Ligand-Mediated Spatially Controllable Superassembly of Asymmetric Hollow Nanotadpoles with Fine-Tunable Cavity as Smart H2O2-Sensitive Nanoswimmers

被引:29
作者
Yan, Miao [1 ]
Xie, Lei [1 ]
Qiu, Beilei [1 ]
Zhou, Shan [1 ]
Liu, Tianyi [1 ]
Zeng, Jie [1 ]
Liang, Qirui [1 ]
Tang, Jinyao [1 ]
Liang, Kang [2 ]
Zhao, Dongyuan [1 ]
Kong, Biao [1 ]
机构
[1] Fudan Univ, Dept Chem, Shanghai Key Lab Mol Catalysis & Innovat Mat, iChEM, Shanghai 200438, Peoples R China
[2] Univ New South Wales, Australian Ctr NanoMed, Sch Chem Engn, Grad Sch Biomed Engn, Sydney, NSW 2052, Australia
基金
上海市自然科学基金; 中国国家自然科学基金;
关键词
direct superassembly; fine-tunable cavity; H2O2-sensitive nanoswimmers; ligand-mediated; nanosynthesis; METAL; NANOPARTICLES; BROMIDE;
D O I
10.1021/acsnano.1c01159
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Ligand-mediated interface control has been broadly applied as a powerful tool in constructing sophisticated nanocomposites. However, the resultant morphologies are usually limited to solid structures. Now, a facile spatially controllable ligand-mediated superassembly strategy is explored to construct monodispersed, asymmetric, hollow, open Au-silica (SiO2) nanotadpoles (AHOASTs). By manipulating the spatial density of ligands, the degree of diffusion of silica can be precisely modulated; thus the diameters of the cavity can be continuously tuned. Due to their highly anisotropic, hollow, open morphologies, we construct a multicompartment nano-container with enzymes held and isolated inside the cavity. Furthermore, the resulting enzyme-AHOASTs are used as biocompatible smart H2O2-sensitive nanoswimmers and demonstrate a higher diffusion coefficient than other nanoscaled swimmers. We believe that this strategy is critical not only in designing sophisticated hollow nanosystem but also in providing great opportunities for applications in nanomaterial assembly, catalysis, sensors, and nanoreactors.
引用
收藏
页码:11451 / 11460
页数:10
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