发光学报
髮光學報
발광학보
CHINESE JOURNAL OF LUMINESCENCE
2012年
7期
729-735
,共7页
王志军%刘冲%杨志平%李盼来%郭庆林
王誌軍%劉遲%楊誌平%李盼來%郭慶林
왕지군%류충%양지평%리반래%곽경림
发光%Eu2+%Ba2Ca(BO3)2%浓度猝灭
髮光%Eu2+%Ba2Ca(BO3)2%濃度猝滅
발광%Eu2+%Ba2Ca(BO3)2%농도졸멸
luminescence%Eu2+%Ba2Ca(BO3)2%concentration quenching
采用高温固相法,以CaCO3(A.R)、BaCO3(A.R)、H3BO3(A.R)和Eu2O3(99.99%)为原料制备了Ba2Ca(BO3)2∶Eu2+绿色发光材料,测量了材料的晶体结构、发光特性及色坐标等.Ba2 Ca(BO3)2∶Eu2+材料的激发光谱覆盖200~500nm的紫外-可见光区.在400nm近紫外光激发下,材料的发射光谱为一主峰位于537nm的非对称宽谱,对应于Eu2+的4f65d1→4f7特征跃迁.研究发现,随Eu2+掺杂浓度的增大,Ba2 Ca(BO3)2∶Eu2+材料的发射强度呈现先增大、后减小的变化趋势,最大发射强度对应的Eu2掺杂摩尔分数为2%.造成发射强度下降的原因为浓度猝灭,其机理为电偶极-电偶极相互作用.依据晶格常数及实验光谱数据,得出临界距离Rc分别为2.64nm和2.11nm.随Eu2+掺杂浓度的增大,Ba2Ca(BO3)2∶Eu2+材料的色坐标变化微小.计算得到Ba2Ca(BO3)2∶2%Eu2+的转换效率约为72%.
採用高溫固相法,以CaCO3(A.R)、BaCO3(A.R)、H3BO3(A.R)和Eu2O3(99.99%)為原料製備瞭Ba2Ca(BO3)2∶Eu2+綠色髮光材料,測量瞭材料的晶體結構、髮光特性及色坐標等.Ba2 Ca(BO3)2∶Eu2+材料的激髮光譜覆蓋200~500nm的紫外-可見光區.在400nm近紫外光激髮下,材料的髮射光譜為一主峰位于537nm的非對稱寬譜,對應于Eu2+的4f65d1→4f7特徵躍遷.研究髮現,隨Eu2+摻雜濃度的增大,Ba2 Ca(BO3)2∶Eu2+材料的髮射彊度呈現先增大、後減小的變化趨勢,最大髮射彊度對應的Eu2摻雜摩爾分數為2%.造成髮射彊度下降的原因為濃度猝滅,其機理為電偶極-電偶極相互作用.依據晶格常數及實驗光譜數據,得齣臨界距離Rc分彆為2.64nm和2.11nm.隨Eu2+摻雜濃度的增大,Ba2Ca(BO3)2∶Eu2+材料的色坐標變化微小.計算得到Ba2Ca(BO3)2∶2%Eu2+的轉換效率約為72%.
채용고온고상법,이CaCO3(A.R)、BaCO3(A.R)、H3BO3(A.R)화Eu2O3(99.99%)위원료제비료Ba2Ca(BO3)2∶Eu2+록색발광재료,측량료재료적정체결구、발광특성급색좌표등.Ba2 Ca(BO3)2∶Eu2+재료적격발광보복개200~500nm적자외-가견광구.재400nm근자외광격발하,재료적발사광보위일주봉위우537nm적비대칭관보,대응우Eu2+적4f65d1→4f7특정약천.연구발현,수Eu2+참잡농도적증대,Ba2 Ca(BO3)2∶Eu2+재료적발사강도정현선증대、후감소적변화추세,최대발사강도대응적Eu2참잡마이분수위2%.조성발사강도하강적원인위농도졸멸,기궤리위전우겁-전우겁상호작용.의거정격상수급실험광보수거,득출림계거리Rc분별위2.64nm화2.11nm.수Eu2+참잡농도적증대,Ba2Ca(BO3)2∶Eu2+재료적색좌표변화미소.계산득도Ba2Ca(BO3)2∶2%Eu2+적전환효솔약위72%.
Ba2 Ca(BO3)2∶Eu2+ phosphor was synthesized by a high temperature solid-state method.CaCO3 (A.R),BaCO3(A.R),H3BO3(A.R) and Eu2O3(99.99%) were used as raw materials.Its crystal structure,luminescent characteristics and Commission International de l'Eclairage (CIE) chromaticity coordinates values were measured.Under the ultraviolet to visible light irradiation,Ba2 Ca( BO3 ) 2 ∶ Eu2 + shows an asymmetrically single green emission band with a maximum at 537 nm,which corresponds to the 4f65d1→4f7 transition of Eu2+.The emission intensity of Ba2Ca(BO3)2∶ Eu2+ was influenced by Eu2+ molefraction,at first,it increases with the increase of Eu2+ mole fraction,and reaches a maximum value at 2%Eu2+,then decreases with further increasing its concentration because of the concentration quenching effect.And the concentration quenching mechanism is verified to be dipole-dipole interaction.According to the crystal structure data and the experimental spectral data,the critical distances( Rc ) can be obtained,and are 2.64 nm and 2.11 nm,respectively.Moreover,with increasing the Eu2+ doped content,the CIE chromaticity coordinates of the samples were slightly varied.For Ba2 Ca( BO3 ) 2∶2% Eu2 +,the quantum efficiency is approximately 72%.