Journal ArticleDOI
Eosin Y-sensitized graphitic carbon nitride fabricated by heating urea for visible light photocatalytic hydrogen evolution: the effect of the pyrolysis temperature of urea
TLDR
The photocatalytic activity for hydrogen evolution from aqueous triethanolamine solution was investigated and the highest activity can be attributed to the pure composition, the higher dye adsorption amount and the lowest defect concentration.Abstract:
Graphitic carbon nitride (g-C3N4) was prepared by pyrolysis of urea at different temperatures (450–650 °C), and characterized by thermogravimetric and differential thermal analysis (TG-DTA), elemental analysis (C/H/N), X-ray diffraction (XRD), UV-vis diffuse reflectance spectra (DRS), Brunauer–Emmett–Teller (BET) analysis, Fourier transform-infrared (FT-IR) spectroscopy, X-ray photoelectron spectroscopy (XPS), and photoluminescence (PL) spectra. The samples prepared at low temperatures (450 and 500 °C) are a mixture of g-C3N4 and impurities, whereas the samples prepared at high temperatures (550, 600 and 650 °C) should be g-C3N4 (polymeric carbon nitride). The polymerization degree of g-C3N4 for the prepared samples increases to a maximum at 600 °C with increasing pyrolysis temperature and then decreases, whereas the defect concentration changes conversely, that is, g-C3N4 prepared at 600 °C has the lowest defect concentration. Using Eosin Y (EY) and the prepared sample as the sensitizer and the matrix, respectively, the photocatalytic activity for hydrogen evolution from aqueous triethanolamine solution was investigated. The g-C3N4 prepared at 600 °C exhibits the highest sensitization activity. Under optimum conditions (1.25 × 10−5 mol L−1 EY and 7.0 wt% Pt), the maximal apparent quantum yield of EY-sensitized g-C3N4 prepared at 600 °C for hydrogen evolution is 18.8%. The highest activity can be attributed to the pure composition, the higher dye adsorption amount and the lowest defect concentration.read more
Citations
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Journal ArticleDOI
Graphitic Carbon Nitride (g-C3N4)-Based Photocatalysts for Artificial Photosynthesis and Environmental Remediation: Are We a Step Closer To Achieving Sustainability?
TL;DR: It is anticipated that this review can stimulate a new research doorway to facilitate the next generation of g-C3N4-based photocatalysts with ameliorated performances by harnessing the outstanding structural, electronic, and optical properties for the development of a sustainable future without environmental detriment.
Journal ArticleDOI
Polymeric Photocatalysts Based on Graphitic Carbon Nitride
TL;DR: The photo-catalytic applications of g-C3N4 -based photocatalysts in the fields of water splitting, CO2 reduction, pollutant degradation, organic syntheses, and bacterial disinfection are reviewed, with emphasis on photocatalysis promoted by carbon materials, non-noble-metal coc atalysts, and Z-scheme heterojunctions.
Journal ArticleDOI
A review on g-C3N4-based photocatalysts
TL;DR: In this paper, the fundamental mechanism of heterogeneous photocatalysis, advantages, challenges and the design considerations of g-C3N4-based photocatalysts are summarized, including their crystal structural, surface phisicochemical, stability, optical, adsorption, electrochemical, photoelectrochemical and electronic properties.
Journal ArticleDOI
Alkali-Assisted Synthesis of Nitrogen Deficient Graphitic Carbon Nitride with Tunable Band Structures for Efficient Visible-Light-Driven Hydrogen Evolution.
Huijun Yu,Run Shi,Yunxuan Zhao,Tong Bian,Yufei Zhao,Chao Zhou,Geoffrey I. N. Waterhouse,Li-Zhu Wu,Chen-Ho Tung,Tierui Zhang +9 more
TL;DR: A facile synthetic strategy for nitrogen-deficient graphitic carbon nitride (g-C3 Nx) is established, involving a simple alkali-assisted thermal polymerization of urea, melamine, or thiourea, with superior visible-light photocatalytic performance compared to pristine g-C2 N4.
Journal ArticleDOI
Sulfur-doped g-C3N4 with enhanced photocatalytic CO2-reduction performance
TL;DR: In this article, a sulfur-doped graphitic carbon nitride (g-C 3 N 4 ) was fabricated by simply calcinating thiourea at 520°C, and it was found to absorb light up to 475nm corresponding to a band gap of 2.63 eV.
References
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Journal ArticleDOI
A metal-free polymeric photocatalyst for hydrogen production from water under visible light
Xinchen Wang,Kazuhiko Maeda,Arne Thomas,Kazuhiro Takanabe,Gang Xin,Johan M. Carlsson,Kazunari Domen,Markus Antonietti +7 more
TL;DR: It is shown that an abundant material, polymeric carbon nitride, can produce hydrogen from water under visible-light irradiation in the presence of a sacrificial donor.
Journal ArticleDOI
Graphitic carbon nitride materials: variation of structure and morphology and their use as metal-free catalysts
Arne Thomas,Anna Fischer,Frédéric Goettmann,Markus Antonietti,Jens Oliver Müller,Robert Schlögl,Johan M. Carlsson +6 more
TL;DR: In this paper, high resolution transmission electron microscopy proves the extended two-dimensional character of the condensation motif of graphitic carbon nitride, and a new family of metal nitride nanostructures can also be accessed from the corresponding oxides.
Journal ArticleDOI
Photodegradation Performance of g-C3N4 Fabricated by Directly Heating Melamine
TL;DR: The results clearly indicate that the metal-free g-C(3)N(4) has good performance in photodegradation of organic pollutant.
Journal ArticleDOI
Unique Electronic Structure Induced High Photoreactivity of Sulfur-Doped Graphitic C3N4
TL;DR: The homogeneous substitution of sulfur for lattice nitrogen and a concomitant quantum confinement effect are identified as the cause of this unique electronic structure and the excellent photoreactivity of C(3)N(4-x)S(x), which may shed light on general doping strategies for designing potentially efficient photocatalysts.
Journal ArticleDOI
Preparation and Enhanced Visible-Light Photocatalytic H2-Production Activity of Graphene/C3N4 Composites
TL;DR: Graphene and graphitic carbon nitride composite photocatalysts were prepared by a combined impregnation−chemical reduction strategy involving polymerization of melamine in the presence of graphene oxide (precursors) and hydrazine hydrate (reducing agent), followed by thermal treatment at 550 °C under flowing nitrogen as mentioned in this paper.