期刊
JOURNAL OF COLLOID AND INTERFACE SCIENCE
卷 597, 期 -, 页码 39-47出版社
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2021.03.159
关键词
Graphitic carbon nitride (g-CN); 2,6-dimethylmorpholine (MP); Pollutant degradation; Hydrogen evolution rate (HER)
资金
- University Grants Commission (UGC) Major Research Project (MRP) New Delhi [37-171/2009(SR)]
- Basic Scientific Research (BRNS) New Delhi [F-25-1/2013-14(BSR)/7-226/2009]
The incorporation of organic electron-rich heterocyclic monomer 2,6-dimethylmorpholine (MP) into electron-poor graphitic carbon nitride (g-CN) semiconductor by solid-state co-polymerization for photocatalytic hydrogen evolution from Rhodamine B dyes (RhB) has been shown to enhance the performance significantly. The results indicate the potential for tailor-designed photocatalysts with effective pollutant degradable capabilities, with the CN-MP copolymer showing six times higher hydrogen evolution rate and two times higher pseudo-order kinetic constant for RhB photodegradation compared to g-CN.
The development of superior heterogeneous catalyst for hydrogen (H-2) evolution is a significant feature and challenging for determining the energy and environmental crises. However, the dumping of numerous lethal colorants (dye) as of textile manufacturing has fascinated widespread devotion-aimed water pollution anticipation and treatment. In this regard, a photocatalytic H-2 evolution by visible light using low-dimensional semiconducting materials having pollutant degradable capacity for Rhodamine B dyes (RhB) has been anticipated as a route towards environmental aspect. Here we fabricated the incorporation of organic electron-rich heterocyclic monomer 2,6-dimethylmorpholine (MP), inside electron-poor graphitic carbon nitride (g-CN) semiconductor by solid-state co-polymerization. The supremacy of copolymerization process was successfully examined via absorbent, calculated band gap, and migration of electrons on the photocatalytic performance of as-constructed CN-MP copolymer. The density functional theory (DFT) calculation provides extra support as evident for the successful integration of MP into the g-CN framework by this means-reduced band gap upon co-polymerization. The hydrogen evolution rate (HER) for g-CN was found as 115.2 lmol/h, whereas for CN-PM0.1 was estimated at 641.2 lmol/h (six times higher). In particular, the pseudo-order kinetic constant of CN-MP0.1 for photodegradation of RhB was two times higher than that of g-CN. Results show an important step toward tailor-designed and explain the vital role of the D-A system for the rational motifs of productive photocatalysts with effective pollutant degradable capability for future demand. (C) 2021 Elsevier Inc. All rights reserved.
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