4.7 Article

Enhancing Charge Transfer in Photocatalytic Hydrogen Production over Dye-Sensitized Pt/TiO2 by Ionic Liquid Coating

期刊

ACS APPLIED ENERGY MATERIALS
卷 4, 期 10, 页码 10931-10939

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsaem.1c01553

关键词

photocatalytic water splitting; hydrogen production; ionic liquid; dye sensitization; photoconversion efficiency

资金

  1. Scientific and Technological Research Council of Turkey (TUBITAK) [217M528]
  2. Bogazici University Scientific Research Projects (BAP) [14002]

向作者/读者索取更多资源

Photocatalytic hydrogen production is considered as a cost-efficient method to produce hydrogen fuel with minimal environmental impact. In this study, a photocatalyst system composed of Pt/TiO2 and dye-sensitized Pt/TiO2 particulates encapsulated by an ionic liquid is proposed, which significantly enhances the efficiency of hydrogen production. Various analyses showed that the ionic liquid coating improves charge transfer and prevents recombination of electron-hole pairs, leading to increased hydrogen production rates.
Photocatalytic hydrogen production from water is considered to be a potentially cost-efficient method to produce hydrogen fuel with little impact on the environment. Nevertheless, hydrogen production efficiencies via photocatalysis remain to be low. Here, a photocatalyst system composed of 1 wt % Pt/TiO2 and dye-sensitized Pt/TiO2 particulates encapsulated by an ionic liquid is proposed. In particular, the enhancement of photocatalytic hydrogen production over 1 wt % Pt/TiO2 particulates sensitized with N719 dye (di-tetrabutylammonium cis-bis(isothiocyanato)bis(2,2'-bipyridyl-4,4'-dicarboxylato) ruthenium(II)) and coated by a thin layer of ionic liquid [BMIM][BF4] (1-butyl-3-methylimidazolium tetrafluoroborate) has been investigated. The Pt was loaded onto the TiO2 surface by incipient wetness impregnation, while the dye and ionic liquid were loaded by solvent evaporation using ethanol and acetone, respectively. The photocatalytic tests were performed in a semibatch glass reactor under visible light irradiation provided by a solar simulator; the hydrogen production rates over Pt/TiO2, dye-sensitized Pt/TiO2, ionic liquid-coated Pt/TiO2, and ionic liquid-coated Pt/TiO2 after dye sensitization were compared. The hydrogen production rate was similar to 21 mu mol/h.gcat on Pt/TiO2, and it increased to similar to 27 mu mol/h.gcat with dye sensitization, while the [BMIM][BF4] coating alone improved hydrogen production three times (similar to 60 mu mol/h.g(cat)). Coating the dye-sensitized particulates with an ionic liquid resulted in another 17% increase in hydrogen production (similar to 70 mu mol/h.g(cat)). Scanning electron microscopy-energy dispersive X-ray analysis (SEM-EDAX), contrast transmission electron microscopy (CTEM), X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, UV-vis characterization of the photocatalysts and electrochemical analysis of the respective photoelectrodes were also performed. The ionic liquid coating increased the performance of Pt/TiO2 by providing better charge transfer between the photocatalyst and the aqueous reaction medium while simultaneously preventing the recombination of photogenerated electron-hole pairs. The improved performance of the dye-sensitized photocatalyst upon the ionic liquid coating indicated that the ionic liquid stabilized the dye on the photocatalyst surface while simultaneously enhancing the charge transfer between the dye and TiO2.

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