4.7 Article

Experimental and modelling studies on the photocatalytic generation of hydrogen during water-splitting over a commercial TiO2 photocatalyst P25

Journal

ENERGY CONVERSION AND MANAGEMENT
Volume 245, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.enconman.2021.114582

Keywords

Photocatalysis; Hydrogen generation; Titanium dioxide; Mathematical modelling; LED irradiation

Funding

  1. ERDF Institute of Environmental Technology - Excellent Research [CZ.02.1.01/0.0/0.0/16_019/0000853]
  2. Large Research Infrastructure ENREGAT [LM2018098, GA CR 20-09914S]
  3. Specific university research (MSMT) [21-SVV/2021]
  4. Universidad Nacional del Litoral (UNL) [CAI + D 50620190100162LI]
  5. Consejo Nacional de Investigaciones Cientificas y Tecnicas (CONICET) [PIP-2015 0100093]
  6. Agencia Nacional de Promocion Cientifica y Tecnologica (ANPCyT) [PICT 2017-2090]

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This study aims to explore the efficiency of photocatalytic hydrogen production by formulating a phenomenological model, and it reveals that the mass transfer of hydrogen significantly influences the dynamics of the photoreactor. Additionally, experimental results indicate the critical roles of photocatalyst concentration and mass transfer in further research and optimization of photocatalytic reactors for hydrogen production in the future.
Hydrogen, generally perceived as an environmentally friendly fuel, possesses the potential to lower society's dependency on fossil energy sources whose utilization leads inherently to global warming problems. Its photocatalytic generation from aqueous solutions is a promising green technology competitive to traditionally employed methods such as steam reforming or water electrolysis. However, the limiting yet achievable efficiencies of this process remain unclear. To address the question of process efficiencies, we formulate a phenomenological model predicting the behavior of an experimental photocatalytic reactor. The model considers the polynomial light intensity distribution, the concentration of photocatalysts, and the finite rate of the mass transfer between liquid and gas phases. We validate the model against experimental data obtained from a study with a commercially available TiO2 P25 photocatalyst used as a gold standard in photocatalysis. The theoretical analysis shows that the mass transfer of hydrogen from the liquid to gas phase significantly affects the photoreactor dynamics. Initial accumulation of hydrogen in the liquid phase and its delayed transport to the gas phase result in a nonlinear time-dependence of the hydrogen concentration in the gas phase. The theoretical average reaction rate reaches a maximum for a photocatalyst concentration of 0.23 g/L, which is in good agreement with an experimentally obtained value of 0.25 g/L. The photonic efficiency, defined as a ratio of the average reaction rate to the average light intensity, also reaches a maximum at the same catalyst concentration and interestingly remains constant for any higher TiO2 loads. Finding the optimal photocatalyst concentration and identifying the critical role of mass transfer shall aid further research in developing and optimizing photocatalytic reactors for hydrogen production in the future.

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