Simulation of CTAB bilayer adsorbed on Au(100), Au(110), and Au(111) surfaces: structure stability and dynamic properties
Received date: 2016-04-13
Revised date: 2016-05-12
Online published: 2017-01-15
Supported by
Supported by the National Basic Research Program (2012CB932504)
金纳米棒的各向异性生长常被认为是由于金表面吸附溴化十六烷基三甲基铵(CTAB)双分子层导致的。利用密度泛函理论(DFT)研究溴离子在(100)、(110)和(111)3种金表面上可能的吸附位点,根据它构建金表面CTAB双分子层模型,再利用分子动力学模拟方法研究这种烷基链互相交错排布的双分子层的结构。此外,动力学性质研究表明外层CTAB有着明显的横向扩散现象,而在法向上则出现上下起伏振动。相比较而言,在(111)表面上的双分子层结构的横向扩散和法向涨落更加显著。用外层单个CTA+脱离双分子层所需要的能量表征金表面CTAB双分子层的稳定性。结果表明(111)表面的CTAB双分子层的稳定性弱于其他两种金表面上的CTAB双分子层。认为这是因为(111)表面上的CTAB双分子层的排布密度相对较低,导致它相对于其他两种表面的双分子层有更高的扩散性和较低的稳定性。这可能是金纳米颗粒倾向于沿(111)表面生长的原因。
潘俊 , 胡中波 . 吸附在Au(100)、Au(110)和Au(111)表面的CTAB双分子层的结构和动力学性质的分子模拟[J]. 中国科学院大学学报, 2017 , 34(1) : 38 -49 . DOI: 10.7523/j.issn.2095-6134.2017.01.006
Anisotropic growth of gold nanorods is often attributed to the adsorption of surfactant cetyltrimethyl ammonium bromide (CTAB) bilayer on gold facets. In this work, we performed DFT (density function theory) calculations to investigate possible binding sites of Br ions on Au(100), Au(110), and Au(111) facets. The CTAB bilayers on these facets were then constructed, and the structures of these interdigitated bilayers were studied by using molecular dynamics simulation. In addition, the dynamic properties of CTAB bilayer were investigated, and the results indicate that the outer layer exhibits noticeable lateral diffusion and undergoes fluctuation along surface normal. Both lateral diffusion and surface normal fluctuation of CTAB bilayer on Au(111) facet are more profound. The stability of CTAB bilayers on gold surfaces was estimated in terms of the required energy for dissociation of a CTA+ ion from the outer layer. The stability of CTAB bilayer on Au(111) is considerably weaker than on Au(100) and Au(110). Higher volatility and weaker stability may be due to lower packing density of CTAB bilayer on Au(111) facet, and both of them induce the growth tendency of gold nanoparticles along the (111) direction.
[1] Dreaden E C, Alkilany A M, Huang X H, et al. The golden age:gold nanoparticles for biomedicine[J]. Chem Soc Rev, 2012, 41(7):2740-2779.
[2] Murphy C J, San T K, Gole A M, et al. Anisotropic metal nanoparticles:synthesis, assembly, and optical applications[J]. J Phys Chem B, 2005, 109(29):13857-13870.
[3] Xiao J Y, Qi L M. Surfactant-assisted, shape-controlled synthesis of gold nanocrystals[J]. Nanoscale, 2011, 3(4):1383-1396.
[4] Smith R K, Lewis P A, Weiss P S. Patterning self-assembled monolayers[J]. Prog Surf Sci, 2004, 75(1/2):1-68.
[5] Daniel M C, Astruc D. Gold nanoparticles:Assembly, supramolecular chemistry, quantum-size-related properties, and applications toward biology, catalysis, and nanotechnology[J]. Chem Rev, 2004, 104(1):293-346.
[6] Ye X C, Gao Y Z, Chen J, et al. Seeded growth of monodisperse gold nanorods using bromide-free surfactant mixtures[J]. Nano Lett, 2013, 13(5):2163-2171.
[7] Jana N R, Gearheart L, Murphy C J. Seed-mediated growth approach for shape-controlled synthesis of spheroidal and rod-like gold nanoparticles using a surfactant template[J]. Adv Mater, 2001, 13(18):1389-1393.
[8] Johnson C J, Dujardin E, Davis S A, et al. Growth and form of gold nanorods prepared by seed-mediated, surfactant-directed synthesis[J]. J Mater Chem, 2002, 12(6):1765-1770.
[9] Murphy C J, Thompson L B, Alkilany A M, et al. The many faces of gold nanorods[J]. J Phys Chem Lett, 2010, 1(19):2867-2875.
[10] Nikoobakht B, El-Sayed M A. Evidence for bilayer assembly of cationic surfactants on the surface of gold nanorods[J]. Langmuir, 2001, 17(20):6368-6374.
