4.7 Article

Direct Z-scheme heterostructure of p-CuAl2O4/n-Bi2WO6 composite nanofibers for efficient overall water splitting and photodegradation

期刊

JOURNAL OF COLLOID AND INTERFACE SCIENCE
卷 550, 期 -, 页码 170-179

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2019.04.099

关键词

p-n heterostructure; Z-scheme; Overall water splitting; Photodegradation

资金

  1. National Natural Science Foundation of China [51572045, 51732003, 61803080, 91233204]
  2. 111 Project [B13013]
  3. China Postdoctoral Science Foundation [2017M610188, 2018T110240]
  4. Science and Technology Development Program of Jilin Province [20180520192JH]
  5. The 13th five-year plan: science and technology research project of the education department of Jilin Province [JJKH20180018KJ]

向作者/读者索取更多资源

Constructing heterostructures can facilitate photoinduced charge separation, leading to enhanced photo catalytic performance. However, spatial separation of charge carriers in traditional type II heterojunctions is at the expense of their redox ability. In this paper, well-designed direct Z-scheme systems (ZSS) of p-CuAl2O4/n-Bi2WO6 composite nanofibers with uniform non-woven web nanostructure was built by electrospinning technique and solvothermal reactions. The formation mechanism of the ZSS and the charge migration pathway is investigated in detail. Results show that as-prepared composite nanofibers exhibit desirable photocatalytic performance for overall water splitting due to its stronger redox power and efficient charge separation. Meantime, it shows great activity for photodegradation of various organic pollutant models (RhB, MO, 4-NP), which is 1 order of magnitude higher than the single-component CuAl2O4 and Bi2WO6. Furthermore, the composite nanofibers exhibit well separable properties by natural sedimentation because of its ultra-long and non-woven web nanostructure. The paper explores CuAl2O4 and its Z-scheme heterostructures in water splitting for the first time, which may highlight its new applications. (C) 2019 Published by Elsevier Inc.

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