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C,N-Codoped TiO₂ with a Nitrogen-Doped Carbon Coating Derived from 2,6-Diaminopyridine for Visible Light-Induced Photocatalytic Hydrogen Evolution

Author:
Xu, Xing, Lai, Lei, Jiang, Jiahong, He, Zhiqiao, Song, Shuang
Source:
Journal of physical chemistry 2019 v.123 no.15 pp. 9702-9712
ISSN:
1932-7455
Subject:
Raman spectroscopy, X-ray photoelectron spectroscopy, absorption, carbon, coatings, dielectric spectroscopy, hydrogen production, hydrolysis, lighting, nitrogen, photocatalysis, photocatalysts, photoluminescence, reflectance spectroscopy, titanium dioxide, transmission electron microscopy
Abstract:
Nitrogen-doped carbon-wrapped C,N-codoped TiO₂ (CN@C,N-TiO₂) was successfully prepared using a facile and efficient method involving hydrolysis and calcination under Ar using tetrabutyl titanate and 2,6-diaminopyridine as the precursors. X-ray photoelectron spectroscopy (XPS) and valence band XPS measurements reveal the successful codoping of interstitial carbon and nitrogen into TiO₂, which leads to a visible-light absorption of up to ∼550 nm in the UV–vis diffuse reflectance spectra. Raman spectra and high-resolution transmission electron microscopy results show that N-doped carbon exists on the surface of C,N-TiO₂, which gives rise to the efficient separation of photoexcited charge carriers, as determined by photoluminescence and electrochemical impedance spectroscopy. Benefiting from the combined effects of a surface-coated N-doped carbon layer and C,N-codoping, the photocatalyst calcined at 450 °C exhibits remarkable visible-light activity toward the hydrogen evolution reaction in the water splitting process with a H₂ production rate of 833.2 μmol h–¹ g–¹ under 94 mW cm–² visible-light illumination (λ > 420 nm). Moreover, the representative CN@C,N-TiO₂ sample can maintain its activity for at least 40 h.
Agid:
6375161