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BiPO4:掺杂镧系离子的更好宿主。

BiPO4: a better host for doping lanthanide ions.

机构信息

Chemistry Division, Bhabha Atomic Research Centre, Trombay, Mumbai, India.

出版信息

Dalton Trans. 2012 Mar 21;41(11):3194-203. doi: 10.1039/c2dt11944g. Epub 2012 Jan 30.

DOI:10.1039/c2dt11944g
PMID:22286329
Abstract

In the present manuscript it is demonstrated that BiPO(4) is a better alternative to lanthanide phosphate host for making lanthanide ion-based luminescent materials. Hexagonal and monoclinic forms of BiPO(4) phase were prepared based on the reaction of Bi(3+) and PO(4)(3-) ions in ethylene glycol medium at 100 and 185 °C, respectively. From the differential thermal analysis (DTA) studies it is confirmed that the difference in the nucleation mechanism rather than the phase transition is responsible for the monoclinic phase formation at low temperatures (125 °C). Monoclinic BiPO(4) is quite stable and forms random solid solutions with lanthanide phosphates having both monoclinic (monazite) and tetragonal (xenotime) structures, as confirmed by XRD, FTIR and (31)P solid state nuclear magnetic resonance studies. On excitation corresponding to the (1)S(0)→(3)P(1) transition of Bi(3+) in BiPO(4):Ln samples, energy transfer from host to lanthanide ions takes place. The studies are quite relevant as there is a growing interest all over the world in replacing lanthanide based host used for different applications with easily available, easily purifiable and cheap main group elements (like Sb, Bi etc.) based hosts.

摘要

在本手稿中,证明了 BiPO(4) 是替代镧磷酸盐宿主用于制造镧离子基发光材料的更好选择。基于 Bi(3+)和 PO(4)(3-)离子在乙二醇介质中的反应,分别在 100 和 185°C 下制备了六方相和单斜相的 BiPO(4)。从差示热分析 (DTA) 研究中可以确认,低温下(125°C)形成单斜相是由于成核机制的差异而不是相变所致。单斜相 BiPO(4)相当稳定,并与具有单斜相(独居石)和四方相(钇石)结构的镧磷酸盐形成随机固溶体,这通过 XRD、FTIR 和 (31)P 固态核磁共振研究得到证实。在 BiPO(4):Ln 样品中对应于 Bi(3+)的 (1)S(0)→(3)P(1)跃迁的激发下,发生了从宿主到镧离子的能量转移。这些研究非常相关,因为全世界都越来越关注用易得、易纯化和廉价的主族元素(如 Sb、Bi 等)基宿主替代用于不同应用的基于镧的宿主。

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