A yellow emitting long afterglow luminescence material SrSc_(2)O_(4):Pr^(3+)was successfully prepared by solid state reaction method.SrSc_(2)O_(4):Pr^(3+)phosphor shows a long afterglow luminescence peak at about 495,...A yellow emitting long afterglow luminescence material SrSc_(2)O_(4):Pr^(3+)was successfully prepared by solid state reaction method.SrSc_(2)O_(4):Pr^(3+)phosphor shows a long afterglow luminescence peak at about 495,545,621,630 and 657 nm,respectively,corresponding to the f–f transitions of Pr^(3+).The afterglow chromaticity coordinates of SrSc_(2)O_(4):1 at%Pr^(3+)were calculated to be(0.35,0.41),indicating that the afterglow emission is close to the light of yellow region.And,the afterglow luminescence of the optimal sample doped by 1 at%Pr^(3+)can persist for over 3 h.The thermoluminescence results suggest that there are three types of traps with depth of 0.61,0.69 and 0.78 eV exiting for all the samples,which are produced by the addition of Pr^(3+)ions.The trap density of SrSc_(2)O_(4):1 at%Pr^(3+)is the maximum when the incorporation of Pr^(3+)ions reaches 1 at%,which thus results in the longest afterglow luminescence.All the results indicate that SrSc_(2)O_(4):Pr^(3+)can be a potential candidate of novel long afterglow phosphors.展开更多
n this work,a series of Zn_(x)Mg_(1.99-x)SnO_(4):0.01Mn^(2+)(x=0,0.01,0.02,0.03,0.04)green long afterglow phosphors are prepared by high-temperature solid-phase reaction.The photoluminescence and long afterglow perfor...n this work,a series of Zn_(x)Mg_(1.99-x)SnO_(4):0.01Mn^(2+)(x=0,0.01,0.02,0.03,0.04)green long afterglow phosphors are prepared by high-temperature solid-phase reaction.The photoluminescence and long afterglow performance of host material doped with Zn^(2+)are investigated.The results show that the emission peak of Mn^(2+)is red-shifted by 5 nm with increasing Zn^(2+)concentration.Zn_(0.03)Mg_(1.96)SnO_(4):0.01Mn^(2+)phosphor has the strongest green luminescence intensity with the chroma-ticity coordinates of(0.0857,0.6083)under 270 nm,and Zn_(0.01)Mg_(1.98)SnO_(4):0.01Mn^(2+)phosphor has su-perior long afterglow performance with average lifetime of 102.41s.The afterglow decay and thermoluminescence curve of phosphor are used to explain the mechanism of long afterglow lumines-cence.Meanwhile,the afterglow intensity distribution of each pixel in Zn_(0.01)Mg_(1.98)SnO_(4):0.01Mn^(2+)coating samples is carried out by hyperspectral imaging,and the optimal luminescence intensity and uniformity of the sample are obtained at a phosphor/epoxy mass ratio of 0.0025.Therefore,Zn_(0.01)Mg_(1.98)SnO_(4):0.01Mn^(2+)can be a potential candidate of novel long afterglow phosphors,and hyperspectral imaging also provides new research approaches for the rational proportioning of luminescent materials.展开更多
基金Project supported by the National Natural Science Foundation of China(11974013,51802137)the State Key Research Projects of Shandong Natural Science Foundation(ZR2020KB019)+1 种基金the fund of"Two-Hundred Talent"plan of Yantai CityMajor Basic Research Projects of Shandong Natural Science Foundation(ZR2020ZD36)。
文摘A yellow emitting long afterglow luminescence material SrSc_(2)O_(4):Pr^(3+)was successfully prepared by solid state reaction method.SrSc_(2)O_(4):Pr^(3+)phosphor shows a long afterglow luminescence peak at about 495,545,621,630 and 657 nm,respectively,corresponding to the f–f transitions of Pr^(3+).The afterglow chromaticity coordinates of SrSc_(2)O_(4):1 at%Pr^(3+)were calculated to be(0.35,0.41),indicating that the afterglow emission is close to the light of yellow region.And,the afterglow luminescence of the optimal sample doped by 1 at%Pr^(3+)can persist for over 3 h.The thermoluminescence results suggest that there are three types of traps with depth of 0.61,0.69 and 0.78 eV exiting for all the samples,which are produced by the addition of Pr^(3+)ions.The trap density of SrSc_(2)O_(4):1 at%Pr^(3+)is the maximum when the incorporation of Pr^(3+)ions reaches 1 at%,which thus results in the longest afterglow luminescence.All the results indicate that SrSc_(2)O_(4):Pr^(3+)can be a potential candidate of novel long afterglow phosphors.
基金supports from the National Key R&D Program of China(No.2019YFC1520500,2019YFC1520104).
文摘n this work,a series of Zn_(x)Mg_(1.99-x)SnO_(4):0.01Mn^(2+)(x=0,0.01,0.02,0.03,0.04)green long afterglow phosphors are prepared by high-temperature solid-phase reaction.The photoluminescence and long afterglow performance of host material doped with Zn^(2+)are investigated.The results show that the emission peak of Mn^(2+)is red-shifted by 5 nm with increasing Zn^(2+)concentration.Zn_(0.03)Mg_(1.96)SnO_(4):0.01Mn^(2+)phosphor has the strongest green luminescence intensity with the chroma-ticity coordinates of(0.0857,0.6083)under 270 nm,and Zn_(0.01)Mg_(1.98)SnO_(4):0.01Mn^(2+)phosphor has su-perior long afterglow performance with average lifetime of 102.41s.The afterglow decay and thermoluminescence curve of phosphor are used to explain the mechanism of long afterglow lumines-cence.Meanwhile,the afterglow intensity distribution of each pixel in Zn_(0.01)Mg_(1.98)SnO_(4):0.01Mn^(2+)coating samples is carried out by hyperspectral imaging,and the optimal luminescence intensity and uniformity of the sample are obtained at a phosphor/epoxy mass ratio of 0.0025.Therefore,Zn_(0.01)Mg_(1.98)SnO_(4):0.01Mn^(2+)can be a potential candidate of novel long afterglow phosphors,and hyperspectral imaging also provides new research approaches for the rational proportioning of luminescent materials.