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Mass-selected aluminum anion clusters, Aln–, were reacted with O2. Rate constants (300 K) for 2 < n < 30 and product branching fractions for 2 < n < 17 are reported. Reactivity is strongly anticorrelated to Aln– electron binding energy (EBE). Al13– reacts more slowly than predicted by EBE but notably is not inert, reacting at a measurable 0.05% efficiency (2.5 ± 1.5 × 10–13 cm3 s–1). Al6– is also an outlier, reacting more slowly than expected after accounting for other factors, suggesting that high symmetry increases stability. Implications of observed Al13– reactivity, contributions of both electronic shell-closing and geometric homogeneity to Aln– resistance to O2 etching, and future directions to more fully unravel the reaction mechanisms are discussed.

The kinetics of MgO + + CH 4 was studied experimentally using the variable ion source, temperature adjustable selected ion flow tube (VISTA-SIFT) apparatus from 300 − 600 K and computationally by running and analyzing reactive atomistic simula- tions. Rate coefficients and product branching fractions were determined as a function of temperature. The reaction proceeded with a rate of k = 5 . 9 ± 1 . 5 × 10 − 10 ( T/ 300 K) − 0 . 5 ± 0 . 2 cm 3 s − 1 . MgOH + was the dominant product at all temperatures, but Mg + , the co-product of oxygen-atom transfer to form methanol, was observed with a product branching fraction of 0 . 08 ± 0 . 03( T/ 300 K) − 0 . 8 ± 0 . 7 . Reactive molecular dynamics simulations using a reactive force field, as well as a neural network trained on thousands of structures yield rate coefficients about one order of magnitude lower. This underestimation of the rates is traced back to the multireference character of the transition state [MgOCH 4 ] + . Statistical modeling of the temperature-dependent kinetics provides further insight into the reactive potential surface. The rate limiting step was found to be consistent with a four-centered activation of the C-H bond, consistent with previous calculations. The product branching was modeled as a competition between dissociation of an insertion intermediate directly after the rate- limiting transition state, and traversing a transition state corresponding to a methyl migration leading to a Mg-CH 3 OH + complex, though only if this transition state is stabilized significantly relative to the dissociated MgOH + + CH 3 product channel. An alternative non-statistical mechanism is discussed, whereby a post-transition state bifurcation in the potential surface could allow the reaction to proceed directly from the four-centered TS to the Mg-CH 3 OH + complex thereby allowing a more robust competition between the product channels .

Mass-selected aluminum anion clusters, Al

We present 300 K rate constants for the ion-ion reactions of O + a n d N + with the atomic halide anions: C l - , B r - , a n d I - measured using a flowing afterglow – Langmuir probe apparatus. All six rate constants were > 1 × 10 - 8 c m 3 s - 1 , larger than those typical for atomic ion – atomic ion reactions, approaching the rate constants of more complex ion-ion systems. Evaluation of literature atomic ion – atomic ion rate constants shows variation over orders of magnitude, but limited to below the expected value for a polyatomic ion-ion reaction of the same reduced mass, fitting into an expected physical picture. Unlike for polyatomic systems, estimation of rate constant for atomic ion – atomic ion reaction rates by simple means does not seem effective.

Rate constants for the reactions of C+ + Cl-, Br-, and I- were measured at 300 K using the variable electron and neutral density electron attachment mass spectrometry technique in a flowing afterglow Langmuir probe apparatus. Upper bounds of

Thermal electron attachment rate coefficients for three interhalogen compounds (ClF, ICl, IBr) have been measured from 300 to 900 K at pressures of 1--2 Torr using a flowing afterglow--Langmuir probe apparatus. ClF attaches somewhat inefficiently ($k=7.5\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}9}\phantom{\rule{0.16em}{0ex}}\mathrm{c}{\mathrm{m}}^{3}\phantom{\rule{0.16em}{0ex}}{\mathrm{s}}^{\ensuremath{-}1}$) at 300 K, with the rate coefficient rising to $1.7\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}8}\phantom{\rule{0.16em}{0ex}}\mathrm{c}{\mathrm{m}}^{3}\phantom{\rule{0.16em}{0ex}}{\mathrm{s}}^{\ensuremath{-}1}$ at 700 K. At higher temperatures the apparent rate coefficient falls steeply; however, this is interpreted as an artifact due to decomposition on the walls of the inlet line. ICl attaches with even lower efficiency ($k=9.5\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}10}\phantom{\rule{0.16em}{0ex}}\mathrm{c}{\mathrm{m}}^{3}\phantom{\rule{0.16em}{0ex}}{\mathrm{s}}^{\ensuremath{-}1}$ at 300 K) and a less steep increase with temperature. Attachment to IBr is too slow to confidently measure with the present experiment, with an upper limit on the rate coefficient of ${10}^{\ensuremath{-}10}\phantom{\rule{0.16em}{0ex}}\mathrm{c}{\mathrm{m}}^{3}\phantom{\rule{0.16em}{0ex}}{\mathrm{s}}^{\ensuremath{-}1}$ from 300 to 600 K. Both ClF and ICl attach dissociatively to yield $\mathrm{C}{\mathrm{l}}^{\ensuremath{-}}$, likely exclusively, though ${\mathrm{F}}^{\ensuremath{-}}$ or ${\mathrm{I}}^{\ensuremath{-}}$ may be produced with limits of $l2%$ and $l5%$, respectively. The ClF attachment was further explored through ab initio calculation of the ClF and $\mathrm{Cl}{\mathrm{F}}^{\ensuremath{-}}$ potential energy curves and $R$-matrix calculations of the resonance parameters which were used then for calculations of the dissociative attachment cross sections and rate coefficients. While the magnitude of the attachment rate coefficient for ClF is similar to those for both $\mathrm{C}{\mathrm{l}}_{2}$ and ${\mathrm{F}}_{2}$, the calculated cross sections show qualitatively different threshold behavior due to the $s$-wave contribution allowed by the lack of inversion symmetry. The $v=1$ and 2 vibrational modes of ClF attach about three to four times faster than $v=0$ and 3 at energies lower than $\ensuremath{\sim}0.2\phantom{\rule{0.16em}{0ex}}\mathrm{eV}$. The calculated rate coefficients are in good agreement with the experiment at 300 K and increase moderately less steeply with temperature.

