光谱学与光谱分析
光譜學與光譜分析
광보학여광보분석
SPECTROSCOPY AND SPECTRAL ANALYSIS
2013年
11期
2921-2925
,共5页
王显盛%万敏华%王银海%赵慧%胡正发%李海玲
王顯盛%萬敏華%王銀海%趙慧%鬍正髮%李海玲
왕현성%만민화%왕은해%조혜%호정발%리해령
β-Ga2 O3%Cr3+%长余辉%近红外
β-Ga2 O3%Cr3+%長餘輝%近紅外
β-Ga2 O3%Cr3+%장여휘%근홍외
β-Ga2 O3%Cr3+%Afterglow%Near-infrared
高温固相法制备了(Ga1- x Alx )2 O3∶Cr3+(x=0,0.1,0.2,0.3,0.4,0.5)系列荧光粉。X射线衍射分析表明Al3+含量增加后,物相依然保持β-Ga2 O3的相。此外随着Al离子含量的逐渐增加,高衍射角峰位向右移动表明Al离子进入了β-Ga2 O3晶格中。激发光谱中258,300,410和550 nm左右的峰位分别对应基质Ga2 O3的带与带的吸收跃迁、电荷迁移带跃迁、Cr3+的4 A2→4 T1以及4 A2→4 T2跃迁。随着Al离子掺杂量的增加,激发光谱峰位都呈现出不同程度的蓝移现象,这分别是由于基质的带隙能量、C r3+与配体之间的电负性以及晶场强度增大所导致的。在发射光谱中,随着Al3+替代Ga3+,Cr3+的发光由宽带发射变为窄带发射,这是由于Al3+的掺入改变了Cr3+周围的晶场,从而Cr3+的红光发射由原来的4 T2→4 A2变为2 E→4 A2跃迁发射。Al离子掺杂改善了样品的长余辉发光特性,并且Al离子含量达到0.5时显示出较长时间的肉眼可见的近红外余辉发射。热释发光曲线显示材料中具有合适的陷阱能级,这也是材料产生长余辉发光的原因。
高溫固相法製備瞭(Ga1- x Alx )2 O3∶Cr3+(x=0,0.1,0.2,0.3,0.4,0.5)繫列熒光粉。X射線衍射分析錶明Al3+含量增加後,物相依然保持β-Ga2 O3的相。此外隨著Al離子含量的逐漸增加,高衍射角峰位嚮右移動錶明Al離子進入瞭β-Ga2 O3晶格中。激髮光譜中258,300,410和550 nm左右的峰位分彆對應基質Ga2 O3的帶與帶的吸收躍遷、電荷遷移帶躍遷、Cr3+的4 A2→4 T1以及4 A2→4 T2躍遷。隨著Al離子摻雜量的增加,激髮光譜峰位都呈現齣不同程度的藍移現象,這分彆是由于基質的帶隙能量、C r3+與配體之間的電負性以及晶場彊度增大所導緻的。在髮射光譜中,隨著Al3+替代Ga3+,Cr3+的髮光由寬帶髮射變為窄帶髮射,這是由于Al3+的摻入改變瞭Cr3+週圍的晶場,從而Cr3+的紅光髮射由原來的4 T2→4 A2變為2 E→4 A2躍遷髮射。Al離子摻雜改善瞭樣品的長餘輝髮光特性,併且Al離子含量達到0.5時顯示齣較長時間的肉眼可見的近紅外餘輝髮射。熱釋髮光麯線顯示材料中具有閤適的陷阱能級,這也是材料產生長餘輝髮光的原因。
고온고상법제비료(Ga1- x Alx )2 O3∶Cr3+(x=0,0.1,0.2,0.3,0.4,0.5)계렬형광분。X사선연사분석표명Al3+함량증가후,물상의연보지β-Ga2 O3적상。차외수착Al리자함량적축점증가,고연사각봉위향우이동표명Al리자진입료β-Ga2 O3정격중。격발광보중258,300,410화550 nm좌우적봉위분별대응기질Ga2 O3적대여대적흡수약천、전하천이대약천、Cr3+적4 A2→4 T1이급4 A2→4 T2약천。수착Al리자참잡량적증가,격발광보봉위도정현출불동정도적람이현상,저분별시유우기질적대극능량、C r3+여배체지간적전부성이급정장강도증대소도치적。재발사광보중,수착Al3+체대Ga3+,Cr3+적발광유관대발사변위착대발사,저시유우Al3+적참입개변료Cr3+주위적정장,종이Cr3+적홍광발사유원래적4 T2→4 A2변위2 E→4 A2약천발사。Al리자참잡개선료양품적장여휘발광특성,병차Al리자함량체도0.5시현시출교장시간적육안가견적근홍외여휘발사。열석발광곡선현시재료중구유합괄적함정능급,저야시재료산생장여휘발광적원인。
The Al doping gallate phosphor (Ga1 - x Alx )2 O3 ∶Cr3+ (x=0 ,0.1 ,0.2 ,0.3 ,0.4 ,0.5) was synthesized by a high temperature solid-state reaction method .The X-ray diffractions show that the phase of the phosphors remains to be Ga2O3 struc-ture with increase in the contents of Al3+ ion .Beside ,the fact that the X-ray diffraction peak shifts towards big angles with in-creasing Al3+ ions content shows that Al3+ ions entered the Ga2 O3 lattice .The peaks of the excitation spectra located at 258 , 300 ,410 and 550 nm are attributed to the band to band transition of the matrix ,charge transfer band transition ,and 4 A2 → 4 T1 and 4 A2 → 4 T2 transition of Cr3+ ions ,respectively .Those excitation spectrum peak positions show different degrees of blue shift with the increase in the Al3+ ions content .The blue shift of the first two peaks are due to the band gap energy of substrate and the electronegativity between Cr3+ ions and ligands increasing ,respectively .The blue shift of the energy level transition of Cr3+ion is attributed to crystal field strength increasing .The Cr3+ ion luminescence changes from a broadband emission to a narrow-band emission with Al3+ doping ,because the emission of Cr3+ ion changed from 4 T2 → 4 A2 to 2 E→ 4 A2 transition with the crystal field change after Al3+ ions doping .The Al3+ ions doping improved the long afterglow luminescence properties of samples ,and the sample showed a longer visible near infrared when Al3+ ions content reaches 0.5 .The thermoluminescence curve shows the sample with suitable trap energy level ,and this is also the cause of the long afterglow luminescence materials .