简介概要

Spectral variations of Ca3Sc2Si3O12:Ce phosphors via substitution and energy transfer

来源期刊:Journal of Rare Earths2012年第4期

论文作者:刘元红 庄卫东 刘荣辉 胡运生 何华强 张书生 高慰

文章页码:339 - 341

摘    要:The luminescence intensity of emission peak at around 525 nm decreased in the Ce3+ and Er3+ co-doped Ca3Sc2Si3O12 phosphors. Mg2+ ion, which was likely incorporated into the Sc3+ position of the host crystal, was co-doped to adjust the crystal field and compensate for the excess positive charge due to the doping of Ce3+. The green emission belonged to the 5d→4f transition of Ce3+ moved toward longer wavelength by addition of Mg2+ in Ce3+ and Er3+ co-doped Ca3Sc2Si3O12 phosphor, which could increase the brightness of the phosphor. However, the position of weakening of luminescence intensity at around 525 nm remained basically unchanged by increasing the amount of Mg2+. The results showed that the weakening of luminescence intensity at around 525 nm caused by the absorption of Er3+, which had little influence on the environment of the crystal field.

详情信息展示

Spectral variations of Ca3Sc2Si3O12:Ce phosphors via substitution and energy transfer

刘元红,庄卫东,刘荣辉,胡运生,何华强,张书生,高慰

Grirem Advanced Materials Co. Ltd., and National Engineering Research Center for Rare Earth Materials, General Research Institute for Nonferrous Metals

摘 要:The luminescence intensity of emission peak at around 525 nm decreased in the Ce3+ and Er3+ co-doped Ca3Sc2Si3O12 phosphors. Mg2+ ion, which was likely incorporated into the Sc3+ position of the host crystal, was co-doped to adjust the crystal field and compensate for the excess positive charge due to the doping of Ce3+. The green emission belonged to the 5d→4f transition of Ce3+ moved toward longer wavelength by addition of Mg2+ in Ce3+ and Er3+ co-doped Ca3Sc2Si3O12 phosphor, which could increase the brightness of the phosphor. However, the position of weakening of luminescence intensity at around 525 nm remained basically unchanged by increasing the amount of Mg2+. The results showed that the weakening of luminescence intensity at around 525 nm caused by the absorption of Er3+, which had little influence on the environment of the crystal field.

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