journal article·2021-01-25

Electrochemical Properties of a Dual-Ion Semiconductor-Ionic Co0.2Zn0.8O-Sm0.20Ce0.80O2−δ Composite for a High-Performance Low-Temperature Solid Oxide Fuel Cell

Sajid Rauf, M. A. K. Yousaf Shah, Bin Zhu, Zuhra Tayyab, Nasir Ali, Sanam Attique, Chen Xia, Rabia Khatoon, Changping Yang, Muhammad Imran Asghar, Peter D. Lund

ACS Applied Energy Materials· Volume 4· Issue 1
Publisher page

Abstract

Semiconductor heterostructures offer a high ionic conduction path enhanced by built-in electric field at the interface, which helps to avoid electronic conduction in low-temperature solid oxide fuel cells (LT-SOFCs). In this study, we synthesized a semiconductor heterostructure based on Co-doped ZnO and Sm0.2Ce0.8O2–δ (SDC) for LT-SOFC application. First, we optimized the composition of the Co-doped ZnO by varying the doping concentration. The cell with Co0.2Zn0.8O composition (σi = 0.158 S cm–1) yielded the best performance of 664 mW cm–2 at 550 °C. This optimized composition of Co-doped ZnO was mixed with a well-known ionic conductor Sm0.2Ce0.8O2−δ (SDC) to further improve the ionic conductivity and performance of the cell. The heterostructure formed between these two semiconductor materials improved the ionic conductivity of this composite material to 0.24 S cm–1 at 550 °C, which is 2 orders higher in magnitude than that of bulk SDC. The fuel cells fabricated with this promising semiconductor-ionic heterostructure material produced an outstanding power density of 928 mW cm–2 at 550 °C. Our further investigation shows protonic conduction (H+) in the Co0.2Zn0.8O-SDC composite, which exhibited protonic conduction 0.088 S cm–1 with a power density of 388 mW cm–2 at 550 °C. A detailed characterization of the material and the fuel cells is performed with the help of different electrochemical (electrochemical impedance spectroscopy (EIS)), spectroscopic (X-ray diffraction (XRD), UV–vis spectroscopy, X-ray photoelectron spectroscopy (XPS)), and microscopic techniques (scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HR-TEM), energy-dispersive X-ray spectrometry (EDX)). The stability of the cell was tested for 35 h to ensure stable operation of these devices. This semiconductor-ionic heterostructure composite provides insight into the development of electrolyte membranes for advanced SOFCs.
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Research context

OpenAlex topics: Advancements in Solid Oxide Fuel Cells · Electronic and Structural Properties of Oxides · Magnetic and transport properties of perovskites and related materials

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

Affiliations

Hubei Collaborative Innovation Centre for Advanced Materialsm, Faculty of Physics and Electronic Science, Hubei University, Wuhan, Hubei 430062, P. R. China

Engineering Research Centre of Nano-Geo Materials of Ministry of Education, Department of Materials Science and Chemistry, China University of Geosciences, 388 Lumo Road, Wuhan 430074, P. R. China

Energy Storage Joint Research Center, School of Energy and Environment, Southeast University, No. 2 Si Pai Lou, Nanjing 210096, P. R. China

Zhejiang Province Key Laboratory of Quantum Technology and Devices and Department of Physics and State Key Laboratory of Silicon Materials, Zhejiang University, Hangzhou 310027, P. R. China

Institute for Composites Science and Innovation (InCSI), School of Material Science and Engineering, Zhejiang University, Hangzhou 310027, P. R. China

State Key Laboratory of Silicon Materials, School of Material Science and Engineering, Zhejiang University, Hangzhou 310027, P. R. China

New Energy Technologies Group, Department of Applied Physics, Aalto University School of Science, P.O. Box 15100, FI-00076 Aalto, Espoo, Finland

Funding

National Laboratory of Solid State Microstructures, Nanjing University · Academy of Finland · National Natural Science Foundation of China · Hubei Province

References (70)