[11] Gao J X, Bender C M, Murphy C J. Dependence of the gold nanorod aspect ratio on the nature of the directing surfactant in aqueous solution[J]. Langmuir, 2003, 19(21):9065-9070.
[12] Sardar R, Funston A M, Mulvaney P, et al. Gold nanoparticles:past, present, and future[J]. Langmuir, 2009, 25(24):13840-13851.
[13] Wang Z L, Mohamed M B, Link S, et al. Crystallographic facets and shapes of gold nanorods of different aspect ratios[J]. Surf Sci, 1999, 440(1/2):L809-L814.
[14] Nakahara H, Shibata O, Moroi Y. Examination of surface adsorption of cetyltrimethylammonium bromide and sodium dodecyl sulfate[J]. J Phys Chem B, 2011, 115(29):9077-9086.
[15] Alkilany A M, Nagaria P K, Hexel C R, et al. Cellular uptake and cytotoxicity of gold nanorods:molecular origin of cytotoxicity and surface effects[J]. Small, 2009, 5(6):701-708.
[16] Perez-Juste J, Liz-Marzan L M, Carnie S, et al. Electric-field-directed growth of gold nanorods in aqueous surfactant solutions[J]. Adv Funct Mater, 2004, 14(6):571-579.
[17] Alkilany A M, Thompson L B, Boulos S P, et al. Gold nanorods:their potential for photothermal therapeutics and drug delivery, tempered by the complexity of their biological interactions[J]. Adv Drug Deliver Rev, 2012, 64(2):190-199.
[18] Khan Z, Singh T, Hussain J I, et al. Au(Ⅲ)-CTAB reduction by ascorbic acid:preparation and characterization of gold nanoparticles[J]. Colloid Surface B, 2013, 104:11-17.
[19] Murphy C J, Jana N R. Controlling the aspect ratio of inorganic nanorods and nanowires[J]. Adv Mater, 2002, 14(1):80-82.
[20] Hu W X, Wiria, Ong W L, et al. High yield shape control of monodispersed Au nanostructures with 3D self-assembly ordering[J]. Colloid Surface A, 2010, 358(1/3):108-114.
[21] Mlambo M, Mdluli P S, Shumbula P, et al. Synthesis and characterization of mixed monolayer protected gold nanorods and their Raman activities[J]. Mater Res Bull, 2013, 48(10):4181-4185.
[22] Merrill N A, Sethi M, Knecht M R. Structural and equilibrium effects of the surface passivant on the stability of Au nanorods[J]. Acs Appl Mater Inter, 2013, 5(16):7906-7914.
[23] Gole A, Murphy C J. Seed-mediated synthesis of gold nanorods:role of the size and nature of the seed[J]. Chem Mater, 2004, 16(19):3633-3640.
[24] Link S, Mohamed M B, El-Sayed M A. Simulation of the optical absorption spectra of gold nanorods as a function of their aspect ratio and the effect of the medium dielectric constant[J]. J Phys Chem B, 1999, 103(16):3073-3077.
[25] Connor E E, Mwamuka J, Gole A, et al. Gold nanoparticles are taken up by human cells but do not cause acute cytotoxicity[J]. Small, 2005, 1(3):325-327.
[26] Qiu Y, Liu Y, Wang L M, et al. Surface chemistry and aspect ratio mediated cellular uptake of Au nanorods[J]. Biomaterials, 2010, 31(30):7606-7619.
[27] Cortesi R, Esposito E, Menegatti E, et al. Effect of cationic liposome composition on in vitro cytotoxicity and protective effect on carried DNA[J]. Int J Pharm, 1996, 139(1/2):69-78.
[28] Mirska D, Schirmer K, Funari S S, et al. Biophysical and biochemical properties of a binary lipid mixture for DNA transfection[J]. Colloid Surface B, 2005, 40(1):51-59.
[29] Takahashi H, Niidome Y, Niidome T, et al. Modification of gold nanorods using phospatidylcholine to reduce cytotoxicity[J]. Langmuir, 2006, 22(1):2-5.
[30] Sreeprasad T S, Samal A K, Pradeep T. One-, two-, and three-dimensional superstructures of gold nanorods induced by dimercaptosuccinic acid[J]. Langmuir, 2008, 24(9):4589-4599.
[31] Zhong L B, Zhou X, Bao S X, et al. Rational design and SERS properties of side-by-side, end-to-end and end-to-side assemblies of Au nanorods[J]. J Mater Chem, 2011, 21(38):14448-14455.
[32] Gomez-Grana S, Hubert F, Testard F, et al. Surfactant (Bi) layers on gold nanorods[J]. Langmuir, 2012, 28(2):1453-1459.
