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Pt促进的负载型Ni催化剂用于快速还原芳香族硝基化合物的活性增强

Enhanced Activity of Supported Ni Catalysts Promoted by Pt for Rapid Reduction of Aromatic Nitro Compounds.

作者信息

Shang Huishan, Pan Kecheng, Zhang Lu, Zhang Bing, Xiang Xu

机构信息

State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Beijing 100029, China.

School of Chemical Engineering, Zhengzhou University, Zhengzhou 450001, China.

出版信息

Nanomaterials (Basel). 2016 Jun 4;6(6):103. doi: 10.3390/nano6060103.

Abstract

To improve the activities of non-noble metal catalysts is highly desirable and valuable to the reduced use of noble metal resources. In this work, the supported nickel (Ni) and nickel-platinum (NiPt) nanocatalysts were derived from a layered double hydroxide/carbon composite precursor. The catalysts were characterized and the role of Pt was analysed using X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), energy dispersive X-ray spectroscopy (EDS) mapping, and X-ray photoelectron spectroscopy (XPS) techniques. The Ni was reduced to metallic Ni⁰ via a self-reduction way utilizing the carbon as a reducing agent. The average sizes of the Ni particles in the NiPt catalysts were smaller than that in the supported Ni catalyst. The electronic structure of Ni was affected by the incorporation of Pt. The optimal NiPt catalysts exhibited remarkably improved activity toward the reduction of nitrophenol, which has an apparent rate constant () of 18.82 × 10 s, 6.2 times larger than that of Ni catalyst and also larger than most of the reported values of noble-metal and bimetallic catalysts. The enhanced activity could be ascribed to the modification to the electronic structure of Ni by Pt and the effect of exposed crystal planes.

摘要

提高非贵金属催化剂的活性对于减少贵金属资源的使用非常可取且具有重要价值。在这项工作中,负载型镍(Ni)和镍 - 铂(NiPt)纳米催化剂由层状双氢氧化物/碳复合前驱体制备而成。使用X射线衍射(XRD)、高分辨率透射电子显微镜(HRTEM)、能量色散X射线光谱(EDS)映射和X射线光电子能谱(XPS)技术对催化剂进行了表征,并分析了Pt的作用。通过以碳作为还原剂的自还原方式,Ni被还原为金属Ni⁰。NiPt催化剂中Ni颗粒的平均尺寸小于负载型Ni催化剂中的尺寸。Ni的电子结构受到Pt掺入的影响。最佳的NiPt催化剂对硝基苯酚还原表现出显著提高的活性,其表观速率常数()为18.82×10 s,比Ni催化剂大6.2倍,也大于大多数已报道的贵金属和双金属催化剂的值。活性增强可归因于Pt对Ni电子结构的修饰以及暴露晶面的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4385/5302623/9495b7be566a/nanomaterials-06-00103-g001.jpg

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