A digital holography (DH) surface erosion/deposition diagnostic is being developed for 3D imaging of plasma facing component surfaces in situ and in real time. Digital holography is a technique that utilizes lasers reflected from a material surface to form an interferogram, which carries information about the topology of the surface when reconstructed. As described in this paper, dual CO2 lasers at 9.271 and 9.250 μm wavelengths illuminate the interrogated surface (at a distance of ∼1 m) in a region of ∼1 cm × 1 cm. The surface feature resolution is ∼0.1 mm in the plane of the surface, and the depth resolution ranges from ∼0.0001 to ∼2 mm perpendicular to the surface. The depth resolution lower limit is set by single-laser and detector optical limitations, while the upper limit is determined by 2π phase ambiguity of the dual-laser synthetic wavelength. Measurements have been made "on the bench" to characterize the single-laser and dual-laser DH configurations utilizing standard resolution targets and material targets that were previously exposed to high flux plasmas in either the Prototype Material Plasma Exposure eXperiment (Proto-MPEX) or the electro-thermal (ET) arc source. Typical DH measurements were made with 0.03 ms integration with an IR camera that can be framed at rates approaching 1.5 kHz. The DH diagnostic system is progressing toward in situ measurements of plasma erosion/deposition either on Proto-MPEX or the ET arc source.

Significant reduction of the breakdown threshold in a DC microdischarge via seeding metal nanoparticles has been demonstrated. Compared to standard Paschen curves in dry air, reductions in the breakdown voltage of 5% to 25% were obtained for PD values (the product of pressure and electrode gap distance) ranging from 20 to 40 Torr-cm by seeding aluminum and iron nanoparticles with mean sizes of 75 nm and 80 nm, respectively. No secondary energy source was required to achieve this breakdown threshold reduction. From high-speed chemiluminescence imaging of the discharge evolution, breakdown was shown to be initiated at reduced voltages. Following breakdown, the increase in temperature ignited some of the nanoparticles near the cathode. Results suggest that possible charging of the nanoparticles within the gap may reduce the effective transient distance, leading to the threshold reduction.

A novel technique is described for the measurement of rate constants and product branching fractions of thermal reactions between cation and radical species. The technique is a variant of the variable electron and neutral density attachment mass spectrometry (VENDAMS) method, employing a flowing afterglow-Langmuir probe apparatus. A radical species is produced in situ via dissociative electron attachment to a neutral precursor; this allows for a quantitative derivation of the radical concentration and, as a result, a quantitative determination of rate constants. The technique is applied to the reactions of Ar(+) and O2(+) with CH3 at 300 K. The Ar(+) + CH3 reaction proceeds near the collisional rate constant of 1.1 × 10(-9) cm(3) s(-1) and has three product channels: → CH3(+) + Ar (k = 5 ± 2 × 10(-10) cm(3) s(-1)), → CH2(+) + H + Ar (k = 7 ± 2 × 10(-10) cm(3) s(-1)), → CH(+) + H2 + Ar (k = 5 ± 3 × 10(-11) cm(3) s(-1)). The O2(+) + CH3 reaction is also efficient, with direct charge transfer yielding CH3(+) as the primary product channel. Several results needed to support these measurements are reported, including the kinetics of Ar(+) and O2(+) with CH3I, electron attachment to CH3I, and mutual neutralization of CH3(+) and CH2(+) with I(-).

A laser-ignition (LI) method is presented that utilizes a high-repetition-rate (HRR) nanosecond laser to reduce minimal ignition energies of individual pulses by ∼10 times while maintaining comparable total energies. The most common LI employs a single nanosecond-laser pulse with energies on the order of tens of millijoules to ignite combustible gaseous mixtures. Because of the requirements of high energy per pulse, fiber coupling of traditional LI systems is difficult to implement in real-world systems with limited optical access. The HRR LI method demonstrated here has an order of magnitude lower per-pulse energy requirement than the traditional single-pulse LI technique, potentially allowing delivery through standard commercial optical fibers. Additionally, the HRR LI approach significantly increases the ignition probability of lean combustible mixtures in high-speed flows while maintaining low individual pulse energies.

Here we report nonintrusive local rotational temperature measurements of molecular oxygen, based on coherent microwave scattering (radar) from resonance-enhanced multiphoton ionization (REMPI) in room air and hydrogen/air flames. Analyses of the rotational line strengths of the two-photon molecular oxygen C(3)Π(v=2)←X(3)Σ(v'=0) transition have been used to determine the hyperfine rotational state distribution of the ground X(3)Σ(v'=0) state. Rotationally resolved 2+1 REMPI spectra of the molecular oxygen C(3)Π(v=2)←X(3)Σ(v'=0) transition at different temperatures were obtained experimentally by radar REMPI. Rotational temperatures have been determined from the resulting Boltzmann plots. The measurements in general had an accuracy of ~±60 K in the hydrogen/air flames at various equivalence ratios. Discussions about the decreased accuracy for the temperature measurement at elevated temperatures have been presented.