Search arXiv⌕ Search

arXiv · 2610.16468

Deterministic positioning accuracy of B centers in hBN by electron irradiation

Abstract

Hexagonal boron nitride (hBN) is a promising material platform for quantum technologies, enabling both the realization of nanophotonic devices and the hosting of point defects that act as high-quality single-photon emitters (SPEs). Among these defects, B centers, which reproducibly emit at 436 nm, can be generated individually at predefined positions using electron beam irradiation, a crucial capability for top-down quantum photonics. Yet, the spatial accuracy of emitter creation strongly conditions the potential applications. Here, we generate arrays of individual B centers in a scanning electron microscope (SEM) with in-situ cathodoluminescence (CL) monitoring. We characterize the sources of random deviations from the target positions to identify the limitations to their deterministic positioning. In particular, we measure the distance between the electron beam and the emitter at the moment the emitter is created based on CL mapping. This approach provides a direct estimation of the spatial extent of the beam-emitter interaction. We find this contribution to be the main constraint to the emitter fabrication accuracy, yielding a standard deviation of 27 nm. Additional contributions, primarily from the finite density of UV-emitting carbon dimer precursors, increase the overall positional standard deviation to 40 nm. Our results highlight the possible improvements to the B center creation technique to reach sub-10 nm accuracy.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

A. Núñez Marcos, C. Arnold, J. Barjon, S. Buil, J. -P. Hermier, A. Delteil. 2026-10-12. Deterministic positioning accuracy of B centers in hBN by electron irradiation. https://arxiv.org/abs/2610.16468

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

KEEP EXPLORING

Related papers

Non-Hermitian Skin Effect from Radiative Coupling in a Reciprocal Chiral Medium

We show that long-range radiative coupling in a passive chiral medium produces an unusual non-Hermitian skin effect in a chain of dipoles. The skin-mode profile consists of a long-range light-line branch-cut contribution, a non-exponential factor $1/[n(\ln n)^2]$ with $n$ being the site number. Finite-chain calculations show that part of the open-boundary spectrum contracts toward the Bloch spectrum, whereas the number of boundary-localized modes remains extensive. The retarded radiative coupling makes both the real-space profile and the finite-size spectral signatures of boundary localization depart from standard finite-range and pure exponential coupling theory.

cond-mat.other↗

Momentum conservation for ab initio calculations with pseudopotentials via a phase space electronic structure formulation

We demonstrate how to build a robust phase space electronic Hamiltonian $\hat{H}_\text{PS}(\boldsymbol{R},\boldsymbol{P})$ that depends on nuclear position $\boldsymbol{R}$ and nuclear momentum $\boldsymbol{P}$ in the presence of ionic pseudopotentials. In particular, we show that in order to account for the non-local component of a pseudopotential while also conserving linear and angular momentum, one is forced to introduce a non-local one-electron operator $\hat{\boldsymbolΓ}^\text{nl}$ that couples electronic and nuclear momenta together. To test the validity of our ansatz, we derive a generalized form of Nafie's exact equality (which relates electronic momentum and electronic position) so as to include the presence of pseudopotentials. We then benchmark our proposed phase space electronic structure theory against this generalized Nafie-like result for a diverse set of diatomic molecules spanning a wide range of elements. We find excellent agreement across this ab initio test set, highlighting the strength of our method in capturing meaningful electronic momentum beyond the Born-Oppenheimer framework.

cond-mat.other↗

A Conservative Darcy-Brinkman-Stokes Formulation for PHREEQC-Coupled Reactive Transport with Cell-Based Surface Complexation

We present a mass-conservative Darcy-Brinkman-Stokes (DBS) formulation for reactive transport with cell-based surface complexation in image-based porous media, coupled to PHREEQC and implemented in GeoChemFoam, an OpenFOAM-based toolbox. Dissolved species are transported in the physical mobile-water fraction, adsorbed species are stored as conservative cell-scale surface inventories, and each reactive cell is coupled to PHREEQC. Reactive surface area is prescribed independently as a cell field, so that internal area left unresolved by segmentation of microporous phases can be represented while DBS flow and transport are retained in the resolved pore space. The implementation is verified with a test suite that isolates the coupling of transport and chemistry from the construction of reactive surface area. Aqueous and adsorbed mass balance is evaluated against a one-dimensional analytical retardation benchmark and closed-system batch calculations. The smooth-interface surface-area algorithms are tested on idealised two- and three-dimensional geometries. In a two-scale lithium micromodel, DBS reproduces fully resolved aqueous and sorbed inventories within 0.6% across Pe=0.1-10. The applications comprise Pb2+ retardation by hydrous ferric oxide coatings in a two-dimensional fracture network, competitive Mn2+/Mg2+ exchange in a three-dimensional Kelvin-cell sorbent, and Sr2+/Ca2+ exchange in Estaillades limestone. In the fracture-network and limestone cases, the formulation yields spatially resolved aqueous and adsorbed inventories even where reactive surface area is only partly resolved at the image scale. The framework therefore supports conservative surface-complexation modelling in both resolved and unresolved pore structures, with relevance to contaminant retention, selective ion capture, and radionuclide transport.

cond-mat.other↗