首页> 外文期刊>RSC Advances >Experimental and theoretical approach to account for green luminescence from Gd2Zr2O7 pyrochlore: exploring the site occupancy and origin of host-dopant energy transfer in Gd2Zr2O7:Eu3+
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Experimental and theoretical approach to account for green luminescence from Gd2Zr2O7 pyrochlore: exploring the site occupancy and origin of host-dopant energy transfer in Gd2Zr2O7:Eu3+

机译:GD2ZR2O7柏树绿色发光的实验与理论方法:探索GD2ZR2O7中的网站占用和主机掺杂能量转移起源:EU3 +

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摘要

Pure and Eu3+-doped Gd2Zr2O7 pyrochlore was synthesized using a gel combustion method using citric acid as a fuel. Samples of Gd2Zr2O7 pyrochlore were characterized systematically using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), energy-dispersive spectroscopy (EDS) and time-resolved photoluminescence spectroscopy (TRPLS). On irradiating the undoped Gd2Zr2O7 pyrochlore with Ultraviolet (UV) light, an intense green emission was observed. Photoluminescence lifetime measurements and X-ray photoelectron spectroscopy (XPS) showed the presence of oxygen vacancies in the pyrochlore sample, which were responsible for the intense green emission in Gd2Zr2O7 . Calculations based on density functional theory (DFT+U) of the electronic density of states in the presence of charged oxygen defects qualitatively explained the origin of the green emission in undoped Gd2Zr2O7 . The emission spectrum of Eu3+ revealed that it was distributed at both Gd3+ and Zr4+ sites in Gd2Zr2O7 , which was also confirmed using lifetime measurements. DFT-based calculations of cohesive energy also showed that doping with Eu is almost equally favorable at Gd and Zr sites. Based on DFT calculations, it is proposed that the distribution of f and d states of Eu3+ atoms matches well with the total density of states (DOS) of ordered Gd2Zr2O7 (o-Gd2Zr2O7 ), which signifies efficient transfer of photon energy from the host to the Eu3+ dopant. The actual site symmetry of europium ions in gadolinium zirconate was also determined based on the Stark splitting pattern and was found to be D-2d, although it is O-h for Gd3+ in Gd2Zr2O7 . Calculations of the Judd-Ofelt parameters revealed that Omega(2) > Omega(4), which indicates high covalency and low symmetry around Eu3+, which is in agreement with the results of emission spectroscopy. The high intensity of the red emission corresponding to the D-5(0) -> F-7(2) transition and good fluorescence yields (51%) highlight the unexplored potential of Gd2Zr2O7 : Eu3+ as a promising red phosphor.
机译:纯和Eu3 +的掺杂Gd2Zr2O7烧绿石,使用用柠檬酸作为燃料的燃烧凝胶法合成。 Gd2Zr2O7烧绿石的样本系统进行了表征使用X射线衍射(XRD),傅里叶变换红外光谱(FTIR),扫描电子显微镜(SEM),能量分散光谱法(EDS)和时间分辨光致发光光谱(TRPLS)。上照射紫外线(UV)光的未掺杂的烧绿石Gd2Zr2O7,观察到强烈的绿色发光。光致发光寿命测量和X射线光电子能谱(XPS)显示氧空位烧绿石样品中,这是负责在Gd2Zr2O7激烈绿色发射的存在。基于状态的在电的氧缺陷的存在的电子密度的密度泛函理论(DFT + U)计算定性的解释绿色发射的原点在未掺杂Gd2Zr2O7。 Eu3 +的的发射光谱表明,它是在两个Gd3 +的和Zr 4+的位点在Gd2Zr2O7,其中还使用寿命测量证实分布。聚能基于DFT的计算也表明:与欧盟方面表示掺杂在Gd和锆网站几乎同样有利。基于DFT计算,所以建议Eu3 +的原子的f和d状态的分布具有有序Gd2Zr2O7(邻Gd2Zr2O7),其表示从主机光子的高效能量传送到的状态(DOS)的总密度匹配良好在Eu3 +的掺杂剂。还确定基于所述Stark分裂图案的铕离子钆锆实际现场对称性和被发现是d-2d中,虽然它是对的Gd 3+中Gd2Zr2O7 O形小时。的贾德-Ofelt理论参数的计算表明,欧米茄(2)>欧米茄(4),其指示周围Eu3 +的,这是在与发射光谱的结果一致的高共价和低对称性。对应于d-5(0)的红色发射的高强度 - > F-7(2)过渡和良好的荧光产率(51%)突出Gd2Zr2O7的未知潜力:Eu3 +的作为有力的红色荧光体。

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  • 来源
    《RSC Advances》 |2016年第50期|共13页
  • 作者单位

    Bhabha Atom Res Ctr Div Radiochem Bombay 400085 Maharashtra India;

    Bhabha Atom Res Ctr Mat Sci Div Bombay 400085 Maharashtra India;

    Inst Sci Educ &

    Res Ctr Santini Ketan 731235 W Bengal India;

    Bhabha Atom Res Ctr Div Radiochem Bombay 400085 Maharashtra India;

    Bhabha Atom Res Ctr Div Radiochem Bombay 400085 Maharashtra India;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
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