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We describe the design and performance of a large magnetic trap for storage and cooling of atomic hydrogen (H). The trap operates in the vacuum space of a dilution refrigerator at a temperature of 1.5 K. Aiming at a large volume of the trap, we implemented the octupole configuration of linear currents (Ioffe bars) for the radial confinement, combined with two axial pinch coils and a 3 T solenoid for the cryogenic H dissociator. The octupole magnet consists of eight race-track segments, which are compressed toward each other with magnetic forces. This provides a mechanically stable and robust construction with a possibility of replacement or repair of each segment. A maximum trap depth of 0.54 K (0.8 T) was reached, corresponding to an effective volume of 0.5 l for hydrogen gas at 50 mK. This is an order of magnitude larger than ever used for trapping atoms. [ABSTRACT FROM AUTHOR]

We describe the design and construction of an experimental cell for the study of free radicals in macroscopically thick films of solidified molecular and rare gases by 128 GHz Electron Spin Resonance (ESR) at temperatures below 1 K. The ESR resonator has an open Fabry–Pérot design, and its frequency can be tuned in situ by adjusting the spacing between the mirrors. The tuning mechanism consists of a piezo positioner and a stainless-steel edge-welded bellows, which can change the resonator frequency by at least 6 GHz. The films of solidified gases can be deposited either directly from a room temperature reservoir or by recondensing from a specially arranged chamber. The free radicals can be created in the solid films by dissociating matrix species by running an rf discharge in a helium vapor. We suggest that such a sample cell design can also be used for a broad range of low-temperature ESR experiments where sample cooling needs to be enhanced by the presence of superfluid helium. [ABSTRACT FROM AUTHOR]

We report on an electron-spin resonance study of nuclear polarization of hydrogen atoms embedded in solid H2 and HD films at temperatures 0.1–1.5 K and in a high magnetic field of 4.6 T. Similar to our previous work [Phys. Rev. Lett. 122, 225301 (2019)], we observed a build-up of the spontaneously (p ≃ 0.35) and highly (p ≃ 0.75) nuclear polarized phases of H atoms in the as-deposited H2 films. However, we did not obtain an enhanced nuclear polarization of H atoms in the regions of their small local concentration. We also failed to observe enhanced nuclear polarization for H atoms in the annealed H2 films as well as in the as-deposited HD sample. These observations tend to support our previous explanation for the build-up of high nuclear polarization due to the formation of weakly-bound triplet H2 molecules. [ABSTRACT FROM AUTHOR]

We present the design and performance of an experimental cell constructed for matrix isolation studies of H and D atoms in solid H2/D2 films, which are created by molecular beam deposition at temperatures below 1 K. The sample cell allows sensitive weighing of the films by a quartz microbalance (QM) and their studies by magnetic resonance techniques in a strong magnetic field of 4.6 T. We are able to regulate the deposition rate in the range from 0.01 to 10 molecular layers/s, and measure the thickness with ≈0.2 monolayer resolution. The upper QM electrode serves as a mirror for a 128 GHz Fabry-Perot resonator connected to an electron spin resonance (ESR) spectrometer. H and D atoms were created by RF discharge in situ in the sample cell, and characterized by ESR and electron-nuclear double resonance. From the magnetic resonance measurements we conclude that the films are smooth and provide homogeneous trapping conditions for embedded atoms. The current sample cell design also makes it possible to calibrate the ESR signal and estimate the average and local concentrations of H and D radicals in the film. [ABSTRACT FROM AUTHOR]

Optical emission studies of a discharged nitrogen-helium gas injected into superfluid helium near 1.5 K are described. Analysis of atomic (α group) and molecular Vegard-Kaplan transitions clearly indicates that the emitting species are embedded inside nitrogen clusters. Cluster formation is most efficient in the crater formed on the liquid surface. Model calculations based on the classical bubble model and density functional theory suggest that under the experimental conditions only clusters consisting of more than 1000 molecules have sufficient kinetic energy for stable cavity formation to occur inside liquid helium. The results obtained suggest that impurity-helium solids formation is a consequence of extensive clustering in the gas jet. [ABSTRACT FROM AUTHOR]

In the present work, we have studied ion-pair states of matrix-isolated I(2) with vacuum-UV absorption and UV-vis-NIR emission, where the matrix environment is systematically changed by mixing Kr with Xe, from pure Kr to a more polarizable Xe host. Particular emphasis is put on low doping levels of Xe that yield a binary complex I(2)-Xe, as verified by coherent anti-Stokes Raman scattering (CARS) measurements. Associated with interaction of I(2) with Xe we can observe strong new absorption in vacuum-UV, redshifted 2400 cm(-1) from the X → D transition of I(2). Observed redshift can be explained by symmetry breaking of ion-pair states within the I(2)-Xe complex. Systematic Xe doping of Kr matrices shows that at low doping levels, positions of I(2) ion-pair emissions are not significantly affected by complexation with Xe, but simultaneous increase of emissions from doubly spin-excited states indicates non-radiative relaxation to valence states. At intermediate doping levels ion-pair emissions shift systematically to red due to change in the average polarizability of the environment. We have conducted spectrally resolved ultrafast pump-probe ion-pair emission studies with pure and Xe doped Kr matrices, in order to reveal the influence of Xe to I(2) dynamics in solid Kr. Strikingly, relaxed emission from the ion-pair states shows no indication of complex presence. It further indicates that the complex escapes detection due to a non-radiative relaxation.

Formation of the unstable cis-formic acid in solid argon matrix is induced by direct excitation of the 6<--0 transition of the nu(OH) vibration of the trans-formic acid. The experiment utilizes strongly focused laser beam that produces relatively high isomerization rate despite the low cross section of the absorption. Raman spectroscopy in a backscattering geometry is used for detection of the reactants and the products. This experimental arrangement allow us to use the same laser source for simultaneous pumping and Raman excitation, and it also guarantees that the excited and probed volumes overlap. The presented method has a high potential for solid state investigations of chemical reactions on the ground electronic state.