Tuning the extent of porosity and composition of N-doped carbon materials by NaNO3 and its effect on electrochemical activity
Source abstract
Abstract
Abstract A facile one-pot method using NaNO 3 as etching agent in a molten salt medium is developed to tune the porous structure and composition of N-doped carbon materials derived from biomass at high temperatures. SEM and TEM analyses reveal that by increasing the amount of NaNO 3 , the structures of the obtained carbons become more open and graphene-like layers are formed. N 2 adsorption/desorption isotherms show that the hierarchical porous structure could be efficiently tuned by adjusting the amount of NaNO 3 in the salt mixture. It is observed that the specific surface area of the as-prepared N-doped carbon using NaNO 3 can reach 1430.1 m 2 g −1 , a much higher value than that of the sample prepared in the absence of NaNO 3 . The micropore ratio decreases with increased amount of NaNO 3 , from 49.42% to 9.98%. Whilst the surface composition of the obtained carbon materials is affected by NaNO 3 . The N content increases and O decreases respectively, by increasing the amount of NaNO 3 . Analysis on the N 1 s high resolution reveals that the sum of pyridinic-N and graphitic-N increased, whereas the sum of pyridinic-N oxide and NO x decreases from NC-0 to NC-0.75. It is also found that the changes of the porous structure and the oxygen-containing groups from NC-0 to NC-0.75 led to changes in hydrophilicity. When the as-prepared carbon materials are used as catalysts for the oxygen reduction reaction, high catalytic activity values are obtained, sample NC-0.5 shows the best performance due to the porous structure and doping effect of N atoms. More importantly, it is concluded that producing N-doped carbon materials from soybean dregs in molten salt medium using NaNO 3 as etching agent could provide a promising approach for the synthesis of opened N-doped carbons of controlled porous structures and large specific surface areas based on biomass precursors.
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Research context
OpenAlex topics: Supercapacitor Materials and Fabrication · Advancements in Battery Materials · Conducting polymers and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (38)
Show source-provided references
1. Chen · J. Phys. Chem. C · 2013 · 117 · 831810.1021/jp4017773 ↗
2. Hojamberdiev · Microporous and Mesoporous Mater. · 2012 · 151 · 33010.1016/j.micromeso.2011.10.015 ↗
3. Fechler · Adv. Mater. · 2013 · 25 · 7510.1002/adma.201203422 ↗
4. Zhao · ACS Appl. Mater. Interfaces · 2016 · 8 · 1802710.1021/acsami.6b03704 ↗
5. Zhu · Chem. Soc. Rev. · 2016 · 45 · 51710.1039/C5CS00670H ↗
6. And · J. Phys. Chem. B · 2000 · 104 · 796010.1021/jp000861u ↗
7. Li · Catal. Sci. Technol. · 2016 · 6 · 367010.1039/C6CY00544F ↗
8. Wang · J. Power Sources · 2014 · 261 · 23810.1016/j.jpowsour.2014.03.057 ↗
9. Wang · J. Electrochem. Soc. · 2014 · 161 · H63710.1149/2.0551410jes ↗
10. Duan · Chem. Commun. · 2017 · 53 · 746510.1039/C7CC03424E ↗
11. Yan · Chem. Commun. · 2012 · 48 · 343010.1039/c2cc00001f ↗
12. Kwon · Small · 2014 · 10 · 50610.1002/smll.201301770 ↗
13. Zhai · Carbon · 2011 · 49 · 54510.1016/j.carbon.2010.09.055 ↗
14. Nishihara · Adv. Mater. · 2012 · 24 · 447310.1002/adma.201201715 ↗
15. Wang · ACS Appl. Mater. Interfaces · 2017 · 9 · 1506810.1021/acsami.7b02712 ↗
16. Li · J. Solid State Electrochem. · 2017 · 1
17. Wang · ACS Appl. Mater. Interfaces · 2012 · 4 · 580010.1021/am302077c ↗
18. Wei · Energy Environ. Sci. · 2011 · 4 · 73610.1039/c0ee00505c ↗
19. Kühnle · Surf. Sci. · 1995 · 340 · 1610.1016/0039-6028(95)00691-5 ↗
20. Ouyang · J. Mater. Chem. A · 2016 · 4 · 983210.1039/C6TA02673G ↗
21. Wang · J. Power Sources · 2015 · 278 · 21310.1016/j.jpowsour.2014.12.072 ↗
22. Dresselhaus · Annu. Rev. Condens. Matter Phys. · 2010 · 1 · 8910.1146/annurev-conmatphys-070909-103919 ↗
23. Song · Electrochim. Acta · 2014 · 147 · 52010.1016/j.electacta.2014.09.146 ↗
24. Ma · Electrochim. Acta · 2014 · 142 · 31710.1016/j.electacta.2014.07.130 ↗
25. Brunauer · J. Am. Chem. Soc. · 1940 · 62 · 172310.1021/ja01864a025 ↗
26. Ding · Electrochim. Acta · 2017 · 255 · 5510.1016/j.electacta.2017.09.159 ↗
27. Chen · Catal. Commun. · 2018 · 107 · 2910.1016/j.catcom.2018.01.013 ↗
28. Arrigo · Chem. Commun. · 2008 · 489110.1039/b812769g ↗
29. Ferrero · J. Mater. Chem. A · 2016 · 4 · 258110.1039/C5TA10063A ↗
30. Wang · J. Power Sources · 2015 · 274 · 74110.1016/j.jpowsour.2014.10.049 ↗
31. Liu · Angew. Chem. Int. Ed. · 2010 · 49 · 256510.1002/anie.200907289 ↗
32. Li · Green Chem. · 2016 · 18 · 54110.1039/C5GC01818H ↗
33. Liu · Small · 2014 · 10 · 19310.1002/smll.201300812 ↗
34. Huang · Carbon · 2014 · 73 · 24410.1016/j.carbon.2014.02.060 ↗
35. Chen · Micro Nano Lett. Inst. Eng. Technol. · 2018
36. Wang · J. Power Sources · 2015 · 297 · 29510.1016/j.jpowsour.2015.07.107 ↗
37. Wu · ECS Trans. · 2008 · 16 · 15910.1149/1.2981852 ↗
38. Yuan · Nanoscale · 2016 · 8 · 870410.1039/C6NR00764C ↗