Show source-provided references
1. 10.1021/acsenergylett.9b0182910.1021/acsenergylett.9b01829 ↗
2. 10.1021/acsami.8b1008710.1021/acsami.8b10087 ↗
3. 10.1016/j.rser.2012.11.03110.1016/j.rser.2012.11.031 ↗
4. 10.3390/app1007248110.3390/app10072481 ↗
5. 10.1021/cr300491e10.1021/cr300491e ↗
6. 10.1002/1439-7641(20001215)1:4<162::AID-CPHC162>3.0.CO;2-Z10.1002/1439-7641(20001215)1:4<162::AID-CPHC162>3.0.CO;2-Z ↗
7. 10.1016/j.jallcom.2020.15631810.1016/j.jallcom.2020.156318 ↗
8. 10.1016/j.nanoen.2017.12.04410.1016/j.nanoen.2017.12.044 ↗
9. 10.1557/mrs.2014.19210.1557/mrs.2014.192 ↗
10. 10.1038/nnano.2011.4310.1038/nnano.2011.43 ↗
11. 10.1002/aenm.20110075110.1002/aenm.201100751 ↗
12. 10.1039/C4EE00748D10.1039/C4EE00748D ↗
13. 10.1016/j.electacta.2017.08.14910.1016/j.electacta.2017.08.149 ↗
14. 10.1016/j.rser.2015.12.03410.1016/j.rser.2015.12.034 ↗
15. 10.1039/b915141a10.1039/b915141a ↗
16. 10.1002/adfm.20080176810.1002/adfm.200801768 ↗
17. 10.1007/s10800-005-9006-x10.1007/s10800-005-9006-x ↗
18. 10.1016/j.nanoen.2013.05.00110.1016/j.nanoen.2013.05.001 ↗
19. 10.1016/j.ijhydene.2011.04.08210.1016/j.ijhydene.2011.04.082 ↗
20. 10.1016/j.pmatsci.2015.01.00110.1016/j.pmatsci.2015.01.001 ↗
21. 10.1016/j.ijhydene.2020.03.14710.1016/j.ijhydene.2020.03.147 ↗
22. 10.1038/nature1765310.1038/nature17653 ↗
23. 10.1021/acsami.9b1304410.1021/acsami.9b13044 ↗
24. 10.1016/j.jpowsour.2019.02.10010.1016/j.jpowsour.2019.02.100 ↗
25. 10.1016/j.ijhydene.2020.05.15510.1016/j.ijhydene.2020.05.155 ↗
26. 10.1021/acsami.0c1006110.1021/acsami.0c10061 ↗
27. 10.1016/S0167-577X(02)00913-810.1016/S0167-577X(02)00913-8 ↗
28. 10.1002/crat.20031016210.1002/crat.200310162 ↗
29. 10.1021/nl900772q10.1021/nl900772q ↗
30. 10.1007/s10800-015-0836-x10.1007/s10800-015-0836-x ↗
31. 10.1016/j.ijhydene.2018.04.12110.1016/j.ijhydene.2018.04.121 ↗
32. 10.1016/j.jpowsour.2018.04.09610.1016/j.jpowsour.2018.04.096 ↗
33. 10.1103/PhysRevLett.93.22550210.1103/PhysRevLett.93.225502 ↗
34. 10.1063/1.205336010.1063/1.2053360 ↗
35. 10.1016/j.ssi.2005.10.00210.1016/j.ssi.2005.10.002 ↗
36. 10.1038/s41467-019-09532-z10.1038/s41467-019-09532-z ↗
37. 10.1021/acsaem.7b0013710.1021/acsaem.7b00137 ↗
38. 10.1016/j.jpowsour.2009.12.03510.1016/j.jpowsour.2009.12.035 ↗
39. 10.1038/ncomms782410.1038/ncomms7824 ↗
40. 10.1002/aenm.20140189510.1002/aenm.201401895 ↗
41. 10.1016/j.jeurceramsoc.2018.07.03710.1016/j.jeurceramsoc.2018.07.037 ↗
42. 10.1021/acsaem.0c0052110.1021/acsaem.0c00521 ↗
43. 10.1039/D0TA04280C10.1039/D0TA04280C ↗
44. 10.1016/j.jpowsour.2015.12.08610.1016/j.jpowsour.2015.12.086 ↗
45. 10.1016/j.ijhydene.2012.11.11210.1016/j.ijhydene.2012.11.112 ↗
46. 10.1016/j.memsci.2014.11.05910.1016/j.memsci.2014.11.059 ↗
47. 10.1021/acssuschemeng.7b0240610.1021/acssuschemeng.7b02406 ↗
48. 10.1039/C9TA00499H10.1039/C9TA00499H ↗
49. 10.1016/j.ijhydene.2018.05.12010.1016/j.ijhydene.2018.05.120 ↗
50. 10.1016/j.ijhydene.2018.03.18410.1016/j.ijhydene.2018.03.184 ↗
51. 10.1016/j.electacta.2019.13534910.1016/j.electacta.2019.135349 ↗
52. 10.1039/C6TA05763B10.1039/C6TA05763B ↗
53. 10.1016/S1388-2481(99)00047-810.1016/S1388-2481(99)00047-8 ↗
54. 10.1016/j.ijhydene.2011.05.05510.1016/j.ijhydene.2011.05.055 ↗
55. 10.1016/j.nanoen.2017.05.00310.1016/j.nanoen.2017.05.003 ↗
56. 10.1016/j.jmatprotec.2007.01.01910.1016/j.jmatprotec.2007.01.019 ↗
57. 10.1111/j.1551-2916.2007.01923.x10.1111/j.1551-2916.2007.01923.x ↗
58. 10.1016/j.ssi.2008.04.00210.1016/j.ssi.2008.04.002 ↗
59. 10.1088/0957-4484/26/30/30400210.1088/0957-4484/26/30/304002 ↗
60. 10.1007/s10853-019-03856-310.1007/s10853-019-03856-3 ↗
61. 10.3390/molecules2421381810.3390/molecules24213818 ↗
62. 10.1016/j.ijhydene.2020.07.01110.1016/j.ijhydene.2020.07.011 ↗
63. 10.1063/1.206187310.1063/1.2061873 ↗
64. 10.1021/jp051525m10.1021/jp051525m ↗
65. 10.1039/D0CE00588F10.1039/D0CE00588F ↗
66. 10.1038/s41467-019-09339-y10.1038/s41467-019-09339-y ↗
67. 10.1166/jnn.2014.872010.1166/jnn.2014.8720 ↗
68. 10.1177/184798041770214410.1177/1847980417702144 ↗
69. 10.1021/acssuschemeng.0c0134410.1021/acssuschemeng.0c01344 ↗
70. 10.1021/acsami.9b0844810.1021/acsami.9b08448 ↗