化学
纳米棒
高分辨率透射电子显微镜
刻面
结晶学
硫系化合物
透射电子显微镜
化学工程
材料科学
表面能
纳米结构
纳米晶
铜
纳米环
六角棱镜
纳米技术
六方晶系
有机化学
物理化学
工程类
作者
Michael B. Sigman,Ali Ghezelbash,Tobias Hanrath,Aaron E. Saunders,Frank Lee,Brian A. Korgel
摘要
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.
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