Improved CO2 Uptake and Supercapacitive Energy Storage Using Heteroatom‐Rich Porous Carbons Derived from Conjugated Microporous Polyaminoanthraquinone Networks
Source abstract
Abstract
Abstract Functionalized porous carbons have received increased attention in both gas and supercapacitive energy storage. We report heteroatom‐rich porous carbons derived from two conjugated microporous polyaminoanthraquinone networks via a straightforward pyrolysis pathway, showing high contents of nitrogen (N, max. 5.2 wt%) and oxygen (O, max. 8.3 wt%), uniform micropore (∼0.6 nm) and large surface area (1165 m2 g−1). In comparison to the polymer precursors, the resulting porous carbons exhibit much improved CO2 uptake capacity of 14.1 wt% at 1 bar maintaining an impressive reversible CO2 uptake after 50 times use. More importantly, they can be applied for efficient supercapacitors with high energy storage capacity (200 F g−1 at 0.5 A g−1), fast charge/discharge rate (charge to 158 F g−1 with only 25 s), and excellent stability (retain 98.5% capacity after 6000 cycles).
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Supercapacitor Materials and Fabrication · Covalent Organic Framework Applications · Advanced battery technologies research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Materials Science and Engineering Liaocheng University Liaocheng 252059 China
State Key Laboratory for Modification of Chemical Fibers and Polymer Materials College of Materials Science and Engineering Donghua University Shanghai 201620 China
Funding
Natural Science Foundation of Shandong Province · Fundamental Research Funds for the Central Universities · National Natural Science Foundation of China · Natural Science Foundation of Shanghai
References (31)
Show source-provided references
1. 10.1016/j.rser.2014.07.09310.1016/j.rser.2014.07.093 ↗
2. 10.1126/science.117224610.1126/science.1172246 ↗
3. 10.1039/C7EE02342A10.1039/C7EE02342A ↗
4. 10.1039/C1CS15060J10.1039/C1CS15060J ↗
5. 10.1021/cr020730k10.1021/cr020730k ↗
6. 10.1021/acs.chemmater.6b0396410.1021/acs.chemmater.6b03964 ↗
7. 10.1016/j.mattod.2017.04.02610.1016/j.mattod.2017.04.026 ↗
8. 10.1002/anie.20140943910.1002/anie.201409439 ↗
9. 10.1039/c3cs60160a10.1039/c3cs60160a ↗
10. 10.1039/C7CS00071E10.1039/C7CS00071E ↗
11. 10.1039/C4CC03026E10.1039/C4CC03026E ↗
12. 10.1021/acs.macromol.6b0090110.1021/acs.macromol.6b00901 ↗
13. 10.1039/C7PY01439B10.1039/C7PY01439B ↗
14. 10.1039/c3ee41906a10.1039/c3ee41906a ↗
15. 10.1021/ja303448r10.1021/ja303448r ↗
16. 10.1002/anie.20140214110.1002/anie.201402141 ↗
17. 10.1021/acsami.7b0955310.1021/acsami.7b09553 ↗
18. 10.1021/acsaem.8b0144410.1021/acsaem.8b01444 ↗
19. 10.1002/adma.20170571010.1002/adma.201705710 ↗
20. 10.1002/aenm.20130038310.1002/aenm.201300383 ↗
21. 10.1021/acsnano.8b0804610.1021/acsnano.8b08046 ↗
22. 10.1002/smll.20180323210.1002/smll.201803232 ↗
23. 10.1021/acs.chemmater.7b0085710.1021/acs.chemmater.7b00857 ↗
24. 10.1002/adma.20150178610.1002/adma.201501786 ↗
25. 10.3389/fchem.2019.0014210.3389/fchem.2019.00142 ↗
26. 10.1021/ja960338m10.1021/ja960338m ↗
27. 10.1016/j.carbon.2018.07.01310.1016/j.carbon.2018.07.013 ↗
28. 10.1021/jacs.6b0764410.1021/jacs.6b07644 ↗
29. 10.1039/c1ee01198g10.1039/c1ee01198g ↗
30. 10.1039/c3ee42366b10.1039/c3ee42366b ↗
31. 10.1016/j.carbon.2013.11.05910.1016/j.carbon.2013.11.059 ↗