Energy and Fuels, cilt.38, sa.14, ss.13228-13244, 2024 (SCI-Expanded)
Complex geometries that are difficult or impossible to achieve with traditional manufacturing techniques can be created through 3D printing today. This method can lead to improved performance and novel designs for gas diffusion electrode (GDE) substrates. In this study, GDE samples are prepared by the 3D printing method and subjected to Pt coating with varying thicknesses using the electron beam evaporation (E-beam) method. GDE samples are denoted BM-C0 (bare), BM-C1 (0.20 μm Cr + 0.20 μm Pt), and BM-C2 (0.20 μm Cr + 0.45 μm Pt). After the coating process, the oxygen evolution reaction (OER) performance of the GDEs is examined in 0.5 M H2SO4. The maximum current density value is obtained as 77.86 mA/cm2 at 1.7 V from the BM-C2 sample. A change in the charge transfer coefficient has been determined in the Tafel curves, resulting from the partial oxidation of Pt. It is determined that the best charge-transfer rate at the electrode/electrolyte interface belongs to the BM-C2 electrode among the GDE samples. According to LSV results, it is revealed that the electrochemical performance of the BM-C2 sample is 14.01 times more improved compared to other GDEs. Furthermore, it is anticipated that a Pt-coated thin film could significantly enhance the performance of GDEs to achieve a competitive performance level in energy conversion devices.