Multistep Wavelength Switching of Near‐Infrared Photoluminescence Driven by Chemical Reactions at Local Doped Sites of Single‐Walled Carbon Nanotubes

2018 ◽  
Vol 24 (72) ◽  
pp. 19162-19165 ◽  
Author(s):  
Tomohiro Shiraki ◽  
Tamehito Shiga ◽  
Tomonari Shiraishi ◽  
Hisashi Onitsuka ◽  
Naotoshi Nakashima ◽  
...  
Keyword(s):  
Carbon Nanotubes ◽  
Chemical Reactions ◽  
Near Infrared ◽  
Single Walled Carbon Nanotubes ◽  
Wavelength Switching ◽  
Single Walled Carbon ◽  
Walled Carbon Nanotubes

scholarly journals In vivo biosensing via tissue-localizable near-infrared-fluorescent single-walled carbon nanotubes

2013 ◽  
Vol 8 (11) ◽  
pp. 873-880 ◽  
Author(s):  
Nicole M. Iverson ◽  
Paul W. Barone ◽  
Mia Shandell ◽  
Laura J. Trudel ◽  
Selda Sen ◽  
...  
Keyword(s):  
Carbon Nanotubes ◽  
Near Infrared ◽  
Single Walled Carbon Nanotubes ◽  
Single Walled Carbon ◽  
Walled Carbon Nanotubes

scholarly journals Enhancing near-infrared photoluminescence from single-walled carbon nanotubes by defect-engineering using benzoyl peroxide

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Lukasz Przypis ◽  
Maciej Krzywiecki ◽  
Yoshiaki Niidome ◽  
Haruka Aoki ◽  
Tomohiro Shiraki ◽  
...  
Keyword(s):  
Carbon Nanotubes ◽  
Conjugated Polymers ◽  
Near Infrared ◽  
Light Emission ◽  
Single Walled Carbon Nanotubes ◽  
Organic Radical ◽  
Defect Engineering ◽  
Single Walled Carbon ◽  
Walled Carbon Nanotubes ◽  
Selection Of

AbstractSingle-walled carbon nanotubes (SWCNTs) have been modified with ester groups using typical organic radical chemistry. Consequently, traps for mobile excitons have been created, which enhanced the optical properties of the material. The proposed methodology combines the benefits of mainstream approaches to create luminescent defects in SWCNTs while it simultaneously avoids their limitations. A step change was achieved when the aqueous medium was abandoned. The selection of an appropriate organic solvent enabled much more facile modification of SWCNTs. The presented technique is quick and versatile as it can engage numerous reactants to tune the light emission capabilities of SWCNTs. Importantly, it can also utilize SWCNTs sorted by chirality using conjugated polymers to enhance their light emission capabilities. Such differentiation is conducted in organic solvents, so monochiral SWCNT can be directly functionalized using the demonstrated concept in the same medium without the need to redisperse the material in water.

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