| Literature DB >> 33191547 |
Hans C Hendrikse1, Arno van der Weijden1, Maria Ronda-Lloret2, Ting Yang3, Roland Bliem4,5, N Raveendran Shiju2, Martin van Hecke1,6, Ling Li3, Willem L Noorduin1.
Abstract
Forging customizable compounds into arbitrary shapes and structures has the potential to revolutionize functional materials, where independent control over shape and composition is essential. Current self-assembly strategies allow impressive levels of control over either shape or composition, but not both, as self-assembly inherently entangles shape and composition. Herein, independent control over shape and composition is achieved by chemical conversion reactions on nanocrystals, which are first self-assembled in nanocomposites with programmable microscopic shapes. The multiscale character of nanocomposites is crucial: nanocrystals (5-50 nm) offer enhanced chemical reactivity, while the composite layout accommodates volume changes of the nanocrystals (≈25%), which together leads to complete chemical conversion with full shape preservation. These reactions are surprisingly materials agnostic, allowing a large diversity of chemical pathways, and development of conversion pathways yielding a wide selection of shape-controlled transition metal chalcogenides (cadmium, manganese, iron, and nickel oxides and sulfides). Finally, the versatility and application potential of this strategy is demonstrated by assembling: 1) a scalable and highly reactive nickel catalyst for the dry reforming of butane, 2) an agile magnetic-controlled particle, and 3) an electron-beam-controlled reversible microactuator with sub-micrometer precision. Previously unimaginable customization of shape and composition is now achievable for assembling advanced functional components.Entities:
Keywords: bioinspired mineralization; ion exchange; nanocomposites; nanocrystals
Year: 2020 PMID: 33191547 DOI: 10.1002/adma.202003999
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849