Visible photocatalysts based on nitrogen and carbon doped nanocrystalline titanium dioxide

Мұқаба

Дәйексөз келтіру

Толық мәтін

Ашық рұқсат Ашық рұқсат
Рұқсат жабық Рұқсат берілді
Рұқсат жабық Тек жазылушылар үшін

Аннотация

Photocatalysts functioning in the visible spectrum range based on nanocrystalline titanium dioxide doped with nitrogen and carbon in the form of microspheres were obtained. Their structural, optoelectronic and photocatalytic properties were studied. The electron paramagnetic resonance method was used to identify spin centers (defects) and determine their concentrations in all the samples under study. Nitrogen atoms with an unpaired electron and Ti3+/oxygen vacancy centers were found in the microspheres doped with nitrogen. Dangling carbon bonds were recorded in the microspheres with carbon impurities. Photocatalysts doped simultaneously with nitrogen and carbon are characterized by both nitrogen and carbon spin centers. It was found that the concentration of defects increases during illumination, which is explained by their recharging. A correlation was established between the concentration of spin centers and the rate of photocatalysis in the obtained structures. It was shown that samples doped with two impurities are characterized by a high photocatalysis rate and prolonged catalysis for more than five hours after the illumination is turned off, as well as stable photocatalytic properties for several years, which determines the novelty of the studies and high prospects for use in ecology and biomedicine.

