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Encapsulating Luminescent Materials in Zeolites. III. Crystal Structure and Scintillation Properties of Cs,Na-LTA Treated with Zirconium Chloride Vapor
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With the purpose of developing a new zeolite scintillator, fully dehydrated Cs,Na-A was exposed to ZrCl4 (g, 3.7 × 103 Pa) at 523 K. The crystal structures of Cs,Na-A and of the product, |Zr0.14Cs5.69Na4.13Cl0.85|[Si12Al12O48]-LTA (Zr,Cs,Na,Cl-A), were determined by single-crystal crystallography using synchrotron X-radiation. The structure of Zr,Cs,Na,Cl-A was refined in the space group Pmm (a = 12.230(1) Å) with all unique data to the final error index R1 = 0.069 for the 639 reflections for which Fo > 4σ(Fo). Its composition was confirmed by scanning electron microscopy energy-dispersive X-ray analysis (SEM-EDX). Octahedral ZrCl62– ions center 14% of the large cavities; each Cl ion bonds to an 8-ring Cs+ ion. These Cs+ ions bridge between ZrCl62– ions to form a continuum with unit cell formula Cs3ZrCl6+ in the near-surface volume of the crystal. Other Cs+ ions lie opposite 6-rings in the sodalite and large cavities; Na+ ions occupy the remaining 6-rings. Upon X-irradiation, Zr,Cs,Na,Cl-A luminesces bright sky blue; the emission band is broad, ranging from 370 to 750 nm, peaking at 480 nm. The integrated intensity of the emission is ca. 16 times greater than that of anthracene, a well documented scintillator. This intense luminescence appears to result from charge transfer within the ZrCl62– ions.

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