Title of article :
Simultaneous synthesis and densification of transparent, photoluminescent polycrystalline YAG by current activated pressure assisted densification (CAPAD)
Author/Authors :
Penilla، نويسنده , , E.H. and Kodera، نويسنده , , Y. and Garay، نويسنده , , J.E.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2012
Pages :
10
From page :
1178
To page :
1187
Abstract :
We report a method for the synthesis and processing of transparent bulk polycrystalline yttrium aluminum garnet (YAG) and photoluminescent Ce-doped YAG ceramics via solid-state reactive-current activated pressure assisted densification (CAPAD). The process uses commercially available γ-Al2O3, Y2O3, and CeO2 nanopowders. The nanopowders were reacted and densified simultaneously at temperatures between 850 °C and 1550 °C and at a maximum pressure of 105 MPa. The solid-state reaction to phase pure YAG occurs in under 4 min at processing temperatures 1100 °C which is significantly faster (on the order of tens of hours) and occurs at much lower temperatures (∼600 °C) compared to conventional reaction sintering. We found that the reaction significantly improves densification – the shrinkage rate of reaction-produced YAG was three times higher than that of YAG using pre-reacted powder. The Ce additions were found to retard the reaction driven shrinkage kinetics by a factor ∼3, but are still faster (by a factor ∼1.6) than those associated with direct densification (no synthesis). Densities >99% were achieved in both pure YAG and Ce doped YAG (Ce:YAG). Results of optical measurements show good transparency in the visible and photoluminescence (PL) in the Ce:YAG. The PL peak is broad and appears white when excited using blue light confirming that the ceramics can be used in solid state lighting to produce white light.
Keywords :
Spark plasma sintering (SPS) , Optical ceramics , YAG , Densification , Photoluminescent ceramics
Journal title :
MATERIALS SCIENCE & ENGINEERING: B
Serial Year :
2012
Journal title :
MATERIALS SCIENCE & ENGINEERING: B
Record number :
2150482
Link To Document :
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