摘要
采用高温固相反应法制备Sr3SiO5∶Eu2+时,往往有Sr2SiO4∶Eu2+共存,从而影响Sr3SiO5∶Eu2+的发光性能。本文采用DSC/TG、淬冷法结合XRD,研究了Sr3SiO5∶Eu2+在降温过程中的分解反应。结果表明,Sr3SiO5是在1 250℃以上稳定存在的化合物,在降温过程中Sr3SiO5在1 250℃分解为Sr2SiO4和SrO。采用快速降温的方法可以抑制Sr3SiO5的分解。当降温速率小于10℃.min-1时,Sr3SiO5全部分解为Sr2SiO4和SrO;当降温速率为15℃.min-1时,样品主要物相为Sr3SiO5,但有少部分Sr3SiO5发生分解,当降温速率增大到20℃.min-1时,Sr3SiO5分解的量更少,即随着降温速率增大,Sr3SiO5分解的量减小,从而获得几近纯相的Sr3SiO5∶Eu2+荧光粉。
When Sr3SiO5∶Eu^2+ was prepared by high temperature solid state method,Sr2SiO4∶Eu2+ phase often coexists and affects the luminescent properties of Sr3SiO5∶Eu2+.In the cooling process,the decompose reaction of Sr3SiO5∶Eu^2+ were studied by DSC/TG,quenching method and XRD.Results indicate that the Sr3SiO5∶Eu^2+ phase is a stable structure above 1 250 ℃.In the cooling process,the Sr3SiO5∶Eu^2+ phosphor will be decomposed down into Sr2SiO4 and SrO at 1 250 ℃,and the decomposition of Sr3SiO5∶Eu^2+ phosphor can be restrained by rapid cooling method.When the cooling rate less than 10 ℃·min^-1,all Sr3SiO5∶Eu2+ decompose into Sr2SiO4 and SrO.When the cooling rate for 15 ℃·min^-1,the main object of samples is Sr3SiO5∶Eu^2+,but there are still a few Sr3SiO5∶Eu2+ decomposition.When the cooling rate is more than 20 ℃·min^-1,decomposition of Sr3SiO5∶Eu2+ phase is less.Sr3SiO5∶Eu^2+ decomposition reduced with increases of the cooling rate,and the pure Sr3SiO5∶Eu2+ phosphor can be obtained.
出处
《无机化学学报》
SCIE
CAS
CSCD
北大核心
2012年第8期1570-1574,共5页
Chinese Journal of Inorganic Chemistry
基金
吉林省科技厅项目(No.20090348,20080511,201201117)
吉林省发改委课题(No.2011FGW03)资助项目