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Effect of tetravalent dopants on hematite nanostructure for enhanced photoelectrochemical water splitting

  • Arunprabaharan Subramanian
  • , Eduardo Gracia-Espino
  • , Alagappan Annamalai*
  • , Hyun Hwi Lee
  • , Su Yong Lee
  • , Sun Hee Choi
  • , Jum Suk Jang
  • *Corresponding author for this work
  • Jeonbuk National University
  • Umeå University
  • Pohang Accelerator Laboratory

Research output: Contribution to journalJournal articlepeer-review

Abstract

In this paper, the influence of tetravalent dopants such as Si 4+ , Sn 4+ , Ti 4+ , and Zr 4+ on the hematite (α-Fe 2 O 3 ) nanostructure for enhanced photoelectrochemical (PEC) water splitting are reported. The tetravalent doping was performed on hydrothermally grown akaganeite (β-FeOOH) nanorods on FTO (fluorine-doped tin-oxide) substrates via a simple dipping method for which the respective metal-precursor solution was used, followed by a high-temperature (800° C) sintering in a box furnace. The photocurrent density for the pristine (hematite) photoanode is ∼0.81 mA/cm 2 at 1.23 V RHE , with an onset potential of 0.72 V RHE ; however, the tetravalent dopants on the hematite nanostructures alter the properties of the pristine photoanode. The Si 4+ -doped hematite photoanode showed a slight photocurrent increment without a changing of the onset potential of the pristine photoanode. The Sn 4+ - and Ti 4+ -doped hematite photoanodes, however, showed an anodic shift of the onset potential with the photocurrent increment at a higher applied potential. Interestingly, the Zr 4+ -doped hematite photoanode exhibited an onset potential that is similar to those of the pristine and Si 4+ -doped hematite, but a larger photocurrent density that is similar to those of the Sn 4+ - and Ti 4+ -doped photoanodes was recorded. The photoactivity of the doped photoanodes at 1.23 V RHE follows the order Zr > Sn > Ti > Si. The onset-potential shifts of the doped photoanodes were investigated using the Ab initio calculations that are well correlated with the experimental data. X-ray diffraction (XRD) and scanning-electron microscopy (FESEM) revealed that both the crystalline phase of the hematite and the nanorod morphology were preserved after the doping procedure. X-ray photoelectron spectroscopy (XPS) confirmed the presence of the tetravalent dopants on the hematite nanostructure. The charge-transfer resistance at the various interfaces of the doped photoanodes was studied using impedance spectroscopy. The doping on the hematite photoanodes was confirmed using the Mott-Schottky (MS) analysis.

Original languageEnglish
Pages (from-to)1203-1212
Number of pages10
JournalApplied Surface Science
Volume427
DOIs
StatePublished - 2018.01.1

Keywords

  • Akaganeite
  • Hematite
  • Nanorods
  • Onset potential
  • Sintering

Quacquarelli Symonds(QS) Subject Topics

  • Materials Science
  • Physics & Astronomy

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