TY - JOUR
T1 - Active and stable plasma-enhanced ALD Pt@Ni-YSZ hydrogen electrode for steam reversible solid oxide cells
AU - Kim, Hyong June
AU - Li, Haoyu
AU - Kim, Daehyun
AU - Park, Geonwoo
AU - Jo, Sung Eun
AU - Ju, Kyoungjae
AU - Han, Geongu
AU - Kwon, Yongchai
AU - Park, Haesun
AU - Lee, Min Hwan
AU - An, Jihwan
N1 - Publisher Copyright:
© 2024 Elsevier B.V.
PY - 2025/3
Y1 - 2025/3
N2 - Designing and fabricating active and thermally stable bifunctional catalysts with minimal noble metal loadings are crucial for reversible solid oxide cells (rSOCs). This study employed Pt nanoparticles fabricated via plasma-enhanced atomic layer deposition (PEALD) to a nickel-yttria stabilized zirconia (Ni-YSZ) electrode to serve as effective catalysts in fuel cell and electrolysis modes. Despite the minimal Pt catalyst loading (<1 μg cm–2), the PEALD Pt@Ni-YSZ catalytic electrode exhibited superior electrochemical performance, (20 % higher than the bare cell), both in the fuel cell and electrolysis modes. Remarkably, this performance is sustained without any degradation over a 50 h duration at 700 °C. Dissimilar stabilization behaviors of the Pt catalysts occurred as distributed fine particles on Ni and anchored coarsened particles at the grain boundaries on YSZ surfaces. Furthermore, the mechanism of the enhanced hydrogen evolution/oxidation reactions with the PEALD Pt@Ni-YSZ electrode was verified using density functional theory simulations.
AB - Designing and fabricating active and thermally stable bifunctional catalysts with minimal noble metal loadings are crucial for reversible solid oxide cells (rSOCs). This study employed Pt nanoparticles fabricated via plasma-enhanced atomic layer deposition (PEALD) to a nickel-yttria stabilized zirconia (Ni-YSZ) electrode to serve as effective catalysts in fuel cell and electrolysis modes. Despite the minimal Pt catalyst loading (<1 μg cm–2), the PEALD Pt@Ni-YSZ catalytic electrode exhibited superior electrochemical performance, (20 % higher than the bare cell), both in the fuel cell and electrolysis modes. Remarkably, this performance is sustained without any degradation over a 50 h duration at 700 °C. Dissimilar stabilization behaviors of the Pt catalysts occurred as distributed fine particles on Ni and anchored coarsened particles at the grain boundaries on YSZ surfaces. Furthermore, the mechanism of the enhanced hydrogen evolution/oxidation reactions with the PEALD Pt@Ni-YSZ electrode was verified using density functional theory simulations.
KW - Hydrogen evolution reaction
KW - Hydrogen oxidation reaction
KW - Plasma enhanced atomic layer deposition
KW - Platinum catalyst
KW - Reversible solid oxide cell
UR - https://www.scopus.com/pages/publications/85207089231
U2 - 10.1016/j.apcatb.2024.124740
DO - 10.1016/j.apcatb.2024.124740
M3 - Article
AN - SCOPUS:85207089231
SN - 0926-3373
VL - 362
JO - Applied Catalysis B: Environmental
JF - Applied Catalysis B: Environmental
M1 - 124740
ER -