Surface Ligands Dictate the Mechanical Properties of Inorganic Nanomaterials

被引:7
|
作者
Rehn, Sarah M. [1 ]
Gerrard-Anderson, Theodor M. [1 ]
Chen, Yu [2 ]
Wang, Peng [2 ]
Robertson, Timothy [1 ]
Senftle, Thomas P. [2 ]
Jones, Matthew R. [2 ]
机构
[1] Rice Univ, Dept Chem, Houston, TX 77005 USA
[2] Rice Univ, Dept Chem & Biomol Engn, Houston, TX 77005 USA
基金
美国国家科学基金会;
关键词
nanoplate; surface chemistry; nanomechanics; chemomechanics; electron microscopy; ligand exchange; GOLD NANOPARTICLE; METAL NANOPARTICLES; QUANTUM DOTS; STRESS; ADSORPTION; SHAPE; SIZE; ALKANETHIOLS; DEFORMATION; TRANSITION;
D O I
10.1021/acsnano.2c12497
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The ability for organic surface chemistry to influence the properties of inorganic nanomaterials is appreciated in some instances but is poorly understood in terms of mechanical behavior. Here we demonstrate that the global mechanical strength of a silver nanoplate can be modulated according to the local binding enthalpy of its surface ligands. A continuum-based core-shell model for nanoplate deformation shows that the interior of a particle retains bulk-like properties while the surface shell has yield strength values that depend on surface chemistry. Electron diffraction experiments reveal that, relative to the core, atoms at the nanoplate surface undergo lattice expansion and disordering directly related to the coordinating strength of the surface ligand. As a result, plastic deformation of the shell is more difficult, leading to an enhancement of the global mechanical strength of the plate. These results demonstrate a size-dependent coupling between chemistry and mechanics at the nanoscale.
引用
收藏
页码:6698 / 6707
页数:10
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