硅酸盐通报
硅痠鹽通報
규산염통보
BULLETIN OF THE CHINESE CERAMIC SOCIETY
2010年
1期
94-97,106
,共5页
孙海鹰%张希艳%王能利%米晓云%刘全生
孫海鷹%張希豔%王能利%米曉雲%劉全生
손해응%장희염%왕능리%미효운%류전생
丙二酸溶胶-凝胶法%YAG:Ce,Gd荧光粉%白光LED%红移
丙二痠溶膠-凝膠法%YAG:Ce,Gd熒光粉%白光LED%紅移
병이산용효-응효법%YAG:Ce,Gd형광분%백광LED%홍이
malonic acid Sol-gel method%YAG:Ce,Gd phosphor%white LED%red-shift
以丙二酸为络合剂,通过溶胶-凝胶法合成了亚微米级YAG:Ce,Gd黄色荧光粉.采用TG/DSC、XRD研究干凝胶热分解和YAG晶相形成的过程;通过荧光光谱分析了Gd~(3+)的掺杂对荧光粉的发光强度的影响规律;通过SEM观察粉体的微观形貌.结果表明:经1200 ℃煅烧3 h得到的荧光粉,粉体粒径为0.3~1 μm,颗粒规则接近球形;随着Gd~(3+)掺杂量的增加,荧光粉的发射光谱由525 nm红移到550 nm.
以丙二痠為絡閤劑,通過溶膠-凝膠法閤成瞭亞微米級YAG:Ce,Gd黃色熒光粉.採用TG/DSC、XRD研究榦凝膠熱分解和YAG晶相形成的過程;通過熒光光譜分析瞭Gd~(3+)的摻雜對熒光粉的髮光彊度的影響規律;通過SEM觀察粉體的微觀形貌.結果錶明:經1200 ℃煅燒3 h得到的熒光粉,粉體粒徑為0.3~1 μm,顆粒規則接近毬形;隨著Gd~(3+)摻雜量的增加,熒光粉的髮射光譜由525 nm紅移到550 nm.
이병이산위락합제,통과용효-응효법합성료아미미급YAG:Ce,Gd황색형광분.채용TG/DSC、XRD연구간응효열분해화YAG정상형성적과정;통과형광광보분석료Gd~(3+)적참잡대형광분적발광강도적영향규률;통과SEM관찰분체적미관형모.결과표명:경1200 ℃단소3 h득도적형광분,분체립경위0.3~1 μm,과립규칙접근구형;수착Gd~(3+)참잡량적증가,형광분적발사광보유525 nm홍이도550 nm.
YAG:Ce,Gd yellow phosphors were synthesized by malonic acid Sol-gel method. The decomposition process of the dry gel and the formation process of crystalline YAG were characterized by TG/DSC and XRD techniques. The influence of Gd~(3+) doping on the luminescent intensity of the phosphor and the microstructure of powders were studied by fluorescence spectrum and SEM. The results indicate that powders calcined at 1200 ℃ for 3 h are about 0.3-1 μm in size with ball morphology. The emission spectrum of phosphor showes gradually red-shift from 525 nm to 550 nm with the increase of doping concentration of Gd~(3+) ion.