4.6 Article

Advanced oxygen-electrode-supported solid oxide electrochemical cells with Sr(Ti,Fe)O3-δ-based fuel electrodes for electricity generation and hydrogen production

期刊

JOURNAL OF MATERIALS CHEMISTRY A
卷 8, 期 48, 页码 25867-25879

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0ta06678h

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资金

  1. Department of Energy [DE-SC0016965, DE-EE0008437]
  2. National Science Foundation [DMR-1912530]
  3. China Scholarship Council [201606285002]
  4. National Natural Science Foundation of China [51602248]
  5. Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource [NSF ECCS-1542205]
  6. MRSEC program at the Materials Research Center [NSF DMR-1121262]
  7. International Institute for Nanotechnology (IIN)
  8. Keck Foundation
  9. State of Illinois, through the IIN
  10. MRSEC Program of the Materials Research Center at Northwestern University [NSF DMR-1720139]
  11. U.S. Department of Energy (DOE) [DE-SC0016965] Funding Source: U.S. Department of Energy (DOE)

向作者/读者索取更多资源

Sr(Ti0.3Fe0.7)O3-delta (STF) and the associated exsolution electrodes Sr-0.95(Ti0.3Fe0.63Ru0.07)O3-delta (STFR), or Sr-0.95(Ti0.3Fe0.63Ni0.07)O3-delta (STFN) are alternatives to Ni-based cermet fuel electrodes for solid oxide electrochemical cells (SOCs). They can provide improved tolerance to redox cycling and fuel impurities, and may allow direct operation with hydrocarbon fuels. However, such perovskite-oxide-based electrodes present processing challenges for co-sintering with thin electrolytes to make fuel electrode supported SOCs. Thus, they have been mostly limited to electrolyte-supported SOCs. Here, we report the first example of the application of perovskite oxide fuel electrodes in novel oxygen electrode supported SOCs (OESCs) with thin YSZ electrolytes, and demonstrate their excellent performance. The OESCs have La0.8Sr0.2MnO3-delta-Zr0.92Y0.16O2-delta (LSM-YSZ) oxygen electrode-supports that are enhanced via infiltration of SrTi0.3Fe0.6Co0.1O3-delta, while the fuel electrodes are either Ni-YSZ, STF, STFN, or STFR. Fuel cell power density as high as 1.12 W cm(-2) is obtained at 0.7 V and 800 degrees C in humidified hydrogen and air with the STFR electrode, 60% higher than the same cell made with a Ni-YSZ electrode. Electrolysis current density as high as -1.72 A cm(-2) is obtained at 1.3 V and 800 degrees C in 50% H2O to 50% H-2 mode; the STFR cell yields a value 72% higher than the same cell made with a Ni-YSZ electrode, and competitive with the widely used conventional Ni-YSZ-supported cells. The high performance is due in part to the low resistance of the thin YSZ electrolyte, and also to the low fuel electrode polarization resistance, which decreases with fuel electrode in the order: Ni-YSZ > STF > STFN > STFR. The high performance of the latter two electrodes is due to exsolution of catalytic metal nanoparticles; the results are discussed in terms of the microstructure and properties of each electrode material, and surface oxygen exchange resistance values are obtained over a range of conditions for STF, STFN, and STFN. The STF fuel electrodes also provide good stability during redox cycling.

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