| Literature DB >> 29889499 |
Noémie Danné1,2, Mijin Kim3, Antoine G Godin1,2, Hyejin Kwon3, Zhenghong Gao1,2, Xiaojian Wu3, Nicolai F Hartmann4, Stephen K Doorn4, Brahim Lounis1,2, YuHuang Wang3,5, Laurent Cognet1,2.
Abstract
The intrinsic near-infrared photoluminescence observed in long single-walled carbon nanotubes is known to be quenched in ultrashort nanotubes due to their tiny size as compared to the exciton diffusion length in these materials (>100 nm). Here, we show that intense photoluminescence can be created in ultrashort nanotubes (∼40 nm length) upon incorporation of exciton-trapping sp3 defect sites. Using super-resolution photoluminescence imaging at <25 nm resolution, we directly show the preferential localization of excitons at the nanotube ends, which separate by less than 40 nm and behave as independent emitters. This unexpected observation opens the possibility to synthesize fluorescent ultrashort nanotubes-a goal that has been long thought impossible-for bioimaging applications, where bright near-infrared photoluminescence and small size are highly desirable, and for quantum information science, where high quality and well-controlled near-infrared single photon emitters are needed.Entities:
Keywords: doping; emission centers; exciton localization; photoluminescence; single molecules; super-resolution microscopy; ultrashort carbon nanotube
Year: 2018 PMID: 29889499 DOI: 10.1021/acsnano.8b02307
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881