光致发光
碳纳米管
激子
材料科学
红外线的
纳米管
荧光
纳米技术
碳纳米管的光学性质
光电子学
光学
物理
凝聚态物理
作者
Noémie Danné,Mijin Kim,Antoine G. Godin,Hyejin Kwon,Zhenghong Gao,Xiaojian Wu,Nicolai F. Hartmann,Stephen K. Doorn,Brahim Lounis,YuHuang Wang,Laurent Cognet
出处
期刊:ACS Nano
[American Chemical Society]
日期:2018-06-11
卷期号:12 (6): 6059-6065
被引量:90
标识
DOI:10.1021/acsnano.8b02307
摘要
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.
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