In this study, visible-light-driven carbon self-doped graphitic carbon nitride photocatalyst was fabricated by a facile method with urea and ammonium citrate, and used for photodegradation of bisphenol A (BPA) in the aqueous environment. The experiments indicated that the prepared photocatalyst (CCN) showed high catalytic activity, and 96.0%, 93.2%, and 95.5% BPA could be photodegraded in 150 min under pH 3, 6, and 11, respectively. The photocatalytic degradation rate (0.018 min) and mineralization (27.6%) of CCN for BPA were about 6.7 and 3.5 times higher than those of the g-CN (0.0027 min, 7.87%), respectively. CCN had high reusability with a photodegradation efficiency of 84.5% for BPA after 3 cycles. Moreover, CCN introduced additional carbon atoms, which generated C-O-C bonds in the g-CN lattice. In contrast to g-CN, carbon doping enhanced the visible light absorption range of CCN, reduced its band gap, and improved the separation efficiency of photogenerated electron-hole pairs. Radical quenching experiment and ESR results revealed that superoxide radicals (•O) and photogenerated holes (h) acted as important parts in the high photodegradation activity under visible light irradiation. This work puts forward a one-pot strategy for the preparation of carbon self-doped g-CN, displacing the high-energy consuming and complicated preparation technology with promising industrial applications.
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http://dx.doi.org/10.1007/s11356-023-26928-z | DOI Listing |
Spectrochim Acta A Mol Biomol Spectrosc
December 2024
College of Chemical Engineering, Hubei University of Arts and Science, Xiangyang 441053, Hubei Province, PR China; Hubei Longzhong Laboratory, Xiangyang 441000, Hubei, PR China. Electronic address:
The rapeseed meal, a type of residual by-product of rapeseed oil production was used as the precursor to prepare nitrogen self-doping carbon dots RM-CDs through an easy hydrothermal process. Thanks to the introduction of nitrogen element and oxygen-containing functional groups, RM-CDs had a fluorescence quantum yield of 18.6 %.
View Article and Find Full Text PDFChem Asian J
December 2024
Materials Research Laboratory, Department of Physics, Indian Institute of Technology, Jammu, Jammu and Kashmir, 181221, India.
The ability to tailor surface area, porosity, and morphologies has driven extensive research into the synthesis of metal-organic frameworks derived carbons and their applications in energy storage. This study presents the development of three-dimensional hierarchically porous carbon derived from polystyrene and small-sized zeolitic imidazolate framework-8 (ZIF-8) particles. Incorporating nanometer-sized ZIF-8 particles forms a core-shell structure in the pre-carbonization stage, transforming into a porous carbon material with a range of pores from micro to macropores after carbonization.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
November 2024
School of Chemistry and Chemical Engineering, Hainan University, Haikou, Hainan, 570228, China.
Int J Biol Macromol
December 2024
Jiangsu Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, Jiangsu Provincial Key Lab of Sustainable Pulp and Paper Technology and Biomass Materials, College of Light Industry and Food Engineering, Nanjing Forestry University, Nanjing 210037, China. Electronic address:
Black liquor, primarily consisting of lignin, polysaccharides, and inorganic substances, is a potential precursor of porous carbon materials for high-performance supercapacitors. However, the laborious purification of black liquor lignin and the introduction of exogenous heteroatoms have hindered their practical applications. Herein, the full components of black liquor were utilized to synthesize hierarchical porous sulfur self-doped lignin carbons (S-LCs) through a self-activation process aimed at improving the performance of supercapacitors.
View Article and Find Full Text PDFSmall
January 2025
State Key Laboratory of Advanced Metallurgy, University of Science and Technology Beijing, Beijing, 100083, China.
Petroleum cokes are largely used as low-cost anodes in aluminum industries and general fuels in cement industries, where large amounts of CO are generated. To reduce CO release, it is challenging to develop green strategies for processing abundant petroleum cokes into high-value products, because there are abundant hetero-atoms in petroleum cokes. To overcome such issues, a sustainable electrochemical approach is proposed to convert ultralow-cost high sulfur petroleum coke and iron powders into high-efficiency catalysts for hydrogen evolution reaction (HER).
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