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Structural and Physicochemical Properties of Carbon Nitride Nanoparticles via Precursor Thermal Treatment: Effect on Methyl Orange Photocatalytic Discoloration

Laura S. Gómez-VelázquezInstituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas (INIFTA), CCT-La Plata-CONICET, Universidad Nacional de La Plata, 1900 La Plata, ArgentinaLorean MadrizEscuela de Bio y Nanotecnologías, Universidad Nacional de San Martín (UNSAM), Chascomús, B7130 Provincia de Buenos Aires, ArgentinaMonica RigolettoDipartimento di Chimica, Università degli Studi di Torino, Torino 10125, ItaliaEnzo LaurentiDipartimento di Chimica, Università degli Studi di Torino, Torino 10125, ItaliaMonserrat BizarroInstituto de Investigaciones en Materiales, Universidad Nacional Autónoma de México, Circuito Exterior S/N, Ciudad Universitaria, Coyoacán 04510, MéxicoMaría Laura Dell′ArcipreteUniversidad Nacional de La PlataMónica C. GonzálezInstituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas (INIFTA), CCT-La Plata-CONICET, Universidad Nacional de La Plata, 1900 La Plata, Argentina
2023en
ABI

Аннотация

In this work, we synthesized and characterized carbon nitride (CN) nanoparticles obtained by the thermal treatment (550 °C) of urea, melamine, dicyandiamine, and dicyandiamine-barbituric acid in an open reactor and evaluated the effect of different precursors on the photocatalytic performance. CNs obtained from melamine, dicyandiamine, and dicyandiamine-barbituric acid were 3D melon-type structures. On the other hand, CN obtained from urea was a 2D microporous, amorphous structure whose melon or graphitic arrangement could not be determined. The presence of structural defective states (mainly C radicals) was corroborated by EPR studies of the solids. The photocatalytic activity of CN powders for methyl orange (MO) discoloration was investigated using 350 nm and simulated solar light (SSL) irradiation. MO removal efficiencies were correlated with the particle’s energy gap, specific surface area, degree of crystallinity, and C radical defects produced upon irradiation. Moreover, the obtained conduction and valence band potentials in the range of −0.60 and + 2.14 V vs NHE (pH = 7), respectively, evidence CN capacity to oxidize water to hydroxyl radicals (HO•) and reduce O2 to superoxide radical anions (O2•–). The formation of both radicals upon SSL irradiation of CN suspensions was confirmed by EPR experiments. The largest specific surface area, the highest charge carrier density, and the amount of C radical defects observed for CN obtained from urea (CNu) account for their highest photocatalytic performance. However, the estimated CNu photonic efficiency of ca. 8% still indicates a deficient separation/migration efficiency of photoinduced charge carriers. Despite CNu performance being higher than those of other CNs obtained from the thermal treatment of simple precursors, further environmentally friendly strategies are still needed to overcome the intrinsic disadvantages of CN before it may be employed in technological applications. A discussion on probable CN mechanisms forming reactive species and leading to MO decolorization is given.

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