A planar ion trapping microdevice with integrated waveguides for optical detection.

A planar ion trap with an integrated waveguide was fabricated and characterized. The microdevice, consisting of a 1 mm-diameter one-hole ring trap and multi-mode optical waveguides, was made on a glass wafer using microfabrication techniques. The experimental results demonstrate that the microdevice can trap 1.5 µm- to 150 µm-diameter charged particles in air under an alternating electric field with the amplitude and frequency varying from 100 V to 750 V, and 100 Hz to 700 Hz, respectively. The on-chip waveguide is capable of detecting the presence of a particle in the trap, and the particle secular motion frequency was found to depend on the input alternating signal amplitude and frequency.

Surface coating effects on the assembly of gold nanospheres.

Optical spectra and atomic force microscopy (AFM) images of individually selected spheres and mechanically assembled silica-coated gold nanosphere pairs were recorded. The shell served as a means of rigid control of the minimum spacing between the metal cores. The spectra of the assembled spheres were simulated using classical electrodynamics. The observed spectra resulted in superior characterization of the particle assembly geometry, relative to the AFM data. Experimental investigations regarding less-rigid polyvinylpyrrolidone (PVP) sphere coatings were also performed and some comparisons were made.

Combined apertureless near-field optical second-harmonic generation/atomic force microscopy imaging and nanoscale limit of detection.

A dual function atomic force/near-field scanning optical microscope (AFM/NSOM) with an ultrafast laser excitation source was used to investigate apertureless, tip enhanced second-harmonic generation (SHG) of ZnO nanowires with spatial resolution below the optical diffraction limit. Single-wire SHG spectra show little to no contribution from bandgap or other emission. Polarization data established values for chi(33)/chi(31) close to previous estimates and confirm the SHG process. Experimental results indicate that the SHG signal was reduced for nanowires after exposure to an atmosphere of carbon dioxide and water vapor. An equation was derived for estimating the minimum chi(2) detectable using apertureless SHG NSOM.

Controlling the expansion into vacuum-the enabling technology for trapping atmosphere-sampled particulate ions.

A new inlet has been designed to control the kinetic energy distributions of ions into a large-radius, frequency-adjusted, linear quadrupole ion trap. The work presented here demonstrates trapping singly-charged, intact proteins in the 10 to 200 kDa range injected from the atmosphere. The trapped ions were held while collisions with a buffer gas removed the remaining amounts of expansion-induced kinetic energy. The ions were then ejected from the trap on-demand into an awaiting detector. There is no low mass limit for ion injection and trapping. The upper limit presented in this study was defined by the limit of the conversion dynode-based detector at approximately 1.5 MDa. Trapping larger masses should be achievable. The transmission and capture efficiency across the entire mass range should be very high because the entire flow from the inlet empties directly into the trap. The kinetic energy distribution of massive ions is the primary reason for the working range limitation of mass spectrometers. Trapping ions with collisional cooling before mass analysis permits the motion of the ions to be completely defined by the applied fields. For this reason, this new inlet and trapping system represents a large step toward sensitive, high-resolution mass spectrometry into the megadalton range and beyond.

Computational and experimental evaluation of nanoparticle coupling.

We present theoretical and experimental studies on the optical properties of dimers composed of octahedron-shaped, gold nanoparticles. The experimental measurements show that the photoluminescence varies quite dramatically as two octahedra are brought into close proximity. AFM images and optical emission have been recorded for dimers in uncoupled and strongly coupled configurations. The former displays a single emission peak, while the latter shows two peaks with the new feature at longer wavelengths. Calculations indicate that the red-shifted peak originates from a strongly coupled plasmon state that oscillates along the extended axis of the dimer. Theoretically, we investigate the distances over which the dimers couple and find this to be particularly plasmon mode dependent. The anisotropic morphology and sharp apexes contribute significantly to the orientational dependence of the interparticle couplings and field properties.

Trapping of intact, singly-charged, bovine serum albumin ions injected from the atmosphere with a 10-cm diameter, frequency-adjusted linear quadrupole ion trap.

High-resolution real-time particle mass measurements have not been achievable because the enormous amount of kinetic energy imparted to the particles upon expansion into vacuum competes with and overwhelms the forces applied to the charged particles within the mass spectrometer. It is possible to reduce the kinetic energy of a collimated particulate ion beam through collisions with a buffer gas while radially constraining their motion using a quadrupole guide or trap over a limited mass range. Controlling the pressure drop of the final expansion into a quadrupole trap permits a much broader mass range at the cost of sacrificing collimation. To achieve high-resolution mass analysis of massive particulate ions, an efficient trap with a large tolerance for radial divergence of the injected ions was developed that permits trapping a large range of ions for on-demand injection into an awaiting mass analyzer. The design specifications required that frequency of the trapping potential be adjustable to cover a large mass range and the trap radius be increased to increase the tolerance to divergent ion injection. The large-radius linear quadrupole ion trap was demonstrated by trapping singly-charged bovine serum albumin ions for on-demand injection into a mass analyzer. Additionally, this work demonstrates the ability to measure an electrophoretic mobility cross section (or ion mobility) of singly-charged intact proteins in the low-pressure regime. This work represents a large step toward the goal of high-resolution analysis of intact proteins, RNA, DNA, and viruses.

