Authors
Vatsala Cilamkoti, Nitika, Ritika Saroha, Shashikant, Deepak Yadav, Monojit Bag, Swastika Banerjee, R K Dutta
Published in
Nanoscale. Jul 10, 2026. Epub Jul 10, 2026.
Abstract
Achieving stable p-type TiO2 with multifunctional catalytic activity remains a long-standing challenge due to intrinsic defect compensation and poor charge transport. Here, we report a hydrothermal strategy to synthesize stable p-type TiO2 nanoparticles via surface modification with nitrogen-functionalized carbon dots (TiO2/N-CD). Density functional theory (DFT)-based studies reveal strong electron transfer from N-CD to Ti- and O-vacancy sites on the Ti143O286 surface, stabilizing defects through electrostatic interaction and modulating Ti and O states near the Fermi level, resulting in titanium-vacancy-driven p-type conductivity. The structure, morphology, composition, texture, and optical and electrochemical properties of TiO2/N-CD are thoroughly characterized. TiO2/N-CD exhibits 96% photocatalytic degradation of tetracycline in water within 90 min (0.030 min-1) attributed to in situ hydroxyl radical generation, which is corroborated by enhanced charge carrier mobility and confirmed by electrochemical impedance spectroscopy and enhanced photocurrent measurements. Additionally, TiO2/N-CD5 exhibited efficient and stable oxygen evolution in alkaline media for 24 h (η10 = 322 mV, corresponding to a Tafel slope of 56 mV dec-1). Computational results further indicate strong H2O adsorption (Eads = -1.37 eV), as corroborated by the wettability of the TiO2/N-CD surface and a favorable pH-dependent lattice oxygen mechanism. This work establishes N-CD-modified p-type TiO2 as a versatile platform for energy and environmental applications.
PMID:
42429034
Bibliographic data and abstract were imported from PubMed on 10 Jul 2026.
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