Modification of relaxation dynamics in Tb3+:Y3Al5O12 nanopowders

被引:0
作者
Lutz, Thomas [1 ,2 ,4 ]
Veissier, Lucile [1 ,2 ,5 ]
Woodburn, Philip J. T. [3 ]
Cone, Rufus L. [3 ]
Barclay, Paul E. [1 ,2 ]
Tittel, Wolfgang [1 ,2 ,6 ,7 ]
Thiel, Charles W. [3 ]
机构
[1] Univ Calgary, Inst Quantum Sci & Technol, Calgary, AB T2N 1N4, Canada
[2] Univ Calgary, Dept Phys & Astron, Calgary, AB T2N 1N4, Canada
[3] Montana State Univ, Dept Phys, Bozeman, MT 59717 USA
[4] Swiss Fed Inst Technol, Zurich, Switzerland
[5] Univ Paris 11, Lab Aime Cotton, CNRS UPR 3321, Orsay, France
[6] Delft Tech Univ, QuTech, Delft, Netherlands
[7] Delft Tech Univ, Fac Elect Engn Math & Comp Sci, Delft, Netherlands
基金
加拿大自然科学与工程研究理事会; 美国国家科学基金会;
关键词
THERMAL-CONDUCTIVITY; PHONON RELAXATION; SOLID-STATE; NANOCRYSTALS; POWDERS; TEMPERATURES; DIAMOND; MEMORY; LIGHT;
D O I
10.1103/PhysRevB.98.054308
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Nanostructured rare-earth-ion-doped materials are increasingly being investigated for on-chip implementations of quantum information processing protocols as well as commercial applications such as fluorescent lighting. However, achieving high-quality and optimized materials at the nanoscale is still challenging. Here we present a detailed study into the restriction of phonon processes in the transition from bulk crystals to small (<= 40-nm) nanocrystals by observing the relaxation dynamics between crystal-field levels of Tb3+:Y3Al5O12. We find that the population relaxation dynamics are modified as the particle size is reduced, consistent with our simulations of inhibited relaxation through a modified vibrational density of states and hence modified phonon emission. However, our experiments also indicate that nonradiative processes not driven by phonons are also present in the smaller particles, causing transitions and rapid thermalization between the levels on a time scale of <100 ns.
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页数:9
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