TY - JOUR
T1 - Photoluminescence properties of YAG:Ce, RE phosphors prepared by citric acid gel combustion method
AU - Zhang, Le
AU - Han, Peng De
AU - Chen, Yan
AU - Wang, Li Xi
AU - Zhang, Qi Tu
PY - 2011/6
Y1 - 2011/6
N2 - (Y0.99-xREx)3 Al5O12:Ce0.03 (RE=Lu, Gd, La) phosphors were successfully synthesized by sol-gel combustion method using citric acid as chelating agent and fuel.Through the analysis of XRD, FTIR, SEM, and photoluminescence spectrum (PL), the crystal structure, particle morphology and luminescent properties of YAG:Ce under different calcination temperatures and RE co-doped concentrations were investigated.The powders with nanocrystalline size were obtained only at 900°C.As the calcination temperatures increasing , the average particle size was from 50 nm to 200 nm. With decreasing ionic radius from La3+, Gd3+, to Lu3+, the ceiling concentration leading to phase transformation was gradually increasing. Doped with only 50 mol% of La3+, to replace Y3+sites, the main phase of sample had transformed into LaAlO3. While the concentration of Gd3+, reached 90 mol%-99 mol%, the main phase of sample remained cubic YAG. Furthermore, Y3+ were completely replaced by Lu3+, with a cubic YAG. The location of the emission peak of Gd-codoped YAG:Ce3+system shifted to the red region, and it had a red shift of 21 nm corresponding to the maximum emission intensity before the appearance of GdAlO3. It reached 33 nm when Y3+ sites were completely replaced by Gd3+. Additionally, it had a blue shift of 24 nm when Y3+ completely replaced by Lu3+. The model of configuration coordinate and the crystal field theory gave this phenomenon a reasonable explanation.
AB - (Y0.99-xREx)3 Al5O12:Ce0.03 (RE=Lu, Gd, La) phosphors were successfully synthesized by sol-gel combustion method using citric acid as chelating agent and fuel.Through the analysis of XRD, FTIR, SEM, and photoluminescence spectrum (PL), the crystal structure, particle morphology and luminescent properties of YAG:Ce under different calcination temperatures and RE co-doped concentrations were investigated.The powders with nanocrystalline size were obtained only at 900°C.As the calcination temperatures increasing , the average particle size was from 50 nm to 200 nm. With decreasing ionic radius from La3+, Gd3+, to Lu3+, the ceiling concentration leading to phase transformation was gradually increasing. Doped with only 50 mol% of La3+, to replace Y3+sites, the main phase of sample had transformed into LaAlO3. While the concentration of Gd3+, reached 90 mol%-99 mol%, the main phase of sample remained cubic YAG. Furthermore, Y3+ were completely replaced by Lu3+, with a cubic YAG. The location of the emission peak of Gd-codoped YAG:Ce3+system shifted to the red region, and it had a red shift of 21 nm corresponding to the maximum emission intensity before the appearance of GdAlO3. It reached 33 nm when Y3+ sites were completely replaced by Gd3+. Additionally, it had a blue shift of 24 nm when Y3+ completely replaced by Lu3+. The model of configuration coordinate and the crystal field theory gave this phenomenon a reasonable explanation.
KW - Co-doping
KW - Photoluminescence
KW - Red shift
KW - Sol-gel combustion method
KW - YAG
UR - http://www.scopus.com/inward/record.url?scp=79960429413&partnerID=8YFLogxK
M3 - 文章
AN - SCOPUS:79960429413
SN - 1000-985X
VL - 40
SP - 677-683+688
JO - Rengong Jingti Xuebao/Journal of Synthetic Crystals
JF - Rengong Jingti Xuebao/Journal of Synthetic Crystals
IS - 3
ER -