4.7 Article

MoSx co-catalytic activation of H2O2 by heterogeneous hemin catalyst under visible light irradiation

期刊

JOURNAL OF COLLOID AND INTERFACE SCIENCE
卷 557, 期 -, 页码 301-310

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2019.09.027

关键词

Molybdenum sulfide; Iron-based catalyst; H2O2 activation; Visible light; Photocatalysis

资金

  1. Natural Science Foundation of China [51573134, 21806121]
  2. Tianjin Research Program of Application Foundation and Advanced Technology [15JCQNJC06300]
  3. National College Students Innovation and Entrepreneurship Training Program [201810058047]

向作者/读者索取更多资源

The slow Fe3+/Fe2+ conversion and difficult reactants contact are the main challenges for H2O2 activation using heterogeneous iron-based catalysts. As a typical two-dimensional layered nanomaterial, molybdenum sulfide holds great promise for promoting such process as co-catalysts, but its combination with solid iron catalysts is rarely reported. In this work, we fabricated a novel heterogeneous photocatalyst by directly anchoring amorphous MoSx onto the PAN fibers with hemin via an adsorption and in-situ transformation method. The detailed characterizations show the successful assembly of hemin and MoSx with the fibrous support through axial coordination and electrostatic bonding, respectively. Taking the degradation of organic dyes as model reactions, the as-prepared catalyst achieved remarkably high and stable catalytic performance in the presence of H2O2 under visible light irradiation, which was much superior to that of the single hemin or MoSx supported fibrous catalyst. The enhanced photocatalytic activity is mainly attributed to (i) the excellent adsorption capability of MoSx, which allows the catalyst to easily capture the reactants and (ii) the accelerated rate-limiting step of Fe3+/Fe2+. conversion. In addition, we also explored the MoSx co-catalytic effect on the other iron-based heterogeneous H2O2 activation systems (such as supported Fe3+ or FePc), and similar enhancing effect was observed. Our findings provide a facile and promising strategy to rationally design the advanced oxidation processes for environmental remediation. (C) 2019 Elsevier Inc. All rights reserved.

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