Facile synthesis of mesoporous carbons with tailored porosity by a fast polymerization
Source abstract
Abstract
Mesoporous carbons (MCs) with controllable pore structure and pore size have been prepared by direct carbonization of composites of reverse compolymer-phloroglucinol/formaldehyde. The microstructure of the MCs was analyzed by small-angle X-ray scattering, nitrogen adsorption isotherms and transmission electron microscope. The results showed the pore size of the obtained MCs can be easily tuned from 6.4 to 11.4 nm. Furthermore, the inkbottle-like or cylindrical pore structure of MCs can be obtained by simply adjusting the ratios of formaldehyde and phloroglucinol.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Mesoporous Materials and Catalysis · Supercapacitor Materials and Fabrication · Covalent Organic Framework Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (18)
Show source-provided references
1. W. Zhou, K. Zhou, X. Liu, R. Hu, H. Liu, S. Chen, J. Mater. Chem. A 2, 7250–7255 (2014)10.1039/C3TA15280D ↗
2. A. Zahoor, M. Christy, Y.J. Hwang, Y.R. Lim, P. Kim, K.S. Nahm, Appl. Catal. B 147, 633–641 (2014)10.1016/j.apcatb.2013.09.043 ↗
3. G. Zu, J. Shen, L. Zou, F. Wang, X. Wang, Y. Zhang, X. Yao, Carbon 99, 203–211 (2016)10.1016/j.carbon.2015.11.079 ↗
4. G. Ramos-Fernandez, M. Canal-Rodríguez, A. Arenillas, J.A. Menendez, I. Rodríguez-Pastor, I. Martin-Gullon, Carbon 126, 456–463 (2018)10.1016/j.carbon.2017.10.025 ↗
5. M. Enterría, J.L. Figueiredo, Carbon 108, 79–102 (2016)10.1016/j.carbon.2016.06.108 ↗
6. J. Gu, Z. Du, C. Zhang, S. Yang, Adv. Energy Mater. 6, 1600917–1600923 (2016)10.1002/aenm.201600917 ↗
7. D. Carriazo, M.C. Gutierrez, M.L. Ferrer, F. del Monte, Chem. Mater. 22, 6146–6152 (2010)10.1021/cm1019684 ↗
8. S.H. Chai, Z.M. Liu, K. Huang., S. Tan, S. Dai, Ind. Eng. Chem. Res. 55, 7355–7361 (2016)10.1021/acs.iecr.6b00823 ↗
9. H. Funabashi, S. Takeuchi, S. Tsujimura, Sci. Rep. 7, 45147–45155 (2017)10.1038/srep45147 ↗
10. K. Zhu, K. Egeblad, C.H. Christensen, Eur. J. Inorg. Chem. 25, 3955–3960 (2007)10.1002/ejic.200700218 ↗
11. C. Liang, Z. Li, S. Dai, Angew. Chem. Int. Ed. 47, 3696–3717 (2008)10.1002/anie.200702046 ↗
12. S. Tanaka, N. Nishiyama, Y. Egashira., K. Ueyama, Chem. Commun. 16, 2125–2127 (2005)10.1039/B501259G ↗
13. M. Florent, C. Xue, D. Zhao, D. Goldfarb, Chem. Mater. 24, 383–392 (2012)10.1021/cm2032493 ↗
14. J. Hou, K. Jiang, M. Tahir, X. Wu, F. Idrees, M. Shen, C. Cao, J. Power Sources 371, 148–155 (2017)10.1016/j.jpowsour.2017.10.045 ↗
15. Y. Zhu, Y. Liu, Y. Liu, T. Ren, T. Chen, Z. Yuan, ChemCatChem 7, 2903–2909 (2015)10.1002/cctc.201500148 ↗
16. P. Li, Y. Song, Z. Tang, G. Yang, J. Yang, J. Sol-Gel. Sci. Technol. 69, 47–51 (2013)10.1007/s10971-013-3183-6 ↗
17. J. Zhang, Z. Qiao, S.M. Mahurin, X. Jiang, S.H. Chai, H. Lu, K. Nelson, S. Dai, Angew. Chem. Int. Ed. 54, 4582–4586 (2017)10.1002/anie.201500305 ↗
18. C.M. Wu, S.Y. Lin, J. Phys. Chem. C 119, 12335–12344 (2015)10.1021/acs.jpcc.5b01461 ↗