Nanophosphors-Based White Light Sources

被引:20
作者
Cesaria, Maura [1 ,2 ]
Di Bartolo, Baldassare [2 ]
机构
[1] Univ Salento, Dept Math & Phys Ennio De Giorgi, Provle Via Arnesano, I-73100 Lecce, Italy
[2] Boston Coll, Dept Phys, Boston, MA 02215 USA
关键词
solid state lighting; white-light emission; size-dependent spectroscopy; nanophosphors; un-doped white-light emitters; UP-CONVERSION LUMINESCENCE; NEAR-INFRARED EMISSION; EMITTING-DIODES; TRIVALENT LANTHANIDES; TRANSITION-METAL; ENERGY-TRANSFER; SPECTROSCOPIC PROPERTIES; CRYSTALLINE ENVIRONMENT; OPTICAL-PROPERTIES; PHONON RELAXATION;
D O I
10.3390/nano9071048
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Miniaturization requests and progress in nanofabrication are prompting worldwide interest in nanophosphors as white-emission mercury-free lighting sources. By comparison with their bulk counterparts, nanophosphors exhibit reduced concentration quenching effects and a great potential to enhance luminescence efficiency and tunability. In this paper, the physics of the nanophoshors is overviewed with a focus on the impact of spatial confinement and surface-to-volume ratio on the luminescence issue, as well as rare earth-activated multicolor emission for white light (WL) output. In this respect, the prominently practiced strategies to achieve WL emission are single nanophosphors directly yielding WL by means of co-doping and superposition of the individual red, green, and blue emissions from different nanophosphors. Recently, a new class of efficient broadband WL emitting nanophosphors has been proposed, i.e., nominally un-doped rare earth free oxide (yttrium oxide, Y2O3) nanopowders and Cr transition metal-doped garnet nanocrystals. In regard to this unconventional WL emission, the main points are: it is strictly a nanoscale phenomenon, the presence of an emitting center may favor WL emission without being necessary for observing it, and, its inherent origin is still unknown. A comparison between such an unconventional WL emission and the existing literature is presented to point out its novelty and superior lighting performances.
引用
收藏
页数:28
相关论文
共 166 条
[1]   Role of the surface in luminescent processes [J].
Abrams, BL ;
Holloway, PH .
CHEMICAL REVIEWS, 2004, 104 (12) :5783-5801
[2]   High-performance phosphorescent white-stacked organic light-emitting devices for solid-state lighting [J].
Adamovich, Vadim I. ;
Levermore, Peter A. ;
Xu, Xin ;
Dyatkin, Alexey B. ;
Elshenawy, Zeinab ;
Weaver, Michael S. ;
Brown, Julie J. .
JOURNAL OF PHOTONICS FOR ENERGY, 2012, 2
[3]   Visible light emission upon near-infrared excitation in a transparent solution of nanocrystalline β-NaGdF4:Yb3+, Er3+ [J].
Aebischer, A ;
Heer, S ;
Biner, D ;
Krämer, K ;
Haase, M ;
Güdel, HU .
CHEMICAL PHYSICS LETTERS, 2005, 407 (1-3) :124-128
[4]   Color-tunable properties of Eu3+- and Dy3+-codoped Y2O3 phosphor particles [J].
Atabaev, Timur Sh ;
Hwang, Yoon-Hwae ;
Kim, Hyung-Kook .
NANOSCALE RESEARCH LETTERS, 2012, 7 :1-7
[5]   Upconversion and anti-stokes processes with f and d ions in solids [J].
Auzel, F .
CHEMICAL REVIEWS, 2004, 104 (01) :139-173
[6]   Temperature Quenching of Yellow Ce3+ Luminescence in YAG:Ce [J].
Bachmann, Volker ;
Ronda, Cees ;
Meijerink, Andries .
CHEMISTRY OF MATERIALS, 2009, 21 (10) :2077-2084
[7]   Size-dependent upconversion luminescence in Er3+/Yb3+-codoped nanocrystalline yttria:: Saturation and thermal effects [J].
Bai, Xue ;
Song, Hongwei ;
Pan, Guohui ;
Lei, Yanqiang ;
Wang, Tie ;
Ren, Xingguang ;
Lu, Shaozhe ;
Dong, Biao ;
Dai, Qilin ;
Fan, Libo .
JOURNAL OF PHYSICAL CHEMISTRY C, 2007, 111 (36) :13611-13617
[8]   Hot emission in Nd3+/Yb3+:YAG nanocrystalline ceramics [J].
Bednarkiewicz, A ;
Hreniak, D ;
Deren, P ;
Strek, W .
JOURNAL OF LUMINESCENCE, 2003, 102 :438-444
[9]   Laser-induced hot emission in Nd3+/Yb3+:YAG nanocrystallite ceramics [J].
Bednarkiewicz, A ;
Strek, W .
JOURNAL OF PHYSICS D-APPLIED PHYSICS, 2002, 35 (20) :2503-2507
[10]   OPTICAL-PROPERTIES OF MANGANESE-DOPED NANOCRYSTALS OF ZNS [J].
BHARGAVA, RN ;
GALLAGHER, D ;
HONG, X ;
NURMIKKO, A .
PHYSICAL REVIEW LETTERS, 1994, 72 (03) :416-419