Enhanced green emission and thermal stability of Ba3Si6O12N2:Eu2+ by Ce3+/P5+-doping: Unity energy transfer, charge compensation and lattice strain release

Описание

Тип публикации: статья из журнала

Год издания: 2020

Идентификатор DOI: 10.1016/j.jlumin.2019.116995

Ключевые слова: Charge compensation, Green phosphor, Oxonitridosilicate, Thermal stability improvement, Unity energy transfer

Аннотация: To optimize luminescence properties of oxonitridosilicate phosphors are extremely necessary for improving lighting quality of white light-emitting diodes (WLEDs). Herein, we designed Ce3+, Eu2+ codoping and P5+↔Si4+ substitution in the presentative Ba3Si6O12N2:Eu2+ green phosphor to realize an enhancement of luminescence efficiencyПоказать полностьюand thermal stability. Rietveld refinement results of Ce3+, Eu2+, P5+-doped Ba3Si6O12N2 (BSON) confirmed the formation of pure trigonal phase (P-3) of Ba3Si6O12N2 and the successful doping of Ce3+, Eu2+, P5+ ions. Ce3+ and Eu2+ ions randomly occupy two Ba crystallographic sites. Interestingly, a near unity energy transfer (ET, ~100%) from Ce3+ ions to Eu2+ ions is observed. Meanwhile, the doping of P5+ ions into BSON also helps improving the luminescence efficiency and thermal stability, which should be attributed to the charge compensation and the relax of lattice strain. In addition, the white light emitting diodes (WLEDs) fabricated by employing P5+-doped BSON: Eu2+ present a better electroluminescence performance than BSON: Eu2+. This study could serve as a guide in developing optimized oxonitridosilicates phosphors with improved luminescence performances based on complete energy transfer and lattice variations in local coordination environments through cation substitutions, and the as-prepared Ce3+/P5+-codoped Ba3Si6O12N2:Eu2+ could be an excellent green-emitting phosphor for UV-to-Visible LED chips pumped WLEDs. © 2019 Elsevier B.V.

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Издание

Журнал: Journal of Luminescence

Выпуск журнала: Vol. 220

Номера страниц: 116995

ISSN журнала: 00222313

Издатель: Elsevier B.V.

Персоны

  • Hao Jiarui (China Univ Geosci, Engn Res Ctr Nanogeomat, Minist Educ, Fac Mat Sci & Chem, 388 Lumo Rd, Wuhan 430074, Peoples R China)
  • Tao Mengxuan (China Univ Geosci, Engn Res Ctr Nanogeomat, Minist Educ, Fac Mat Sci & Chem, 388 Lumo Rd, Wuhan 430074, Peoples R China)
  • Gao Zhiyu (China Univ Geosci, Engn Res Ctr Nanogeomat, Minist Educ, Fac Mat Sci & Chem, 388 Lumo Rd, Wuhan 430074, Peoples R China)
  • Chen Shuoting (China Univ Geosci, Engn Res Ctr Nanogeomat, Minist Educ, Fac Mat Sci & Chem, 388 Lumo Rd, Wuhan 430074, Peoples R China)
  • Liu Yixin (China Univ Geosci, Engn Res Ctr Nanogeomat, Minist Educ, Fac Mat Sci & Chem, 388 Lumo Rd, Wuhan 430074, Peoples R China)
  • Wang Hongquan (China Univ Geosci, Engn Res Ctr Nanogeomat, Minist Educ, Fac Mat Sci & Chem, 388 Lumo Rd, Wuhan 430074, Peoples R China)
  • Wei Yi (China Univ Geosci, Engn Res Ctr Nanogeomat, Minist Educ, Fac Mat Sci & Chem, 388 Lumo Rd, Wuhan 430074, Peoples R China)
  • Molokeev Maxim S. (SB RAS, Lab Crystal Phys, Kirensky Inst Phys, Krasnoyarsk 660036, Russia; Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia; Siberian Fed Univ, Krasnoyarsk 660041, Russia)
  • Li Guogang (China Univ Geosci, Engn Res Ctr Nanogeomat, Minist Educ, Fac Mat Sci & Chem, 388 Lumo Rd, Wuhan 430074, Peoples R China)