Transformation of Metal–Organic Frameworks into Huge-Diameter Carbon Nanotubes with High Performance in Proton Exchange Membrane Fuel Cells
Source abstract
Abstract
Herein, we report an efficient strategy to transfer metal organic frameworks into huge-diameter carbon nanotubes (CNTs) at high production by using Fe-citrate-functionalized zeolitic imidazolium frameworks-8 (ZIF-8) as precursors. The constructed porous Fe–N-decorated CNTs represent a tube diameter of >0.1 μm and a length of >5 μm. We find that the use of Fe-citrate could not only facilitate the agglomeration of Fe to generate huge-diameter CNTs by the bottom-up organic strategy but also induce the formation of Fe–N sites by the ligand substitution of 2-methylimidazole with citrate ions in ZIF-8, making it a promising class of Pt-alternative catalysts for oxygen reduction reaction (ORR). Such an ideal architecture is endowed with highly intrinsic activity from Fe–N and the faster mass transport from huge-diameter tubes, leading to an excellent ORR performance with a maximum power density of 665 mW cm–2.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Fuel Cells and Related Materials · Advanced battery technologies research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
The State Key Laboratory of Power Transmission Equipment & System Security and New Technology, College of Chemistry and Chemical Engineering, Chongqing University, Chongqing 400044, China
College of Chemistry, Chongqing Normal University, Chongqing 401331, P. R. China
Funding
Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China
References (28)
Show source-provided references
1. 10.1021/jacs.5b0029210.1021/jacs.5b00292 ↗
2. 10.1016/j.nanoen.2016.04.04210.1016/j.nanoen.2016.04.042 ↗
3. 10.1039/c3sc51052b10.1039/c3sc51052b ↗
4. 10.1039/c4cs00484a10.1039/c4cs00484a ↗
5. 10.1126/science.aaf905010.1126/science.aaf9050 ↗
6. 10.1039/c8ta07380e10.1039/c8ta07380e ↗
7. 10.1021/acsami.6b1685110.1021/acsami.6b16851 ↗
8. 10.1002/anie.20130392410.1002/anie.201303924 ↗
9. 10.1039/c5ta09859a10.1039/c5ta09859a ↗
10. 10.1002/adma.20140184810.1002/adma.201401848 ↗
11. 10.1021/jacs.7b0651410.1021/jacs.7b06514 ↗
12. 10.1016/j.jpowsour.2018.11.02410.1016/j.jpowsour.2018.11.024 ↗
13. 10.1039/c8ta06743k10.1039/c8ta06743k ↗
14. 10.1016/j.jpowsour.2018.12.04710.1016/j.jpowsour.2018.12.047 ↗
15. 10.1126/science.116804910.1126/science.1168049 ↗
16. 10.1021/acsami.6b1217810.1021/acsami.6b12178 ↗
17. 10.1021/acs.accounts.6b0054110.1021/acs.accounts.6b00541 ↗
18. 10.1039/c7cs00104e10.1039/c7cs00104e ↗
19. 10.1039/c4ta01237b10.1039/c4ta01237b ↗
20. 10.1021/jacs.7b0194210.1021/jacs.7b01942 ↗
21. 10.1039/c8ee02656d10.1039/c8ee02656d ↗
22. 10.1007/s00706-014-1394-310.1007/s00706-014-1394-3 ↗
23. 10.1016/j.nanoen.2017.05.04210.1016/j.nanoen.2017.05.042 ↗
24. 10.1002/anie.20130302510.1002/anie.201303025 ↗
25. 10.1002/ejic.20150078210.1002/ejic.201500782 ↗
26. 10.1039/c7ta09435c10.1039/c7ta09435c ↗
27. 10.1002/anie.20171041810.1002/anie.201710418 ↗
28. 10.1002/adma.20160445610.1002/adma.201604456 ↗