Synthesis features of LiRF4 (R = Er–Lu) nanoparticles by the high-temperature co-precipitation method and their photoluminescent properties

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Аннотация

Nanoparticles of LiRF4 (R = Y, Yb, Lu), activated with Yb3+/Er3+ and Yb3+/Tm3+ ions, were obtained by the high-temperature co-precipitation method. The influence of the precursor molar ratio and the cationic composition of matrices on their dimensionality and morphology was studied. A method for the heterogeneous crystallization of these compounds using LiYF4 nanoseeds was optimized, which opens up opportunities for controlled synthesis of LiRF4 nanoparticles with controllable characteristics. Among the studied objects, LiYF4@LiYbF4:Tm3+@LiYF4 nanoparticles demonstrate the most intense anti-Stokes photoluminescence in the UV (λ = 362 nm) and blue (λ = 450 nm) ranges, exceeding similar indicators for β-NaYF4:Yb3+/Tm3+@NaYF4 particles. LiYF4@LiLuF4:Yb3+/Er3+@LiYF4 nanoparticles are the most efficient converters of IR radiation in the λ = 1530 nm range among the investigated isostructural matrices and exhibit similar spectral-luminescent properties to the β-NaYF4:Yb3+/Er3+@NaYF4 compound with an equivalent degree of codoping. The obtained results allow considering LiYF4@LiYbF4:Tm3+@LiYF4 and LiYF4@LiLuF4:Yb3+/Er3+@LiYF4 nanoparticles as a real alternative to the most widely used phosphors based on the hexagonal matrix β-NaYF4 for photonics and biotechnology applications.

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Авторлар туралы

A. Koshelev

Shubnikov Institute of Crystallography of Kurchatov Complex of Crystallography and Photonics of NRC “Kurchatov Institute”

Хат алмасуға жауапты Автор.
Email: avkoshelev03@gmail.com
Ресей, Moscow

V. Artemov

Shubnikov Institute of Crystallography of Kurchatov Complex of Crystallography and Photonics of NRC “Kurchatov Institute”

Email: avkoshelev03@gmail.com
Ресей, Moscow

N. Arkharova

Shubnikov Institute of Crystallography of Kurchatov Complex of Crystallography and Photonics of NRC “Kurchatov Institute”

Email: avkoshelev03@gmail.com
Ресей, Moscow

M. Seyed Dorraji

University of Zanjan

Email: avkoshelev03@gmail.com
Иран, Zanjan

D. Karimov

Shubnikov Institute of Crystallography of Kurchatov Complex of Crystallography and Photonics of NRC “Kurchatov Institute”

