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相转移催化剂驱动由离子型、半导体聚合物螺旋包裹的单壁碳纳米管具有不同的有机溶剂溶解性。

Phase transfer catalysts drive diverse organic solvent solubility of single-walled carbon nanotubes helically wrapped by ionic, semiconducting polymers.

机构信息

Department of Chemistry, French Family Science Center, 124 Science Drive, Duke University, Durham, North Carolina 27708, USA.

出版信息

Nano Lett. 2010 Oct 13;10(10):4192-9. doi: 10.1021/nl102540c.

Abstract

Use of phase transfer catalysts such as 18-crown-6 enables ionic, linear conjugated poly[2,6-{1,5-bis(3-propoxysulfonicacidsodiumsalt)}naphthylene]ethynylene (PNES) to efficiently disperse single-walled carbon nanotubes (SWNTs) in multiple organic solvents under standard ultrasonication methods. Steady-state electronic absorption spectroscopy, atomic force microscopy (AFM), and transmission electron microscopy (TEM) reveal that these SWNT suspensions are composed almost exclusively of individualized tubes. High-resolution TEM and AFM data show that the interaction of PNES with SWNTs in both protic and aprotic organic solvents provides a self-assembled superstructure in which a PNES monolayer helically wraps the nanotube surface with periodic and constant morphology (observed helical pitch length = 10 ± 2 nm); time-dependent examination of these suspensions indicates that these structures persist in solution over periods that span at least several months. Pump-probe transient absorption spectroscopy reveals that the excited state lifetimes and exciton binding energies of these well-defined nanotube-semiconducting polymer hybrid structures remain unchanged relative to analogous benchmark data acquired previously for standard sodium dodecylsulfate (SDS)-SWNT suspensions, regardless of solvent. These results demonstrate that the use of phase transfer catalysts with ionic semiconducting polymers that helically wrap SWNTs provide well-defined structures that solubulize SWNTs in a wide range of organic solvents while preserving critical nanotube semiconducting and conducting properties.

摘要

使用相转移催化剂,如 18-冠-6,可使离子型、线性共轭聚[2,6-{1,5-双(3-丙磺酸钠)萘ylene]乙炔](PNES)在标准超声方法下有效地将单壁碳纳米管(SWNTs)分散在多种有机溶剂中。稳态电子吸收光谱、原子力显微镜(AFM)和透射电子显微镜(TEM)表明,这些 SWNT 悬浮液几乎完全由单个管组成。高分辨率 TEM 和 AFM 数据表明,PNES 与质子和非质子有机溶剂中的 SWNTs 的相互作用提供了一种自组装超结构,其中 PNES 单层螺旋缠绕在纳米管表面上,具有周期性和恒定的形态(观察到的螺旋螺距长度=10±2nm);对这些悬浮液的时变研究表明,这些结构在溶液中至少持续几个月。泵浦探针瞬态吸收光谱表明,这些结构明确的纳米管-半导体聚合物杂化结构的激发态寿命和激子结合能与以前获得的类似标准十二烷基硫酸钠(SDS)-SWNT 悬浮液的基准数据相比保持不变,无论溶剂如何。这些结果表明,使用离子半导体聚合物与 SWNTs 螺旋缠绕的相转移催化剂提供了明确的结构,可在广泛的有机溶剂中溶解 SWNTs,同时保持关键的纳米管半导体和导电性能。

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