光子上转换
发光
材料科学
激发态
激发
镧系元素
光电子学
离子
人口
激活剂(遗传学)
化学
原子物理学
物理
社会学
基因
人口学
有机化学
量子力学
生物化学
作者
Heng Jia,Nan Li,Huiyu He,Xucheng Zhang,Yingyue Teng,Weiping Qin
标识
DOI:10.1002/adom.202302583
摘要
Abstract Precise control over multicolor luminescence of upconversion nanoparticles (UCNPs) is of significant importance for their applications in widespread fields of research. However, realizing the tunable emissions in single UCNPs with a single lanthanide element remains a great challenge. Herein, without multiple lanthanide elements, a new strategy for the regulation of the excited‐state level population pathways of the same lanthanide activator Er 3+ ion to obtain multicolor‐tunable upconversion luminescence is proposed through utilizing 980 nm coupled 1973 nm synergistic excitation. Unlike typical single wavelength excitation, the synergistic excitation may affect population pathways of the excited‐state level of Er 3+ ion by adjusting excitation wavelength and power density, resulting in a dynamically adjustable change in luminescence color output. Notably, multicolor luminescence involving green, chartreuse, yellow, orange, and red can be tuned dynamically in the NaYF 4 :Er 3+ single UCNPs by using the tunable 980/1973 nm synergistic excitation. This dynamic luminescence color variation from these UCNPs has demonstrated promising potential applications in volumetric color display. The results provide a new approach to achieve multicolor‐tunable upconversion luminescence at single nanoparticles level and open up the possibility of developing true three‐dimensional volumetric color display technologies with resolution at the nanometer range.
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