TY - GEN
T1 - Electric field process for the fabrication of higher order structures form biomolecule derivatized nanoparticles (#1030)
AU - Heller, M. J.
AU - Dehlinger, D.
AU - Sullivan, B.
AU - Esener, S.
PY - 2007/8/24
Y1 - 2007/8/24
N2 - An electronic microarray has been used to carry out directed self-assembly of higher order 3D structures from Biotin/Streptavidin and DNA derivatized nanoparticles. Structures with up to fifty layers of alternating biotin and streptavidin and DNA nanoparticles were fabricated using a 400 site CMOS microarray system. In this process, reconfigurable electric fields produced by the microarray device were used to rapidly transport, concentrate and accelerate the binding of 40 nanometer biotin, streptavidin and DNA derivatized nanoparticles to selected sites on the microarray. The nanoparticle layering process takes less than one minute per layer (10-20 seconds for addressing and binding nanoparticles, 40 seconds for washing). The nanoparticle addressing/binding process was monitored by changes in fluorescence intensity as each nanoparticle layer was deposited. The final multilayered 3-D structures are about two microns in thickness and 50 microns in diameter. Active structures with chemical to luminescent to fluorescent properties are now being fabricated. The use of a microelectronic array device for assisted self-assembly represents a unique example of combining "top-down" and "bottom-up" technologies into a unique nanofabrication process. Such a process will be useful for the hierarchal assembly of 3D nano, micro, and macrostructures for a variety of electronic/photonic, nanomaterials, energy and biosensor applications.
AB - An electronic microarray has been used to carry out directed self-assembly of higher order 3D structures from Biotin/Streptavidin and DNA derivatized nanoparticles. Structures with up to fifty layers of alternating biotin and streptavidin and DNA nanoparticles were fabricated using a 400 site CMOS microarray system. In this process, reconfigurable electric fields produced by the microarray device were used to rapidly transport, concentrate and accelerate the binding of 40 nanometer biotin, streptavidin and DNA derivatized nanoparticles to selected sites on the microarray. The nanoparticle layering process takes less than one minute per layer (10-20 seconds for addressing and binding nanoparticles, 40 seconds for washing). The nanoparticle addressing/binding process was monitored by changes in fluorescence intensity as each nanoparticle layer was deposited. The final multilayered 3-D structures are about two microns in thickness and 50 microns in diameter. Active structures with chemical to luminescent to fluorescent properties are now being fabricated. The use of a microelectronic array device for assisted self-assembly represents a unique example of combining "top-down" and "bottom-up" technologies into a unique nanofabrication process. Such a process will be useful for the hierarchal assembly of 3D nano, micro, and macrostructures for a variety of electronic/photonic, nanomaterials, energy and biosensor applications.
KW - Electric field
KW - Higher order structures
KW - Nanofabrication
KW - Nanoparticles
KW - Self-assembly
UR - http://www.scopus.com/inward/record.url?scp=34548018072&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=34548018072&partnerID=8YFLogxK
M3 - Conference contribution
AN - SCOPUS:34548018072
SN - 1420063421
SN - 9781420063424
SN - 1420061828
SN - 9781420061826
T3 - 2007 NSTI Nanotechnology Conference and Trade Show - NSTI Nanotech 2007, Technical Proceedings
SP - 269
EP - 270
BT - 2007 NSTI Nanotechnology Conference and Trade Show - NSTI Nanotech 2007, Technical Proceedings
T2 - 2007 NSTI Nanotechnology Conference and Trade Show - NSTI Nanotech 2007
Y2 - 20 May 2007 through 24 May 2007
ER -