摘要
用碳酸盐作沉淀剂,采用无机体系共沉淀法制备了钆镓石榴石Gd3Ga5O12(GGG)前驱体.由TG-DTA和IR光谱分析表明,合成的沉淀为碱式碳酸盐,煅烧过程中失重为28.06%.XRD分析表明在1000℃煅烧3h可以得到晶化完全的GGG多晶料,通过与固相反应比较可知,碳酸盐共沉淀法制备GGG多晶料具有反应时间短、晶化程度高、煅烧温度低、Ga2O3挥发量少等优点.GGG晶体提拉生长表明,Gd2O3和Ga2O3的组分失配问题已经得到基本解决,从而大大提高了单晶的光学质量.
Gd3Ga5O12 (GGG) precursor was synthesized by a co-precipitation method using ammonium hydrogen carbonate as precipitator. TG-DTA and IR spectra indicated that the precursor was alkaline and the weight loss during calcination was 28.06%. The results of XRD analysis indicated that the polycrystalline powder was well-crystallized after calcination at 1000degreesC for 3h. Compared with the solid-state reaction, the carbonate co-precipitation had the merits of short reaction period, well-crystallization, low calcining temperature, and less volatilization. As a result, the volatilization and disproportion of Gd2O3 and Ga2O3 could be well controlled during crystal growth and the optical quality of single crystal was also improved.
出处
《无机材料学报》
SCIE
EI
CAS
CSCD
北大核心
2004年第6期1423-1426,共4页
Journal of Inorganic Materials