Stress-induced ordering evolution of 1D segmented heteronanostructures and their chemical post-transformations

Investigations of one-dimensional segmented heteronanostructures (1D-SHs) have recently attracted much attention due to their potentials for applications resulting from their structure and synergistic effects between compositions and interfaces. Unfortunately, developing a simple, versatile and cont...

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Veröffentlicht in:Nature communications 2024-04, Vol.15 (1), p.3208-12, Article 3208
Hauptverfasser: Chen, Qing-Xia, Lu, Yu-Yang, Yang, Yang, Chang, Li-Ge, Li, Yi, Yang, Yuan, He, Zhen, Liu, Jian-Wei, Ni, Yong, Yu, Shu-Hong
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Sprache:eng
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Zusammenfassung:Investigations of one-dimensional segmented heteronanostructures (1D-SHs) have recently attracted much attention due to their potentials for applications resulting from their structure and synergistic effects between compositions and interfaces. Unfortunately, developing a simple, versatile and controlled synthetic method to fabricate 1D-SHs is still a challenge. Here we demonstrate a stress-induced axial ordering mechanism to describe the synthesis of 1D-SHs by a general under-stoichiometric reaction strategy. Using the continuum phase-field simulations, we elaborate a three-stage evolution process of the regular segment alternations. This strategy, accompanied by easy chemical post-transformations, enables to synthesize 25 1D-SHs, including 17 nanowire-nanowire and 8 nanowire-nanotube nanostructures with 13 elements (Ag, Te, Cu, Pt, Pb, Cd, Sb, Se, Bi, Rh, Ir, Ru, Zn) involved. This ordering evolution-driven synthesis will help to investigate the ordering reconstruction and potential applications of 1D-SHs. The formation mechanisms for periodic heterostructures are still poorly understood. Here, the authors propose a versatile approach to synthesize one-dimensional segmented heterostructures and reveal a stress-induced ordering mechanism through phase-field simulations.
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-024-47446-7