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通过电化置换反应由钯纳米线形成钯/金纳米结构。

Formation of Pd/Au nanostructures from Pd nanowires via galvanic replacement reaction.

作者信息

Teng Xiaowei, Wang Qi, Liu Ping, Han Weiqiang, Frenkel Anatoly I, Wen Wen, Marinkovic Nebojsa, Hanson Jonathan C, Rodriguez Jose A

机构信息

Center for Functional Nanomaterials, Brookhaven National Laboratory, Upton, New York 11973, USA.

出版信息

J Am Chem Soc. 2008 Jan 23;130(3):1093-101. doi: 10.1021/ja077303e.

DOI:10.1021/ja077303e
PMID:18161978
Abstract

Bimetallic nanostructures with non-random metal atoms distribution are very important for various applications. To synthesize such structures via benign wet chemistry approach remains challenging. This paper reports a synthesis of a Au/Pd alloy nanostructure through the galvanic replacement reaction between Pd ultrathin nanowires (2.4 +/- 0.2 nm in width, over 30 nm in length) and AuCl3 in toluene. Both morphological and structural changes were monitored during the reaction up to 10 h. Continuous changes of chemical composition and crystalline structure from Pd nanowires to Pd68Au32 and Pd45Au55 alloys, and to Au nanoparticles were observed. More interestingly, by using combined techniques such as high-resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), energy dispersive X-ray spectrometry (EDS), UV-vis absorption, and extended X-ray absorption fine structure (EXAFS) spectroscopy, we found the formation of Pd68Au32 non-random alloy with Au-rich core and Pd-rich shell, and random Pd45Au55 alloy with uniformly mixed Pd and Au atom inside the nanoparticles, respectively. Density functional theory (DFT) calculations indicated that alkylamine will strongly stabilize Pd to the surface, resulting in diffusion of Au atoms into the core region to form a non-random alloy. We believe such benign synthetic techniques can also enable the large scale preparation of various types of non-random alloys for several technically important catalysis applications.

摘要

具有非随机金属原子分布的双金属纳米结构对于各种应用非常重要。通过良性湿化学方法合成此类结构仍然具有挑战性。本文报道了通过钯超薄纳米线(宽度为2.4±0.2纳米,长度超过30纳米)与甲苯中的AuCl3之间的电化置换反应合成Au/Pd合金纳米结构。在长达10小时的反应过程中监测了形态和结构变化。观察到从钯纳米线到Pd68Au32和Pd45Au55合金,再到金纳米颗粒的化学成分和晶体结构的连续变化。更有趣的是,通过使用高分辨率透射电子显微镜(HRTEM)、X射线衍射(XRD)、能量色散X射线光谱(EDS)、紫外可见吸收和扩展X射线吸收精细结构(EXAFS)光谱等组合技术,我们分别发现形成了具有富金核心和富钯壳的Pd68Au32非随机合金,以及纳米颗粒内部钯和金原子均匀混合的随机Pd45Au55合金。密度泛函理论(DFT)计算表明,烷基胺将强烈地将钯稳定在表面,导致金原子扩散到核心区域形成非随机合金。我们相信,这种良性合成技术还能够大规模制备用于几种技术上重要的催化应用的各种类型的非随机合金。

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