[33] Weidemaier K, Tavernier H L, Fayer M D. Photoinduced electron transfer on the surfaces of micelles[J]. J Phys Chem B, 1997, 101(45):9352-9361.
[34] Henkel A, Schubert O, Plech A, et al. Growth Kinetic of a Rod-Shaped Metal Nanocrystal[J]. J Phys Chem C, 2009, 113(24):10390-10394.
[35] Bakshi M S, Kaur G, Thakur P, et al. Surfactant selective synthesis of gold nanowires by using a DPPC-surfactant mixture as a capping agent at ambient conditions[J]. J Phys Chem C, 2007, 111(16):5932-5940.
[36] Meena S K, Sulpizi M. Understanding the microscopic origin of gold nanoparticle anisotropic growth from molecular dynamics simulations[J]. Langmuir, 2013, 29(48):14954-14961.
[37] Yuan S L, Ma L X, Zhang X Q, et al. Molecular dynamics studies on monolayer of cetyltrimethylammonium bromide surfactant formed at the air/water interface[J]. Colloid Surface A, 2006, 289(1/3):1-9.
[38] Wandlowski T, Wang J X, Magnussen O M, et al. Structural and kinetic aspects of bromide adsorption on Au(100)[J]. J Phys Chem-Us, 1996, 100(24):10277-10287.
[39] Magnussen O M, Ocko B M, Wang J X, et al. In-situ X-ray diffraction and STM studies of bromide adsorption on Au(111) electrodes[J]. J Phys Chem-Us, 1996, 100(13):5500-5508.
[40] Heinz H, Vaia R A, Farmer B L, et al. Accurate simulation of surfaces and interfaces of face-centered cubic metals using 12-6 and 9-6 Lennard-Jones potentials[J]. J Phys Chem C, 2008, 112(44):17281-17290.
[41] Feng J, Pandey R B, Berry R J, et al. Adsorption mechanism of single amino acid and surfactant molecules to Au {111} surfaces in aqueous solution:design rules for metal-binding molecules[J]. Soft Matter, 2011, 7(5):2113-2120.
[42] Wang L M, Li J Y, Pan J, et al. Revealing the binding structure of the protein corona on gold nanorods using synchrotron radiation-based techniques:understanding the reduced damage in cell membranes[J]. J Am Chem Soc, 2013, 135(46):17359-17368.
[43] Lybrand T P, Ghosh I, Mccammon J A. Hydration of chloride and bromide anions-determination of relative free-energy by computer-simulation[J]. J Am Chem Soc, 1985, 107(25):7793-7794.
[44] Thomas A S, Elcock A H. Molecular dynamics simulations of hydrophobic associations in aqueous salt solutions indicate a connection between water hydrogen bonding and the Hofmeister effect[J]. J Am Chem Soc, 2007, 129(48):14887-14898.
[45] Ferrer-Tasies L, Moreno-Calvo E, Cano-Sarabia M, et al. Quatsomes:vesicles formed by self-assembly of sterols and quaternary ammonium surfactants[J]. Langmuir, 2013, 29(22):6519-6528.
[46] Mackerell A D, Bashford D, Bellott M, et al. All-atom empirical potential for molecular modeling and dynamics studies of proteins[J]. J Phys Chem B, 1998, 102(18):3586-3616.
[47] Mackerell A D, Feig M, Brooks C L. Extending the treatment of backbone energetics in protein force fields:limitations of gas-phase quantum mechanics in reproducing protein conformational distributions in molecular dynamics simulations[J]. J Comput Chem, 2004, 25(11):1400-1415.
[48] Darden T, York D, Pedersen L. Particle mesh Ewald:an NlogN method for Ewald sums in large systems[J]. J Chem Phys, 1993, 98(12):10089-10092.
[49] Phillips J C, Braun R, Wang W, et al. Scalable molecular dynamics with NAMD[J]. J Comput Chem, 2005, 26(16):1781-1802.
[50] Humphrey W, Dalke A, Schulten K. VMD:visual molecular dynamics[J]. J Mol Graph Model, 1996, 14(1):33-38.
[51] Alkilany A M, Frey R L, Ferry J L, et al. Gold nanorods as nanoadmicelles:1-naphthol partitioning into a nanorod-bound surfactant bilayer[J]. Langmuir, 2008, 24(18):10235-10239.
[52] Bockmann R A, Hac A, Heimburg T, et al. Effect of sodium chloride on a lipid bilayer[J]. Biophys J, 2003, 85(3):1647-1655.
[53] Xia Y N, Xiong Y J, Lim B, et al. Shape-controlled synthesis of metal nanocrystals:simple chemistry meets complex physics?[J]. Angew Chem Int Edit, 2009, 48(1):60-103.
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