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Synthesis of Au@Pt Core—Shell Nanoparticles as Efficient Electrocatalyst for Methanol Electro-Oxidation

机译:Au @ Pt核壳纳米粒子的合成作为甲醇电氧化的高效电催化剂

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摘要

Bimetallic Au@Pt nanoparticles (NPs) with Pt monolayer shell are of much interest for applications in heterogeneous catalysts because of enhanced catalytic activity and very low Pt-utilization. However, precisely controlled synthesis with uniform Pt-monolayers and stability on the AuNPs seeds remain elusive. Herein, we report the controlled deposition of Pt-monolayer onto uniform AuNPs seeds to obtain Au@Pt core–shell NPs and their Pt-coverage dependent electrocatalytic activity for methanol electro-oxidation. The atomic ratio between Au/Pt was effectively tuned by varying the precursor solution ratio in the reaction solution. The morphology and atomic structure of the Au@Pt NPs were analyzed by high-resolution scanning transmission electron microcopy (HR-STEM) and X-ray diffraction (XRD) techniques. The results demonstrated that the Au@Pt core–shell NPs with Pt-shell thickness (atomic ratio 1:2) exhibit higher electrocatalytic activity for methanol electro-oxidation reaction, whereas higher and lower Pt ratios showed less overall catalytic performance. Such higher catalytic performance of Au@Pt NPs (1:2) can be attributed to the weakened CO binding on the Pt/monolayers surface. Our present synthesis strategy and optimization of the catalytic activity of Au@Pt core–shell NPs catalysts provide promising approach to rationally design highly active catalysts with less Pt-usage for high performance electrocatalysts for applications in fuel cells.
机译:具有Pt单层壳的双金属Au @ Pt纳米粒子(NPs)由于其增强的催化活性和极低的Pt利用率而引起了在非均相催化剂中的广泛应用。但是,精确控制的具有均匀Pt单层的合成以及AuNPs种子的稳定性仍然难以捉摸。在本文中,我们报道了将Pt单层受控沉积到均匀的AuNPs种子上以获得Au @ Pt核壳NP及其对甲醇电氧化的依赖于Pt覆盖率的电催化活性。通过改变反应溶液中的前体溶液比例,可以有效地调节Au / Pt之间的原子比。通过高分辨率扫描透射电子显微镜(HR-STEM)和X射线衍射(XRD)技术分析了Au @ Pt纳米颗粒的形貌和原子结构。结果表明,具有Pt-壳层厚度(原子比为1:2)的Au @ Pt核壳NPs对甲醇电氧化反应具有较高的电催化活性,而Pt比值的较高和较低则显示出较低的总体催化性能。 Au @ Pt NPs(1:2)的这种较高的催化性能可归因于Pt /单层表面上CO结合力的减弱。我们目前的合成策略和Au @ Pt核壳NPs催化剂的催化活性的优化提供了一种有前途的方法,可以合理设计具有较少Pt用量的高活性催化剂,用于燃料电池中的高性能电催化剂。

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