Affiliations 

  • 1 Institute of Atomic and Molecular Sciences , Academia Sinica , Taipei 10617 , Taiwan
  • 2 Department of Materials Science and Engineering , National Chiao Tung University , Hsinchu 30010 , Taiwan
  • 3 School of Materials Science and Engineering , University of Science and Technology Beijing , Beijing 100083 , China
  • 4 Department of Physics , National Cheng Kung University , Tainan 70101 , Taiwan
  • 5 Center for Theoretical Physics, Department of Physics, Faculty of Science , University of Malaya , Kuala Lumpur 50603 , Malaysia
  • 6 Department of Mechanical Engineering , Ming Chi University of Technology , New Taipei City 24301 , Taiwan
ACS Appl Mater Interfaces, 2019 Jan 09;11(1):1655-1664.
PMID: 30561192 DOI: 10.1021/acsami.8b17758

Abstract

The ability of band offsets at multiferroic/metal and multiferroic/electrolyte interfaces in controlling charge transfer and thus altering the photoactivity performance has sparked significant attention in solar energy conversion applications. Here, we demonstrate that the band offsets of the two interfaces play the key role in determining charge transport direction in a downward self-polarized BFO film. Electrons tend to move to BFO/electrolyte interface for water reduction. Our experimental and first-principle calculations reveal that the presence of neodymium (Nd) dopants in BFO enhances the photoelectrochemical performance by reduction of the local electron-hole pair recombination sites and modulation of the band gap to improve the visible light absorption. This opens a promising route to the heterostructure design by modulating the band gap to promote efficient charge transfer.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.