Search

The orthosilicate phosphors SrxBa2–xSiO4:Eu2+ have now been known for over four decades and have found extensive recent use in solid-state white lighting. It is well-recognized in the literature and in practice that intermediate compositions in the solid-solutions between the orthosilicates Sr2SiO4 and Ba2SiO4 yield the best phosphor hosts when the thermal stability of luminescence is considered. We employ a combination of synchrotron X-ray diffraction, total scattering measurements, density functional theory calculations, and low-temperature heat capacity measurements, in conjunction with detailed temperature- and time-resolved studies of luminescence properties to understand the origins of the improved luminescence properties. We observe that in the intermediate compositions, the two cation sites in the crystal structure are optimally bonded as determined from bond valence sum calculations. Optimal bonding results in a more rigid lattice, as established by the intermediate compositions possessing the hi...

Ce3+-substituted aluminum garnet compounds of yttrium (Y3Al5O12) and lutetium (Lu3Al5O12)—both important compounds in the generation of (In,Ga)N-based solid state white lighting—have been prepared using a simple microwave heating technique involving the use of a microwave susceptor to provide the initial heat source. Carbon used as the susceptor additionally creates a reducing atmosphere around the sample that helps stabilize the desired luminescent compound. High quality, phase-pure materials are prepared within a fraction of the time and using a fraction of the energy required in a conventional ceramic preparation; the microwave technique allows for a reduction of about 95% in preparation time, making it possible to obtain phase pure, Ce3+-substituted garnet compounds in under 20 min of reaction time. It is estimated that the overall reduction in energy compared with ceramic routes as practised in the lab is close to 99%. Conventionally prepared material is compared with material prepared using microwav...

A new, highly efficient green oxyfluoride phosphor family Sr2.975−xBaxCe0.025AlO4F (SBAF:Ce3+) has been developed as a component of solid state white light emitting diodes (LED). The phosphor emits with a maximum at 502 nm when excited by 405 nm excitation, with a quantum efficiency approaching 100%. When SBAF:Ce3+ (x = 1.0) is incorporated with encapsulant on an ultraviolet (405 nm) LED, greenish-white light with a color rendering index of 62 under a forward bias current of 20 mA is obtained. The results suggest that phosphors deriving from SBAF:Ce3+ have potential for incorporation in formulations for white LEDs and related applications. The preparation and structural and optical characterization of the phosphor family is described. Attempts to understand the origins of the high efficiency on the basis of the thermal quenching characteristics of SBAF:Ce3+ in comparison with related compounds are presented.

Two dense inorganic−organic frameworks were prepared using the intrinsically luminescent organic ligand 9-fluorenone-2,7-dicarboxylic acid (H2FDC) in combination with the alkaline earth metals calcium and strontium. Ca(FDC)(H2O)2 (1) and Sr(FDC)(H2O)5·2H2O (2) were prepared hydrothermally and both adopt three-dimensional framework structures. They absorb strongly between 380 and 460 nm and show broad visible emission with peaks at 503 and 526 nm, respectively. Structure 1 shows a quantum yield at room temperature of 7.8% which increases to 15% at −196 °C, while structure 2 shows a room temperature quantum yield of 2.8%, increasing to 3.3% at −196 °C.

We report a novel strategy for writing volume holograms by photoacid generation and subsequent acid-catalyzed degradation leading to increased free volume/refractive index modulation in the exposed regions of a cross-linked rigid polymeric matrix. This strategy offers nondestructive read out and high diffraction efficiency and allows optical-quality, millimeter thick films to be fabricated that possess excellent thermal and dimensional stability. A key feature of this approach is the efficient acid-catalyzed degradation of functional groups in the cross-linked matrix leading to release of volatile products which diffuse readily out of the thick films. Furthermore, the reported data storage material is lightweight and inexpensive and can be easily processed into different shapes, making it an attractive candidate for data storage applications.