Near-Infrared-to-Blue Upconversion in Colloidal BaYF5:Tm3+, Yb3+ Nanocrystals

Near-Infrared-to-Blue Upconversion in Colloidal BaYF5:Tm3+, Yb3+ Nanocrystals
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DOI:
10.1021/cm900313s
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发表时间:
2009-05-12
影响因子:
8.6
通讯作者:
Capobianco, John A.
Capobianco, John A.
中科院分区:
材料科学2区
文献类型:
--
作者:
Vetrone, Fiorenzo;Mahalingam, Venkataramanan;Capobianco, John A.

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使用热分解方法合成了掺杂有0.5摩尔% Tm 3+和15摩尔% Yb 3+的四氟化钇钡(BaYF 5)纳米晶体(BaYF 5:Tm 3+,Yb 3+),产生矩形纳米晶体(15 nm x 5 nm),其可以通过称为上转换的过程将近红外光(上)转换为更高能量(例如蓝光)。BaYF 5:Tm 3+,Yb 3+纳米晶体在980 tun激发后的上转换光谱显示,在高激发密度(90 W/cm(2))下,来自(1)G(4)-> H-3(6)跃迁的上转换蓝光发射比红外H-3(4)-> H-3(6)发射更强,这与Tm 3 +/Yb 3+共掺杂纳米材料通常观察到的情况相反。另一方面,红外发射在较低的激发密度(15 W/cm(2))下占主导地位,这表明缺乏激发的Yb 3+离子来进行超过H-3(4)激发态到(1)G(4)激发态的上转换。在激发密度高于57 W/cm(2)的功率依赖性研究中观察到上转换过程的饱和,导致上转换过程所需的预期光子数出现偏差。对BaYF_5:Tm ~(3+),Yb ~(3+)纳米晶体的上转换发光特性进行了分析和讨论。
Tetragonal barium yttrium fluoride (BaYF5) nanocrystals doped with 0.5 mol % Tm3+ and 15 mol % Yb3+ (BaYF5:Tm3+, Yb3+) were synthesized using the thermal decomposition method yielding rectangular-shaped nanocrystals (15 nm x 5 nm) that can (up)convert near-infrared light to higher energies such as blue, via a process known as upconversion. The upconversion spectrum of the BaYF5:Tm3+, Yb3+ nanocrystals, following excitation with 980 tun, revealed that the upconverted blue emission from the (1)G(4) -> H-3(6) transition was more intense than the infrared H-3(4) -> H-3(6) emission at high excitation densities (90 W/cm(2)) contrary to what is normally observed for Tm3+/Yb3+ codoped nanomaterials. On the other hand, the infrared emission dominates at lower excitation densities (15 W/cm(2)) demonstrating a lack of excited Yb3+ ions to carry on the upconversion beyond the H-3(4) excited state to the (1)G(4) excited state. A saturation of the upconversion process was observed in the power dependence studies at excitation densities above 57 W/cm(2), causing a deviation in the expected number of photons required for the upconversion process. The upconversion properties of BaYF5:Tm3+, Yb3+ nanocrystals are elucidated and discussed.