Synthesizing Functional Ceramic Powders for Solid Oxide Cells in Minutes through Thermal Shock
Source abstract
Abstract
Ceramic fuel/electrolysis cells are key energy/material conversion devices. Here, we report that, by thermal shock, mixed ionic and electronic conducting electrode powders with a perovskite structure can be successfully synthesized within 2 min, while this procedure requires a two-step calcination and almost 40 h when a conventional furnace is used. This benefits from the high temperature supplied to the system, greatly enhancing the reaction kinetics among the raw materials. Moreover, typical electrolyte powders with a fluorite structure, such as (Y2O3)0.08(ZrO2)0.92 (YSZ) and Sm0.2Ce0.8O1.95 (SDC), are also synthesized in several minutes through a thermal shock, which significantly reduces the fabrication time of a solid oxide cell. Also, one can easily prepare multiple samples at one time via tailoring the carbon support size. The availability of fast synthesis of the thermal-shock technique enables the development of new functional ceramic powders for solid-oxide cells in a high-throughput and economical manner.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Solid Oxide Fuel Cells · Nuclear Materials and Properties · Chemical Looping and Thermochemical Processes
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Nuclear Science and Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, United States
Department of Materials Science and Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, United States
State Key Laboratory of Electrical Insulation and Power Equipment, Xi’an Jiaotong University, Xi’an 710049, People’s Republic of China
Funding
Basic Energy Sciences · Massachusetts Institute of Technology
References (25)
Show source-provided references
1. 10.1038/s41586-021-03264-110.1038/s41586-021-03264-1 ↗
2. 10.1038/nature0286310.1038/nature02863 ↗
3. 10.1126/science.120409010.1126/science.1204090 ↗
4. 10.1038/s41563-020-00854-810.1038/s41563-020-00854-8 ↗
5. 10.1038/s41929-019-0310-y10.1038/s41929-019-0310-y ↗
6. 10.1038/nature1909010.1038/nature19090 ↗
7. 10.1038/ncomms912010.1038/ncomms9120 ↗
8. 10.1126/science.112587710.1126/science.1125877 ↗
9. 10.1038/nchem.177310.1038/nchem.1773 ↗
10. 10.1039/C2EE22547F10.1039/C2EE22547F ↗
11. 10.1021/acsami.9b0428610.1021/acsami.9b04286 ↗
12. 10.1016/j.compositesa.2015.10.03510.1016/j.compositesa.2015.10.035 ↗
13. 10.1016/j.jallcom.2010.01.06810.1016/j.jallcom.2010.01.068 ↗
14. 10.1002/adem.20130040910.1002/adem.201300409 ↗
15. 10.1016/j.actamat.2016.12.01510.1016/j.actamat.2016.12.015 ↗
16. 10.1126/science.aaz768110.1126/science.aaz7681 ↗
17. 10.1007/s10971-015-3778-110.1007/s10971-015-3778-1 ↗
18. 10.1016/j.jpowsour.2017.02.09010.1016/j.jpowsour.2017.02.090 ↗
19. 10.1039/C7RA11337D10.1039/C7RA11337D ↗
20. 10.1016/j.jpowsour.2016.02.06910.1016/j.jpowsour.2016.02.069 ↗
21. 10.1007/s11664-019-07193-810.1007/s11664-019-07193-8 ↗
22. 10.1038/srep1959310.1038/srep19593 ↗
23. 10.1039/C4DT01430H10.1039/C4DT01430H ↗
24. 10.1016/j.susc.2011.12.01310.1016/j.susc.2011.12.013 ↗
25. 10.1038/s41565-019-0367-410.1038/s41565-019-0367-4 ↗