4.6 Article

Controllable synthesis of uniform CaMoO4:Eu3+, M+ (M = Li, Na, K) microspheres and optimum luminescence properties

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RSC ADVANCES
卷 5, 期 13, 页码 9441-9454

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c4ra12183j

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资金

  1. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Education, Science and Technology [2010-0029634]
  2. National Natural Science Foundations of China [21301053]
  3. Natural Science Fund for Creative Research Groups of Hubei Province of China [2014CFA015]

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High-quality and monodisperse CaMoO4:Eu3+, M+ (M = Li, Na, K) microspheres have been synthesized with the assistance of poly-(diallyldimethylammonium chloride) (PDDA) via a facile coprecipitation hydrothermal route. X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), transmission electron microscopy (TEM), thermogravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS), as well as photoluminescence (PL) spectroscopy are used to characterize the resulting samples. The results show that the CaMoO4:Eu3+, M+ (M = Li, Na, K) can be directly indexed to a tetragonal CaMoO4 phase with high purity. A series of controlled experiments indicate that PDDA as a shape modifier introduced into the reaction system plays a critical role in the morphology of the final products. Furthermore, the shape and size of the products can be further manipulated by adjusting the concentration of PDDA and pH values in the initial solution. The prepared microspheres are stable at a suitable annealing temperature. The possible formation mechanism for these microspheres is presented. Additionally, the PL properties of CaMoO4:Eu3+, M+ (M = Li, Na, K) were investigated in detail. The results reveal that the red emission peak intensities of CaMoO4:Eu3+, Li+ and CaMoO4:Eu3+, Na+ are higher than that of CaMoO4:Eu3+, K+. The particle size and shape have a remarkable effect on the photoluminescence properties of the phosphor. The luminescence intensity is observably enhanced with increasing of the annealing temperature due to eliminating PDDA and/or H2O present in the samples and to the improved crystal quality.

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