Site Occupation and Luminescence of Novel Orange-Red Ca3M2Ge3O12:Mn2+Mn4+ (M = Al, Ga) Phosphors

被引:92
作者
Dong, Langping [1 ,2 ]
Zhang, Liang [1 ,2 ]
Jia, Yongchao [3 ]
Shao, Baiqi [1 ]
Lu, Wei [1 ]
Zhao, Shuang [1 ,2 ]
You, Hongpeng [1 ,2 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Rare Earth Resource Utilizat, Changchun 130022, Peoples R China
[2] Univ Sci & Technol China, Hefei 230026, Peoples R China
[3] Catholic Univ Louvain, Inst Condensed Matter & Nanosci, European Theoret Spect Facil, B-1348 Louvain La Neuve, Belgium
基金
中国国家自然科学基金;
关键词
Site occupation; Luminescence; Self-reduction; Thermal stability; WLEDs; EMITTING PHOSPHOR; ENERGY-TRANSFER; ENHANCED LUMINESCENCE; MN4+ EMISSION; WHITE; BAND; PHOTOLUMINESCENCE; EU3+; GENERATION; EFFICIENCY;
D O I
10.1021/acssuschemeng.9b07281
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Novel orange-red-emitting phosphors Ca3M2Ge3O12:Mn2+,Mn4+ (M = AI, Ga) with sufficient red light component were developed, and their lattice occupancy and luminescent properties of different color centers have been studied. In Ca3M2Ge3O12:Mn, the abnormal self-reduction of Mn4+ to Mn2+ occurs. The doped manganese ion (using MnO2 as Mn source) occupies dodecahedron Ca2+ site forming Mn2+(I) color center with orange emission, while it occupies octahedral Al3+/Ga3+ site forming Mn2+(II) and Mn4+ color centers with red and deep red light emission. The thermal quenching properties show that Ca3M2Ge3O12:Mn (M = Al, Ga) samples have low thermal quenching, and the thermal quenching of Mn2+(I) is lower than that of Mn2+(II) due to existence of more defects nearby the Mn2+(II) providing additional nonradiative recombination decay path. Ca3Al2Ge3O12:Mn has a lower thermal quenching than Ca3Ga2Ge3O12:Mn because the former possesses higher rigidity. The obtained results reveal that Ca3M2Ge3O12:Mn2+,Mn4+ (M = Al, Ga) has potential practical value in WLEDs. Moreover, the luminescence of Mn2+ and Mn4+ ions in a matrix provides a new strategy for designing and synthesizing new luminescent materials.
引用
收藏
页码:3357 / 3366
页数:19
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