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金上不对称一维钯双金属纳米结构的合成。

Synthesis of Asymmetric One-Dimensional Pd on Au Bimetallic Nanostructures.

作者信息

Khanal Bishnu P, Zubarev Eugene R

机构信息

Department of Chemistry, Rice University, 6100 Main Street, Houston, Texas 77005, United States.

出版信息

Langmuir. 2021 Aug 17;37(32):9901-9909. doi: 10.1021/acs.langmuir.1c01640. Epub 2021 Aug 9.

DOI:10.1021/acs.langmuir.1c01640
PMID:34369149
Abstract

Nanostructures composed of a gold nanorod (AuNR) core and a Pd/Pt shell are of great interest due to their potential application as plasmon resonance-enhanced catalysts. However, the synthesis of well-defined one-dimensional bimetallic nanostructures with precise control over shell thickness and length remains a challenge. In this study, we report a detailed and systematic study on the chemical synthesis of a uniform Pd shell on single crystalline and pentahedrally twinned (PHT) AuNRs of various lengths. AuNRs were used as a template, and the slow and controlled reduction of Pd(II) ions on preformed AuNRs was carried out for the formation of rectangular-shaped Au@Pd bimetallic nanorods. The Pd shell thickness around the AuNRs was controlled by the supply of Pd(II) ions in the growth solution. We were able to grow a ∼20 nm uniform Pd shell around the AuNR, keeping the rod-like morphology intact without local nucleation to form irregular shapes and randomly overgrown nanostructures. The formation of bimetallic nanorods was also extended beyond typical single crystalline nanorods to PHT high aspect ratio gold nanorods and nanowires, using them as templates. To our surprise, unusually curved asymmetric nanorods were formed when the Pd deposition was carried out on AuNRs longer than ∼800 nm which could be possibly due to a Pd and Au lattice mismatch at the interface and higher flexibility of the nanorods when they exceeded certain lengths.

摘要

由金纳米棒(AuNR)核和Pd/Pt壳组成的纳米结构因其作为等离子体共振增强催化剂的潜在应用而备受关注。然而,合成具有精确壳层厚度和长度控制的明确一维双金属纳米结构仍然是一个挑战。在本研究中,我们报告了一项关于在各种长度的单晶和五面体孪晶(PHT)AuNRs上化学合成均匀Pd壳的详细系统研究。以AuNRs为模板,通过在预先形成的AuNRs上缓慢且可控地还原Pd(II)离子来形成矩形Au@Pd双金属纳米棒。AuNRs周围的Pd壳厚度通过生长溶液中Pd(II)离子的供应来控制。我们能够在AuNR周围生长出约20 nm的均匀Pd壳,保持棒状形态完整,不会局部成核形成不规则形状和随机过度生长的纳米结构。双金属纳米棒的形成也从典型的单晶纳米棒扩展到了PHT高纵横比的金纳米棒和纳米线,并以它们为模板。令我们惊讶的是,当在长度超过约800 nm的AuNRs上进行Pd沉积时,会形成异常弯曲的不对称纳米棒,这可能是由于界面处Pd和Au晶格不匹配以及纳米棒超过一定长度时具有更高的柔韧性所致。

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