journal article·2019-05-22Open access

Synergistic Coupling of Proton Conductors BaZr0.1Ce0.7Y0.1Yb0.1O3−δ and La2Ce2O7 to Create Chemical Stable, Interface Active Electrolyte for Steam Electrolysis Cells

Wenyuan Li, Bo Guan, Liang Ma, Hanchen Tian, Xingbo Liu

ACS Applied Materials & Interfaces· Volume 11· Issue 20

Abstract

For the first time, proton conductors BaZr0.1Ce0.7Y0.1Yb0.1O3−δ (BZCYYb) and La2Ce2O7 (LCO) are combined to create an interface active and steam-tolerant electrolyte for high-performance proton-conducting solid oxide electrolysis cells. LCO shows good chemical compatibility with BZCYYb. The readily fabricated LCO/BZCYYb bilayer electrolyte can be densified at a temperature of as low as 1300 °C versus ∼1600 °C for the benchmark steam-stable BaZr0.8Y0.2O3−δ electrolyte. With Pr2NiO4+δ as the anode and Ni as the cathode catalyst, this bilayer electrolyte cell yields a current density of 975 and 300 mA/cm2 under a 1.3 V applied potential at 700 and 600 °C, respectively. This performance is among the best of all H-SOECs equipped with a chemically stable electrolyte so far. A BZCYYb layer in the bilayer electrolyte promotes the hydrogen evolution reaction at the cathode side, resulting in a 108% improvement over the cell without this layer. The LCO layer, on the other hand, effectively protects this functional BZCYYb layer from the high concentration of steam in a practical SOEC operation condition. The cell without the LCO layer shows degradation in terms of an increased electrolyzing potential from 1.07 to 1.29 V during a constant 400 mA/cm2 operation at 700 °C. In contrast, the bilayer electrolyte cell maintains the same electrolyzing potential of 1.13 V under the same conduction for a 102 h operation. These findings demonstrate that this synergic bilayer electrolyte design is a vital strategy to overcome the dilemma between performance and stability faced by the current benchmark Zr- or Ce-rich Ba(CeZr)O3−δ electrolysis cells to achieve excellent performance and stability at the same time.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advancements in Solid Oxide Fuel Cells · Chemical Looping and Thermochemical Processes · Electronic and Structural Properties of Oxides

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Mechanical & Aerospace Engineering Department, Benjamin M. Statler College of Engineering & Mineral Resources, West Virginia University, Morgantown, West Virginia 26506, United States

School of Materials Science and Engineering, Hebei University of Engineering, Handan 056038, China

Funding

Office of Energy Efficiency and Renewable Energy

References (46)

Show source-provided references
1. 10.1039/C4CS00194J10.1039/C4CS00194J ↗
2. 10.1016/j.ssi.2015.03.00610.1016/j.ssi.2015.03.006 ↗
3. 10.1039/C8TA04018D10.1039/C8TA04018D ↗
4. 10.1149/2.1541709jes10.1149/2.1541709jes ↗
5. 10.1016/j.jpowsour.2011.12.01910.1016/j.jpowsour.2011.12.019 ↗
6. 10.1146/annurev.matsci.33.022802.09182510.1146/annurev.matsci.33.022802.091825 ↗
7. 10.1039/C7CP05899C10.1039/C7CP05899C ↗
8. 10.1039/b612060c10.1039/b612060c ↗
9. 10.1002/advs.20180036010.1002/advs.201800360 ↗
10. 10.1021/acsami.7b1670310.1021/acsami.7b16703 ↗
11. 10.1149/1.139188810.1149/1.1391888 ↗
12. 10.1149/1.183664710.1149/1.1836647 ↗
13. 10.1088/1468-6996/11/4/04430110.1088/1468-6996/11/4/044301 ↗
14. 10.1016/S0167-2738(00)00777-310.1016/S0167-2738(00)00777-3 ↗
15. 10.1016/j.ssi.2010.07.02610.1016/j.ssi.2010.07.026 ↗
16. 10.1039/C6RA13347A10.1039/C6RA13347A ↗
17. 10.1016/j.jpowsour.2015.02.02710.1016/j.jpowsour.2015.02.027 ↗
18. 10.1016/S0167-2738(01)00839-610.1016/S0167-2738(01)00839-6 ↗
19. 10.1016/j.jallcom.2015.11.04110.1016/j.jallcom.2015.11.041 ↗
20. 10.1016/j.ceramint.2017.09.01310.1016/j.ceramint.2017.09.013 ↗
21. 10.1016/j.ijhydene.2013.04.05110.1016/j.ijhydene.2013.04.051 ↗
22. 10.1126/science.117481110.1126/science.1174811 ↗
23. 10.1149/2.096404jes10.1149/2.096404jes ↗
24. 10.1016/j.jpowsour.2016.04.02210.1016/j.jpowsour.2016.04.022 ↗
25. 10.1016/j.pmatsci.2011.08.00210.1016/j.pmatsci.2011.08.002 ↗
26. 10.1002/fuce.20110010910.1002/fuce.201100109 ↗
27. 10.1016/j.jpowsour.2013.04.10710.1016/j.jpowsour.2013.04.107 ↗
28. 10.1039/C7CP04103A10.1039/C7CP04103A ↗
29. 10.1039/C8EE02865F10.1039/C8EE02865F ↗
30. 10.1016/j.electacta.2018.07.03210.1016/j.electacta.2018.07.032 ↗
31. 10.1103/PhysRevB.84.05411010.1103/PhysRevB.84.054110 ↗
32. 10.1103/PhysRevB.85.13210110.1103/PhysRevB.85.132101 ↗
33. 10.1016/S0955-2219(03)00499-010.1016/S0955-2219(03)00499-0 ↗
34. 10.1038/s41560-018-0230-010.1038/s41560-018-0230-0 ↗
35. 10.1016/j.ijhydene.2018.06.07610.1016/j.ijhydene.2018.06.076 ↗
36. 10.1016/j.jpowsour.2009.12.07910.1016/j.jpowsour.2009.12.079 ↗
37. 10.1016/j.ssi.2011.09.00810.1016/j.ssi.2011.09.008 ↗
38. 10.1039/C4TA07202B10.1039/C4TA07202B ↗
39. 10.1039/C7TA05841A10.1039/C7TA05841A ↗
40. 10.1016/j.ijhydene.2015.05.16210.1016/j.ijhydene.2015.05.162 ↗
41. 10.1039/C6TA06414K10.1039/C6TA06414K ↗
42. 10.1016/j.jpowsour.2010.02.01210.1016/j.jpowsour.2010.02.012 ↗
43. 10.1126/science.120409010.1126/science.1204090 ↗
44. 10.1016/j.jpowsour.2005.01.03810.1016/j.jpowsour.2005.01.038 ↗
45. 10.1016/j.jpowsour.2009.06.00710.1016/j.jpowsour.2009.06.007 ↗
46. 10.1111/jace.1588110.1111/jace.15881 ↗