journal article·2023-06-23Open access

Plasma-Assisted N-Doped TiO2 Nanotube Array as an Active UV–vis Photoanode

Marcin Pisarek, Mirosław Krawczyk, Magdalena Gurgul, Leszek Zaraska, Krzysztof Bieńkowski, Marcin Hołdyński, Renata Solarska

ACS Applied Nano Materials· Volume 6· Issue 12

Abstract

High Resolution Image Download MS PowerPoint Slide This work shows the possibility of using plasma nitriding under ultra-high-vacuum conditions to introduce nitrogen into a titanium dioxide structure in the form of nanotubes with a diameter of about 110 nm. Nanotubes were produced by the anodic oxidation of Ti foil in a solution based on glycerine and water with the addition of ammonium fluoride at a voltage of 25 V. Based on experimental evidence obtained by X-ray photoelectron spectroscopy (XPS, in situ), it has been shown that alternating nitriding and annealing processes at 450 °C leads to formation of Ti-N-O, Ti-N, and Ti-O-N chemical bonds in the TiO 2 crystal structure (anatase). The observed changes were identified as interstitial or substitutional admixtures or variations of these. The spectrophotometric and spectrophotoelectrochemical tests performed showed that the photoactivity of the photoanodes doped with nitrogen and annealed at 450 °C in the UV–vis range was significantly greater than that of the photoanodes without nitrogen. The highest maximum photocurrent density, of about 30.0 μA·cm –2 at a wavelength of λ = 350 nm, was obtained for the double-nitrided and once-annealed sample, where nitrogen was mainly incorporated in the interstitial positions in the TiO 2 lattice. For the materials not nitrided as well as annealed only at 450 °C and pristine, the worse photoresponse was received at the levels of ∼16 and ∼0.2 μA·cm –2, respectively. The thermo-chemical treatment applied also effectively extended the operational range of the photoanodes toward visible light, where a wide maximum of light absorption was observed from ∼400 to ∼700 nm, with a maximum wavelength of 550 nm and an estimated bandgap energy of 2.5 eV. Our investigations confirmed that photoelectrochemical (PEC) performance for TiO 2 NT-based photoanodes was achieved by the optimum annealing condition and concentration of nitrogen, where the narrowed bandgap was observed by generating a new N 2p energy level above the O 2p valence band. The following research techniques were used to identify the changes taking place in the materials produced: XPS spectroscopy, UV–vis spectroscopy, PEC measurements, X-ray diffraction structural measurements, and scanning electron microscopic observations.
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Research context

OpenAlex topics: Advanced Photocatalysis Techniques · TiO2 Photocatalysis and Solar Cells · Ga2O3 and related materials

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Institute of Physical Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, 01-224 Warsaw, Poland

Faculty of Chemistry, Jagiellonian University in Kraków, Gronostajowa 2, 30-387 Kraków, Poland

Laboratory of Molecular Research for Solar Energy Innovations, Centre of New Technologies University of Warsaw, Banacha 2c, 02-097 Warsaw, Poland

Funding

Instytut Chemii Fizycznej PAN · National Center for Research and Development

References (70)

