Abstract
Porous
metal nanofoams have made significant contributions to a diverse set of
technologies from separation and filtration to aerospace. Nonetheless, finer control over nano and
microscale features must be gained to reach the full potential of these
materials in energy storage, catalytic, and sensing applications. As biologics naturally occur and assemble
into nano and micro architectures, templating on assembled biological materials
enables nanoscale architectural control without the limited chemical scope or
specialized equipment inherent to alternative synthetic techniques. Here, we rationally assemble 1D biological
templates into scalable, 3D structures to fabricate metal nanofoams with a
variety of genetically programmable architectures and material
chemistries. We demonstrate that
nanofoam architecture can be modulated by manipulating viral assembly,
specifically by editing the viral surface coat protein, as well as altering
templating density. These architectures
were retained over a broad range of compositions including monometallic and
bi-metallic combinations of noble and transition metals of copper, nickel,
cobalt, and gold. Phosphorous and boron
incorporation was also explored. In addition to increasing the surface area
over a factor of 50, as compared to the nanofoam’s geometric footprint, this
process also resulted in a decreased average crystal size and altered phase
composition as compared to non-templated controls. Finally, templated hydrogels
were deposited on the centimeter scale into an array of substrates as well as
free standing foams, demonstrating the scalability and flexibility of this
synthetic method towards device integration.
As such, we anticipate that this method will provide a platform to
better study the synergistic and de-coupled effects between nano-structure and
composition for a variety of applications including energy storage, catalysis,
and sensing.