4.8 Article

General Programmable Growth of Hybrid Core-Shell Nanostructures with Liquid Metal Nanodroplets

Journal

ADVANCED MATERIALS
Volume 33, Issue 11, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.202008024

Keywords

core-shell structures; galvanic reaction; liquid metals; nanofabrication

Funding

  1. ARC [LE0882813, LE120100104]
  2. Australian Research Council (ARC) [DP170101467, FT180100585, FT160100207, LP180100722]
  3. National Key Research & Development Program of China [2018YFE0202700]
  4. National Natural Science Foundation of China [11874003, 21822302, 12074021, 51672018, 11874316]
  5. Beijing Natural Science Foundation [Z180007]
  6. BUAA-UOW Joint Research Centre Small Grant
  7. AIIM
  8. Natural Science Foundation of Hunan Province [2019JJ50602]
  9. Scientific Research Fund of Hunan Provincial Education Department [18C0105]
  10. Innovative Research Team in University [IRT13093]
  11. Centre for Materials Science in QUT

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This study presents a general route for programmable preparation of complex core-shell nanostructures using liquid metal droplets as reformable templates. By triggering a localized galvanic replacement reaction in an ultrasonication system, high-level compositional diversity control and quantitative regulation of both the core and shell layers of the heterogeneous products are achieved, offering a method that cannot be realized with a solid-template synthetic route.
Core-shell and hollow nanostructures have been receiving significant interest due to their potential in wide scientific and technological fields. Given such large scope, however, they still lag far behind in terms of the ambition toward controllably, or even programmatically, synthesizing libraries of core-shell structures on a large scale. Here, a general route for the programmable preparation of complex core-shell nanostructures by using liquid metal (LM) droplets as reformable templates is presented, and the triggering of a localized galvanic replacement reaction in one ultrasonication system is demonstrated. Benefiting from the activity and mobility of the metal components in LM templates, high-level compositional diversity control and quantitative regulation of both the core and the shell layers of the heterogeneous products are achieved, which cannot be realized with a solid-template synthetic route.

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