LA/C14DMAO/H2O体系多结构自组装体及其模板金纳米材料制备与性能

doi:10.3866/PKU.WHXB201511193

物理化学学报 >> 2016, Vol. 32 >> Issue (1): 380-390.doi: 10.3866/PKU.WHXB201511193

论文上一篇

LA/C₁₄DMAO/H₂O体系多结构自组装体及其模板金纳米材料制备与性能

冯磊,郝京诚*()

山东大学，胶体与界面化学教育部重点实验室，济南 250100

收稿日期:2015-10-12 发布日期:2016-01-13
通讯作者: 郝京诚 E-mail:jhao@sdu.edu.cn
基金资助:
国家自然科学基金(2140102006, 21273134);山东省自然科学基金(ZR2013BQ025)

Preparation and Property of Gold Nanoparticles from Muliple Self-Assembled Structures as Templates in LA/C₁₄DMAO/H₂O System

Lei FENG,Jing-Cheng HAO*()

Key Laboratory of Colloid and Interface Chemistry, Shandong University, Jinan 250100, P. R. China

Received:2015-10-12 Published:2016-01-13
Contact: Jing-Cheng HAO E-mail:jhao@sdu.edu.cn
Supported by:
the National Natural Science Foundation of China(2140102006, 21273134);Shandong Provincial Natural ScienceFoundation, China(ZR2013BQ025)

摘要/Abstract

摘要：

月桂酸(LA)与十四烷基二甲基氧化胺(C₁₄DMAO)形成的无盐阴/阳离子表面活性剂混合体系表现出丰富的相行为。运用冷冻蚀刻透射电子显微镜(FF-TEM)和偏光显微镜(POM)、差示扫描量热(DSC)、流变和[2]H NMR测定对体系相行为和微观结构进行了研究，发现水溶液中可自聚集形成胶束(L₁)、层状(L_αl)、囊泡(L_αν)和凝胶相。以胶束相和层状相为软模板制备了金纳米材料，运用透射电子显微镜(TEM)和能谱仪(EDS)表征了金纳米材料。与用传统阳离子表面活性剂溶液制备金纳米材料相比，该体系由于具有自身还原性而不需要加入还原剂NaBH₄。实验证明：还原过程不会破坏模板溶液原有微观结构，且可通过调控聚集体结构实现控制制备金纳米材料形貌的目的。HK-2细胞的噻唑蓝(MTT)比色法实验进一步证明，本体系制备的球形金纳米材料作为基因载体具有高效和低毒的特点，在基因治疗中具有潜在的实际应用价值，可为寻求安全可靠的基因治疗途径提供实验数据和理论参考。

关键词: 月桂酸, 十四烷基二甲基氧化胺, 相行为, 模板, 金纳米材料

Abstract:

Rich phase behavior was observed in salt-free cationic/anionic (catanionic) surfactant mixtures of lauric acid (LA) with a nonionic surfactant, tetradecyldimethylamine oxide (C₁₄DMAO), in water. The phase behavior and microstructures of the LA/C₁₄DMAO/H₂O system were investigated by freeze-fracture transmission electron microscope (FF-TEM), polarized optical microscope (POM), differential scanning calorimetry (DSC), rheological measurements, and [2]H NMR. A variety of self-assembled microstructures were determined, including micelles (L₁ phase), lamellae (L_αl phase), vesicles (L_αν phase) and gels. Using the L₁ and L_αl phases as the templates, gold nanoparticles could be produced, as confirmed by transmission electron microscope (TEM) and energy dispersive spectrometer (EDS). Compared with the traditional method of preparing Au nanomaterials in aqueous solutions, this method can avoid the addition of NaBH₄ as a reducing agent. The sample solution plays roles as a template and a reductant and the reduction process does not destroy the original self-assembled microstructures in the solution. Hence, by controlling the aggregate structures of the template solution, one can achieve the goal of regulating the morphology of Au nanomaterials, which provides a new path for the preparation of noble metal nanostructured materials with different shapes and structures. The results of the methyl thiazolyl tetrazolium (MTT) assay with HK-2 cells show that, as a gene carrier, spherical Au-nanoparticles prepared in a micellar phase possess the characteristics of higher loading efficiency and lower toxicity than those obtained in traditional surfactant systems, demonstrating potential applications in gene therapy.

Key words: Lauric acid, Tetradecyldimethylamine oxide, Phase behavior, Template, Au nanomaterial

MSC2000:

O648

冯磊,郝京诚. LA/C₁₄DMAO/H₂O体系多结构自组装体及其模板金纳米材料制备与性能[J]. 物理化学学报, 2016, 32(1): 380-390.

Lei FENG,Jing-Cheng HAO. Preparation and Property of Gold Nanoparticles from Muliple Self-Assembled Structures as Templates in LA/C₁₄DMAO/H₂O System[J]. Acta Phys. -Chim. Sin., 2016, 32(1): 380-390.

