The technology of solid-state lighting has developed for decades in various industries.Phosphor,as an element part,determines the application domain of lighting products.For instance,blue and redemitting phosphors are...The technology of solid-state lighting has developed for decades in various industries.Phosphor,as an element part,determines the application domain of lighting products.For instance,blue and redemitting phosphors are required in the process of plant supplementing light,arrow-band emitting phosphors are applied to backlight displays,etc.In this work,a Bi^(3+)-activated blue phosphor was obtained in a symmetrical and co mpact crystal structure of Gd3Sb07(GSO).Then,the co-doping strategy of alkali metal ions(Li^(+),Na^(+),and K^(+))was used to optimize the performance.The result shows that the photoluminescence intensity is increased by 2.1 times and 1.3 times respectively by introducing Li~+and K^(+)ions.Not only that,it also achieves narrow-band emitting with the full width of half-maximum(FWHM)reaching 42 nm through Na^(+)doping,and its excitation peak position also shifts from 322 to 375 nm,which can be well excited by near-ultraviolet(NUV)light emitting diode(LED)chips(365 nm).Meanwhile,the electroluminescence spectrum of GSO:0.6 mol%Bi^(3+),3 wt%Na^(+)matches up to 93.39%of the blue part of the absorption spectrum of chlorophyll a.In summary,the Bi^(3+)-activated blue phosphor reported in this work can synchronously meet the requirements of plant light replenishment and field emission displays.展开更多
Blue-violet light can not only enhance the total content of biomass and glucoside but also enrich the taste of the fruit.Thus,it is meaningful to study the blue-violet luminescent materials for plant cultivation.In th...Blue-violet light can not only enhance the total content of biomass and glucoside but also enrich the taste of the fruit.Thus,it is meaningful to study the blue-violet luminescent materials for plant cultivation.In this study,titanium(IV)-activated CaYAlO4(CYAO) phosphors were synthesized by conventional hightemperature solid-state reaction.X-ray powder diffraction was employed to analyze the crystalstructure of CYAO.It is found that the doped Ti^4+ ions do not change obviously the crystal structure of phosphors.Upon 246 nm excitation,CaYAl1-xO4:xTi^4+phosphors exhibit broad blue-violet emission band peaking at 395 nm,which can be attributed to the charge transfer of Ti^4+-O^2-.Moreover,this phosphor exhibits strong thermal stability.The luminescence emission intensity at 150℃maintained about 91 mol% of its initial value at room temperature.Additionally,the electron transition process and concentration quenching mechanism of CaYAl1-xO4:xTi^4+are discussed in detail.The excellent luminescent properties indicate that CaYAl1-xO4:xTi^4+phosphor may have promising application in indoor plant cultivation.展开更多
Nowadays,due to uncontrolled synthesis and lack of more direct and systematic evidences,the photoluminescence origin of“zero-dimensional”Cs4PbI6 remains great controversy and the luminescence cannot be controlled.He...Nowadays,due to uncontrolled synthesis and lack of more direct and systematic evidences,the photoluminescence origin of“zero-dimensional”Cs4PbI6 remains great controversy and the luminescence cannot be controlled.Here we propose a controllable dissolution-recrystallization method to synthesize“emissive”and“non-emissive”Cs4PbI6 nanocrystals(NCs)respectively.Through comparing“emissive”and“non-emissive”Cs4PbI6 NCs,it is clearly proved that the visible emission in“emissive”Cs4PbI6 NCs comes from embedded CsPbI3 quantum dots(QDs).It is found for CsPbI3@Cs4PbI6 nanocomposites,methyl acetate(MeAC)and cyclohexane play an important role in dissolution and recrystallization respectively to obtain Cs4PbI6 matrix and CsPbI3 cores.Benefiting from this two-step method,the as-synthesized CsPbI3@Cs4PbI6 nanocomposites with CsPbI3 QDs uniformly distributed in Cs4PbI6 matrix are bright with photoluminescence quantum yield(PLQY)up to 71.4%and exhibit improved stability than CsPbI3 NCs.Moreover,utilizing its formation mechanism,the size of embedded CsPbI3 QDs can be controlled by reasonable designing the“dissolution”process,so that the luminescence of this CsPbI3@Cs4PbI6 nanocomposites can be adjusted in a wide range from green to red(554–630 nm).Our finding not only provides a novel method for synthesizing tunable“emissive”Cs4PbI6 NCs,but also makes clear the photoluminescence origin of“emissive”Cs4PbI6.展开更多
基金Project supported by the Key R&D Projects in Hunan Province(2021SK2047,2022NK2044)Science and Technology Innovation Program of Hunan Province(2022WZ1022)Superior Youth Project of the Science Research Project of Hunan Provincial Department of Education(22B0211)。
文摘The technology of solid-state lighting has developed for decades in various industries.Phosphor,as an element part,determines the application domain of lighting products.For instance,blue and redemitting phosphors are required in the process of plant supplementing light,arrow-band emitting phosphors are applied to backlight displays,etc.In this work,a Bi^(3+)-activated blue phosphor was obtained in a symmetrical and co mpact crystal structure of Gd3Sb07(GSO).Then,the co-doping strategy of alkali metal ions(Li^(+),Na^(+),and K^(+))was used to optimize the performance.The result shows that the photoluminescence intensity is increased by 2.1 times and 1.3 times respectively by introducing Li~+and K^(+)ions.Not only that,it also achieves narrow-band emitting with the full width of half-maximum(FWHM)reaching 42 nm through Na^(+)doping,and its excitation peak position also shifts from 322 to 375 nm,which can be well excited by near-ultraviolet(NUV)light emitting diode(LED)chips(365 nm).Meanwhile,the electroluminescence spectrum of GSO:0.6 mol%Bi^(3+),3 wt%Na^(+)matches up to 93.39%of the blue part of the absorption spectrum of chlorophyll a.In summary,the Bi^(3+)-activated blue phosphor reported in this work can synchronously meet the requirements of plant light replenishment and field emission displays.
