Contact angle and adsorption energies of nanoparticles at the air-liquid interface determined by neutron reflectivity and molecular dynamics

被引:48
|
作者
Reguera, Javier [1 ,2 ,3 ]
Ponomarev, Evgeniy [1 ]
Geue, Thomas [4 ]
Stellacci, Francesco [1 ]
Bresme, Fernando [5 ]
Moglianetti, Mauro [6 ]
机构
[1] Ecole Polytech Fed Lausanne, Inst Mat, CH-1015 Lausanne, Switzerland
[2] CIC BiomaGUNE, Donostia San Sebastian 20009, Spain
[3] Basque Fdn Sci, Ikerbasque, Bilbao 48011, Spain
[4] Paul Scherrer Inst, Lab Neutron Scattering & Imaging, CH-5232 Villigen, Switzerland
[5] Univ London Imperial Coll Sci Technol & Med, Dept Chem, London SW7 2AZ, England
[6] Ist Italiano Tecnol, CBN, I-73010 Arnesano, Italy
基金
瑞士国家科学基金会; 英国工程与自然科学研究理事会;
关键词
SCANNING-TUNNELING-MICROSCOPY; GOLD; MONOLAYERS; SURFACE; WATER; FABRICATION; SCATTERING; PARTICLES; PLANAR; SHELL;
D O I
10.1039/c5nr00620a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Understanding how nanomaterials interact with interfaces is essential to control their self-assembly as well as their optical, electronic, and catalytic properties. We present here an experimental approach based on neutron reflectivity (NR) that allows the in situ measurement of the contact angles of nanoparticles adsorbed at fluid interfaces. Because our method provides a route to quantify the adsorption and interfacial energies of the nanoparticles in situ, it circumvents problems associated with existing indirect methods, which rely on the transport of the monolayers to substrates for further analysis. We illustrate the method by measuring the contact angle of hydrophilic and hydrophobic gold nanoparticles, coated with perdeuterated octanethiol (d-OT) and with a mixture of d-OT and mercaptohexanol (MHol), respectively. The contact angles were also calculated via atomistic molecular dynamics (MD) computations, showing excellent agreement with the experimental data. Our method opens the route to quantify the adsorption of complex nanoparticle structures adsorbed at fluid interfaces featuring different chemical compositions.
引用
收藏
页码:5665 / 5673
页数:9
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