Structural Characterization of Carbon‐Doped and Carbon‐Coated Core–Shell TiO2 Nanoparticles

  • Carbon‐doped TiO2 nanoparticles were prepared by a facile carbothermal treatment at different temperatures. The synthesis was conducted in a rotary tube furnace under an acetylene/nitrogen gas flow. A detailed analysis of the morphology of the particles revealed a layered graphene structure surrounding the TiO2core with a temperature‐shell thickness of 1–1.5 nm. The material exhibits a significant shift in the Raman Eg(1) mode toward higher wavenumbers. High carbon contents were determined by X‐ray photoelectron spectroscopy. This led to the conclusion that in addition to the carbon in the shell, carbon is also incorporated into the TiO2 structure. Substitutional doping in favor of titanium or oxygen atoms could be excluded based on XPS measurements due to the absence of Ti–C bonds and the lack of changes in lattice parameters of the unit cell or microstrain. An interstitial incorporation of carbon is therefore most likely. Either the incorporation of carbon or the carbon shell suppressed the phase transition from anatase to theCarbon‐doped TiO2 nanoparticles were prepared by a facile carbothermal treatment at different temperatures. The synthesis was conducted in a rotary tube furnace under an acetylene/nitrogen gas flow. A detailed analysis of the morphology of the particles revealed a layered graphene structure surrounding the TiO2core with a temperature‐shell thickness of 1–1.5 nm. The material exhibits a significant shift in the Raman Eg(1) mode toward higher wavenumbers. High carbon contents were determined by X‐ray photoelectron spectroscopy. This led to the conclusion that in addition to the carbon in the shell, carbon is also incorporated into the TiO2 structure. Substitutional doping in favor of titanium or oxygen atoms could be excluded based on XPS measurements due to the absence of Ti–C bonds and the lack of changes in lattice parameters of the unit cell or microstrain. An interstitial incorporation of carbon is therefore most likely. Either the incorporation of carbon or the carbon shell suppressed the phase transition from anatase to the thermodynamically stable rutile which is expected above 600 Celsius. Additionally, the process inhibits the crystallite growth at higher treatment temperatures.…show moreshow less

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Author:Dominik EitelORCiD, Sabrina PanzerORCiD, Ulrich HagemannORCiD, Markus HeidelmannORCiD, Fabio JosephORCiD, Jens HelbigORCiD, Uta HelbigORCiD, Melanie KaliwodaORCiD, Ulrich Teipel
DOI:https://doi.org/10.1002/admi.202500770
ISSN:2196-7350
Parent Title (English):Advanced Materials Interfaces
Publisher:Wiley
Document Type:Article
Language:English
Date of first Publication:2025/12/08
Reviewed:Begutachtet/Reviewed
Release Date:2026/03/02
Volume:13
Issue:2
Article Number:e00770
Pagenumber:12
institutes:Fakultät Werkstofftechnik
Institut für Angewandte Wasserstoffforschung, Elektro- und Thermochemische Energiesysteme (H2Ohm)
Institut für Chemie, Material- und Produktentwicklung
Research Themes:Materialien & Produktionstechnik
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