拉曼光谱
光致发光
煅烧
材料科学
焦绿石
X射线光电子能谱
发光
晶体结构
光谱学
分析化学(期刊)
纳米颗粒
结晶学
化学
纳米技术
化学工程
相(物质)
催化作用
色谱法
有机化学
生物化学
工程类
物理
光学
光电子学
量子力学
作者
Madhab Pokhrel,Kareem A. Wahid,Yuanbing Mao
标识
DOI:10.1021/acs.jpcc.6b04798
摘要
A series of 5 mol % Eu3+-doped rare earth (RE) hafnium oxide RE2Hf2O7 (RE = Y, La, Pr, Gd, Er, and Lu) nanoparticles (NPs) have been synthesized, calcinated, and systematically investigated using X-ray diffraction (XRD), Raman spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy, Fourier transform infrared spectroscopy, and optically excited luminescence. Effects of the A-site RE3+ cation and calcination on the crystal structure of the RE2Hf2O7:5%Eu NPs were distinguished using XRD and Raman studies. Spectroscopic analysis showed that the La2Hf2O7:5%Eu3+ and Pr2Hf2O7:5%Eu3+ possessed ordered pyrochlore structures while the RE2Hf2O7:5%Eu3+ compositions (RE = Y, Er, and Lu) possessed disordered fluorite structure and were thermodynamically stable up to the highest calcination temperature employed in this study (1500 °C); however, a disordered–ordered transition observed in the Gd2Hf2O7:5%Eu3+ composition indicated that it was not thermodynamically stable. Detailed photoluminescence (PL) studies, including quantum yield and decay properties of each sample before and after calcination, were performed and correlated with their compositions and crystal structures. These results suggest that the A site RE3+ cations and calcination of these RE2Hf2O7:5%Eu NPs play important roles in their PL properties.
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