Compact microcubic structures platform based on self-assembly Prussian blue nanoparticles with highly tuneable conductivity

被引:13
作者
Cantanhede Silva, Welter [1 ,2 ]
Guix, Maria [1 ]
Alarcon Angeles, Georgina [1 ,3 ]
Merkoci, Arben [1 ,3 ,4 ]
机构
[1] Univ Autonoma Barcelona, Inst Catala Nanotecnol, Barcelona, Catalonia, Spain
[2] Univ Fed Piaui, Dept Chem, BR-64049550 Teresina, Piaui, Brazil
[3] Autonomous Metropolitan Univ, Dept Basic Sci, Unit Azcapotzalco, Mexico City 02200, DF, Mexico
[4] Passeig Lluis Co, Inst Catalana Recerca & Estudis Avancats, Barcelona 2308010, Spain
关键词
ELECTROCATALYTIC REDUCTION; SUPRAMOLECULAR CHEMISTRY; NANOCOMPOSITE FILMS; BETA-CYCLODEXTRIN; IMMOBILIZATION; ORGANIZATION; COMPOSITES; DEPOSITION; ELECTRODE;
D O I
10.1039/c0cp00960a
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
Control of molecular and supramolecular properties is used to obtain a new advanced hybrid material based on Prussian blue nanoparticles (PB NPs). This hybrid material is obtained through a self-assembled Layer-by-Layer (LbL) approach combining the advantageous features of beta-cyclodextrin (beta-CD) polysaccharides, PB NPs and poly(allylamine hydrochloride) from electrostatic interaction between the deposited layers. Transmission electronic microscopy images suggested that PB NPs were protected by beta-CD polysaccharides that prevent the aggregation phenomena. In addition, as confirmed by scanning electronic microscopy images, it was found that PB NPs are organized in microcubic supramolecular like structures via a mesoscale self-assembly process. Interestingly, the 3-bilayer {PAH/PB-CD} film exhibited a higher density of microcubic structures and a high electrochemical response with PB sites available for redox reactions at a supramolecular level. By utilizing fewer bilayers and consequently less material deposition, the formed {PAH/PB-CD} multilayer films of a tuneable conductivity can be expected to have interesting future applications for host-guest like dependent electrochemical biosensing designs.
引用
收藏
页码:15505 / 15511
页数:7
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