journal article·2017-07

Effects of B‐site doped elements in the electronic‐conducting perovskite phase on the property of dual‐phase membranes

Hongwei Cheng, Xiaolu Xiong, Hongbin Zhao, Ziqin Gu, Xionggang Lu, Qian Xu, Weilin Yao

Publisher page

Abstract

Abstract A series of dense oxygen permeable dual‐phase membranes with a composition of 60 wt% Ce 0.8 Gd 0.2 O 2−δ ‐40 wt% Ba 0.95 La 0.05 Fe 0.9 M 0.10 O 3−δ ( CGO ‐ BLFM 0.10 , M=Fe, Nb, Zr, Zn, Sc, Y) were successfully synthesized and evaluated as potential ceramic membranes for oxy‐fuel combustion. The effects of B‐site doped elements in electronic‐conducting phase ( BLFM 0.10 ) on the crystal structure, microstructure, chemical compatibility, oxygen permeability, as well as chemical stability of CGO ‐ BLFM 0.10 were systematically investigated. All electronic‐conducting phase BLFM 0.10 oxides exhibited a pure cubic perovskite structure and showed good chemical compatibility with ionic‐conducting phase CGO . CGO ‐ BLFS c 0.10 showed the best oxygen permeation stability under a pure CO 2 atmosphere. CO 2 ‐corrosion on the perovskite phase is the main reason for the property deterioration of fluorite‐perovskite‐typed dual‐phase membrane materials. The stability of dual‐phase membrane materials can be effectively enhanced by reducing the basicity of electronic‐conducting phase of perovskite materials.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Advancements in Solid Oxide Fuel Cells · Chemical Looping and Thermochemical Processes · Catalytic Processes in Materials Science

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

Affiliations

State Key Laboratory of Advanced Special Steel & School of Materials Science and Engineering Shanghai University Shanghai China

College of Sciences Shanghai University Shanghai China

Funding

National Natural Science Foundation of China

References (36)

Show source-provided references
1. 10.1126/science.117224610.1126/science.1172246 ↗
2. 10.1016/j.energy.2006.02.00610.1016/j.energy.2006.02.006 ↗
3. 10.1016/j.energy.2006.07.03910.1016/j.energy.2006.07.039 ↗
4. 10.1016/j.enpol.2007.03.00910.1016/j.enpol.2007.03.009 ↗
5. 10.1111/j.1744-7402.2010.02507.x10.1111/j.1744-7402.2010.02507.x ↗
6. 10.1039/C1EE02539B10.1039/C1EE02539B ↗
7. 10.1016/j.memsci.2013.04.06710.1016/j.memsci.2013.04.067 ↗
8. 10.1039/C1CC16631J10.1039/C1CC16631J ↗
9. 10.1246/cl.1985.174310.1246/cl.1985.1743 ↗
10. 10.1016/j.ssi.2011.06.01010.1016/j.ssi.2011.06.010 ↗
11. 10.1016/S0927-5193(96)80013-110.1016/S0927-5193(96)80013-1 ↗
12. 10.1016/S0376-7388(02)00005-410.1016/S0376-7388(02)00005-4 ↗
13. 10.1016/j.memsci.2011.02.03710.1016/j.memsci.2011.02.037 ↗
14. 10.1021/cm101665r10.1021/cm101665r ↗
15. 10.1016/j.memsci.2013.02.05110.1016/j.memsci.2013.02.051 ↗
16. 10.1016/j.memsci.2009.05.02310.1016/j.memsci.2009.05.023 ↗
17. 10.1016/j.memsci.2013.02.04910.1016/j.memsci.2013.02.049 ↗
18. 10.1016/j.ssi.2011.06.01110.1016/j.ssi.2011.06.011 ↗
19. 10.1016/j.memsci.2011.10.03010.1016/j.memsci.2011.10.030 ↗
20. 10.1021/ie300083r10.1021/ie300083r ↗
21. 10.1016/j.memsci.2014.07.02810.1016/j.memsci.2014.07.028 ↗
22. 10.1021/acssuschemeng.5b0069310.1021/acssuschemeng.5b00693 ↗
23. 10.1016/j.memsci.2015.05.05710.1016/j.memsci.2015.05.057 ↗
24. 10.1016/j.memsci.2011.08.05910.1016/j.memsci.2011.08.059 ↗
25. 10.1016/j.ijhydene.2010.10.00210.1016/j.ijhydene.2010.10.002 ↗
26. 10.1021/am200892b10.1021/am200892b ↗
27. 10.1016/j.jmst.2014.09.00110.1016/j.jmst.2014.09.001 ↗
28. 10.1039/C4TA00658E10.1039/C4TA00658E ↗
29. 10.1016/j.susc.2011.12.01310.1016/j.susc.2011.12.013 ↗
30. 10.1039/C4TA01593B10.1039/C4TA01593B ↗
31. 10.1016/j.memsci.2009.03.01210.1016/j.memsci.2009.03.012 ↗
32. 10.1016/S0376-7388(99)00211-210.1016/S0376-7388(99)00211-2 ↗
33. 10.1016/j.memsci.2011.07.00810.1016/j.memsci.2011.07.008 ↗
34. 10.1002/aic.1280210.1002/aic.12802 ↗
35. 10.1016/j.ssi.2013.08.04010.1016/j.ssi.2013.08.040 ↗
36. 10.1016/j.ijhydene.2013.01.04410.1016/j.ijhydene.2013.01.044 ↗