荧光粉
光致发光
材料科学
青色
离子
发光
光谱学
发射光谱
光电子学
晶体结构
分析化学(期刊)
光学
结晶学
谱线
化学
物理
天文
量子力学
色谱法
作者
Freia Ruegenberg,Amador García‐Fuente,Markus Seibald,Dominik Baumann,Simon Peschke,Werner Urland,Andries Meijerink,Hubert Huppertz,Markus Suta
标识
DOI:10.1002/adom.202101643
摘要
Abstract Eu 2+ ‐activated phosphors of the UCr 4 C 4 structure type have emerged as promising new (ultra‐)narrow band phosphors. Especially the UCr 4 C 4 ‐type alkali lithosilicates have caused a sensation in the field of phosphor research in the recent years due to their consistent (ultra)narrow‐band luminescence in the cyan and green range that can pave the way to novel backlighting LEDs with high color gamut. The compound “K 2 Na 2 [Li 3 SiO 4 ] 4 :Eu 2+ ” stands out with a strikingly narrow emission in the cyan range (<0.2 eV or <30 nm full width at half maximum in the energy or wavelength scale, respectively) but the position of the Eu 2+ ions within this structure has been so far controversial. High‐resolution photoluminescence spectroscopy at 10 K reveals a complex emission spectrum with seven emission bands in the violet to green range. Combination with single‐crystal X‐ray diffraction (SCXRD) demonstrates that the cation channels in the structure also contain Li + ions. The presence of emission bands in the violet and blue spectral range reveals that the Eu 2+ ions also occupy the available K sites in the structure independently confirmed by advanced ligand field calculations. This study demonstrates that a combination of SCXRD, photoluminescence spectroscopy, and theory can help elucidate advanced structural problems.
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