Applications of microelectromagnetic traps.

Microelectromagnetic traps (METs) have been used for almost two decades to manipulate magnetic fields. Different trap geometries have been shown to produce distinct magnetic fields and field gradients. Initially, microelectromagnetic traps were used mainly to separate and concentrate magnetic material at small scales. Recently such traps have been implemented for unique applications, for example filterless bioseparations, inductive heat generation, and biological detection. In this review, we describe recent reports in which MET geometry, current density, or external fields have been used. Descriptions of recent applications in which METs have been used to develop sensors, manipulate DNA, or block ion current are also provided.

Magnetically gated microelectrodes.

Microelectrodes fabricated in the center of single-coil microelectromagnetic traps are described. Magnetic particles are then used to reversibly gate transport of an electroactive species to the surface of the electrode or as a means to produce an ON/OFF bioelectrocatalytic glucose sensor.

Electromagnetic micropores: fabrication and operation.

We describe the fabrication and characterization of electromagnetic micropores. These devices consist of a micropore encompassed by a microelectromagnetic trap. Fabrication of the device involves multiple photolithographic steps, combined with deep reactive ion etching and subsequent insulation steps. When immersed in an electrolyte solution, application of a constant potential across the micropore results in an ionic current. Energizing the electromagnetic trap surrounding the micropore produces regions of high magnetic field gradients in the vicinity of the micropore that can direct motion of a ferrofluid onto or off of the micropore. This results in dynamic gating of the ion current through the micropore structure. In this report, we detail fabrication and characterize the electrical and ionic properties of the prepared electromagnetic micropores.

UV photodissociation of η5-C5H5NiNO: an excited-state Jahn-Teller distortion produces a cartwheeling NO.

The 225 nm photodissociation of cyclopentadienylnickel nitrosyl was studied using velocity-mapped ion imaging with 1 + 1' REMPI detection of the NO (X (2)Π(1/2,3/2), v'' = 0) photofragment. The product recoil energy and angular distributions were measured for selected rotational states of NO. The NO product displays two speeds, a slow product peaked at the center of the ion image and a fast anisotropic product that has an inverted rotational population. In rotational states above J'' = 40.5, an even faster anisotropic NO photofragment appears, most likely because the metal-containing dissociation partner emerges in a lower electronic state, increasing the available energy. The µ-v-j vector correlations were measured and are consistent with the orientation µâˆ¥v⊥ j. The observed vector correlations arise from an excited-state Jahn-Teller distortion of the parent, a distortion that bends the Ni-NO coordinate prior to dissociation.