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The application of photolithographic techniques further provides elastomer materials with precisely and spatially controlled tribological properties.
Genetically engineered protein polymers (GEPP) are a class of multifunctional materials with precisely controlled molecular structure and property profile.
Recent advances in the handling of DNA have made it possible to use DNA as a building block of nano-sized materials with precisely designed architectures.
The well-defined (co polymers self-assembly or can be pre-assembled to materials with precisely controlled morphologies which can be affected and fixed by processing.
Ligands inspired by the natural extracellular matrix, cell cell contacts, and growth factors have been incorporated into synthetic materials with precisely engineered density and presentation.
We describe the systematic use of coupled quantum and statistical mechanical calculations to design materials with precisely controlled charge perturbation and charge transport (under the influence of applied electric fields) critical to the realization of desired photonic and electronic properties.
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The well-established structure-property relationship shown in this paper could further provide guidance for fabrication of high performance recyclable material with precisely controllable microstructures and behaviors.
Since existing atomic layer deposition (ALD) shows ultrahigh conformity and compatibility to semiconductor processing [21], it is a powerful tool for plasmonic material deposition with precisely controlled thickness.
Compared with chemical synthesis, genetic engineering has enabled the protein materials with uniform composition, precisely controlled molecular weight and tunable structures for use in drug delivery.
Nanostructured materials can be synthesized with precisely controlled morphologies, sizes, and seemingly limitless chemical functional groups [42].
With advancements in synthetic methods, nanostructured materials can be synthesised with precisely controlled morphologies, sizes and seemingly limitless chemical functional groups.
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