4.7 Article

Surfactant and TiO2 underlayer derived porous hematite nanoball array photoanode for enhanced photoelectrochemical water oxidation

期刊

CHEMICAL ENGINEERING JOURNAL
卷 320, 期 -, 页码 81-92

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2017.03.040

关键词

Hematite; Photoelectrochemical; Water oxidation; TiO2 underlayer; CTAB surfactant; Porous nanoballs

资金

  1. BK21 Plus program, the basic science research programs of the National Research Foundation of Korea (NRF) [2012R1A6A3A04038530]
  2. Korea Ministry of Environment (MOE) [2014000160001]
  3. Korea Research Institute of Standards and Science (KRISS) under the project Establishing Measurement Standards for Inorganic Analysis [15011044]

向作者/读者索取更多资源

Controlling the morphology of semiconductors at the nanoscale level is the key for efficient photoelectrochemical (PEC) water splitting systems. Herein, we report for the first time the fabrication of porous hematite nanoball array film on conducting FTO via a facile pulse reverse electrodeposition method using cetyltrimethylammonium bromide (CTAB) surfactant and a TiO2 underlayer (UL) on FTO. A prolonged low-temperature-annealing treatment is employed to convert iron into hematite (alpha-Fe2O3) and to remove the surfactant molecules gradually. Annihilation of surfactant molecules led to the creation of pores during crystallization of hematite nanoballs, thereby providing low-resistant diffusion pathways for the migration and incorporation of cations (TO4+ from UL and Sn4+ from FTO) in hematite. The hematite photoanode with porous nanoball array exhibited significantly higher PEC performance than the flat hematite due to sixfold enrichment in the donor density, improved charge-transfer properties, and higher light absorption. The enhancement in photocurrent and water oxidation performance of porous hematite photoanode is also feasible when coupled with well-known Co and CoPi catalysts. Thus, our new approach allowed the simple fabrication of hematite films with nanoporous architecture for enabling high photon harvesting and maximized interfacial charge transfer to facilitate water oxidation reaction. (C) 2017 Elsevier B.V. All rights reserved.

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