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Open Access

Combining SnO2-x and g-C3N4 nanosheets toward S-scheme heterojunction for high selectivity into green products of NO degradation reaction under visible light

Pham Van Vieta,b, Thanh-Dat Nguyena,b, Dai-Phat Buia,b, Cao Minh Thic( )
Faculty of Materials Science and Technology, University of Science, VNU-HCM, 227 Nguyen Van Cu Street, District 5, Ho Chi Minh City, 700000, Viet Nam
Vietnam National University – Ho Chi Minh City, Thu Duc District, Ho Chi Minh City, 700000, Viet Nam
Ho Chi Minh City University of Technology (HUTECH), 475A Dien Bien Phu Street, Binh Thanh District, Ho Chi Minh City, 700000, Viet Nam
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Abstract

NOx emissions cause many negative impacts on the living environment. The photocatalysis of semiconductors is superior for nitric oxide (NO) degradation due to their low redox potential. In this report, we combine SnO2-x/g-C3N4 heterojunction photocatalyst toward the high selectivity into green products under visible light illumination. Results show that SnO2-x/g-C3N4 heterojunction degraded 40.8% of NO, which is 1.6 times higher than that of g-C3N4. In addition, the selectivity coefficient of SnO2-x/g-C3N4 is higher 3 times than both pure SnO2-x and g-C3N4. Furthermore, SnO2-x/g-C3N4 expresses a superior stability for NO photocatalytic-degradation after five cycles. The scavenger trapping test results, and electron spin resonance (ESR) analysis also provide more understanding of the charge transfer mechanism of materials. SnO2-x/g-C3N4 heterojunction shows a high removal efficiency of NO gas, making it an up-and-coming environmental treatment candidate.

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Journal of Materiomics
Pages 1-8

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Cite this article:
Van Viet P, Nguyen T-D, Bui D-P, et al. Combining SnO2-x and g-C3N4 nanosheets toward S-scheme heterojunction for high selectivity into green products of NO degradation reaction under visible light. Journal of Materiomics, 2022, 8(1): 1-8. https://doi.org/10.1016/j.jmat.2021.06.006

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Received: 12 April 2021
Revised: 01 June 2021
Accepted: 11 June 2021
Published: 17 June 2021
© 2021 The Chinese Ceramic Society.

This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).