Predicting the Excitation Dynamics in Lanthanide Nanoparticles

verfasst von

Simon Spelthann, Jonas Thiem, Oliver Melchert, Rajesh Komban, Christoph Gimmler, Ayhan Demicran, Axel Ruehl, Detlev Ristau

Abstract

With their dipole-forbidden 4f transitions, lanthanides doped in nanoparticles promise high excited state lifetimes and quantum yields that are required for applications such as composite lasers or nanoscale quantum memories. Quenching at the nanoparticle surface, however, severely reduces the lifetime and quantum yield and requires resource-consuming experimental optimization that could not be replaced by simulations due to the limitations of existing approaches until now. Here, a versatile approach is presented that fully accounts for spatiotemporal dynamics and reliably predicts the lifetimes and quantum yields of lanthanide nanoparticles. LiYF₄:Pr³⁺nanoparticles are synthesized as a model system, and the lifetimes of a concentration series (≈10 nm, 0.7−1.47 at%) are used to match the model parameters to the experimental conditions. Employing these parameters, the lifetimes and quantum yields of a size series (≈5 at%, 12−21 nm) are predicted with a maximum uncertainty of 12.6%. To demonstrate the potential of the model, a neutral shell is added around the core particles in the model which extends the lifetime by up to 44%. Furthermore, spatiotemporal analysis of single nanoparticles points toward a new type of energy trapping in lanthanide nanoparticles. Consequently, the numerical optimization brings applications such as efficient nanoparticle lasers or quantum memories within reach.

Organisationseinheit(en)

Institut für Quantenoptik
PhoenixD: Simulation, Fabrikation und Anwendung optischer Systeme
QUEST Leibniz Forschungsschule

Externe Organisation(en)

Fraunhofer-Zentrum für Angewandte Nanotechnologie (CAN)

Typ

Artikel

Journal

Advanced optical materials

Band

11

ISSN

2195-1071

Publikationsdatum

18.07.2023

Publikationsstatus

Veröffentlicht

Peer-reviewed

Ja

ASJC Scopus Sachgebiete

Elektronische, optische und magnetische Materialien, Atom- und Molekularphysik sowie Optik

Elektronische Version(en)

https://doi.org/10.1002/adom.202300096 (Zugang: Offen)