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Project Title Self-Assembly of Biological Nanostructures |
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Research Program |
Project # NM4 |
Participating Faculty: Esther R. Angert, Carl A. Batt NBTC Students/Postdocs: Soazig Delamarre, Yajaira Sierra, Sandra Saldana Other Students/Postdocs: Leonardo Maestri |
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Objectives
Methods We investigated the optical properties of two-dimensional nanoparticle arrays biotemplated using S-layers. These experiments were initially performed on gold nanoparticle arrays formed on HPI-layers, but may eventually be extended to include the characterization of nanoparticle arrays patterned onto other types of S-layers displaying a variety of different lattice parameters. Nanoparticle array structures as catalysts for nanofiber/nanowire growth The nanoparticle arrays obtained using the above approaches were then subjected to plasma-enhanced chemical vapor deposition (PECVD) processes to synthesize the nanofiber/tube and nanowire arrays. We collaborated closely with Michael Simpson (Oakridge National Laboratories, ORNL) and used facilities in the Center for Nanoscale Material Science at ORNL. In addition we have explored the use of S-layers as etch resists in collaboration with Oxford Instruments. Cloning and expression of S-layers Using native and recombinant S-layer proteins (derived from the gene sbpA in Bacillus sphaericus, as described in our progress report), we studied their surface interaction and reassembly characteristics on various solid substrates in more detail. Pattered substrates used for our surface-interaction and reassembly studies will be fabricated using the advanced electron-beam lithography systems. Summary These S-layers have been used to demonstrate on a preliminary basis their ability to serve both as scaffolds for the growth of semiconductor structures and as ultra-high resolution etch resist materials. In both cases similar approaches have been used and are based upon our expansive foundation in understanding how to assemble S-layers on the surface and to then use them to create ordered arrays. The first test was carried out in conjunction with Mike Simpson at ORNL where carbon nanofibers were grown from nickel catalyst particles held in place by the S-layers (Figure 2). In the second test, gold nanoparticles biotemplated on the S-layers were used as a nanoetch mask in a SiCl4 inductively-coupled plasma (ICP) etch process. This plasma etch process resulted in the successful formation of silicon nanopillars ~100 nm high and ~30 nm wide at the base. This work was carried out in collaboration with Oxford Scientific (Figure 3). Accomplishments
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Figure 1: Brightfield TEM images and corresponding 2-D FFT power spectra of unstained SAS S-layers after incubation in citrate-capped gold nanoparticle (Au NP) or functionalized CdSe/ZnS quantum dot (QD) solutions. (a) Au NPs. (b) DMAET-QDs. (c) C3-QDs. (d) C8-QDs. (e) C16-QDs. To the right of each TEM image is a plot of the fast Fourier transform (FFT) calculated for a 305 nm-diameter circular region of the pattern. Scale bars represent 100 nm in all TEM images and 0.21 nm-1 in the FFT plots. |
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Figure 2: Carbon nanofibers fabricated using a plasma-enhanced CVD process with nickel catalyst particles biotemplated on HPI S-layer. |
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Figure 3: Silicon nanopillars fabricated using SiCl4 ICP etch process with gold nano-particles biotemplated on HPI S-layer as an etch mask. |
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