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通过改变核尺寸和壳层厚度来控制核/壳结构的金/铂铁纳米颗粒的电催化作用。

Controlling core/shell Au/FePt nanoparticle electrocatalysis via changing the core size and shell thickness.

作者信息

Sun Xiaolian, Li Dongguo, Guo Shaojun, Zhu Wenlei, Sun Shouheng

机构信息

Department of Chemistry, Brown University, Providence, Rhode Island 02912, USA and State Key Laboratory of Molecular Vaccinology and Molecular Diagnostics & Center for Molecular Imaging and Translational Medicine, School of Public Health, Xiamen University, Xiamen 261005, China.

Department of Chemistry, Brown University, Providence, Rhode Island 02912, USA.

出版信息

Nanoscale. 2016 Feb 7;8(5):2626-31. doi: 10.1039/c5nr06492a.

Abstract

Using a modified seed-mediated method, we synthesized core/shell Au/FePt nanoparticles (NPs) with Au sizes of 4, 7, and 9 nm and the FePt shell was controlled to have similar FePt compositions and 0.5, 1, and 2 nm thickness. We studied both core and shell effects on electrochemical and electrocatalytic properties of the Au/FePt NPs, and found that the Au core did change the redox chemistry of the FePt shell and promoted its electrochemical oxidation of methanol. The catalytic activity was dependent on the FePt thicknesses, but not much on the Au core sizes, and the 1 nm FePt shell was found to be the optimal thickness for catalyzing methanol oxidation in 0.1 M HClO4 + 0.1 M methanol, offering not only high activity (1.19 mA cm(-2) at 0.5 V vs. Ag/AgCl), but also enhanced stability. Our studies demonstrate a general approach to the design and tuning of shell catalysis in the core/shell structure to achieve optimal catalysis for important electrochemical reactions.

摘要

我们采用改进的种子介导法合成了核壳结构的Au/FePt纳米颗粒(NPs),其中Au核的尺寸分别为4、7和9 nm,FePt壳层的成分相似,厚度分别控制为0.5、1和2 nm。我们研究了核壳结构对Au/FePt NPs电化学和电催化性能的影响,发现Au核确实改变了FePt壳层的氧化还原化学性质,并促进了其对甲醇的电化学氧化。催化活性取决于FePt壳层的厚度,而对Au核尺寸的依赖性不大,发现在0.1 M HClO4 + 0.1 M甲醇中催化甲醇氧化的最佳FePt壳层厚度为1 nm,不仅具有高活性(在0.5 V相对于Ag/AgCl时为1.19 mA cm(-2)),而且稳定性增强。我们的研究展示了一种在核壳结构中设计和调节壳层催化以实现对重要电化学反应最佳催化的通用方法。

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