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高压下Y2O2S中Tb(3+)和Eu(3+)能级的光谱性质及位置

Spectroscopic properties and location of the Tb(3+) and Eu(3+) energy levels in Y2O2S under high hydrostatic pressure.

作者信息

Behrendt M, Mahlik S, Szczodrowski K, Kukliński B, Grinberg M

机构信息

Institute of Experimental Physics, Faculty of Mathematics, Physics and Informatics, University of Gdańsk, 80-308 Gdańsk, Poland.

出版信息

Phys Chem Chem Phys. 2016 Aug 10;18(32):22266-75. doi: 10.1039/c6cp03075k.

Abstract

In this contribution, an extensive spectroscopic study of Y2O2S doped with Eu(3+) and Tb(3+) is presented. Steady-state luminescence and luminescence excitation spectra as well as the time-resolved spectra and luminescence kinetics were obtained at high hydrostatic pressures up to 240 kbar. It was found that pressure quenches the luminescence from the (5)D3 excited state of Tb(3+) and recovers additional luminescence related to transitions from the (5)D3 state of Eu(3+). These effects are related to the pressure-induced increases in the energies of the ground electronic manifold 4f(n) of Eu(3+) and Tb(3+) ions with respect to the band edges. Analysis of the emission and excitation spectra allowed the estimation of the energies of the ground states of all lanthanide (Ln) ions (Ln(3+) and Ln(2+)) with respect to the valence and conduction bands edges of the Y2O2S host. The bandgap energy and difference between energies of the ground states of Ln(2+) and Ln(3+) have been calculated as functions of pressure. The experimental high-pressure spectroscopy results allow the calculation of the absolute values (calculated with respect to the vacuum level) of the energies and pressure-induced shifts of the conduction and valence band edges and the ground states of Ln(3+) and Ln(2+) ions in Y2O2S.

摘要

在本论文中,我们对掺杂了Eu(3+)和Tb(3+)的Y2O2S进行了广泛的光谱研究。在高达240 kbar的高静水压力下,我们获得了稳态发光和发光激发光谱以及时间分辨光谱和发光动力学。研究发现,压力淬灭了Tb(3+)的(5)D3激发态的发光,并恢复了与Eu(3+)的(5)D3态跃迁相关的额外发光。这些效应与压力诱导的Eu(3+)和Tb(3+)离子的基电子多重态4f(n)相对于能带边缘的能量增加有关。对发射光谱和激发光谱的分析使得我们能够估计所有镧系(Ln)离子(Ln(3+)和Ln(2+))的基态相对于Y2O2S主体的价带和导带边缘的能量。计算了带隙能量以及Ln(2+)和Ln(3+)基态能量之间的差值作为压力的函数。实验高压光谱结果使得我们能够计算Y2O2S中导带和价带边缘以及Ln(3+)和Ln(2+)离子基态的能量绝对值(相对于真空能级计算)以及压力诱导的位移。

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