Eu2+ activated pyrosilicate phosphor were prepared under a reducing atmosphere by solid-state reaction.The crystal structure of Ba2 MgSi2 O7: Eu2+ was analyzed by XRD method.The excitation spectrum of Ba2MgSi2 O7; Eu2...Eu2+ activated pyrosilicate phosphor were prepared under a reducing atmosphere by solid-state reaction.The crystal structure of Ba2 MgSi2 O7: Eu2+ was analyzed by XRD method.The excitation spectrum of Ba2MgSi2 O7; Eu2+ is composed of two broad bands centered at about 310 nm and 395 nm respectively.In the emission spectra, the peak wavelength is at about 507 nm under 380 nm UV excitation.It was found that the introduction of Zn2+ into Ba2MgSi2O7: Eu2+ Can effectively increase its emission intensity without changing the position of emission peak.And the Eu2 + and Ce3 + codoped pyrosilicate phosphor is the efficient bluish green phosphor under the excitation of long UV light and its emission intensity is stronger than Eu2+ doped pyrosilicate phosphor.展开更多
A series of phosphor of MO-RE2 O3-B2 O3: Eu, Mn ( M = Mg, Ca, Sr; RE = Y, La, Gd) were prepared and studied.Excitation spectra exhibited high absorption in UV region (370 ~ 400 nm).There existed two valence states for...A series of phosphor of MO-RE2 O3-B2 O3: Eu, Mn ( M = Mg, Ca, Sr; RE = Y, La, Gd) were prepared and studied.Excitation spectra exhibited high absorption in UV region (370 ~ 400 nm).There existed two valence states for europium ions Eu2+ and Eu 3+, the broad emission band peaking at 515 nm correspond to the 5d-4f emission transition of Eu2+ , the sharp emission peaking at 590 and 610 nm correspond to the 5D0→7FJ(J = 1,2,3,4) emission transition of Eu 3 + By the introduction of Mg and Y into MO-RE2O3-B2O3: Eu, blue-green emission was restrained ultimately and red emission peaking at 610 nm was enhanced strongly, intensity and colorimetric purity of red light were both enhanced.Furthermore, Mg1-xSrxO-Y2O3-B2O3: Eu was also researched, the introduction of Sr into MgO-Y2O3-B2O3:Eu gives rise to a shift to longer wavelengths of the position of the excitation peak, and the emission spectra varies with the increasing of x simultaneously.展开更多
基金Project supported by the National Natural Foundation of China (59982001)and Natural Science Foundation of Beijing(4012010)
文摘Eu2+ activated pyrosilicate phosphor were prepared under a reducing atmosphere by solid-state reaction.The crystal structure of Ba2 MgSi2 O7: Eu2+ was analyzed by XRD method.The excitation spectrum of Ba2MgSi2 O7; Eu2+ is composed of two broad bands centered at about 310 nm and 395 nm respectively.In the emission spectra, the peak wavelength is at about 507 nm under 380 nm UV excitation.It was found that the introduction of Zn2+ into Ba2MgSi2O7: Eu2+ Can effectively increase its emission intensity without changing the position of emission peak.And the Eu2 + and Ce3 + codoped pyrosilicate phosphor is the efficient bluish green phosphor under the excitation of long UV light and its emission intensity is stronger than Eu2+ doped pyrosilicate phosphor.
基金Project supported by the National Natural Foundation of China (59982001) and Natural Science Foundation of Beijing(4012010)
文摘A series of phosphor of MO-RE2 O3-B2 O3: Eu, Mn ( M = Mg, Ca, Sr; RE = Y, La, Gd) were prepared and studied.Excitation spectra exhibited high absorption in UV region (370 ~ 400 nm).There existed two valence states for europium ions Eu2+ and Eu 3+, the broad emission band peaking at 515 nm correspond to the 5d-4f emission transition of Eu2+ , the sharp emission peaking at 590 and 610 nm correspond to the 5D0→7FJ(J = 1,2,3,4) emission transition of Eu 3 + By the introduction of Mg and Y into MO-RE2O3-B2O3: Eu, blue-green emission was restrained ultimately and red emission peaking at 610 nm was enhanced strongly, intensity and colorimetric purity of red light were both enhanced.Furthermore, Mg1-xSrxO-Y2O3-B2O3: Eu was also researched, the introduction of Sr into MgO-Y2O3-B2O3:Eu gives rise to a shift to longer wavelengths of the position of the excitation peak, and the emission spectra varies with the increasing of x simultaneously.
