arXiv subjects

Benjamin S. Kamerin

Publications and source records attributed to Benjamin S. Kamerin.

8 recordsLinked to original sources

arXiv2025

Stern-Gerlach deflection of cryogenically cold polyatomic molecules in superfluid nanodroplets

Beam deflection is capable of providing valuable information about the magnetic moments of molecules and clusters as well as the relaxation dynamics of their spins. However, observations have been hampered by magnetic couplings to excited vibrational and rotational states of polyatomic systems, which are challenging to control, characterize, and systematize. In this work, we carried out deflection measurements on superfluid helium nanodroplets doped with high-spin FeCl2 and CoCl2 molecules and their complexes. This enabled quantitative determination of the magnetic moments of molecules and clusters at extremely low, and fully defined, temperature of all of their degrees of freedom. The spin magnetic moments become thermalized and oriented along the applied field. Dimers and trimers are found to be antiferromagnetically ordered. The issue of rates and mechanisms of molecular spin relaxation within the cryogenic helium matrix is highlighted.

physics.atm-clus↗

arXiv2025

Magnetic deflection of high-spin sodium dimers formed on helium nanodroplets

Spectroscopic data on alkali-atom dimers residing on the surface of liquid helium nanodroplets have revealed that they are detected primarily in the weakly bound, metastable, spin-triplet state. Here, by measuring the magnetic Stern-Gerlach deflection of a sodium-doped nanodroplet beam, we transparently demonstrate the abundance of high-magnetic-moment dimers. Their electron spins thermalize with the cryogenic superfluid droplets and become fully oriented by the external magnetic field.

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arXiv2025

Shift of nanodroplet and nanocluster size distributions induced by dopant pick-up statistics

In pick-up experiments using nanodroplet and nanocluster beams, the size distribution of hosts carrying a specified number of dopants changes when the vapor density in the pick-up region is altered. This change, analyzed here, has quantitative consequences for the interpretation of data that are sensitive to host size, such as mass spectrometric, spectroscopic, and deflection measurements.

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arXiv2022

Shells in CO$_2$ Clusters

Abundance spectra of (CO$_2$)$_N$ clusters (up to $N \approx$ 500) acquired under a wide range of adiabatic expansion conditions are analyzed within the evaporative ensemble framework. Analysis reveals that cluster stability functions display strikingly universal patterns for all expansion conditions. These patterns reflect the inherent properties of individual clusters. From this analysis the size-dependent cluster binding energies are determined, shell and subshell closing sizes identified, and cuboctahedral packing ordering for sizes above $N \approx 130$ is confirmed. It is demonstrated that a few percent variation in the dissociation energies translates into significant abundance variations, especially for the larger clusters.

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arXiv2022

Probing the presence and absence of metal-fullerene electron transfer reactions in helium nanodroplets by deflection measurements

Metal-fullerene compounds are characterized by significant electron transfer to the fullerene cage, giving rise to an electric dipole moment. We use the method of electrostatic beam deflection to verify whether such reactions take place within superfluid helium nanodroplets between an embedded C$_{60}$ molecule and either alkali (heliophobic) or rare-earth (heliophilic) atoms. The two cases lead to distinctly different outcomes: C$_{60}$Na$_n$ ($n$=1-4) display no discernible dipole moment, while C$_{60}$Yb is strongly polar. This suggests that the fullerene and small alkali clusters fail to form a charge-transfer bond in the helium matrix despite their strong van der Waals attraction. The C$_{60}$Yb dipole moment, on the other hand, is in agreement with the value expected for an ionic complex.

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arXiv2020

Electric deflection of imidazole dimers and trimers in helium nanodroplets: Dipole moments, structure, and fragmentation

Deuterated imidazole (IM) molecules, dimers and trimers formed in liquid helium nanodroplets are studied by the electrostatic beam deflection method. Monitoring the deflection profile of (IM)D+ provides a direct way to establish that it is the primary product of the ionization-induced fragmentation both of (IM)2 and (IM)3. The magnitude of the deflection determines the electric dipole moments of the parent clusters: nearly 9 D for the dimer and 14.5 D for the trimer. These very large dipole values confirm theoretical predictions and derive from a polar chain bonding arrangement of the heterocyclic imidazole molecules.

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arXiv2019

Direct detection of polar structure formation in helium nanodroplets by beam deflection measurements

Long-range intermolecular forces are able to steer polar molecules submerged in superfluid helium nanodroplets into highly polar metastable configurations. We demonstrate that the presence of such special structures can be identified, in a direct and determinative way, by electrostatic deflection of the doped nanodroplet beam. The measurement also establishes the structures' electric dipole moments. In consequence, the introduced approach is complementary to spectroscopic studies of low-temperature molecular assembly reactions. It is enabled by the fact that within the cold superfluid matrix the molecular dipoles become nearly completely oriented by the applied electric field. As a result, the massive (tens of thousands of helium atoms) nanodroplets undergo significant deflections. The method is illustrated here by an application to dimers and trimers of dimethyl sulfoxide (DMSO) molecules. We interpret the experimental results with ab initio theory, mapping the potential energy surface of DMSO complexes and simulating their low temperature aggregation dynamics.

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arXiv2019

Oriented polar molecules trapped in cold helium nanodroplets: Electrostatic deflection, size separation, and charge migration

Helium nanodroplets doped with polar molecules are studied by electrostatic deflection. This broadly applicable method allows even polyatomic molecules to attain sub-Kelvin temperatures and nearly full orientation in the field. The resulting intense force from the field gradient strongly deflects even droplets with tens of thousands of atoms, the most massive neutral systems studied by beam "deflectometry." We use the deflections to extract droplet size distributions. Moreover, since each host droplet deflects according to its mass, spatial filtering of the deflected beam translates into size filtering of neutral fragile nanodroplets. As an example, we measure the dopant ionization probability as a function of droplet radius and determine the mean free path for charge hopping through the helium matrix. The technique will enable separation of doped and neat nanodroplets and size-dependent spectroscopic studies.

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