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In-situ synthesis of AgNbO3/g-C3N4 photocatalyst via microwave heating method for efficiently photocatalytic H2 generation
[Display omitted] This paper is designed for elevating the photocatalytic H2-evoultion performance of g-C3N4 through the modification of AgNbO3 nanocubes. Via the microwave heating method, g-C3N4 was in-situ formed on AgNbO3 surface to fabricate a close contact between the two semiconductors in fort...
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Published in: | Journal of colloid and interface science 2019-01, Vol.534, p.163-171 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | [Display omitted]
This paper is designed for elevating the photocatalytic H2-evoultion performance of g-C3N4 through the modification of AgNbO3 nanocubes. Via the microwave heating method, g-C3N4 was in-situ formed on AgNbO3 surface to fabricate a close contact between the two semiconductors in forty minutes. X-ray diffraction (XRD), Fourier transform-infrared (FT-IR), X-ray photoelectron spectroscopy (XPS) experiments were performed to confirm the binary structure of the synthesized AgNbO3/g-C3N4 composite. N2-adsorption and visible diffuse reflection spectroscopy (DRS) analyses indicated that the addition of AgNbO3 to g-C3N4 showed nearly negligible influence on the specific surface area and the optical property. Photoluminescence (PL) spectroscopy experiment suggested that the AgNbO3/g-C3N4 displayed reduced PL emission and longer lifetime of photoexcited charge carriers than g-C3N4, which could be ascribed to the suitable band potential and the intimate contact of g-C3N4 and AgNbO3. This result was also confirmed by the transient photocurrent response experiment. The influence of the enhanced charge separation was displayed in their photocatalytic reaction. AgNbO3/g-C3N4 sample showed enhanced performance in photocatalytic H2-generation under visible light illumination. The H2-evolution rate is determined to be 88 μmol·g−1·h−1, which reaches 2.0 times of g-C3N4. This study provides a feasible and rapid approach to fabricate g-C3N4 based composite. |
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ISSN: | 0021-9797 1095-7103 |
DOI: | 10.1016/j.jcis.2018.09.025 |