共 52 条
Regioselective surface encoding of nanoparticles for programmable self-assembly
被引:172
作者:
Chen, Gang
[1
,5
]
Gibson, Kyle J.
[1
]
Liu, Di
[1
]
Rees, Huw C.
[1
]
Lee, Jung-Hoon
[1
]
Xia, Weiwei
[2
]
Lin, Ruoqian
[2
]
Xin, Huolin L.
[2
]
Gang, Oleg
[2
,3
,4
]
Weizmann, Yossi
[1
]
机构:
[1] Univ Chicago, Dept Chem, 5735 S Ellis Ave, Chicago, IL 60637 USA
[2] Brookhaven Natl Lab, Ctr Funct Nanomat, Upton, NY 11973 USA
[3] Columbia Univ, Dept Chem Engn, New York, NY USA
[4] Columbia Univ, Dept Appl Phys & Appl Math, New York, NY USA
[5] Univ Cent Florida, Dept Chem, Orlando, FL 32816 USA
关键词:
GOLD;
GROWTH;
NANOSTRUCTURES;
CLUSTERS;
SILVER;
FUNCTIONALIZATION;
NANOCUBES;
SHAPE;
D O I:
10.1038/s41563-018-0231-1
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Surface encoding of colloidal nanoparticles with DNA is fundamental for fields where recognition interaction is required, particularly controllable material self-assembly. However, regioselective surface encoding of nanoparticles is still challenging because of the difficulty associated with breaking the identical chemical environment on nanoparticle surfaces. Here we demonstrate the selective blocking of nanoparticle surfaces with a diblock copolymer (polystyrene-b-polyacrylic acid). By tuning the interfacial free energies of a ternary system involving the nanoparticles, solvent and copolymer, controllable accessibilities to the nanoparticles' surfaces are obtained. Through the modification of the polymer-free surface region with single-stranded DNA, regioselective and programmable surface encoding is realized. The resultant interparticle binding potential is selective and directional, allowing for an increased degree of complexity of potential self-assemblies. The versatility of this regioselective surface encoding strategy is demonstrated on various nanoparticles of isotropic or anisotropic shape and a total of 24 distinct complex nanoassemblies are fabricated.
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页码:169 / +
页数:8
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