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让旧前驱体玩新花样:室温快速合成无表面活性剂的胶体铂纳米颗粒

Teaching old precursors new tricks: Fast room temperature synthesis of surfactant-free colloidal platinum nanoparticles.

作者信息

Quinson J, Mathiesen J K, Schröder J, Dworzak A, Bizzotto F, Zana A, Simonsen S B, Theil Kuhn L, Oezaslan M, Jensen K M Ø, Arenz M

机构信息

University of Copenhagen, Chemistry Department, Universitetsparken 5, 2100 Copenhagen Ø, Denmark.

University of Copenhagen, Chemistry Department, Universitetsparken 5, 2100 Copenhagen Ø, Denmark.

出版信息

J Colloid Interface Sci. 2020 Oct 1;577:319-328. doi: 10.1016/j.jcis.2020.05.078. Epub 2020 May 25.

DOI:10.1016/j.jcis.2020.05.078
PMID:32497917
Abstract

A fast, simple, instrument-free room temperature synthesis of stable electroactive surfactant-free colloidal Pt nanoparticles in alkaline methanol and methanol-water mixtures is presented. Pair distribution function (PDF) analysis suggests that methoxy substitution of chloride ligands from HPtCl occurs in methanol. X-ray absorption spectroscopy (XAS) studies and UV-vis measurements show that solutions of HPtCl in methanol age and are reduced to Pt(II) species over time. These species are ideal precursors to significantly reduce the induction period typically observed in colloidal Pt nanoparticle syntheses as well as the temperature needed to form nanoparticles. The room temperature synthesis presented here allows designing simple in situ studies of the nanoparticle formation. In situ infra-red spectroscopy gives insight into the formation and stabilization mechanism of surfactant-free nanoparticles by CO surface groups. Finally, the surfactant-free nanoparticles ca. 2-3 nm in diameter obtained are shown to be readily active electrocatalysts e.g. for methanol oxidation. The synthesis approach presented bears several advantages to design new studies and new syntheses of surfactant-free colloidal nanomaterials.

摘要

本文介绍了一种在碱性甲醇和甲醇 - 水混合物中快速、简单、无需仪器的室温合成稳定的无电活性表面活性剂胶体铂纳米颗粒的方法。对分布函数(PDF)分析表明,在甲醇中,HPtCl的氯配体发生了甲氧基取代。X射线吸收光谱(XAS)研究和紫外 - 可见测量表明,HPtCl在甲醇中的溶液会随着时间老化并还原为Pt(II)物种。这些物种是理想的前体,可显著缩短胶体铂纳米颗粒合成中通常观察到的诱导期以及形成纳米颗粒所需的温度。本文提出的室温合成方法允许设计简单的纳米颗粒形成原位研究。原位红外光谱揭示了由CO表面基团形成和稳定无表面活性剂纳米颗粒的机制。最后,所获得的直径约2 - 3 nm的无表面活性剂纳米颗粒被证明是易于活性的电催化剂,例如用于甲醇氧化。所提出的合成方法在设计无表面活性剂胶体纳米材料的新研究和新合成方面具有几个优点。

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