Email: avkoshelev03@gmail.com
Ресей, Moscow

Әдебиет тізімі

  1. Combes C.M., Dorenbos P., Van Eijk C.W. et al. // J. Luminescence. 1997. V. 71. № 1. P. 65. https://doi.org/10.1016/S0022-2313(96)00118-4
  2. Каминский А.А., Ляшенко А.И., Исаев Н.П. и др. // Квантовая электроника. 1998. Т. 25. № 3. С. 195.
  3. Loiko P., Soulard R., Guillemot L. et al. // IEEE J. Quantum Electron. 2019. V. 55. № 6. P. 1. https://doi.org/10.1109/JQE.2019.2943477
  4. Yokota Y., Yamaji A., Kawaguchi N. et al. // Phys. Status Solidi. С. 2012. V. 9. № 12. P. 2279. https://doi.org/10.1002/pssc.201200290
  5. Kamada K., Hishinuma K., Kurosawa S. et al. // Opt. Mater. 2016. V. 61. P. 134. https://doi.org/10.1016/j.optmat.2016.09.019
  6. Qiu Z., Wang S., Wang W., Wu S. // ACS Appl. Mater. Interfaces. 2020. V. 12. № 26. P. 29835. https://doi.org/10.1021/acsami.0c07765
  7. Vasyliev V., Villora E.G., Nakamura M. et al. // Opt. Express. 2012. V. 20. № 13. P. 14460. https://doi.org/10.1364/OE.20.014460
  8. Romanova I.V., Tagirov M.S. // Magnetic Resonance in Solids. Electronic J. 2019. V. 21. № 4. P. 13. https://doi.org/10.26907/mrsej-19412
  9. Zelmon D.E., Erdman E.C., Stevens K.T. et al. // Appl. Opt. 2016. V. 55. № 4. P. 834. https://doi.org/10.1364/AO.55.000834
  10. Khaydukov E.V., Mironova K.E., Semchishen V.A. et al. // Sci. Rep. 2016. V. 6. № 1. P. 35103. https://doi.org/10.1038/srep35103
  11. Hao S., Shang Y., Li D. et al. // Nanoscale. 2017. V. 9. № 20. P. 6711. https://doi.org/10.1039/C7NR01008G
  12. Zheng K., Han S., Zeng X. et al. // Adv. Mater. 2018. V. 30. № 30. P. 1801726. https://doi.org/10.1002/adma.201801726
  13. Guo Q., Wu J., Yang Y. et al. // J. Power Sources. 2019. V. 426. P. 178. https://doi.org/10.1016/j.jpowsour.2019.04.039
  14. Zhou Y., Wu S., Wang F. et al. // Chemosphere. 2020. V. 238. P. 124648. https://doi.org/10.1016/j.chemosphere.2019.124648
  15. Каримов Д.Н., Демина П.А., Кошелев А.В. и др. // Российские нанотехнологии. 2020. Т. 15. № 6. С. 699. https://doi.org/10.1134/S1992722320060114
  16. Huang R., Liu S., Huang J. et al. // Nanoscale. 2021. V. 13. № 9. P. 4812. https://doi.org/10.1039/D0NR09068A
  17. Yang Y., Huang J., Wei W. et al. // Nature Commun. 2022. V. 13. № 1. P. 3149. https://doi.org/10.1038/s41467-022-30713-w
  18. Федоров П.П. // Журн. неорган. химии. 1999 Т. 44. № 11. С. 1792.
  19. Mai H.X., Zhang Y.W., Si R. et al. // J. Am. Chem. Soc. 2006. V. 128. № 19. P. 6426. https://doi.org/10.1021/ja060212h
  20. Naccache R., Yu Q., Capobianco J.A. // Adv. Opt. Mater. 2015. V. 3. № 4. P. 482. https://doi.org/10.1002/adom.201400628
  21. Wang J., Deng R., MacDonald M.A. et al. // Nat. Mater. 2014. V. 13. № 2. P. 157. https://doi.org/10.1038/NMAT3804
  22. Rojas‐Gutierrez P.A., DeWolf C., Capobianco J.A. // Part. Part. Syst. Charact. 2016. V. 33. № 12. P. 865. https://doi.org/10.1002/ppsc.201600218
  23. Cheng T., Marin R., Skripka A., Vetrone F. // J. Am. Chem. Soc. 2018. V. 140. № 40. P. 12890. https://doi.org/10.1021/jacs.8b07086
  24. Wang J., Wang F., Xu J. et al. // C.R. Chim. 2010. V. 13. № 6–7. P. 731. https://doi.org/10.1016/j.crci.2010.03.021
  25. Liu S., An Z., Huang J., Zhou B. // Nano Res. 2023. V. 16. № 1. P. 1626. https://doi.org/10.1007/s12274-022-5121-9
  26. Kaczmarek A.M., Suta M., Rijckaert H. et al. // J. Mater. Chem. C. 2021. V. 9. № 10. P. 3589. https://doi.org/10.1039/d0tc05865c
  27. Zhang X., Wang M., Ding J. et al. // CrystEngComm. 2012. V. 14. № 24. P. 8357. https://doi.org/10.1039/c2ce26159f
  28. He E., Zheng H., Gao W. et al. // Mater. Res. Bull. 2013. V. 48. № 9. P. 3505. https://doi.org/10.1016/j.materresbull.2013.05.046
  29. Chen B., Wang F. // Inorg. Chem. Front. 2020. V. 7. № 5. P. 1067. https://doi.org/10.1039/C9QI01358J
  30. Zhang L., Wang Z., Lu Z. et al. // J. Nanosci. Nanotechnol. 2014. V. 14. № 6. P. 4710. https://doi.org/10.1166/jnn.2014.8641
  31. Jiang X., Cao C., Feng W. et al. // J. Mater. Chem. B. 2016. V. 4. № 1. P. 87. https://doi.org/10.1039/c5tb02023a
  32. Carl F., Birk L., Grauel B. et al. // Nano Res. 2021. V. 14. P. 797. https://doi.org/10.1007/s12274-020-3116-y
  33. Gao W., Zheng H., He E. et al. // J. Luminescence. 2014. V. 152. P. 44. https://doi.org/10.1016/j.jlumin.2013.10.046
  34. Li W., He Q., Xu J. et al. // J. Luminescence. 2020. V. 227. P. 117396. https://doi.org/10.1016/j.jlumin.2020.117396
  35. Zou Q., Huang P., Zheng W. et al. // Nanoscale. 2017. V. 9. № 19. P. 6521. https://doi.org/10.1039/C7NR02124K
  36. Liu J., Rijckaert H., Zeng M. et al. // Adv. Funct. Mater. 2018. V. 28. № 17. P. 1707365. https://doi.org/10.1002/adfm.201707365
  37. Dong J., Zhang J., Han Q. et al. // J. Luminescence. 2019. V. 207. P. 361. https://doi.org/10.1016/j.jlumin.2018.11.041
  38. Wang F., Deng R., Liu X. // Nat. Protoc. 2014. V. 9. № 7. P. 1634. https://doi.org/10.1038/nprot.2014.111
  39. Boyer J.C., Cuccia L.A., Capobianco J.A. // Nano Lett. 2007. V. 7. № 3. P. 847. https://doi.org/10.1021/nl070235+
  40. Koshelev A.V., Arkharova N.A., Khaydukov K.V. et al. // Crystals. 2022. V. 12. № 5. P. 599. https://doi.org/10.3390/cryst12050599
  41. Wang F., Han Y., Lim C.S. et al. // Nature. 2010. V. 463. № 7284. P. 1061. https://doi.org/10.1038/nature08777
  42. Liu Q., Sun Y., Yang T. et al. // J. Am. Chem. Soc. 2011. V. 133. № 43. P. 17122. https://doi.org/10.1021/ja207078s
  43. Damasco J.A., Chen G., Shao W. et al. // ACS Appl. Mater. Interfaces. 2014. V. 6. № 16. P. 13884. https://doi.org/10.1021/am503288d
  44. Huang X. // Opt. Mater. Express. 2016. V. 6. № 7. P. 2165. https://doi.org/10.1364/OME.6.002165
  45. Alyatkin S., Asharchuk I., Khaydukov K. et al. // Nanotechnology. 2016. V. 28. № 3. P. 035401. https://doi.org/10.1088/1361-6528/28/3/035401
  46. Gao D., Zhang X., Chong B. et al. // Phys. Chem. Chem. Phys. 2017. V. 19. № 6. P. 4288. https://doi.org/10.1039/C6CP06402G
  47. Schroter A., Märkl S., Weitzel N., Hirsch T. // Adv. Funct. Mater. 2022. V. 32. № 26. P. 2113065. https://doi.org/10.1002/adfm.202113065

