4.7 Article

Construction of α-Fe2O3 and Fe/Co-N4 structures with faceted TiO2 nanocrystals for highly efficient degradation of sulfathiazole in water

期刊

JOURNAL OF CLEANER PRODUCTION
卷 220, 期 -, 页码 668-676

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.jclepro.2019.02.168

关键词

TiO2 nanosheets; n-p-n heterojunction; Charge separation; Oxygen activation; Sulfathiazole

资金

  1. Foundation of National Key Scientific Instruments and Equipment Development Project of China [2014YQ060773]
  2. Priority Academic Program Development of Jiangsu Higher Education Institutions

向作者/读者索取更多资源

The severe pollution and scarcity of clean water occurred worldwide. The photocatalysis on semiconductors is highly expected in decontamination or purification of water, although the performance of current semiconductors is extremely restricted by the low efficiency in utilization of sustainable solar energy. An effective strategy for this restriction is the construction of their surface heterojunctions. Unfortunately, the constructed heterojunctions have to be heterotypic because of the band discontinuities at the isotypic interface. Moreover, in most of cases, the constructing does not necessarily improve their performance efficiently due to the inertness of the ground state oxygen in trapping of the separated electrons. In this work, well-faceted TiO2 with coexposed (001) and (101) and selective deposition of alpha-Fe2O3 and Fe/Co-N-4 on the (001) facets was acquired. The overall photocatalytic activity of the well designed composite in degradation of sulfathiazole has enhanced significantly by as much as 5.91 times compared to the bare faceted TiO2, and remained almost the same in 40 recycle usages. The significant performance of the designedly constructed composite was attributed to the remarkably enhanced light absorption, efficient separation of photo-induced charge carriers, oxygen activation and trapping of separated electrons through the Fe/Co-N-4 structure and the n-p-n dual heterojunction. (C) 2019 Elsevier Ltd. All rights reserved.

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