Толық мәтін

Рұқсат жабық

Авторлар туралы

E. Kytina

Lomonosov Moscow State University

Email: zaytsevvb@my.msu.ru

Физический факультет

Ресей, Moscow, 119991

V. Zaitsev

Lomonosov Moscow State University; Sνenzhen MSU-BIT University

Хат алмасуға жауапты Автор.
Email: zaytsevvb@my.msu.ru

Физический факультет

Ресей, Moscow, 119991; China, Shenzhen, 518172

Е. Konstantinova

Lomonosov Moscow State University

Email: liza35@mail.ru

Физический факультет

Ресей, Moscow, 119991

V. Kulbachinskii

Lomonosov Moscow State University

Email: zaytsevvb@my.msu.ru

Физический факультет

Ресей, Moscow, 119991

Әдебиет тізімі

  1. Khan A.U., Tahir K., Shah M.Z.U. et al. // Nanomaterials. 2024. V. 14. № 13. P. 1136. https://doi.org/10.3390/nano14131136
  2. Hwang I., Schmuki P., Mazare A. // Physica Status Solidi A. 2024. V. 221. № 16. P. 2400335. https://doi.org/10.1002/pssa.202400335
  3. Dongmei He, Du L., Wang K. et al. // Russ. J. Inorg. Chem. 2021. V. 66. № 13. P. 1986. https://doi.org/10.1134/S0036023621130040
  4. Mokrushin A.S., Gorban Yu.M., Nagornov I.A. et al. // Russ. J. Inorg. Chem. 2022. V. 67. № 12. P. 2099. https://doi.org/10.1134/S0036023622601520
  5. Zheleznov V.V., Tkachenko I.A., Ziatdinov A.M. et al. // Russ. J. Inorg. Chem. 2023. V. 68. № 1. P. 95. https://doi.org/10.1134/S0036023622602045
  6. Wang N., Ma W., Jin Y. // Mater. Res. Express. 2024. V. 11. № 7. P. 075506. https://doi.org/10.1088/2053-1591/ad5fe1
  7. Wang Q., Yuan Y., Li C. et al. // Renew Energy. 2024. V. 231. P. 120997. https://doi.org/10.1016/j.renene.2024.120997
  8. Chang Y.-C., Lai P.-R., Yang J.H.C. et al. // J Alloys Compd. 2024. V. 1002. P. 175443. https://doi.org/10.1016/j.jallcom.2024.175443
  9. Hu L., Huo K., Chen R. et al. // Anal. Chem. 2011. V. 83. № 21. P. 8138. https://doi.org/10.1021/ac201639m
  10. Jaafar H., Ahmad Z.A., Ain M.F. // Optik. 2017. V. 144. P. 91. https://doi.org/10.1016/j.ijleo.2017.06.097
  11. Wang X., Liu X., Liu L. et al. // Appl. Catal., B: Environment and Energy. 2024. V. 358. P. 124338. https://doi.org/10.1016/j.apcatb.2024.124338
  12. Schneider J., Matsuoka M., Takeuchi M. et al. // Chem. Rev. 2014. V. 114. № 19. P. 9919. https://doi.org/10.1021/cr5001892
  13. Rangel-Contreras V., Reyes-Vallejo O., Subramaniam V. // J. Mater. Sci. — Mater. Electron. 2024. V. 35. № 19. P. 1301. https://doi.org/10.1007/s10854-024-12986-7
  14. Wei Y., Huang Y., Fang Y. et al. // Mater. Res. Bull. 2019. V. 119. P. 110571. https://doi.org/10.1016/j.materresbull.2019.110571
  15. Liu Z., Zhang X., Nishimoto S. et al. // Environ. Sci. Technol. 2008. V. 42. № 22. P. 8547. https://doi.org/10.1021/es8016842
  16. Haghighi P., Haghighat F. // Build. Environ. 2024. V. 249. P. 111108. https://doi.org/10.1016/j.buildenv.2023.111108
  17. Kerstner Baldin E., Marasca Antonini L., De León M.A. et al. // Bull. Mater. Sci. 2024. V. 47. № 3. P. 133. https://doi.org/10.1007/s12034-024-03238-9
  18. Motola M., Čaplovičová M., Krbal M. et al. // Electrochim. Acta. 2020. V. 331. P. 135374. https://doi.org/10.1016/j.electacta.2019.135374
  19. Low J., Yu J., Jaroniec M. et al. // Adv. Mater. 2017. V. 29. № 20. https://doi.org/10.1002/adma.201601694
  20. Konstantinova E.A., Minnekhanov A.A., Kytina E.V. et al. // JETP Lett. 2020. V. 112. № 8. P. 527. https://doi.org/10.1134/S0021364020200060
  21. Tang T., Yin Z., Chen J. et al. // Chem. Eng. J. 2021. V. 417. P. 128058. https://doi.org/10.1016/j.cej.2020.128058
  22. Zubair M., Kim H., Razzaq A. et al. // J. CO2 Utilization. 2018. V. 26. P. 70. https://doi.org/10.1016/j.jcou.2018.04.004
  23. Piedra-López J., Calzada L.A., Guerra-Blanco P. et al. // Catal. Today. 2024. V. 432. P. 114610. https://doi.org/10.1016/j.cattod.2024.114610
  24. Shabalina A., Golubovskaya A., Fakhrutdinova E. et al. // Nanomaterials. 2022. V. 12. № 22. P. 4101. https://doi.org/10.3390/nano12224101
  25. Stoll S., Schweiger A. // J. Magn. Reson. 2006. V. 178. № 1. P. 42. https://doi.org/10.1016/j.jmr.2005.08.013
  26. Byung-Hyun K., Mina P., Gyubong K. et al. // J. Phys. Chem. C. 2018. V. 122. № 27. P. 15297. https://doi.org/10.1021/acs.jpcc.8b02239
  27. Kytina E.V., Savchuk T.P., Gavrilin I.M. et al. // Russ. J. Inorg. Chem. 2023. V. 68. № 3. P. 357. https://doi.org/10.1134/S003602362260229X
  28. Morimoto A., Miura T., Kumeda M. et al. // J. Appl. Phys. 1982. V. 53. № 11. P. 7299. https://doi.org/10.1063/1.329879
  29. Livraghi S., Chierotti M.R., Giamello E. et al. // J. Phys. Chem. C. 2008. V. 112. № 44. P. 17244. https://doi.org/10.1021/jp803806s
  30. Li Y., Peng Y.-K., Hu L. et al. // Nat. Commun. 2019. V. 10. № 1. P. 4421. https://doi.org/10.1038/s41467-019-12385-1
  31. Konstantinova E.A., Minnekhanov A.A., Kokorin A.I. et al. // J. Phys. Chem. C. 2018. V. 122. № 18. P. 10248. https://doi.org/10.1021/acs.jpcc.8b01621

Қосымша файлдар

Қосымша файлдар
Әрекет
1. JATS XML
2. Fig. 1. Microphotographs of N-C-TiO2 microspheres. Scale bars are 100 nm (a), 1 μm (b).

Жүктеу (519KB)
3. Fig. 2. Diffractogram of N-C-TiO2 samples.

Жүктеу (27KB)
4. Fig. 3. Determination of the forbidden band width of doped N-C-TiO2 microspheres and TiO2 samples without impurities.

Жүктеу (26KB)
5. Fig. 4. Kinetics of photocatalysis for TiO2 (1), N-TiO2 (2), C-TiO2 (3), N-C-TiO2 (4), N-C-TiO2_old (5) microspheres under photoexcitation in the visible range of the spectrum. The arrows show the moments of illumination on (τ = 0) and illumination off (τ = 20 min). C0 is the dye concentration at time τ = 0, C is the dye concentration at time τ.

Жүктеу (27KB)
6. Fig. 5. EPR spectra of a series of microspheres under dark conditions and illumination: N-C-TiO2 (1 and 2), N-TiO2 (3 and 4), C-TiO2 (5 and 6), TiO2 (7).

Жүктеу (28KB)
7. Fig. 6. Relaxation kinetics of the EPR signal amplitude relaxation from broken carbon bonds in N-C-TiO2. The inset shows the kinetics for carbon-doped TiO2.

Жүктеу (27KB)

© Russian Academy of Sciences, 2025