TY - JOUR
T1 - Exploring mixed proton/electron conducting air electrode materials in protonic electrolysis cell
AU - Leonard, Kwati
AU - Druce, John
AU - Thoreton, Vincent
AU - Kilner, John A.
AU - Matsumoto, Hiroshige
N1 - Funding Information:
This work was supported by JSPS Core-to-Core Program, Advance research Network and by World Premier International Research (WPI), MEXT Japan.
Funding Information:
This work was supported by JSPS Core-to-Core Program, Advance research Network and by World Premier International Research (WPI), MEXT Japan.
Publisher Copyright:
© 2018 Elsevier B.V.
PY - 2018/6
Y1 - 2018/6
N2 - In this work, we investigate and compare the performance and cell polarization resistance of Ba0.5La0.5CoO3−δ (BLC) and double perovskite oxide BaGd0.8La0.2Co2O6−δ (BGLC) anode on cathode supported protonic steam electrolysis cells using a 20 μm SrZr0.5Ce0.4Y0.1O3−δ electrolyte with Ni-SZCY541 composite as the cathode. The kinetics of protons through the bulk and across the gas electrolyte interfaces of both anode materials were also studied by direct measurement of their tracer diffusions using time-of-flight secondary ion mass spectrometry depth profiling (TOF-SIMS). Cell terminal voltages of 1.74 and 1.93 V, were observed at a current density of 0.5 A cm−2 for both BLC and BGLC whereas a hydrogen evolution rate of 121.85 and 111.15 μmol cm−2 every minute was also obtained at the same current density, translating to a current efficiency of 78 and 72% respectively. Hydrogen tracer diffusion studies confirm BGLC can incorporate protons into the bulk relative to BLC even though the present steam electrolysis results show a better performance for BLC at 600 °C.
AB - In this work, we investigate and compare the performance and cell polarization resistance of Ba0.5La0.5CoO3−δ (BLC) and double perovskite oxide BaGd0.8La0.2Co2O6−δ (BGLC) anode on cathode supported protonic steam electrolysis cells using a 20 μm SrZr0.5Ce0.4Y0.1O3−δ electrolyte with Ni-SZCY541 composite as the cathode. The kinetics of protons through the bulk and across the gas electrolyte interfaces of both anode materials were also studied by direct measurement of their tracer diffusions using time-of-flight secondary ion mass spectrometry depth profiling (TOF-SIMS). Cell terminal voltages of 1.74 and 1.93 V, were observed at a current density of 0.5 A cm−2 for both BLC and BGLC whereas a hydrogen evolution rate of 121.85 and 111.15 μmol cm−2 every minute was also obtained at the same current density, translating to a current efficiency of 78 and 72% respectively. Hydrogen tracer diffusion studies confirm BGLC can incorporate protons into the bulk relative to BLC even though the present steam electrolysis results show a better performance for BLC at 600 °C.
UR - http://www.scopus.com/inward/record.url?scp=85041811661&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85041811661&partnerID=8YFLogxK
U2 - 10.1016/j.ssi.2018.02.016
DO - 10.1016/j.ssi.2018.02.016
M3 - Article
AN - SCOPUS:85041811661
SN - 0167-2738
VL - 319
SP - 218
EP - 222
JO - Solid State Ionics
JF - Solid State Ionics
ER -