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1. JATS XML
2. Fig. 1. Phase diagram of the LiF–YF3 binary system [18]

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3. Fig. 2. Radiographs of LiRF4 LPS synthesized with a different ratio of precursors n(Li+):n(R3+):n(F-) (a): 1:1:4 (1), 1.75:1:4 (2), 2.5:1:4 (3); the cationic composition of the crystal matrix (b): R = Y (1), Yb (2), Lu (3) and the precursor ratio 1.75:1:4

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4. Fig. 3. SEM and TEM images of LiRF4 LPS with corresponding histograms of the dimensional distribution obtained with different ratios of precursors: a – 1:1:4, b – 1.75:1:4, c – 2.5:1:4, and the cationic composition of the matrix: R = Y (d), Yb (E), Lu (E)

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5. Fig. 4. X-ray images of LiYF4 (1) nanotubes and structures obtained after applying one (2), three (3) and five (4) epitaxial LiYF4 shells:Yb3+/Er3+ (a); a TEM image of LiYF4 primers is shown in the box. Dependence of the LF dimension LiYF4:Yb3+/Er3+ on the ratio nprek:nzatr (b)

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6. Fig. 5. Low frequency radiographs LiYF4@LiYF4:Yb3+/Tm3+@LiYF4 (nΣprek:pp = 20) (1), LiYF4@LiLuF4:Yb3+/Er3+@LiYF4 (NΣPRECK:psatr = 160) (2) with a seed/core/shell structure and reference woofers β-NaYF4:Yb3+/Tm3+@NaYF4 (a). Low frequency SAM images LiYF4@LiYF4:Yb3+/Tm3+@LiYF4 (b), LiYF4@LiLuF4:Yb3+/Er3+@LiYF4 (c), β-NaYF4:Yb3+/Tm3+@NaYF4 (d), β-NaYF4:Yb3+/Er3+@NaYF4 (e) with corresponding histograms of the dimensional distribution

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7. Fig. 6. Spectra of LF FL LiYF4 (1), LiYbF4 (2), LiLuF4 (3), β-NaYF4 (4) doped with Yb3+/Tm3+ (a) and Yb3+/Er3+ (b) ions. Appearance and observed LF of LF colloids LiYF4@LiYF4:Yb3+/Tm3+@LiYF4 and LiYF4@LiLuF4:Yb3+/Er3+@LiLuF4 , obtained by excitation by radiation λ = 975 nm, shown in the inserts

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