We use polarization-entangled photon pairs to demonstrate quantum nonlocality in an experiment suitable for advanced undergraduates. The photons are produced by spontaneous parametric downconversion using a violet diode laser and two nonlinear crystals. The polarization state of the photons is tunable. Using an entangled state analogous to that described in the Einstein-PodolskyRosen "paradox," we demonstrate strong polarization correlations of the entanged photons. Bell's idea of a hidden variable theory is presented by way of an example and compared to the quantum prediction. A test of the Clauser, Horne, Shimony and Holt version of the Bell inequality finds S = 2.307 ± 0.035, in clear contradiciton of hidden variable theories. The experiments described can be performed in an afternoon.

We present detailed instructions for constructing and operating an apparatus to produce and detect polarization-entangled photons. The source operates by type-I spontaneous parametric downconversion in a two-crystal geometry. Photons are detected in coincidence by single-photon counting modules and show strong angular and polarization correlations. We observe more than 100 entangled photon pairs per second. A test of a Bell inequality can be performed in an afternoon.

The separation of nanoparticles from micron size particles in high conductance buffers was achieved using an AC dielectrophoretic (DEP) microarray device with hydrogel over-coated microelectrodes. While nanoparticles could be selectively concentrated into high field regions directly over the platinum microelectrodes, micro-bubbling and electrode darkening was also observed. For similar experiments using un-coated microelectrodes, SEM analysis showed severe erosion of the platinum microelectrodes and fusion of nanoparticles due to the aggressive electrochemistry.

Multilayered structures composed of biomolecule-derivatized nanoparticles can be fabricated by electric-field-directed self-assembly. A microelectrode-array device facilitates the rapid parallel electrophoretic transport and binding of biotin and streptavidin fluorescent nanoparticles to specific sites on the microarray. Control of the current, voltage, and activation time of each of the 400-microarray electrodes allows a combinatorial approach to optimize nanoparticle binding. Under optimal conditions, nanoparticle layers form within 15 s of microelectrode activation, and the directed assembly of more than 50 alternate layers of nanoparticles is complete within an hour. The final multilayered structures are removed from the support by a relatively simple lift-off process. The electric-field process allows the parallel patterned assembly of multilayer structures using extremely low concentrations of nanoparticles and produces minimal nonspecific binding to unactivated sites. These results are significant for the development of rapid, maskless nanofabrication and hierarchical integration of biomolecular-derivatized nanocomponents into higher-order materials and devices.

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We have developed an automated cell counting method that uses images obtained at multiple focal heights to enumerate cells in confluent culture. By taking the derivative of image intensity with respect to focal height using two complementary images, we are able to count high-density monolayers of cells over a large image area. Our method resists errors arising from variability in the focal plane caused by flatness or tilt non-uniformities with a minimal amount of focal plane alignment, allowing the automated collection of images across a large area.

A fully automated electronic microarray control system (Nanochip 400 System) was used to carry out a combinatorial process to determine optimal conditions for fabricating higher order three-dimensional nanoparticle structures. Structures with up to 40 layers of bioderivatized nanoparticles were fabricated on a 400test site CMOS microarray using the automated Nanochip 400 System. Reconfigurable electric fields produced on the surface of the CMOS microarray device actively transport, concentrate, and promote binding of 40 nm biotin-and streptavidin-derivatized nanoparticles to selected test sites on the microarray surface. The overall fabrication process including nanoparticle reagent delivery to the microarray device, electronic control of the CMOS microarray and the optical/fluorescent detection, and monitoring of nanoparticle layering are entirely controlled by the Nanochip 400 System. The automated nanoparticle layering process takes about 2 minutes per layer, with 10e20 seconds required for the electronic addressing and binding of nanoparticles, and roughly 60 seconds for washing. The addressing and building process is monitored by changes in fluorescence intensity as each nanoparticle layer is deposited. The final multilayered 3D structures are about 2 mm in thickness and 55 mm in diameter. Multilayer nanoparticle structures and control sites on the microarray were verified by SEM analysis.

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