基金supported by the National Natural Science Foundation of China(21706060,51703061)Natural Science Foundation of Hunan Province(2017JJ3103)+1 种基金Youth Project of Hunan Education Department(17B1118)Hunan Provincial Engineering Technology Research Center for Optical Agriculture(2018TP2003).
文摘Blue-violet light can not only enhance the total content of biomass and glucoside but also enrich the taste of the fruit.Thus,it is meaningful to study the blue-violet luminescent materials for plant cultivation.In this study,titanium(IV)-activated CaYAlO4(CYAO) phosphors were synthesized by conventional hightemperature solid-state reaction.X-ray powder diffraction was employed to analyze the crystalstructure of CYAO.It is found that the doped Ti^4+ ions do not change obviously the crystal structure of phosphors.Upon 246 nm excitation,CaYAl1-xO4:xTi^4+phosphors exhibit broad blue-violet emission band peaking at 395 nm,which can be attributed to the charge transfer of Ti^4+-O^2-.Moreover,this phosphor exhibits strong thermal stability.The luminescence emission intensity at 150℃maintained about 91 mol% of its initial value at room temperature.Additionally,the electron transition process and concentration quenching mechanism of CaYAl1-xO4:xTi^4+are discussed in detail.The excellent luminescent properties indicate that CaYAl1-xO4:xTi^4+phosphor may have promising application in indoor plant cultivation.
基金This work was financially supported by the Joint Funds of the National Natural Science Foundation of China and Yunnan Province(No.U1902222)the National Natural Science Foundation of China(Nos.51961145101 and 52102195)+3 种基金China Postdoctoral Science Foundation(Nos.2020M672960 and 2021M703656)Guangzhou Science&Technology Project(No.202007020005)Hunan High Level Talent Gathering Project(Nos.2019RS1077 and 2020RC5007)the Guangdong Provincial Key Laboratory of Semiconductor Micro Display(No.2020B121202003)。
文摘Nowadays,due to uncontrolled synthesis and lack of more direct and systematic evidences,the photoluminescence origin of“zero-dimensional”Cs4PbI6 remains great controversy and the luminescence cannot be controlled.Here we propose a controllable dissolution-recrystallization method to synthesize“emissive”and“non-emissive”Cs4PbI6 nanocrystals(NCs)respectively.Through comparing“emissive”and“non-emissive”Cs4PbI6 NCs,it is clearly proved that the visible emission in“emissive”Cs4PbI6 NCs comes from embedded CsPbI3 quantum dots(QDs).It is found for CsPbI3@Cs4PbI6 nanocomposites,methyl acetate(MeAC)and cyclohexane play an important role in dissolution and recrystallization respectively to obtain Cs4PbI6 matrix and CsPbI3 cores.Benefiting from this two-step method,the as-synthesized CsPbI3@Cs4PbI6 nanocomposites with CsPbI3 QDs uniformly distributed in Cs4PbI6 matrix are bright with photoluminescence quantum yield(PLQY)up to 71.4%and exhibit improved stability than CsPbI3 NCs.Moreover,utilizing its formation mechanism,the size of embedded CsPbI3 QDs can be controlled by reasonable designing the“dissolution”process,so that the luminescence of this CsPbI3@Cs4PbI6 nanocomposites can be adjusted in a wide range from green to red(554–630 nm).Our finding not only provides a novel method for synthesizing tunable“emissive”Cs4PbI6 NCs,but also makes clear the photoluminescence origin of“emissive”Cs4PbI6.
