Nonhydrolytic sol–gel and gram-scale synthesis of surfactant-free maghemite nanoparticles with high surface area
Source abstract
Abstract
An organic molecule was used as a surfactant for nanoparticle synthesis in liquid phase. However, residual molecules on the surface of the nanoparticles limit their catalytic applications, because the interaction of a reactant with the nanoparticle surface is interrupted. Therefore, it is favorable for catalytic applications that the organic molecule used in the synthesis of nanoparticles only induces a sol–gel reaction of the metal precursors and the formation of nanoparticles and hardly adheres to the resulting nanoparticles. Herein, we report surfactant-free and high-surface area maghemite nanostructures via nonhydrolytic sol–gel reaction. Using Fe(acetylacetonate)3 as an iron precursor and hexylamine as a solvent and growth inhibitor, Fe2O3 nanoparticles were generated by nonhydrolysis of the iron complex and condensation at 140 °C under an air atmosphere. Characterization revealed monodisperse nanoparticles with an average size of 2.3 nm and a crystalline phase of maghemite. Residual hexylamine is hardly observed, and thus their specific surface area is 403.7 m2/g. An experimental comparison of the Fe2O3 synthesis with hexylamine and benzylamine indicates that the cone angle of an organic molecule is an important factor in the synthesis of nanoparticles with a small size and high surface area.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Iron oxide chemistry and applications · Nanomaterials for catalytic reactions · Nanoparticle-Based Drug Delivery
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (28)
Show source-provided references
1. Cushing BL, Kolesnichenko VL, O’Connor CJ (2004) Chem Rev 104:389310.1021/cr030027b ↗
2. Park J, Lee E, Hwang N-M, Kang M, Kim SC, Hwang Y, Park JG, Noh HJ, Kim JY, Park JH, Hyeon T (2005) Angew Chem Int Ed 44:287210.1002/anie.200461665 ↗
3. Shen C, Hui C, Yang T, Xiao C, Tian T, Bao L, Chen S, Ding H, Gao H (2008) Chem Mater 20:693910.1021/cm800882n ↗
4. Liu Y, Walker ARH (2010) Angew Chem Int Ed 122:693310.1002/ange.201001931 ↗
5. Zhou X, Xie ZX, Jiang ZY, Kuang Q, Zhang SH, Xu T, Huang RB, Zheng LS (2005) Chem Comm 557210.1039/b510287a ↗
6. Wang H, Uehara M, Nakamura H, Miyazaki M, Maeda H (2005) Adv Mater 17:250610.1002/adma.200500503 ↗
7. Buonsanti R, Grillo V, Carlino E, Giannini C, Kipp T, Cingolani R, Cozzoli PDJ (2008) J Am Chem Soc 130:1122310.1021/ja803559b ↗
8. Wang C, Hu Y, Lieber CM, Sun S (2008) J Am Chem Soc 130:890210.1021/ja803408f ↗
9. Park J, An K, Hwang Y, Park JG, Noh HJ, Kim JY, Park JH, Hwang NM, Hyeon T (2004) Nat Mater 3:89110.1038/nmat1251 ↗
10. Seo WS, Lee JH, Sun X, Suzuki Y, Mann D, Liu Z, Terashima M, Yang PC, Mcconnell MV, Nishimura DG, Dai H (2006) Nat Mater 5:97110.1038/nmat1775 ↗
11. Park MH, Li JH, Kumar A, Li G, Yang Y (2009) Adv Funct Mater 19:124110.1002/adfm.200801639 ↗
12. Huynh WU, Dittmer JJ, Alivisatos AP (2002) Science 295:242510.1126/science.1069156 ↗
13. Park JC, Kim J, Kwon H, Song H (2009) Adv Mater 21:80310.1002/adma.200800596 ↗
14. Lee G, Shim JH, Kang H, Nam KM, Song H, Park JT (2009) Chem Comm 503610.1039/b911068b ↗
15. Garnweitner G, Niederberger M (2006) J Am Ceram Soc 6:180110.1111/j.1551-2916.2006.01005.x ↗
16. Pinna N, Garnweitner G, Antonietti M, Niederberger M (2005) J Am Chem Soc 127:560810.1021/ja042323r ↗
17. Kang HW, Lee SC, Kweon K, Kim HJ, Lee G (2010) J Anal Sci Technol 1:13010.5355/JAST.2010.130 ↗
18. Martin RL, Shirley DA (1974) J Am Chem Soc 96:529910.1021/ja00824a001 ↗
19. Garnweitner G, Antonietti M, Niederberger M (2005) Chem Comm 39710.1039/b414510k ↗
20. Zhao ZW, Guo ZP, Liu HK (2005) J Power Sources 147:26410.1016/j.jpowsour.2005.01.021 ↗
21. Melcarne G, Marco LD, Carlino E, Martina F, Manca M, Cingolani R, Gigli G, Ciccarella G (2010) J Mater Chem 20:724810.1039/c0jm01167c ↗
22. Rao Y, Trudeau M, Antonelli D (2006) J Am Chem Soc 128:1399610.1021/ja0647147 ↗
23. Asadi M, Kianfar AH, Torabi S, Mohammadi K (2008) J Chem Thermodyn 40:52310.1016/j.jct.2007.08.003 ↗
24. Romeo R, Arena G, Scoiaro LM (1992) Inorg Chem 31:487910.1021/ic00049a029 ↗
25. Eckhardt B, Ortel E, Polte J, Bernsmeier D, Görke O, Strasser P, Kraehnert R (2012) Adv Mater 24:311510.1002/adma.201104984 ↗
26. Schüth F (2003) Angew Chem Int Ed 42:360410.1002/anie.200300593 ↗
27. Chen D, Huang F, Cheng Y-B, Caruso RA (2009) Adv Mater 21:220610.1002/adma.200802603 ↗
28. Terribile D, Trovarelli A, Llorca J, Leitenburg CD, Dolcetti G (1998) J Catal 178:29910.1006/jcat.1998.2152 ↗