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溶剂介导的核壳 PdAu@Pd 纳米晶壳层尺寸重构用于稳健的 C1 和 C2 醇电催化。

Solvent-Mediated Shell Dimension Reconstruction of Core@Shell PdAu@Pd Nanocrystals for Robust C1 and C2 Alcohol Electrocatalysis.

机构信息

College of Chemistry Chemical Engineering and Materials Science Soochow University, Suzhou, 215123, China.

出版信息

Small. 2021 Aug;17(32):e2101428. doi: 10.1002/smll.202101428. Epub 2021 Jul 2.

DOI:10.1002/smll.202101428
PMID:34213824
Abstract

The core@shell structure dimension of the Pd-based nanocrystals deeply impacts their catalytic properties for C1 and C2 alcohol oxidation reactions. However, the precise simultaneous control on the synthesis of core@shell nanocrystals with different shell dimensions is difficult, and most synthesis on Pd-based core@shell nanocatalysts involves the surfactants participation by multiple steps, thus leads to limited catalytic properties. Herein, for the first time, a facile one-step surfactant-free strategy is developed for shell dimension reconstruction of PdAu@Pd core@shell nanocrystals by altering volume ratios of mixed solvents. The Pd-based sunflower-like (SL) and coral grass-like (CGL) nanocrystals are obtained with different 2D hexagonal nanosheet assembles and 3D network shells, respectively. Benefitting from the clean surface shell of 2D ultrathin nanosheets structure, high atom utilization efficiency, and robust electronic effect. The PdAu@Pd SL achieves the ascendant methanol/ethanol/ethylene glycol oxidation reaction (MOR/EOR/EGOR) activities, much higher than Pd/C catalysts, as well as the improved antipoisoning ability. Notably, this one-step construction shell dimension of PdAu@Pd core@shell catalysts not only provide a significant reference for the improvement of surfactant-free synthetic routes, but also shed light on the advanced engineering on shell dimensions in core@shell nanostructures for electrocatalysis and so forth.

摘要

钯基纳米晶体的核壳结构尺寸对其催化 C1 和 C2 醇氧化反应的性能有深远影响。然而,精确地同时控制不同壳尺寸的核壳纳米晶体的合成具有挑战性,而且大多数关于钯基核壳纳米催化剂的合成都涉及使用表面活性剂的多步参与,从而导致其催化性能受限。在此,首次开发了一种简便的无表面活性剂一步策略,通过改变混合溶剂的体积比来重构 PdAu@Pd 核壳纳米晶体的壳层尺寸。得到了具有不同二维六方纳米片组装和三维网络壳的钯基向日葵状(SL)和珊瑚草状(CGL)纳米晶体。得益于清洁的表面壳的二维超薄纳米片结构、高原子利用率和强电子效应,PdAu@Pd SL 实现了优越的甲醇/乙醇/乙二醇氧化反应(MOR/EOR/EGOR)活性,明显高于 Pd/C 催化剂,以及提高了抗中毒能力。值得注意的是,这种一步构建 PdAu@Pd 核壳催化剂的壳层尺寸不仅为无表面活性剂合成路线的改进提供了重要参考,而且为核壳纳米结构中壳层尺寸的先进工程学在电催化等领域提供了启示。

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