Covalent Functionalization of Short, Single-Wall Carbon Nanotubes: Photophysics of 2,4,6-Triphenylpyrylium Attached to the Nanotube Walls

被引:22
作者
Aprile, Carmela [1 ]
Martin, Roberto [1 ]
Alvaro, Mercedes [1 ]
Garcia, Hermenegildo [1 ]
Scaiano, J. C. [2 ]
机构
[1] Univ Politecn Valencia, Inst Tecnol Quim, CSIC UPV, Valencia 46022, Spain
[2] Univ Ottawa, Dept Chem, Ctr Catalysis Res & Innovat, Ottawa, ON K1N 6N5, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
PHOTOINDUCED ELECTRON-TRANSFER; OPTICAL-PROPERTIES; ZINC PORPHYRIN; CHEMISTRY; PHOTOCHEMISTRY; NANOHYBRIDS; FULLERENES; COMPLEXES; UNITS;
D O I
10.1021/cm803037g
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
2,4,6-Triarylpyrylium units (TP+) have been attached covalently to the walls of short, water-soluble single-wall carbon nanotubes (sSWNT) to give TP-sSWNT sample (6.8 wt % on TP+). The high loading achieved in this manner has allowed characterization of the material by a wide range of techniques, including AFM (about 1 mu m length), thermogravimetric analyses (absence of inorganic particles in the sample), Raman spectroscopy (radial breathing vibration mode at 180 cm(-1)), and solution H-1 NMR spectroscopy (up to 0.5 ppm variation in the delta of the protons upon attachment to the graphene walls). Optical spectroscopy reveals the absence of the van Hove singularities in the TP-sSWNT sample. Fluorescence spectroscopy indicates sSWNT quenching of the otherwise intense TP+ emission. Laser flash photolysis has allowed detecting a transient species characterized by a broad absorption from 400 to 700 nm that decays with a fast (<500 ns) and a slow (a few microsecond) kinetics. TP-sSWNT emits NIR luminescence with an estimated 2.3 x 10(-3) quantum yield.
引用
收藏
页码:884 / 890
页数:7
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