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• W2049554443 abstract "Due to the presence of high-density twinned-defects and diffuse elastic strain, pentagonal cyclic twinning (PCT) structures may have more fascinating properties than the corresponding single crystalline structure. Although there are a lot of reports concerning the PCT nanocrystals of many monometals and bimetal alloys, the established growth mechanisms of PCT structures are still not straightforward and usually inconsistent with each other. In this Letter, using dodecanethiol-capped Au nanocrystals (NCs) as building blocks, taking self-assembly of Au NCs into their colloidal crystals as the crystallization model, we found the competition of crystal cohesive energy and surface free energy plays an important role in the formation of PCT colloidal crystal. By rationally selecting the solvent to tailor the crystal cohesive energy, the structure of the colloidal crystals can be tuned. PCT structures are more likely to form when the interaction between building blocks is weak, while the single crystal structure is formed when the interaction is strong. The results demonstrate that the thermodynamic factors are the origin of pentagonal cyclic twinning." @default.
• W2049554443 created "2016-06-24" @default.
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• W2049554443 date "2013-09-30" @default.
• W2049554443 modified "2023-10-14" @default.
• W2049554443 title "Understanding the Formation of Pentagonal Cyclic Twinned Crystal from the Solvent Dependent Assembly of Au Nanocrystals into Their Colloidal Crystals" @default.
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• W2049554443 doi "https://doi.org/10.1021/jz401682q" @default.
• W2049554443 hasPublicationYear "2013" @default.
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