Search arXivSearch

arXiv · 2607.25077

Electron-Stimulated Desorption of D Atoms from Gibbsite (Al(OD)3) and D2O Ice: Energy and Temperature Dependence of Translational Energy Distributions

Abstract

The electron-stimulated desorption (ESD) of neutral D atoms from gibbsite (\ce{Al(OD)3}) nanoplatelets and amorphous \ce{D2O} ice has been investigated using $2+1$ resonance-enhanced multiphoton ionization (REMPI) time-of-flight mass spectroscopy in a high vacuum chamber at temperatures 15 and 300\,K. Electron irradiation at 540, 250, and 150\,eV produces similar translational energy distributions at $\sim$300\,K, with a dominant intermediate-temperature component ($T \sim 1500$--$2100$\,K). Cooling to 15\,K suppresses the D atom yield by approximately 50\% and removes the lowest-temperature (slowest) component. This decrease in yield is consistent with diminished hole mobility and restricted diffusion at cryogenic temperatures. Under identical conditions, \ce{D2O} amorphous solid water ice films produce approximately 20 times greater D atom signal than bare gibbsite, with significantly hotter translational distributions, reflecting the higher deuterium surface density and distinct bonding environments of bulk ice relative to the terminal hydroxyl groups on gibbsite. These results identify hole transport to terminal hydroxyl sites as the rate-limiting step for nonthermal D atom production and provide a mechanistic framework for understanding atomic hydrogen release from aluminum hydroxide phases relevant to radioactive waste storage at the Hanford Site.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

William T. P. Denman, Brant M. Jones, Jacob Messner, Xin Zhang, Micah P. Prange, Greg A. Kimmel, Jay A. LaVerne, Thomas M. Orlando. 2026-07-27. Electron-Stimulated Desorption of D Atoms from Gibbsite (Al(OD)3) and D2O Ice: Energy and Temperature Dependence of Translational Energy Distributions. https://arxiv.org/abs/2607.25077

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Intrinsic Matching Frustration in Fluctuating Finite Systems

We formulate intrinsic matching frustration (IMF), a fluctuation-induced, kinetics-independent reduction in the mean capacity permitted by a prescribed matching rule. For complementary one-to-one matching, the instantaneous capacity is set by the minority population, so fluctuations produce a nonzero mean deficit even when the two populations are balanced on average. At finite size, this deficit depends on the full distribution of the population difference and is determined by its variance alone only in the Gaussian limit. Compartmentalization hides matching capacity by preventing cancellation between local imbalances of opposite sign. Fusion releases this hidden capacity monotonically under coarse graining, producing a measurable recovery of product yield following local reaction to completion.

physics.chem-ph

Phonon chirality as an additive control of CISS: a symmetry-protected law

Chirality-induced spin selectivity (CISS) is usually associated with molecular handedness. The possible contribution of chiral phonons is less established. We study a helical tight-binding model in which local phonon angular momentum modulates spin-dependent nearest-neighbor hopping. Fewest-switches surface hopping calculations give the transmitted spin polarization $\mathrm{SP}=aC+b\mathrm{PH}$. Here $C$ is the molecular chirality and $\mathrm{PH}$ is the phonon chirality. A mirror symmetry reverses $C$, $\mathrm{PH}$, and $\mathrm{SP}$ simultaneously. This symmetry excludes both a chirality-independent offset and a $C\cdot\mathrm{PH}$ term. The phonon contribution can therefore enhance, cancel, or reverse the molecular CISS signal.

physics.chem-ph

A fast physics-based matrix model for the impedance of a PEM fuel cell: Incorporating functionally graded catalyst layer and channel impedances

We extend a recent physics-based matrix model for calculating PEM fuel cell impedance (doi:10.1149/2754-2734/ad6ce8) to cases of low air flow stoichiometry and functionally graded cathode catalyst layers (CCLs). We demonstrate that the matrix model produces accurate spectra and is almost three orders of magnitude faster than a model based on the standard boundary-value problem solver. The physics-based matrix model can compete with equivalent circuit models for fitting experimental EIS spectra, particularly those measured from cells with functionally graded CCL.

physics.chem-ph