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无溶剂合成单分散Cu2S纳米棒、纳米盘和纳米片。

Solventless synthesis of monodisperse Cu2S nanorods, nanodisks, and nanoplatelets.

作者信息

Sigman Michael B, Ghezelbash Ali, Hanrath Tobias, Saunders Aaron E, Lee Frank, Korgel Brian A

机构信息

Department of Chemical Engineering, Texas Materials Institute, Center for Nano- and Molecular Science and Technology, The University of Texas at Austin, Austin, Texas 78712-1062, USA.

出版信息

J Am Chem Soc. 2003 Dec 24;125(51):16050-7. doi: 10.1021/ja037688a.

Abstract

Cu(2)S nanocrystals with disklike morphologies were synthesized by the solventless thermolysis of a copper alkylthiolate molecular precursor. The nanodisks ranged from circular to hexagonal prisms from 3 to 150 nm in diameter and 3 to 12 nm in thickness depending on the growth conditions. High resolution transmission electron microscopy (HRTEM) revealed the high chalcocite (hexagonal) crystal structure oriented with the c-axis ([001] direction) orthogonal to the favored growth direction. This disk morphology is thermodynamically favored as it allows the extension of the higher energy [100] and [110] surfaces with respect to the [001] planes. The hexagonal prism morphology also appears to relate to increased C-S bond cleavage of adsorbed dodecanethiol along the more energetic [100] facets relative to [001] facets. Monodisperse Cu(2)S nanodisks self-assemble into ribbons of stacked platelets. This solventless approach provides a new technique to synthesize anisotropic metal chalcogenide nanostructures with shapes that depend on both the face-sensitive thermodynamic surface energy and the surface reactivity.

摘要

通过铜烷基硫醇盐分子前驱体的无溶剂热解合成了具有盘状形态的Cu₂S纳米晶体。根据生长条件,纳米盘的形状从圆形到六棱柱形不等,直径为3至150纳米,厚度为3至12纳米。高分辨率透射电子显微镜(HRTEM)显示,其具有高辉铜矿(六方)晶体结构,c轴([001]方向)与有利生长方向正交。这种盘状形态在热力学上是有利的,因为相对于[001]平面,它允许更高能量的[100]和[110]表面扩展。六棱柱形态似乎也与十二烷硫醇在相对于[001]晶面更具能量的[100]晶面上的吸附导致的C-S键断裂增加有关。单分散的Cu₂S纳米盘自组装成堆叠薄片的带状物。这种无溶剂方法提供了一种新技术,可用于合成形状取决于表面敏感的热力学表面能和表面反应性的各向异性金属硫族化物纳米结构。

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