中山大学学报(自然科学版)
中山大學學報(自然科學版)
중산대학학보(자연과학판)
ACTA SCIENTIARUM NATURALIUM UNIVERSITATIS SUNYATSENI
2009年
z2期
109-112
,共4页
王飞%刘利军%王其洪%于凯立%邵泽
王飛%劉利軍%王其洪%于凱立%邵澤
왕비%류리군%왕기홍%우개립%소택
红色长余辉%Gd2O2S%Eu3+%Si4+%Ti4+%激发光谱%发射光谱%发光材料
紅色長餘輝%Gd2O2S%Eu3+%Si4+%Ti4+%激髮光譜%髮射光譜%髮光材料
홍색장여휘%Gd2O2S%Eu3+%Si4+%Ti4+%격발광보%발사광보%발광재료
red long afterglow%Gd2O2S: Eu3+,Si4+,Ti4+%excitation spectrum%emission spectrum%phosphor
采用高温固相反应法首次合成了新型红色长余辉发光材料Gd2O2S:Eu3+,Si4+,Ti4+.用X射线粉末衍射(XRD)、扫描电镜(SEM)、分光光度计等对合成产物进行了分析与表征.结果表明:Gd2O2S:Eu3+,Si4+,Ti4+的晶体结构与Gd2O2S相同,为六方晶系.颗粒的形貌为类球形.Gd2O2S:Eu3+,Si4+,Ti4+的激发光谱呈250~400 nm宽带状,激发光谱主峰位于365 nm;发射光谱为线状光谱,归属于Eu3+的5DJ(J=0,1)→7FJ(K=0,1,2,4)跃迁.最强的发射峰为627 nm和617 nm,均属于5D0→7F2跃迁,且627 nm的发射峰明显远强于617nm,显示出纯正的红色发光;并且Si4+和Ti4+离子的共掺杂可显著延长样品Cd2O2S:Eu3+的余辉时间.
採用高溫固相反應法首次閤成瞭新型紅色長餘輝髮光材料Gd2O2S:Eu3+,Si4+,Ti4+.用X射線粉末衍射(XRD)、掃描電鏡(SEM)、分光光度計等對閤成產物進行瞭分析與錶徵.結果錶明:Gd2O2S:Eu3+,Si4+,Ti4+的晶體結構與Gd2O2S相同,為六方晶繫.顆粒的形貌為類毬形.Gd2O2S:Eu3+,Si4+,Ti4+的激髮光譜呈250~400 nm寬帶狀,激髮光譜主峰位于365 nm;髮射光譜為線狀光譜,歸屬于Eu3+的5DJ(J=0,1)→7FJ(K=0,1,2,4)躍遷.最彊的髮射峰為627 nm和617 nm,均屬于5D0→7F2躍遷,且627 nm的髮射峰明顯遠彊于617nm,顯示齣純正的紅色髮光;併且Si4+和Ti4+離子的共摻雜可顯著延長樣品Cd2O2S:Eu3+的餘輝時間.
채용고온고상반응법수차합성료신형홍색장여휘발광재료Gd2O2S:Eu3+,Si4+,Ti4+.용X사선분말연사(XRD)、소묘전경(SEM)、분광광도계등대합성산물진행료분석여표정.결과표명:Gd2O2S:Eu3+,Si4+,Ti4+적정체결구여Gd2O2S상동,위륙방정계.과립적형모위류구형.Gd2O2S:Eu3+,Si4+,Ti4+적격발광보정250~400 nm관대상,격발광보주봉위우365 nm;발사광보위선상광보,귀속우Eu3+적5DJ(J=0,1)→7FJ(K=0,1,2,4)약천.최강적발사봉위627 nm화617 nm,균속우5D0→7F2약천,차627 nm적발사봉명현원강우617nm,현시출순정적홍색발광;병차Si4+화Ti4+리자적공참잡가현저연장양품Cd2O2S:Eu3+적여휘시간.
Gd2O2S:Eu3+,Si4+ ,Ti4+ , as a novel red long afterglow phosphor, was first synthesized by high-temperature solid-state reac-tion method. The synthesized phosphors were investigated respectively by XRD, SEM and fluorescence speetrophotometer. The results showed that: Gd2 O2 S: Eu;3+, Si4+ , Ti4+ possess hexagonal crystal structure, which is similar to that of Gd202 S matrix. The particles of Gd2O2S: Eu3+, Si4+, Ti4+are basically spherical in shape,with good dispersion. The excitation spectrum is a broad band, from 250 nm to 400 nm, and the main peak is at 365 nm. The emission spectrum shows that Gd2O2S:Eu3+, Si4+, Ti4+has narrow emissionpeaks which belong to Eu3+ ions transition from 5DJ(J=0,1,2) to 7FJ(J= 0,1,2,3,4). The strongest emission peak is at 627nm and 617 nm, which belongs to the Eu3+ ions transition from 5D0→7F2. Moreover, the relative intensity of the emission peak (λ =627nm)is markedly stronger than that of the emission peak (λ=617 nm). Therefore, Gd2O2S:Eu3+ , Si4+, Ti4+emits the pure red light. What's more, the afterglow time of Gd2O2S:Eu3+ can be significantly increased when the Si4+ and Ti4+ are co-doped.