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用于固态照明设备的新型镝和铽激活的Ca(PO)Cl荧光粉的结构与发光特性

Structure and Luminescence Properties of Novel Dyand Tb Activated Ca(PO)Cl Phosphors for Solid-State Lighting Devices.

作者信息

Maske Roshana T, Yerpude A N, Wandhare Rupesh S, Parshuramkar D M, Pawar N R

机构信息

Department of Physics, N.H. College, Chandrapur, India.

Department of Physics, ACS College, Yavatmal, India.

出版信息

Luminescence. 2025 Jul;40(7):e70241. doi: 10.1002/bio.70241.

Abstract

The novel Dy-and Tb-doped Ca(PO)Cl phosphor is synthesized by the conventional wet chemical technique. The XRD pattern of prepared Dy and Tb doped in host material is in well agreement with the PDF card no. 7032212. The SEM image shows that the size of the particle is non-uniform in size and shape; it ranges in submicrometers. FTIR analysis confirms phosphate (PO) and Ca-O group bonding present in Ca(PO)Cl phosphor. The photoluminescence spectra of the prepared Ca(PO)Cl:Dy phosphor, under the excitation at 350 nm, it exhibit two emission peaks located at 474 nm (F → H) and 572 nm (F → H), emitting blue and orange color respectively. The high-intensity peak is located at 474 nm. The PLE spectra of Ca(PO)Cl:Tb phosphor contain two strong emission peaks centered at 470 (blue) nm and 543 (green) nm, these ascribed due to D → F & D → F transition of Tb ions monitored at 354 and 379 nm excitation. The concentration quenching mechanism between the Dy-Dy ions and Tb-Tb ions is primarily attributed to dipole-dipole (d-d) interactions. The results suggest that Ca(PO)Cl:RE (RE = Dy, Tb) phosphor shows promise for use as a near-UV phosphor in solid-state lighting applications.

摘要

采用传统湿化学技术合成了新型Dy和Tb掺杂的Ca(PO)Cl荧光粉。在主体材料中掺杂Dy和Tb后制备的XRD图谱与PDF卡号7032212完全吻合。SEM图像显示颗粒的尺寸和形状不均匀,范围在亚微米级别。FTIR分析证实了Ca(PO)Cl荧光粉中存在磷酸盐(PO)和Ca-O基团键合。制备的Ca(PO)Cl:Dy荧光粉在350 nm激发下的光致发光光谱显示出两个发射峰,分别位于474 nm(F→H)和572 nm(F→H),分别发射蓝色和橙色光。高强度峰位于474 nm。Ca(PO)Cl:Tb荧光粉的PLE光谱包含两个强发射峰,中心分别位于470(蓝色)nm和543(绿色)nm,这归因于在354和379 nm激发下监测到的Tb离子的D→F和D→F跃迁。Dy-Dy离子和Tb-Tb离子之间的浓度猝灭机制主要归因于偶极-偶极(d-d)相互作用。结果表明,Ca(PO)Cl:RE(RE = Dy,Tb)荧光粉有望用作固态照明应用中的近紫外荧光粉。

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