<![CDATA[Enhanced photoluminescence property of single-component CaAlSiN <ce:inf loc='post'>3</ce:inf>: Ce <ce:sup loc='post'>3+</ce:sup>, Eu <ce:sup loc='post'>2+</ce:sup> multicolor phosphor through Ce <ce:sup loc='post'>3+</ce:sup>-Eu <ce:sup loc='post'>2+</ce:sup> energy transfer]]>
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3: Ce 3+, Eu 2+ multicolor phosphor through Ce 3+-Eu 2+ energy transfer]]>

机译:<![CDATA [单个组件CALASIN的增强光致发光属性 3 :什么:sup place =“post”> 3 + , I <那是什么:supplace =“post”> 2 + 多色码头通过什么:sup place =“post”> 3 + -eu 2 + 能量转印]]>

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AbstractA series of single-component CaAlSiN3: Ce3+, Eu2+phosphors with dual emission colors (yellow and red) were successfully preparedviaa direct-nitriding method to achieve spectral tuning and broadening of CaAlSiN3: Eu2+red phosphor. Crystal structure, morphology, photoluminescence properties and energy transfer mechanism were thoroughly investigated. The particular plate-like morphology of CaAlSiN3: Ce3+, Eu2+phosphor was obtained due to the lattice distortion and preferential orientation growth of host lattice originated from the introduction of Ce3+into CaAlSiN3. More interestingly, the luminescent intensity of red emission peak was enhanced through an energy transfer process between Ce3+and Eu2+ions. Under excitation of 460?nm, CaAlSiN3: 0.02Ce3+, 0.001Eu2+phosphor exhibited intense and broad emission peaks centered at 580?nm (yellow) and 618?nm (closely near to the red isochromatic region around 615?nm). Furthermore, the energy transfer mechanism from Ce3+to Eu2+ion was determined to be electric dipole-dipole interaction and the energy transfer efficiency was 94%. The CaAlSiN3: Ce3+, Eu2+phosphors showed super broad excitation spectra from 270 to 500?nm, high external quantum efficiency (74%) and small thermal quenching. Evidently, CaAlSiN3: Ce3+, Eu2+samples may be potential candidates of red phosphor for improving optical performance of illumination-grade light sources.Highlights?Spectral tuning and broadening for CaAlSiN3based red emitting phosphor are achieved.?Single-component CaAlSiN3: Ce3+, Eu2+multicolor phosphors have been prepared.?Ce3+doping results in lattice distortion and plate-like morphology of host crystal.?Energy transfer mechanism is determined to be electric dipole-dipole interaction.]]>
机译:<![CDATA [ 抽象 一系列单组件caalsin 3 :ce 3 + ,eu 2 + 双发射颜色的磷光体(黄色和红色通过斜体>一种直接氮化的方法来成功制备,以实现光谱调谐和扩大Caalsin 3 :eu 2 + 红色磷光体。彻底研究了晶体结构,形态,光致发光性能和能量转移机制。 Caalsin的特定板式形态 3 :ce 3 + ,eu 2 + 由于晶格畸变而获得的磷光体源于CE 3 + 进入caalsin 3 。更有意义地,通过CE 3 + 和EU 2,通过能量转移过程来增强红色发射峰的发光强度。 + / Ce:sup>离子。在激励460?nm,caalsin 3 :0.02ce 3 + ,0.001eu < CE:Sup =“post”> 2 + 磷光体表现出在580Ω(黄色)和618Ω(黄色)和618Ω·nm(靠近615Ω·纳米的红色等象区紧密的宽度的发射峰。此外,来自CE 3 + 到eu 2 + 离子的能量转移机制是电偶极子 - 偶极相互作用,能量转移效率为94%。 Caalsin 3 :ce 3 + ,eu 2 + 磷光体显示出超宽易激谱,从270至500〜500Ω,高外部量子效率(74%)和小的热淬火。显然,Caalsin 3 :ce 3 + ,eu 2 + 样品可以是红色磷光体的潜在候选者,用于改善照明级光源的光学性能。 亮点 Caalsin的光谱调谐和扩大为Caalsin 3 基于红色的发射实现荧光粉。 单组件爪子 3 :ce 3 + ,eu 2 + 多色荧光粉已准备好。 ce 3 + 掺杂导致镜片变形和宿主水晶的板状形态。 能量传输机制被确定为电偶极 - 偶极交互。 ]]>

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