Abstract
Commercial Pt/C (Com. Pt/C) electrocatalysts are considered optimal for oxygen reduction and hydrogen evolution reactions (ORR and HER). However, their high Pt content and poor stability restrict their large-scale application. In this study, photocatalytic synthesis was used to reduce ultrafine Pt nanoparticles in-situ on a composite support of TiO2-decorated nitrogen-doped carbon (TiO2−NC). The nitrogen-doped carbon had a large surface area and electronic effects that ensured the uniform dispersion of TiO2 nanoparticles to form a highly photoactive and stable support. TiO2−NC served as a composite support that enhanced the dispersibility and stability of ultrafine Pt electrocatalyst, owing to the presence of N sites and the strong metal-support interaction. Relative to Com. Pt/C, the as-obtained Pt/TiO2−NC had positive shifts of 44 and 10 mV in the ORR half-wave potential and HER overpotential at −10 mA cm−2, respectively. After an accelerated durability test, Pt/TiO2−NC had lower losses in electrochemical specific area (0.7 %) and electrocatalytic activity (0 mV shift) than Com. Pt/C (25.6 %, 22 mV shift). These results indicate that the developed strategy enabled the facile synthesis and stabilization of ultrafine Pt nanoparticles, which improved the utilization efficiency and long-term stability of Pt-based electrocatalysts.
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Shen, L., Wang, Z., Gong, Q., Zhang, Y., & Wang, J. (2023). Photocatalytic Synthesis of Ultrafine Pt Electrocatalysts with High Stability Using TiO2-Decorated N-Doped Carbon as Composite Support. ChemSusChem, 16(18). https://doi.org/10.1002/cssc.202300393
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