Influence of oxygen vacancy defect on photoelectrochemical performance in interstitial nitrogen doped titanium dioxide photocatalyst

An interstitial nitrogen doped titanium dioxide (N-TiO 2 ) photocatalyst with high concentration of oxygen vacancies (O v ) defect was synthesised using a dry physical method. The successful O v defect was confirmed by PL, XPS and ESR analyses, where the wavelength at 468 nm representing as band-to-sub-band energy, binding energies at 398.7 and 400.3 eV proving the Ti−O−N−O, Ti−O−N or N−O bonding and g-value was obtained at about 1.988 ± 0.01 and 2.045 ± 0.01, attributed to the trapped electron at the surface of Ti 3+ and confirming the presence of hole trapping site. The presence of O v defects in interstitial N-TiO 2 photocatalyst has been extensively studied by researchers; however, their influence on photoelectrochemical (PEC) activity is not yet fully elucidated. In this work, the O v defect demonstrated a lower resistivity, ca. 2.513 ×103 Ω, which promoted rapid electron transfer, thus lowering the rate of electron-hole recombination proven by PL, EIS, and photocurrent responses. Besides, it proved a larger accumulation of electrons at the interface due to contribution as an electron donor, where the carrier concentration ca. 4.27 ×1018 cm -3 . Hence, the photocatalytic degradation for N-TiO 2 photocatalyst was achieved 3.4 times higher as compared to the unmodified TiO 2 photocatalyst, where the rate photoactivity of N-TiO 2 photocatalyst was determined about 0.138 min -1 .

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Publication Details

Journal
Desalination and Water Treatment
Published
2025-10-01
DOI
https://doi.org/10.1016/j.dwt.2025.101537
Primary Topic
TiO2 Photocatalysis and Solar Cells
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article
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article

Influence of oxygen vacancy defect on photoelectrochemical performance in interstitial nitrogen doped titanium dioxide photocatalyst

Mohd Azlan Mohd Ishak, Nadiah Natar, W.I. Nawawi, Mohd Fairul Sharin Abdul Razak et al.
Desalination and Water Treatment
TiO2 Photocatalysis and Solar Cells
article

Influence of oxygen vacancy defect on photoelectrochemical performance in interstitial nitrogen doped titanium dioxide photocatalyst

Mohd Azlan Mohd Ishak, Nadiah Natar, W.I. Nawawi, Mohd Fairul Sharin Abdul Razak, N.A. Muhamad
article en

Abstract

An interstitial nitrogen doped titanium dioxide (N-TiO 2 ) photocatalyst with high concentration of oxygen vacancies (O v ) defect was synthesised using a dry physical method. The successful O v defect was confirmed by PL, XPS and ESR analyses, where the wavelength at 468 nm representing as band-to-sub-band energy, binding energies at 398.7 and 400.3 eV proving the Ti−O−N−O, Ti−O−N or N−O bonding and g-value was obtained at about 1.988 ± 0.01 and 2.045 ± 0.01, attributed to the trapped electron at the surface of Ti 3+ and confirming the presence of hole trapping site. The presence of O v defects in interstitial N-TiO 2 photocatalyst has been extensively studied by researchers; however, their influence on photoelectrochemical (PEC) activity is not yet fully elucidated. In this work, the O v defect demonstrated a lower resistivity, ca. 2.513 ×103 Ω, which promoted rapid electron transfer, thus lowering the rate of electron-hole recombination proven by PL, EIS, and photocurrent responses. Besides, it proved a larger accumulation of electrons at the interface due to contribution as an electron donor, where the carrier concentration ca. 4.27 ×1018 cm -3 . Hence, the photocatalytic degradation for N-TiO 2 photocatalyst was achieved 3.4 times higher as compared to the unmodified TiO 2 photocatalyst, where the rate photoactivity of N-TiO 2 photocatalyst was determined about 0.138 min -1 .

Desalination and Water TreatmentVol. 324
Universiti Malaysia Perlis (MY), Universiti Teknologi MARA (MY)
Openalex Percentile: Top 79%
TiO2 Photocatalysis and Solar Cells
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Influence of oxygen vacancy defect on photoelectrochemical performance in interstitial nitrogen doped titanium dioxide photocatalyst — Mohd Azlan Mohd Ishak, Nadiah Natar, et al. · Desalination and Water Treatment (2025) | TGRS Research Map | TGRS