TY - JOUR
T1 - BaO-modified finger-like nickel-based anode for enhanced performance and durability of direct carbon solid oxide fuel cells
AU - Li, Lin
AU - Xie, Yujiao
AU - Han, Tingting
AU - Zhang, Jinjin
AU - Yu, Fangyong
AU - Li, Gen
AU - Sunarso, Jaka
AU - Yang, Naitao
AU - Li, Yongdan
N1 - Publisher Copyright:
© 2024 Elsevier Ltd
PY - 2024/7/15
Y1 - 2024/7/15
N2 - Direct carbon solid oxide fuel cells (DC-SOFCs) are hopeful high-temperature energy conversion devices with all-solid-state structure, high efficiency, and low emission. The anode catalytic activity is a direct limiting factor in the electrochemical performance of DC-SOFCs. Here, we successfully fabricated a finger-like Ni-based anode/electrolyte in one step, followed by infiltrating BaO within the anode, which significantly improved the anodic reaction and DC-SOFC performance. At 850 °C, the BaO/Ni-YSZ anode-supported DC-SOFC gave the optimal output of 505 and 825 mW cm−2 powering by activated carbon and hydrogen, respectively, which were significantly superior to those of the cell with traditional Ni-YSZ anode. Moreover, DC-SOFC with BaO/Ni-YSZ anode exhibited more stable operation for 20.9 h under 100 mA at 850 °C, giving a relatively high fuel utilization of 23.4 %. These excellent performances can be partially attributed to the smaller particle sizes and more grain boundaries of the BaO/Ni-YSZ anode due to the BaO infiltration, which effectively enhanced the ionic conductivity and mechanical strength of the anode. More importantly, density functional theory simulation revealed that the infiltrated BaO in the Ni-YSZ anode enhanced the adsorption ability of Ni sites for carbon monoxide and oxygen ions, which led to the increased differential charge densities and the reduction in the energy barrier of electrochemical oxidation reaction, thus effectively improving DC-SOFC performance and conversion efficiency.
AB - Direct carbon solid oxide fuel cells (DC-SOFCs) are hopeful high-temperature energy conversion devices with all-solid-state structure, high efficiency, and low emission. The anode catalytic activity is a direct limiting factor in the electrochemical performance of DC-SOFCs. Here, we successfully fabricated a finger-like Ni-based anode/electrolyte in one step, followed by infiltrating BaO within the anode, which significantly improved the anodic reaction and DC-SOFC performance. At 850 °C, the BaO/Ni-YSZ anode-supported DC-SOFC gave the optimal output of 505 and 825 mW cm−2 powering by activated carbon and hydrogen, respectively, which were significantly superior to those of the cell with traditional Ni-YSZ anode. Moreover, DC-SOFC with BaO/Ni-YSZ anode exhibited more stable operation for 20.9 h under 100 mA at 850 °C, giving a relatively high fuel utilization of 23.4 %. These excellent performances can be partially attributed to the smaller particle sizes and more grain boundaries of the BaO/Ni-YSZ anode due to the BaO infiltration, which effectively enhanced the ionic conductivity and mechanical strength of the anode. More importantly, density functional theory simulation revealed that the infiltrated BaO in the Ni-YSZ anode enhanced the adsorption ability of Ni sites for carbon monoxide and oxygen ions, which led to the increased differential charge densities and the reduction in the energy barrier of electrochemical oxidation reaction, thus effectively improving DC-SOFC performance and conversion efficiency.
KW - BaO
KW - DFT
KW - Direct carbon
KW - Finger-like pore
KW - Nickel-based anode
KW - Solid oxide fuel cell
UR - http://www.scopus.com/inward/record.url?scp=85189437840&partnerID=8YFLogxK
U2 - 10.1016/j.fuel.2024.131656
DO - 10.1016/j.fuel.2024.131656
M3 - Article
AN - SCOPUS:85189437840
SN - 0016-2361
VL - 368
JO - Fuel
JF - Fuel
M1 - 131656
ER -