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通过核/壳结构的形成与转化实现多金属磷化物纳米棒的可编程合成

Programmable Synthesis of Multimetallic Phosphide Nanorods Mediated by Core/Shell Structure Formation and Conversion.

作者信息

Zhang Yulu, Li Na, Zhang Zhiyong, Li Shuang, Cui Meiyang, Ma Lu, Zhou Hua, Su Dong, Zhang Sen

机构信息

Department of Chemistry, University of Virginia, Charlottesville, Virginia 22904, United States.

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

出版信息

J Am Chem Soc. 2020 May 6;142(18):8490-8497. doi: 10.1021/jacs.0c02584. Epub 2020 Apr 22.

Abstract

Generalized synthetic strategies for nanostructures with well-defined physical dimensions and broad-range chemical compositions are at the frontier of advanced nanomaterials design, functionalization, and application. Here, we report a composition-programmable synthesis of multimetallic phosphide CoMP nanorods (NRs) wherein M can be controlled to be Fe, Ni, Mn, Cu, and their binary combinations. Forming CoP/MP core/shell NRs and subsequently converting them into CoMP solid-solution NRs through thermal post-treatment are essential to overcome the obstacle of morphology/structure inconsistency faced in conventional synthesis of CoMP with the different M compositions. The resultant CoMP with uniform one-dimensional (1-D) structure provides us a platform to unambiguously screen the M synergistic effects in improving the electrocatalytic activity, as exemplified by the oxygen evolution reaction. This new approach mediated by core/shell nanostructure formation and conversion can be extended to other multicomponent nanocrystal systems (metal alloy, mixed oxide, and chalcogenide, etc.) for diverse applications.

摘要

具有明确物理尺寸和广泛化学组成的纳米结构的通用合成策略处于先进纳米材料设计、功能化及应用的前沿。在此,我们报道了一种多金属磷化物CoMP纳米棒(NRs)的组成可编程合成方法,其中M可被控制为Fe、Ni、Mn、Cu及其二元组合。形成CoP/MP核壳纳米棒并随后通过热后处理将其转化为CoMP固溶体纳米棒,对于克服传统合成不同M组成的CoMP时面临的形态/结构不一致障碍至关重要。所得具有均匀一维(1-D)结构的CoMP为我们提供了一个平台,以明确筛选M在提高电催化活性方面的协同效应,以析氧反应为例。这种由核壳纳米结构形成和转化介导的新方法可扩展到其他多组分纳米晶体系统(金属合金、混合氧化物和硫族化物等)以用于多种应用。

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