A multilayer core–shell architecture capable of selectively capturing distinct nanomaterials into a predetermined layer is anticipated to facilitate multifunctional isolation or cascade processes at the microscale. However, fabricating single‐crystal architectures featuring numerous shells with intricate distribution patterns remains challenging. In this study, we employed DNA nanotechnology to construct microscale multilayer core–shell DNA origami crystals. The internal layers exhibit tunable properties, including size, quantity, self‐similarity, and morphology. The shell size can be regulated from 700 to 1800 µm3, and the layer quantity can be extended to five. We also fabricated eight distinct crystals exhibiting non‐self‐similarity and two types of heteromorphic core–shell crystals. Each layer has operational independence, allowing the customized capture of nanomaterials and implementation of compartmentalized reactions. These multilayer core–shell crystals have potential for serving as compartmentalization templates for functional units, which may provide possibilities for simulating cell work or constructing artificial organelles.
A perspective on polymer-ligand functionalization is provided, charting how macromolecular-level binding chemistry translates into multiscale structure-property relationships and ultimately governs material function, and how these precise surfaces and assembly concepts dictate biomedical performance.
Debasmita Muhuri, Xiao-Yi Sun, Xi Mao et al.· ACS Applied Materials and In...· 0 citations
Biological systems solve energy conversion, fluidic, mechanical, and optical problems using hierarchically ordered architectures whose functional feature sizes fall in the nanometer‐to‐micrometer range. Translating these architectures into synthetic devices requires transferable design rules rather than morphological a...
Nafeesa Sarfraz, Sadaf Bibi, MuhammadIbrar Ahmed et al.· Aggregate· 0 citations
The self-assembly of colloidal particles enables the creation of structured materials with programmable functionalities; however, controlling interaction specificity and aggregate morphology in a reversible and scalable manner remains a major challenge. Here, we investigate the selective depletion-induced self-assembly...
D. Sahu, Jude Ann Vishnu, Lisa Shafroth et al.· 0 citations
Crystalline self-assembly offers a powerful route to ordered organic materials with well-defined structures and morphologies. Despite substantial advances in controlling crystal habit, organic single crystals with precisely engineered architectures, particularly those with fully enclosed internal cavities, remain exc...
Lin Chen, Fei Tong, Rizwan Ali et al.· Journal of the American Chem...· 0 citations
Hybrid polymer nanocomposites have become central to the development of lightweight, high-performance, and sustainable materials in response to growing demands from electrification, advanced manufacturing, and multifunctional device technologies. In this context, hybrid nanoparticles, single nanoscale entities integrat...
Tasnim Alam Subah, Hasan Tasnim Salehin, Rakibul Hasan Rafi et al.· RSC Advances· 0 citations
Shape-programmable particles offer significant opportunities for microrobotic systems at the individual level and for hierarchical materials with emergent functionalities arising from collective particle behavior. However, fabricating shape-changing stimuli-responsive particles with complex three-dimensional geometries...
Hamed Almohammadi, Gurminder K. Paink, Vasumathi Venkat et al.· 0 citations
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