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三元杂化纳米粒子异构体:通过固态保护基团引导 Ag 在 Pt-Fe(3)O(4)上的成核。

Ternary hybrid nanoparticle isomers: directing the nucleation of Ag on Pt-Fe(3)O(4) using a solid-state protecting group.

机构信息

Department of Chemistry and Materials Research Institute, The Pennsylvania State University , University Park, Pennsylvania 16802, United States.

出版信息

ACS Nano. 2014 Jan 28;8(1):1047-55. doi: 10.1021/nn405943z. Epub 2013 Dec 20.

Abstract

Colloidal hybrid nanoparticles are an important class of materials that incorporate multiple nanoparticles into a single system through solid-state interfaces, which can result in multifunctionality and the emergence of synergistic properties not found in the individual components. These hybrid structures are typically produced using seeded-growth methods, where preformed nanoparticles serve as seeds onto which additional domains are added through subsequent reactions. For hybrid nanoparticles that contain more than two domains, multiple configurations with distinct connectivities and functionalities are possible, and these can be considered as nanoparticle analogues of molecular isomers. However, accessing one isomer relative to others in the same hybrid nanoparticle system is challenging, particularly when the formation of a target isomer is disfavored relative to more stable or synthetically accessible configurations. Here, we show that an iron oxide shell installed onto the Pt domain of Pt-Fe3O4 hybrid nanoparticles serves as a solid-state protecting group that can direct the nucleation of a third domain to an otherwise disfavored site. Under traditional conditions, Ag nucleates exclusively onto the Pt domain of Pt-Fe3O4 heterodimers, resulting in the formation of the Ag-Pt-Fe3O4 heterotrimer isomer. When the Pt surface is covered with an iron oxide protecting group, the nucleation of Ag is redirected onto the Fe3O4 domain, producing the distinct and otherwise inaccessible Pt-Fe3O4-Ag isomer. Similar results are obtained for the Au-Pt-Fe3O4 system, where formation of the favored Au-Pt-Fe3O4 configuration is blocked by the iron oxide protecting group. The thickness of the iron oxide shell that protects the Pt domain can be systematically tuned by adjusting the ratio of oleic acid to iron pentacarbonyl during the synthesis of the Pt-Fe3O4 heterodimers, and this insight is important for controllably implementing the protecting group chemistry.

摘要

胶体杂化纳米粒子是一类重要的材料,通过固态界面将多个纳米粒子整合到单个体系中,从而产生多功能性和协同特性,这些特性在单个组件中是找不到的。这些杂化结构通常采用种子生长法制备,其中预形成的纳米粒子作为种子,通过后续反应在其上添加额外的畴。对于包含两个以上畴的杂化纳米粒子,可以有多种具有不同连接性和功能的构型,这些可以被视为分子异构体的纳米粒子类似物。然而,在同一杂化纳米粒子体系中相对于其他异构体来获取一个异构体是具有挑战性的,特别是当目标异构体的形成相对于更稳定或更易合成的构型不利时。在这里,我们表明,安装在 Pt-Fe3O4 杂化纳米粒子的 Pt 畴上的氧化铁壳可以作为固态保护基团,引导第三畴在原本不利的位置进行成核。在传统条件下,Ag 仅在 Pt-Fe3O4 异质二聚体的 Pt 畴上优先成核,从而形成 Ag-Pt-Fe3O4 杂三聚物异构体。当 Pt 表面被氧化铁保护基团覆盖时,Ag 的成核被重新引导到 Fe3O4 畴上,生成独特且原本无法进入的 Pt-Fe3O4-Ag 异构体。对于 Au-Pt-Fe3O4 体系也得到了类似的结果,其中氧化铁保护基团阻止了有利的 Au-Pt-Fe3O4 构型的形成。通过调整合成 Pt-Fe3O4 异质二聚体过程中油酸与五羰基铁的比例,可以系统地调节保护 Pt 畴的氧化铁壳的厚度,这一见解对于可控实施保护基团化学非常重要。

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