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Porous WO 3 monolith-based photoanodes for high-efficient photoelectrochemical water splitting

  • Yina Wang
  • , Fangfang Zhang
  • , Guoyan Zhao
  • , Yingao Zhao
  • , Yangyang Ren
  • , Huijun Zhang
  • , Linyu Zhang
  • , Jimin Du
  • , Yumin Han
  • , Dae Joon Kang
  • Anyang Normal University
  • Zhengzhou University
  • International Joint Laboratory of Henan Photoelectric Functional Materials
  • Sungkyunkwan University
  • Henan Province Key Laboratory of New Opto-Electronic Functional Materials

Research output: Contribution to journalArticlepeer-review

Abstract

We report a successful fabrication of low-cost, high-efficient, structurally-rigid, porous WO 3 photoelectrochemical (PEC) catalysts using polystyrene as the template by a sol-gel method and a high-temperature annealing treatment. The scanning electron microscopy and Brunauer-Emmett-Teller surface analysis results indicate that such WO 3 monoliths possess a porous structure and a large specific surface area, which can supply lots of photogenerated charge transfer pathways as well as more surface PEC active sites. Compared with a commercially available WO 3 , our highly porous WO 3 PEC catalysts show an excellent PEC water splitting activity. Particularly, the porous WO 3 photoanodes calcinated in the presence of oxygen atmosphere at 450 °C for 7 h show the best PEC performance exhibiting the photocurrent density of 0.97 mA/cm 2 at 1.23 V versus reversible the hydrogen electrode and the incident photon-to-current conversion efficiency up to 48.9% at 420 nm in 0.5 M Na 2 SO 4 electrolyte under AM 1.5 G irradiation. Such excellent PEC performance is due to the high porosity of the WO 3 , promoting the fast transfer and the separation rate of photogenerated carriers during the PEC water splitting process.

Original languageEnglish
Pages (from-to)7302-7308
Number of pages7
JournalCeramics International
Volume45
Issue number6
DOIs
StatePublished - 15 Apr 2019

Keywords

  • Energy conversion
  • Photoanode
  • Porous structures
  • Water splitting
  • WO

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