Search arXiv⌕ Search

arXiv · 2610.39623

Origin and photoluminescence of a shallow hydrogen-related donor in silicon

Abstract

Paramagnetic color centers in silicon are being investigated recently for use in quantum technologies. While the origin of most of the prominent photoluminescence (PL) lines are well understood, that is not the case for those connected to hydrogen, even though it is almost always present in silicon, e.g., shallow hydrogen-related donors (SHDs), but their atomic structure remains elusive. Recent experiments suggested connection between the SHDs and the so-called X and the B$_i$ (or X$_i$) PL-lines. An SHD, termed the MT2 center, was tentatively assigned to a bistable, negative-U defect, arising due to the interaction of hydrogen with the self-interstitial complex I$_4$. Using high-level density functional theory calculations, we investigate the interaction of hydrogen with self-interstitial complexes In. A shallow effective-mass-theory donor arises when hydrogen attacks a Si-Si bond in I$_n$, inserting itself as a bond-center interstitial (I$_n$H$_{BC}$) in an exothermic reaction. We demonstrate this in the case of a single self-interstitial and of a complex of four. The latter I$_\mathrm{4}$H$_\mathrm{BC}$ complex shows electronic, spin and PL properties remarkably close to MT2. We find that hydrogen in the presence of I$_4$ follows the same behavior as in pristine silicon, i.e., it is a negative-U bistable defect, only detectable under illumination. In the I$_4$H$_{BC}$ complex, H can hop via photo-assisted mechanism between equivalent BC sites of the I$_4$ complex, leading to a motional averaged tetragonal symmetry as experimentally observed for MT2. The zero-phonon line is distinct from the X-line (attributed to the bare I$_4$ complex), and falls well into the range of the X$_i$ lines. Our results identify the I$_4$H complex as a prototype for a class of SHDs, inferring that similar SHDs may arise, with the X$_i$ lines as their PL fingerprints, when H attacks I$_n$ clusters.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Miaomiao Han, Peter Deak, Bing Huang, Adam Gali. 2026-10-29. Origin and photoluminescence of a shallow hydrogen-related donor in silicon. https://arxiv.org/abs/2610.39623

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

KEEP EXPLORING

Related papers

Dynamic Peach-Koehler self-force, inertia, and radiation damping of a regularized dislocation

The elastodynamic Peach-Koehler force is computed for a fully-regularized straight dislocation with isotropic core in continuum isotropic elastic elasticity, in compact forms involving partial mass or impulsion functions relative to shear and compressional waves. The force accounts for both dynamic radiation damping and inertia. The expressions are valid indifferently for subsonic or supersonic velocities. Results are compared with the case of a flat-core dislocation of the Peierls-Eshelby type, for a motion of jump from rest to constant velocity. In the steady-state limit, the Lagrangian function relevant to expressing the force in the flat-core case must be replaced by a related but different function for the regularized dislocation. However, by suitably defining the regularizing dislocation width, the steady-state limits of the force for the fully-regularized and flat-core dislocations can be matched exactly.

cond-mat.mtrl-sci↗

LightPFP: A Lightweight Route to Ab Initio Accuracy at Scale

Machine learning interatomic potentials (MLIPs) bridge the gap between quantum-mechanical accuracy and scalable molecular simulations. However, a fundamental trade-off persists: universal MLIPs (u-MLIPs) offer broad transferability but are computationally expensive, whereas task-specific MLIPs (ts-MLIPs) achieve high efficiency at the expense of costly DFT training data. Here we introduce LightPFP, a data-efficient knowledge distillation framework. Instead of relying on expensive DFT calculations, LightPFP constructs a distilled ts-MLIP by using a u-MLIP to generate high-quality, material-specific training data, while employing a pre-trained lightweight model to further improve data efficiency. Across diverse material systems, LightPFP reduces model development time by approximately three orders of magnitude compared with DFT-based workflows, while maintaining DFT-level accuracy. Combined with a LAMMPS/Kokkos inference backend, LightPFP achieves more than three orders of magnitude higher inference efficiency than u-MLIP baselines while enabling simulations of systems thousands of times larger. When the teacher exhibits systematic bias, LightPFP supports few-shot precision correction using as few as 10 high-accuracy DFT configurations, as demonstrated by reproducing MgO's experimental melting point. This u-MLIP-driven distillation establishes a scalable route to high-fidelity, data-efficient MLIPs, accelerating the pace of materials discovery and design.

cond-mat.mtrl-sci↗

First-order polarization process as an alternative to antiferroelectricity

Antiferroelectrics generate significant interest since their polarization versus electric field (P-E) curves show typical double-hysteresis loops appealing for various applications. Unfortunately, antiferroelectrics are rare. In magnetic compounds, magnetization versus magnetic field (M-H) curves can show analogous double hysteresis loops not only in antiferromagnets but also in systems exhibiting field-induced first-order reorientation of the magnetization through a so-called first-order magnetization process. Here, we show that appealing double-hysteresis P-E loops can also appear from an unprecedented first-order polarization process. Focusing on non-polar CaTiO3, which can be turned ferroelectric under tensile strain, we study epitaxial thin films on differently-oriented NdGaO3 substrates using a combination of theoretical and experimental techniques. We uncover that a certain configuration exhibits double-hysteresis P-E loops that we rationalize from a field-induced abrupt rotation of the polarization. Such a first-order polarization process establishes a promising alternative pathway to achieve double hysteresis P-E loops appealing for practical applications.

cond-mat.mtrl-sci↗