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原子精确金属纳米团簇的融合生长模式。

Fusion growth patterns in atomically precise metal nanoclusters.

机构信息

Department of Chemistry, Carnegie Mellon University, Pittsburgh, PA 15213, USA.

出版信息

Nanoscale. 2019 Nov 7;11(41):19158-19165. doi: 10.1039/c9nr05789g. Epub 2019 Sep 11.

Abstract

Atomically precise nanoclusters of coinage metals in the 1-3 nm size regime have been intensively pursued in recent years. Such nanoclusters are attractive as they fill the gap between small molecules (<1 nm) and regular nanoparticles (>3 nm). This intermediate identity endows nanoclusters with unique physicochemical properties and provides nanochemists opportunities to understand the fundamental science of nanomaterials. Metal nanoparticles are well known to exhibit plasmon resonances upon interaction with light; however, when the particle size is downscaled to the nanocluster regime, the plasmons fade out and step-like absorption spectra characteristic of cluster sizes are manifested due to strong quantum confinement effects. Recent research has revealed that nanoclusters are commonly composed of a distinctive kernel and a surface-protecting shell (or staple-like metal-ligand motifs). Understanding the kernel configuration and evolution is one of the central topics in nanoscience research. This Review summarizes the recent progress in identifying the growth patterns of atomically precise coinage nanoclusters. Several basic kernel units have been observed, such as the M, M and M polyhedrons (where, M = metal atom). Among them, the tetrahedral M and icosahedral M units are the most common ones, which are adopted as building blocks to construct larger kernel structures via various fusion or aggregation modes, including the vertex- and face-sharing mode, the double-strand and alternate single-strand growth, and cyclic fusion of units, as well as the fcc-based cubic growth pattern. The identification of the kernel growth pathways has led to deeper understanding of the evolution of electronic structure and optic properties.

摘要

近年来,人们对尺寸在 1-3nm 范围内的贵金属原子精确纳米团簇进行了深入研究。这类纳米团簇之所以具有吸引力,是因为它们填补了小分子(<1nm)和常规纳米粒子(>3nm)之间的空白。这种中间特性赋予了纳米团簇独特的物理化学性质,并为纳米化学家提供了机会,使其能够深入理解纳米材料的基础科学。众所周知,金属纳米粒子在与光相互作用时会表现出等离子体共振;然而,当粒子尺寸缩小到纳米团簇范围时,由于强量子限域效应,等离子体消失,表现出特征于团簇尺寸的阶跃式吸收光谱。最近的研究表明,纳米团簇通常由独特的核和表面保护壳(或类似订书钉的金属配体图案)组成。了解核的结构和演化是纳米科学研究的核心课题之一。本综述总结了近年来在确定原子精确的贵金属纳米团簇生长模式方面的进展。已经观察到了几种基本的核结构单元,例如 M、M 和 M 多面体(其中,M=金属原子)。其中,四面体 M 和二十面体 M 单元最为常见,它们被用作构建更大核结构的构建块,通过各种融合或聚集模式,包括顶点和面共享模式、双链和交替单链生长以及单元的循环融合,以及基于 fcc 的立方生长模式。核生长途径的确定加深了对电子结构和光学性质演化的理解。

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