参考文献

1	Kaler E. W. ; Murthy A. K. ; Rodriguez B. E. ; Zasadzinski J. A. N. Science 1989, 245, 1371.
2	Morigaki K. ; Dallavalle S. ; Walde P. ; Colonna S. ; Luisi P. L. J. Am. Chem. Soc 1997, 119, 292.
3	Bergstrøm M. P. ; Pedersen J. S. Langmuir 1999, 15, 2250.
4	Horbaschek K. H. ; Hoffmann H. ; Hao J. J. Phys. Chem. B 2000, 104, 2781.
5	Campbell S. E. ; Zhang Z. ; Friberg S. E. ; Patel R. Langmuir 1998, 14, 590.
6	Horbaschek K. ; Hoffmann H. ; Thunig C. J. Colloid Interface Sci 1998, 206, 439.
7	Hao J. ; Li H. ; Liu W. ; Hirsch A. Chem. Commun 2004, No 5, 602.
8	Song S. ; Feng L. ; Song A. ; Hao J. J. Phys. Chem. B 2012, 116, 12850.
9	Song, S.; Zheng, Q.; Song, A.; Hao, J. Langmuir 2012, 28, 219.
10	Jiang Y. ; Geng T. ; Li Q. ; Li G. ; Ju H. Colloids Surf. A 2014, 462, 27.
11	Ghosh S. ; Ray A. Ind. Eng. Chem. Res 2015, 54, 1953.
12	Gao J. ; Bender C. M. ; Murphy C. J. Langmuir 2003, 19, 9065.
13	Murphy C. J. ; Jana N. R. Adv. Mater 2002, 14, 80.
14	Lu C. ; Wu N. ; Jiao X. ; Luo C. ; Cao W. Chem. Commun 2003, No 9, 1056.
15	Huang X. ; El-Sayed M. A. Lasers Med. Sci 2008, 23, 217.
16	Wei Q. ; Ji J. ; Shen J. J. Nanosci. Nanotechnol 2008, 8, 5708.
17	Xiao J. ; Qi L. Nanoscale 2011, 3, 1383.
18	Cai W. ; Fu G. ; Li C. ; Zhang L. ; Kan C. Appl. Phys. A 2004, 78, 1187.
19	Loubat A. ; Lacroix L. M. ; Robert A. ; Impéror-Clerc M. ; Poteau R. ; Maron L. ; Arenal R. ; Pansu B. ; Viau G. J. Phys. Chem. C 2015, 119, 4422.
20	Jana N. R. ; Gearheart L. ; Murphy C. J. Adv. Mater 2001, 13, 1389.
21	Xu L. ; Feng L. ; Dong R. ; Hao J. ; Dong S. Biomacromolecules 2013, 14, 2781.
22	Teng M. ; Song A. ; Liu L. ; Hao J. J. Phys. Chem. B 2008, 112, 1671.
23	Leontidis E. K. K. ; Kyprianidou-Leodidou T. ; Bekiari V. ; Lianos P. Langmuir 2002, 18, 3659.
24	Zanchet D. ; Micheel C. M. ; Parak W. J. ; Gerion D. ; Alivisatos A. P. Nano Lett 2001, 1, 32.
25	Gao H. ; Kong Y. ; Cui D. ; Ozkan C. S. Nano Lett 2003, 3, 471.
26	Wu H. ; Liu H. ; Tan S. ; Yu J. ; Zhao W. ; Wang L. ; Liu Q. J. Phys. Chem. C 2014, 118, 26825.
27	Maeda H. Colloids Surf. A 1996, 109, 263.
28	Song A. ; Dong S. ; Jia X. ; Hao J. ; Liu W. ; Liu T. Angew. Chem. Int. Edit 2005, 117, 4086.
29	Hoffmann H. Adv. Mater 1994, 6, 116.
30	Wang L. ; Liu J. ; Exarhos G. J. ; Flanigan K. Y. ; Bordia R. J. Phys. Chem. B 2000, 104, 2810.
31	Li Q. ; Li T. ; Wu J. J. Phys. Chem. B 2000, 104, 9011.
32	Kondo, Y.; Miyazawa, H.; Sakai, H.; Abe, M.; Yoshino, N. J. Am. Chem. Soc. 2002, 124, 6516. doi: 10.1021/ja0178564.
33	Medronho B. ; Shafaei S. ; Szopko R. ; Miguel M. G. ; Olsson U. ; Schmidt C. Langmuir 2008, 24, 6480.
34	Liu C. ; Hao J. ; Wu Z. J. Phys. Chem. B 2010, 114, 9795.
35	Alexandridis P. ; Zhou D. ; Khan A. Langmuir 1996, 12, 2690.
36	Niu J. ; Wang D. ; Qin H. ; Xiong X. ; Tan P. ; Li Y. ; Liu R. ; Lu X. ; Wu J. ; Zhang T. ; Ni W. ; Jin J. Nature Commun 2014, 5, 3313.
37	Pileni M. P. Nat. Mater 2003, 2, 145.
38	Dong, R.; Liu, W.; Hao, J. Accounts Chem. Res. 2012, 45, 504. doi: 10.1021/ar200124g.

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LA/C₁₄DMAO/H₂O体系多结构自组装体及其模板金纳米材料制备与性能

Preparation and Property of Gold Nanoparticles from Muliple Self-Assembled Structures as Templates in LA/C₁₄DMAO/H₂O System

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