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首页> 外文期刊>Journal of Materials Science >Non-covalent stabilization and functionalization of boron nitride nanosheets (BNNSs) by organic polymers: formation of complex BNNSs-containing structures
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Non-covalent stabilization and functionalization of boron nitride nanosheets (BNNSs) by organic polymers: formation of complex BNNSs-containing structures

机译:有机聚合物对氮化硼纳米片(BNNSs)的非共价稳定和功能化:复杂的含BNNSs结构的形成

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摘要

The straightforward non-covalent functionalization and solubilization of hexagonal boron nitride nanosheets (BNNSs) has been achieved by reacting either polythiophene or polyvinylpyrrolidone polymers with exfoliated BNNSs. The BNNSs apparently form strong pi-pi stacking interactions with the polymers to yield stable derivatized nanosheets with modified properties. A number of polythiophene polymers functionalized with carboxylic acid groups that are connected to the thiophene subunit by varying numbers of CH2-hydrocarbon linker units have also been tethered to the exfoliated BNNSs. These BNNS-polythiophene-(CH2)(n)-COOH structures have been further coordinated to pre-formed TiO2 nanoparticles to form more complex BNNS-polythiophene(CH2)(n)-COO-TiO2 hybrid nanomaterials through covalent binding between the TiO2 nanoparticle surface and the carboxylic acid functional group of the BNNS-polythiophene unit. These novel structures have been characterized by SEM, TEM, FTIR, UV-Vis, and other spectroscopic data.
机译:通过使聚噻吩或聚乙烯吡咯烷酮聚合物与脱落的BNNS反应,已经实现了六方氮化硼纳米片(BNNS)的直接非共价官能化和增溶作用。 BNNS显然与聚合物形成了强烈的pi-pi堆积相互作用,从而产生具有改性特性的稳定的衍生化纳米片。许多通过羧酸基团官能化的聚噻吩聚合物也被束缚在脱落的BNNS上,该羧酸基团通过不同数量的CH2-烃基连接单元与噻吩亚基连接。这些BNNS-聚噻吩-(CH2)(n)-COOH结构已进一步与预先形成的TiO2纳米粒子协调,以通过TiO2纳米粒子之间的共价结合形成更复杂的BNNS-聚噻吩(CH2)(n)-COO-TiO2杂化纳米材料。 BNNS-聚噻吩单元的表面和羧酸官能团。这些新颖的结构已通过SEM,TEM,FTIR,UV-Vis和其他光谱数据进行了表征。

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