Low-lying excited state energy trap induced by cross-relaxation - The main origin of concentration quenching in lanthanide upconversion nanoparticlesShow others and affiliations
2023 (English)In: Journal of Alloys and Compounds, ISSN 0925-8388, E-ISSN 1873-4669, Vol. 936, article id 168149Article in journal (Refereed) Published
Abstract [en]
In lanthanide-doped upconversion nanoparticles (UCNPs), the concentration of emitter ions, also known as activator ions, is usually limited to 1 - 5 mol% due to concentration quenching effects. This circumstance limits the luminescent efficiency of UCNPs' and their use in a variety of application areas. Earlier studies have attributed the activator concentration quenching to migration of energy to the nanoparticle surface, while indicating that cross-relaxation between activator ions had a minor role therein. In this work, we carried out comparative studies on Er3+-doped and Yb3+-Er3+ codoped UCNPs and could, in contrast to this notion, prove a general adverse effect of cross-relaxation between activator ions, here Er3+ ions, on up -conversion luminescence (UCL). The direct result of the cross-relaxation is that the energy of the excitation light is accumulated into a low-lying excited state of Er3+ in the infrared region, so forming a "low-lying excited state energy trap ". As a result, the excitation energy is used for generating down-conversion lu-minescence or for indirectly facilitating UCL channels that are directly related to the low-lying excited state energy trap. The identified effect can be used to regulate UCL channels to achieve a concentrated UCL band that is more favorable for certain applications, e.g., biological imaging.
Place, publisher, year, edition, pages
Elsevier BV , 2023. Vol. 936, article id 168149
Keywords [en]
Upconversion nanoparticles, Cross-relaxation, Concentration quenching, Energy trap
National Category
Theoretical Chemistry Physical Chemistry
Identifiers
URN: urn:nbn:se:kth:diva-323433DOI: 10.1016/j.jallcom.2022.168149ISI: 000907705500002Scopus ID: 2-s2.0-85145608798OAI: oai:DiVA.org:kth-323433DiVA, id: diva2:1732413
Note
QC 20230131
2023-01-312023-01-312023-01-31Bibliographically approved