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Electro-catalytically active Au@Pt nanoparticles for hydrogen evolution reaction: an insight into a tryptophan mediated supramolecular interface towards a universal core-shell synthesis approach

机译:用于氢释放反应的电催化活性Au @ Pt纳米颗粒:色氨酸介导的超分子界面对通用核壳合成方法的见解

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摘要

We report an eco-friendly, one-pot, room-temperature method for the rapid synthesis of electrocatalytically active Au@Pt (50 nm) bimetallic nanoparticles via a tryptophan (Trp) mediated supramolecular interface in an aqueous environment. Our results demonstrate a simple universal approach for high shell-metal loading where a pre-stabilized tryptophan polymerized-Au core serves as a template to facilitate subsequent deposition of Pt. We observed that the amine-stabilized poly-Trp bi-layer has an enhancing effect on the electrocatalytic potential of Au@Pt NPs by the virtue of an amine stabilized interface, thereby enhancing the HER activity over glassy carbon electrodes. Several characterization techniques were used to confirm the inherent core-shell morphology of the resulting Au@Pt NPs. This Trp mediated facile green synthesis strategy has the potential to synthesize an array of Au-core containing bimetallic nanoparticles with enhanced catalytic activity and stable structure integration.
机译:我们报告了一种环保的单锅室温方法,可通过色氨酸(Trp)介导的超分子界面在水性环境中快速合成电催化活性Au @ Pt(50 nm)双金属纳米颗粒。我们的结果证明了一种简单的通用方法,可用于高壳金属负载,其中预先稳定的色氨酸聚合的Au核用作模板,以促进随后的Pt沉积。我们观察到,通过胺稳定的界面,胺稳定的多Trp双层对Au @ Pt NPs的电催化潜力具有增强作用,从而增强了玻璃碳电极上的HER活性。几种表征技术被用于确认所得Au @ Pt NP的固有核-壳形态。这种由Trp介导的简便的绿色合成策略具有合成具有增强催化活性和稳定结构整合性的,含Au核的双金属纳米粒子阵列的潜力。

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