Electronic and Structural Properties of Lanthanide-Doped MoS$_2$: Impact of Ionic Size and Orbital Configuration Mismatch

TL;DR

This study uses density functional theory to explore how lanthanide dopants affect the structural and electronic properties of MoS2 monolayers, revealing insights into their potential as infrared single-photon emitters for quantum technologies.

Contribution

It provides a detailed theoretical analysis of lanthanide doping in MoS2, highlighting the role of vacancies in stabilizing dopants and predicting their optical emission properties.

Findings

S vacancies improve thermodynamic stability of doped MoS2

Ce4+ likely does not emit in infrared due to empty f-shell

Er3+ doped MoS2 is predicted to emit in the infrared

Abstract

Single-photon emitters (SPEs) are crucial for quantum technologies such as quantum simulation, secure quantum communication, and precision measurements. Two-dimensional transition metal dichalcogenides (TMDCs) are promising SPE candidates due to their atomically thin nature and efficient photon extraction. However, their emission wavelengths limit compatibility with existing telecommunication technologies. Lanthanide doping in TMDCs, such as \defect{MoS}{2}, offers a potential solution by introducing sharp, $f$-orbital derived emissions in the infrared range. Yet, the feasibility of introducing these dopants remains uncertain due to their large ionic radii of the lanthanides. We employ density functional theory (DFT) calculations to investigate the structural and electronic properties of lanthanide-doped \defect{MoS}{2} monolayers (Ln=Ce, Er). By evaluating formation energies with up to three adjacent S vacancies, we assess how these vacancies mitigate lattice strain caused by the size mismatch of Ce and Er with Mo. Our results show that while \defect{Ln}{Mo} destabilizes the pristine lattice, S vacancies enhance thermodynamic stability. Charge state analysis indicates that defect states introduced by \defect{Ln}{Mo} localize near the valence band and remain stable across a wide Fermi energy range. Electronic structure analysis shows that Ce$^{4+}$ and Er$^{3+}$ maintain their oxidation states upon electron doping due to additional acceptor states from host-induced dangling bonds. These states arise from an orbital filling mismatch between dopants and Mo. Consequently, \defect{Ce}{Mo} is unlikely to exhibit infrared emissions due to its empty $f$-shell, whereas \defect{Er}{Mo} is expected to emit in the infrared. These findings demonstrate the potential of lanthanide-doped TMDCs as tunable SPEs and provide design strategies for optimizing their optical and electronic properties.