4.7 Article

Interfacial coupling perovskite CeFeO3 on layered graphitic carbon nitride as a multifunctional Z-scheme photocatalyst for boosting nitrogen fixation and organic pollutants demineralization

期刊

CHEMICAL ENGINEERING JOURNAL
卷 427, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2021.131406

关键词

Perovskite; Carbon graphitic nitride; Z-scheme; Photocatalysis

资金

  1. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Education [2021R1A6A1A03038785]
  2. National Research Foundation [2020R1F1A1075839]
  3. National Research Foundation of Korea [2020R1F1A1075839, 00000001] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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The study successfully synthesized a PCN@CFO1 photocatalyst with excellent catalytic performance and stable reusability through a simple one-step calcination strategy, which efficiently removed organic micropollutants.
The application of pristine graphitic carbon nitride (PCN, g-C3N4)/cerium ferrite (CeFeO3, CFO) composites as photocatalysts for energy production and water treatment has not yet been reported despite its great potential. In this study, CFO, an orthorhombic perovskite-type oxide, was covalently coupled to PCN via a facile single-step calcination strategy. Compared to PCN, optimized 1% CFO-doped PCN (PCN@CFO1) exhibited wide ranges of organic-micropollutant removal (sulfamethoxazole (SMX), atrazine, and bisphenol A) and achieved approximately 49.9% of total-organic-carbon (TOC) removal for SMX in 4 h with 5 stable reusable performances. Further, scavenger experiments and the electron paramagnetic resonance (EPR) spin-trap analysis revealed that PCN@CFO1 could produce superoxide (O-2(-center dot)) and hydroxyl radicals (center dot OH) for organic-pollutant degradation. Meanwhile, the intermediate species of organic pollutants were investigated using liquid chromatography-tandem mass spectrometry to identify the degradation pathways. Of note, PCN@CFO1 achieved up to 573.12 mu mol(-1) g(-1) of ammonia production rate and 2.92% of apparent quantum efficiency of nitrogen photo-fixation at 400 nm, which was 8 times higher than that of PCN. Through coupling CFO and PCN, the flat band potential was found to be upshifted, and a high ratio of the Ce3+ interface associated with oxygen vacancies was generated, resulting in the formation of a Z-scheme system. Remarkably, the formation of the Z-scheme structure on PCN@CFO1 showed enhancement in charge transfer, hydrophilicity, and charge separation, significantly improving the photocatalytic performance for organic-micropollutant demineralization and nitrogen photo-fixation under UVA-LED (400 nm) light irradiation. Our study provided a facile and scalable preparation strategy for multifunctional photocatalysts that could be effectively activated under energy-efficient UVA-LED irradiation for energy production and emerging pollutants degradation.

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