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Lanthanide-Activated Phosphors Based on 4f-5d Optical Transitions: Theoretical and Experimental Aspects

  • Xian Qin
  • , Xiaowang Liu
  • , Wei Huang
  • , Marco Bettinelli
  • , Xiaogang Liu
  • National University of Singapore
  • Nanjing Tech University
  • Nanjing University of Posts and Telecommunications
  • University of Verona

科研成果: 期刊稿件文章同行评审

945 引用 (Scopus)

摘要

The synthesis of lanthanide-activated phosphors is pertinent to many emerging applications, ranging from high-resolution luminescence imaging to next-generation volumetric full-color display. In particular, the optical processes governed by the 4f-5d transitions of divalent and trivalent lanthanides have been the key to enabling precisely tuned color emission. The fundamental importance of lanthanide-activated phosphors for the physical and biomedical sciences has led to rapid development of novel synthetic methodologies and relevant tools that allow for probing the dynamics of energy transfer processes. Here, we review recent progress in developing methods for preparing lanthanide-activated phosphors, especially those featuring 4f-5d optical transitions. Particular attention will be devoted to two widely studied dopants, Ce3+ and Eu2+. The nature of the 4f-5d transition is examined by combining phenomenological theories with quantum mechanical calculations. An emphasis is placed on the correlation of host crystal structures with the 5d-4f luminescence characteristics of lanthanides, including quantum yield, emission color, decay rate, and thermal quenching behavior. Several parameters, namely Debye temperature and dielectric constant of the host crystal, geometrical structure of coordination polyhedron around the luminescent center, and the accurate energies of 4f and 5d levels, as well as the position of 4f and 5d levels relative to the valence and conduction bands of the hosts, are addressed as basic criteria for high-throughput computational design of lanthanide-activated phosphors.

源语言英语
页(从-至)4488-4527
页数40
期刊Chemical Reviews
117
5
DOI
出版状态已出版 - 8 3月 2017
已对外发布

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