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Post-synthetic modification of graphitic carbon nitride with PCl3 and POCl3 for enhanced photocatalytic degradation of organic compounds
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SYSNO ASEP 0564314 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Článek ve WOS Title Post-synthetic modification of graphitic carbon nitride with PCl3 and POCl3 for enhanced photocatalytic degradation of organic compounds Author(s) Praus, P. (CZ)
Smýkalová, A. (CZ)
Cvejn, D. (CZ)
Losertová, M. (CZ)
Koštejn, Martin (UCHP-M) RID, SAI, ORCID
Novák, V. (CZ)Number of authors 6 Article number 109439 Source Title Diamond and Related Materials. - : Elsevier - ISSN 0925-9635
Roč. 130, DEC 2022 (2022)Number of pages 12 s. Language eng - English Country CH - Switzerland Keywords surface modification ; P doping ; photocatalysis ; POCl3 OECD category Physical chemistry Method of publishing Open access with time embargo (01.01.2025) Institutional support UCHP-M - RVO:67985858 UT WOS 000880001100003 EID SCOPUS 85139844247 DOI 10.1016/j.diamond.2022.109439 Annotation Graphitic carbon nitride (g-C3N4) was synthesised from melamine at 550 degrees C in the air for a period of 4 h. As such prepared g-C3N4 was dispersed in PCl3 and POCl3 with and without pyridine at an ambient temperature for us to dope g-C3N4 with phosphorus. The bulk structural properties of g-C3N4 examined by X-ray diffraction (XRD) and Fourier transformed infrared (FTIR) spectroscopy were not changed. On the contrary, a surface modification in terms of pore size distribution studied using physisorption of nitrogen and electron microscopy was observed. Using PCl3 (in the presence of pyridine), nitrogen vacancies were filled with phosphorus and phosphoramidate groups were formed (with and without pyridine). When POCl3 was used nitrogen vacancies were removed and the surface structure was rearranged, but no phosphorus was doped in g-C3N4. The band gap energies varied from 2.69 to 2.73 eV and specific surface areas varied from 8 to 11 m2 g-1.The g-C3N4 surface structure rearrangement was associated with altered electronic properties which led to higher photocatalytic activity observed by the degradation of Ofloxacin, Amoxicillin and Rhodamine B (RhB) under LED irradiation of 420 nm. A degradation efficiency decreased in the order: Ofloxacin > RhB > Amoxi-cillin. Superoxide radicals were found to be able to react with all the organic compounds, but holes could react only with Ofloxacin and RhB. All the modified materials were more active than the pristine g-C3N4 and the best photocatalyst was prepared through the reaction with PCl3 in the presence of pyridine. Workplace Institute of Chemical Process Fundamentals Contact Eva Jirsová, jirsova@icpf.cas.cz, Tel.: 220 390 227 Year of Publishing 2023 Electronic address https://hdl.handle.net/11104/0336162
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