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Facet-selective growth of organic heterostructured architectures via sequential crystallization of structurally complementary π-conjugated molecules

机译:通过结构互补的π共轭分子的顺序结晶,有机异质结构的面选择性生长

摘要

In contrast to those for their polymeric counterparts, the controlled construction of organic heterostructured architectures derived from π-conjugated organic molecules has been rare and remains a great challenge. Herein, we develop a simple single-step solution strategy for the realization of organic heterostructures comprising coronene and perylene. Under a sequential crystallization process, an efficient doping step for coronene and perylene domains enables their perfect lattice matching, which facilitates facet-selective epitaxial growth of perylene domains on both the tips and the side surfaces of the preformed seed microwires by manipulating the growth pathways of the two pairs of materials. The present synthetic route provides a promising platform to investigate the detailed formation mechanism of complex organic heterostructures with specific topological configurations, further directing the construction of more functional heterostructured materials.
机译:与它们的聚合物对应物相比,衍生自π共轭有机分子的有机异质结构的受控结构很少见,仍然是一个巨大的挑战。本文中,我们开发了一种简单的单步解决方案策略,以实现包含异戊二烯和per的有机异质结构。在顺序结晶过程中,高效的ron烯和ylene域掺杂步骤使它们能够实现完美的晶格匹配,这有助于通过操纵籽晶微丝的生长路径在预成型种子微丝的尖端和侧面上选择性地进行epi域的面选择性外延生长。两对材料。本合成途径为研究具有特定拓扑构型的复杂有机异质结构的详细形成机理提供了有希望的平台,进一步指导了功能更强的异质结构材料的构建。

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