General Recyclable Redox-Metallothermic Reaction Route to Hierarchically Porous Carbon/Metal Composites
Source abstract
Abstract
Herein, we develop a general synthetic route to obtain composites of porous carbon and electrochemically active metal particles such as Ge, In, Bi, and Sn. The thermolysis of a Zn-based metal–organic framework (MOF) produces hierarchically porous carbon (HPC) and metallic Zn at high temperatures, which can act as a reducing agent of metal oxides. In the reaction system of a Zn-based MOF with GeO 2, in situ evolved Zn reduces GeO 2, producing Ge and ZnO. Interestingly, ZnO is automatically reduced to Zn via a carbothermic reduction during the conversion process, which returns reducing agent to the reaction. Thus, the repeated occurrence of the zincothermic and carbothermic reduction reactions promotes a recyclable redox-metallothermic reaction. After complete reduction of GeO 2, Zn metal is spontaneously vaporized to yield Ge/HPC composites. This facile method can be successfully extended to other metal oxides including In 2 O 3, Bi 2 O 3, and SnO. The as-synthesized Ge/HPC is tested as a rechargeable battery anode material, which exhibits a reversible capacity as high as ∼600 mA h g –1 after 300 cycles at a rate of 0.5 C and a low electrode volume expansion (less than 30%).
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Advanced battery technologies research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, School of Natural Science, Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919, Republic of Korea
Department of Energy Engineering, School of Energy and Chemical Engineering, Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919, Republic of Korea
Funding
National Research Foundation of Korea
References (40)
Show source-provided references
1. 10.1002/anie.20080481610.1002/anie.200804816 ↗
2. 10.1002/chem.20100308010.1002/chem.201003080 ↗
3. 10.1002/anie.20130801310.1002/anie.201308013 ↗
4. 10.1021/ja401869h10.1021/ja401869h ↗
5. 10.1039/C5DT00690B10.1039/C5DT00690B ↗
6. 10.1038/ncomms745110.1038/ncomms7451 ↗
7. 10.1002/chem.20150486710.1002/chem.201504867 ↗
8. 10.1039/C5SC04425A10.1039/C5SC04425A ↗
9. 10.1021/ja203184k10.1021/ja203184k ↗
10. 10.1021/cm202554j10.1021/cm202554j ↗
11. 10.1039/c3cc38955c10.1039/c3cc38955c ↗
12. 10.1021/ja710614610.1021/ja7106146 ↗
13. 10.1038/ncomms626110.1038/ncomms6261 ↗
14. 10.1039/C4TA02501F10.1039/C4TA02501F ↗
15. 10.1021/ja208940u10.1021/ja208940u ↗
16. 10.1039/C5NR00244C10.1039/C5NR00244C ↗
17. 10.1039/c3cc47620k10.1039/c3cc47620k ↗
18. 10.1021/ja508412810.1021/ja5084128 ↗
19. 10.1039/C4TA01272K10.1039/C4TA01272K ↗
20. 10.1002/adma.20150231510.1002/adma.201502315 ↗
21. 10.1039/C5CC01123J10.1039/C5CC01123J ↗
22. 10.1039/c2cc33439a10.1039/c2cc33439a ↗
23. 10.1007/s11837-010-0190-810.1007/s11837-010-0190-8 ↗
24. Bash E. · 2015 · 1 · 1
25. 10.1021/cr500207g10.1021/cr500207g ↗
26. 10.1021/ja047435x10.1021/ja047435x ↗
27. 10.1038/3510464410.1038/35104644 ↗
28. 10.1016/j.mser.2011.06.00110.1016/j.mser.2011.06.001 ↗
29. 10.1039/b919877f10.1039/b919877f ↗
30. 10.1021/acsnano.5b0038910.1021/acsnano.5b00389 ↗
31. 10.1039/C0EE00552E10.1039/C0EE00552E ↗
32. 10.1002/adfm.20140088810.1002/adfm.201400888 ↗
33. 10.1021/am502867f10.1021/am502867f ↗
34. 10.1021/acsnano.5b0081710.1021/acsnano.5b00817 ↗
35. 10.1002/1521-3749(200205)628:4<829::AID-ZAAC829>3.0.CO;2-A10.1002/1521-3749(200205)628:4<829::AID-ZAAC829>3.0.CO;2-A ↗
36. 10.1021/ja01345a01910.1021/ja01345a019 ↗
37. 10.1007/BF0020922810.1007/BF00209228 ↗
38. 10.1021/nl304716e10.1021/nl304716e ↗
39. 10.1021/acs.nanolett.5b0447610.1021/acs.nanolett.5b04476 ↗
40. 10.1021/am504687310.1021/am5046873 ↗