Single Nanoparticle to 3D Supercage: Framing for an Artificial Enzyme System

被引:113
作者
Cai, Ren [1 ,2 ,3 ]
Yang, Dan [6 ]
Peng, Shengjie [6 ]
Chen, Xigao [1 ,2 ,3 ]
Huang, Yun [1 ,2 ,3 ]
Liu, Yuan [1 ,2 ,3 ]
Hou, Weijia [1 ,2 ,3 ]
Yang, Shengyuan [1 ,2 ,3 ,7 ]
Liu, Zhenbao [1 ,2 ,3 ]
Tan, Weihong [1 ,2 ,3 ,4 ,5 ]
机构
[1] Univ Florida, Dept Chem, Ctr Res Bio Nano Interface, Gainesville, FL 32611 USA
[2] Univ Florida, UF Genet Inst, Hlth Canc Ctr, Dept Physiol & Funct Genom, Gainesville, FL 32611 USA
[3] Univ Florida, McKnight Brain Inst, Gainesville, FL 32611 USA
[4] Hunan Univ, Coll Biol, Coll Chem & Chem Engn, Mol Sci & Biomed Lab,State Key Lab Chemo Bio Sen, Changsha 410082, Hunan, Peoples R China
[5] Hunan Univ, Collaborat Res Ctr Mol Engn Theranost, Changsha 410082, Hunan, Peoples R China
[6] Nanyang Technol Univ, Sch Mat Sci & Engn, Singapore 639798, Singapore
[7] Univ South China, Coll Publ Hlth, Hengyang 421001, Peoples R China
基金
美国国家卫生研究院;
关键词
GRAPHENE QUANTUM DOTS; SUPERLATTICES; NANOMATERIALS; NANOCLUSTERS; NANOCRYSTALS; TEMPERATURE; GENERATION; NANOWIRES; MECHANISM; NANOZYMES;
D O I
10.1021/jacs.5b09337
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A facile strategy has been developed to fabricate Cu(OH)(2) supercages (SCs) as an artificial enzyme system with intrinsic peroxidase-mimic activities (PMA). SCs with high catalytic activity and excellent recyclability were generated via direct conversion of amorphous Cu(OH)(2) nanoparticles (NPs) at room temperature. More specifically, the process that takes a single nanoparticle to a 3D supercage involves two basic steps. First, with addition of a copper ammonia complex, the Cu2+ ions that are located on the surface of amorphous Cu(OH)(2) NPs would evolve into a fine lamellar structure by coordination and migration and eventually convert to ID nanoribbons around the NPs. Second, accompanied by the migration of Cu2+, a hollow cavity is generated in the inner NPs, such that a single nanoparticle eventually becomes a nanoribbon-assembled 3D hollow cage. These Cu(OH)(2) SCs were then engineered as an artificial enzymatic system with higher efficiency for intrinsic PMA than the peroxidase activity of a natural enzyme, horseradish peroxidase.
引用
收藏
页码:13957 / 13963
页数:7
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