Optical absorption measurements with parametric down-converted photons.

It has been known for some time that correlated detection of pairs of photons generated by parametric down-conversion can eliminate several sources of error that occur in single-beam measurements. In the correlated photon measurements, the down-converted photons are separated into two beams with one photon of a pair in each beam. The absolute detection efficiency of a detector in one beam can be determined from the count rate of a detector in the other beam and the coincidence rate for the two detectors. These ideas can be used to measure the optical absorbance of a sample placed in front of one of the detectors. Errors due to stray light and dark counts are substantially reduced and fluctuations in pump intensity largely eliminated.

Detection of chemical warfare-related species on complex aerosol particles deposited on surfaces using an ion trap-based aerosol mass spectrometer.

A new type of aerosol mass spectrometer was developed by minimal modification of an existing commercial ion trap to analyze the semivolatile components of aerosols in real time. An aerodynamic lens-based inlet system created a well-collimated particle beam that impacted into the heated ionization volume of the commercial ion trap mass spectrometer. The semivolatile components of the aerosols were thermally vaporized and ionized by electron impact or chemical ionization in the source. The nascent ions were extracted and injected into the ion trap for mass analysis. The utility of this instrument was demonstrated by identifying semivolatile analytes in complex aerosols. This study is part of an ongoing effort to develop methods for identifying chemical species related to CW agent exposure. Our efforts focused on detection of CW-related species doped on omnipresent aerosols such as house dust particles vacuumed from various surfaces found in any office building. The doped aerosols were sampled directly into the inlet of our mass spectrometer from the vacuumed particle stream. The semivolatile analytes were deposited on house dust and identified by positive ion chemical ionization mass spectrometry up to 2.5 h after deposition. Our results suggest that the observed semivolatile species may have been chemisorbed on some of the particle surfaces in submonolayer concentrations and may remain hours after deposition. This research suggests that identification of trace CW agent-related species should be feasible by this technique.

MALDI of individual biomolecule-containing airborne particles in an ion trap mass spectrometer.

Individual airborne biomolecule-containing particles were detected and characterized in near real-time by matrix-assisted laser desorption/ionization (MALDI) with an ion trap mass spectrometer. Biomolecule-containing particles were laboratory-generated and passed through a heated region containing a solution of matrix in equilibrium with the gas phase. Passage into a cooler region created a supersaturation, resulting in rapid deposition of the matrix vapor onto the biomolecule-containing particles, whereupon they were sampled into the inlet of our spectrometer. The coated particles were collimated and individually sized by light-scattering-based time-of-flight. When the sized particle reached the center of the ion trap, it was irradiated with a focused 266-nm laser, and the resulting ions were mass-analyzed. Mass spectra of leucine enkephalin, bradykinin, substance P, and polylysine-containing particles were determined with attomole sensitivity. Structural information of the peptides contained in an individual particle was obtained by tandem mass spectrometry. Analysis of the results yields insights into the aerosol laser ablation ionization process that suggests an optically limited mechanism for ion production that has interesting ramifications on the utility of aerosol-based MALDI as an analytical technique.

High-pressure ion trap mass spectrometry.

The effects of buffer gas pressure on ion trap stability, mass resolution/calibration, and choice of mass scanning are described. Pressure effects were treated phenomenologically by adding a drag term to the ion equations of motion. The resulting collisional damping enlarges the mass-dependent stability region but reduces the region in which mass-selective resonance ejection can be performed. The pressure effects can be reduced by increasing the frequency of the alternating quadrupole field.

Analysis of volatile organic compounds in air with a micro ion trap mass analyzer.

Analysis of several volatile organic compounds in air has been demonstrated with a micro ion trap mass analyzer equipped with a semipermeable membrane sampling inlet. MS/MS of selected compounds was also shown to be feasible with the miniature ion trap and could be used to improve sensitivity by reducing background noise.

Double resonance ejection in a micro ion trap mass spectrometer.

Ion ejection from a cylindrical micro ion trap by resonance excitation of the secular motion is observed to be strongly dependent on the frequency of the secular motion at resonance. Both the intensity of the ion signal and the mass resolution of the resulting mass spectrum are increased when the ion secular frequency is approximately that of a nonlinear resonance of the trap. The resonances are attributed to electrical as well as geometrical considerations.