Repozytorium

Combining XRD and SEM techniques with site selective spectroscopy for structural and spectroscopic studies of Nd3+-doped LuPO4 micro-powders.

Autorzy

Kacper Albin Prokop

Małgorzata Guzik

Yannick Guyot

Georges Boulon

Joanna Cybińska

Rok wydania

2020

Czasopismo

Ceramics International

Numer woluminu

46

Strony

26350-26360

DOI

10.1016/j.ceramint.2020.03.169

Kolekcja

Naukowa

Język

Angielski

Typ publikacji

Artykuł

Streszczenie

We present and discuss the structural and spectroscopic properties of micro-crystalline Nd3+-doped LuPO4 zircon-(xenotime)-type orthophosphates (0.5–20 mol% of Nd3+ ions) synthesized by high-temperature solid-state reaction, in which Nd3+ optical rare earth ion plays the role of a structural probe. Surprisingly, in the literature there are not many studies performed for this optical material. The basic structural research with detailed information about the non-equivalent symmetry sites for the powdered samples with different Nd3+ ion concentrations is still missing. It is very important to fulfill this gap in order to properly apply this optical material. A series of Nd3+-doped LuPO4 micro-powders were obtained by using molar ratio of Lu2O3, Nd2O3, and NH4H2PO4 as the starting materials. Also, for some samples the 10% of ammonium dihydrogen phosphate excess was applied. The XRD and SEM analysis reveal some dependence of Nd3+ ion concentration and synthesis route on the crystal structure. The low-temperature high-resolution techniques like absorption spectroscopy at 4.2 K and site-selective tuneable laser spectroscopy at 77 K allowed to take advantage of Nd3+ ion as a probe for local ordering due to the close relation between its spectroscopic properties and the local structure at the ion site. To the best of our knowledge such a study has not been reported for micro-powdered Nd3+-doped LuPO4.

Słowa kluczowe

Lutetium orthophosphates, Nd3+ ions, Micro-powders, NIR emitting optical materials, Nd3+ symmetry site

Adres publiczny

http://dx.doi.org/10.1016/j.ceramint.2020.03.169

Strona internetowa wydawcy

http://www.elsevier.com

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