Show source-provided references
1. 10.1039/C5NJ03478G10.1039/C5NJ03478G ↗
2. 10.1039/C4EE00147H10.1039/C4EE00147H ↗
3. 10.3390/photochem103002410.3390/photochem1030024 ↗
4. 10.1016/j.physe.2017.02.00310.1016/j.physe.2017.02.003 ↗
5. 10.1002/cphc.20100027610.1002/cphc.201000276 ↗
6. 10.1016/j.apcatb.2018.04.04510.1016/j.apcatb.2018.04.045 ↗
7. 10.1186/s40580-022-00323-910.1186/s40580-022-00323-9 ↗
8. 10.1038/238037a010.1038/238037a0 ↗
9. 10.1007/s12209-021-00303-w10.1007/s12209-021-00303-w ↗
10. 10.1039/C4EE02169J10.1039/C4EE02169J ↗
11. 10.1155/2015/52707010.1155/2015/527070 ↗
12. 10.1063/1.35630610.1063/1.356306 ↗
13. 10.1016/j.materresbull.2016.10.03110.1016/j.materresbull.2016.10.031 ↗
14. 10.3390/ma1104058410.3390/ma11040584 ↗
15. 10.1021/ja903781h10.1021/ja903781h ↗
16. 10.1103/PhysRevB.70.08511610.1103/PhysRevB.70.085116 ↗
17. 10.1063/1.327227210.1063/1.3272272 ↗
18. 10.1021/jp068503010.1021/jp0685030 ↗
19. 10.1016/j.ceramint.2012.12.06810.1016/j.ceramint.2012.12.068 ↗
20. 10.1002/celc.20150007810.1002/celc.201500078 ↗
21. 10.1021/acsanm.2c0453410.1021/acsanm.2c04534 ↗
22. 10.1016/j.apsusc.2023.15647210.1016/j.apsusc.2023.156472 ↗
23. 10.1557/jmr.2006.034410.1557/jmr.2006.0344 ↗
24. 10.1016/j.apsusc.2016.03.12810.1016/j.apsusc.2016.03.128 ↗
25. 10.1021/acsomega.0c0009410.1021/acsomega.0c00094 ↗
26. 10.1021/acs.jpcc.5b0840310.1021/acs.jpcc.5b08403 ↗
27. 10.1039/C5CP02888D10.1039/C5CP02888D ↗
28. 10.1016/j.apcatb.2016.05.00610.1016/j.apcatb.2016.05.006 ↗
29. 10.1039/c1jm10274e10.1039/c1jm10274e ↗
30. 10.1016/j.jhazmat.2010.08.12110.1016/j.jhazmat.2010.08.121 ↗
31. 10.1002/anie.20100137410.1002/anie.201001374 ↗
32. 10.1016/j.envpol.2020.11617010.1016/j.envpol.2020.116170 ↗
33. 10.1016/j.apsusc.2013.05.02110.1016/j.apsusc.2013.05.021 ↗
34. 10.1039/C5NJ00127G10.1039/C5NJ00127G ↗
35. 10.1016/j.apsusc.2018.02.15310.1016/j.apsusc.2018.02.153 ↗
36. 10.3390/mi912061810.3390/mi9120618 ↗
37. 10.1016/j.jallcom.2011.08.00310.1016/j.jallcom.2011.08.003 ↗
38. 10.1016/j.wri.2021.10016310.1016/j.wri.2021.100163 ↗
39. 10.1016/j.cattod.2010.11.08610.1016/j.cattod.2010.11.086 ↗
40. 10.1021/la400586r10.1021/la400586r ↗
41. 10.1038/s41598-017-14463-010.1038/s41598-017-14463-0 ↗
42. 10.1021/acs.jpcc.1c0045910.1021/acs.jpcc.1c00459 ↗
43. 10.1016/j.ceramint.2016.06.11710.1016/j.ceramint.2016.06.117 ↗
44. 10.1016/j.cej.2018.05.12210.1016/j.cej.2018.05.122 ↗
45. 10.1016/j.chemphys.2007.07.04110.1016/j.chemphys.2007.07.041 ↗
46. 10.1016/j.chemphys.2007.07.02010.1016/j.chemphys.2007.07.020 ↗
47. 10.1002/chem.20100167210.1002/chem.201001672 ↗
48. 10.1021/cr500073810.1021/cr5000738 ↗
49. 10.1016/j.apsusc.2015.07.19010.1016/j.apsusc.2015.07.190 ↗
50. 10.1016/j.materresbull.2012.09.06110.1016/j.materresbull.2012.09.061 ↗
51. 10.1016/j.matlet.2014.03.05010.1016/j.matlet.2014.03.050 ↗
52. 10.1039/C5RA05818J10.1039/C5RA05818J ↗
53. 10.1021/jp111198210.1021/jp1111982 ↗
54. 10.1016/0166-9834(83)80076-110.1016/0166-9834(83)80076-1 ↗
55. 10.1016/j.apcata.2010.05.03910.1016/j.apcata.2010.05.039 ↗
56. 10.1016/j.cattod.2016.07.00910.1016/j.cattod.2016.07.009 ↗
57. 10.1021/jp014192b10.1021/jp014192b ↗
58. 10.1088/0957-4484/20/23/23570110.1088/0957-4484/20/23/235701 ↗
59. 10.1088/0022-3719/20/28/02810.1088/0022-3719/20/28/028 ↗
60. 10.1063/1.327227210.1063/1.3272272 ↗
61. 10.1016/j.susc.2010.10.03910.1016/j.susc.2010.10.039 ↗
62. 10.1039/c3nr00476g10.1039/c3nr00476g ↗
63. 10.1021/jp400082u10.1021/jp400082u ↗
64. 10.1021/cr500189210.1021/cr5001892 ↗
65. Powell C. J. · 2010
66. 10.1016/j.electacta.2015.07.02310.1016/j.electacta.2015.07.023 ↗
67. 10.1016/j.electacta.2012.10.09610.1016/j.electacta.2012.10.096 ↗
68. 10.1111/j.1551-2916.2011.04692.x10.1111/j.1551-2916.2011.04692.x ↗
69. 10.1038/s41598-021-01165-x10.1038/s41598-021-01165-x ↗
70. 10.1063/1.214008510.1063/1.2140085 ↗