pd-Au / MWCNTs前体在H_2-Ar中的退火导致形成新型Pd-Au / MWCNTs催化剂。形成了高度分散的Pd-Au固溶体(平均XRD粒径4.8 nm),该新型催化剂比Pd / MWCNT更具活性。事实证明,Pd-Au / MWCNTs和Pd / MWCNTs催化剂都比市售的高度分散的Pt-Ru / Vulcan催化剂更具活性。

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