Surface States Induced Photoluminescence Enhancement of Nitrogen-Doped Carbon Dots Via Post-Treatments
Abstract The tunable photoluminescence (PL) of nitrogen-doped carbon dots (NCDs) has attracted much attention in recent years while the specific mechanism is still in dispute. Herein, NCDs with yellow emission were successfully synthesized via a facile hydrothermal approach. Three kinds of post-trea...
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doaj-37926c61c0c94f2baff6b2e4753bb0932020-11-25T03:14:57ZengSpringerOpenNanoscale Research Letters1931-75731556-276X2019-05-011411910.1186/s11671-019-3008-9Surface States Induced Photoluminescence Enhancement of Nitrogen-Doped Carbon Dots Via Post-TreatmentsXian Wei0Shiliang Mei1Dan Yang2Guilin Zhang3Fengxian Xie4Wanlu Zhang5Ruiqian Guo6Engineering Research Center of Advanced Lighting Technology, Ministry of Education; Institute for Electric Light Sources, Fudan UniversityEngineering Research Center of Advanced Lighting Technology, Ministry of Education; Institute for Electric Light Sources, Fudan UniversityEngineering Research Center of Advanced Lighting Technology, Ministry of Education; Institute for Electric Light Sources, Fudan UniversityEngineering Research Center of Advanced Lighting Technology, Ministry of Education; Institute for Electric Light Sources, Fudan UniversityEngineering Research Center of Advanced Lighting Technology, Ministry of Education; Institute for Electric Light Sources, Fudan UniversityEngineering Research Center of Advanced Lighting Technology, Ministry of Education; Institute for Electric Light Sources, Fudan UniversityEngineering Research Center of Advanced Lighting Technology, Ministry of Education; Institute for Electric Light Sources, Fudan UniversityAbstract The tunable photoluminescence (PL) of nitrogen-doped carbon dots (NCDs) has attracted much attention in recent years while the specific mechanism is still in dispute. Herein, NCDs with yellow emission were successfully synthesized via a facile hydrothermal approach. Three kinds of post-treatment routes were investigated to verify the influence of surface states on the PL emission of NCDs including solvent-dependent, reduced-reaction and metal-enhanced effect. The interaction mechanism was studied by absorption spectrum, structural characterizations, steady-state and time-resolved spectroscopy. When dispersed in different solvents, the as-prepared NCDs show tunable emission and PL enhancement attributed to hydrogen bonding between solvents and NCDs. Besides, the addition of NaBH4 can induce the reduction of the C=O bonds existing in original NCDs to C–O bonds and thus result in the enhancement of the intrinsic (n–π*) emission. Moreover, metal-enhanced fluorescence of NCDs can also be observed when adding Ag+ into initial NCD solution, which might be ascribed to aggregation-induced emission enhancement. These results for post-treated NCDs demonstrate that surface functional groups are responsible for PL emission and provide new possibilities like multi-image sensing and lighting application.http://link.springer.com/article/10.1186/s11671-019-3008-9Carbon dotsN-dopedSurface statesPL enhancementSolvent-dependent effectReduced-reaction effect |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Xian Wei Shiliang Mei Dan Yang Guilin Zhang Fengxian Xie Wanlu Zhang Ruiqian Guo |
spellingShingle |
Xian Wei Shiliang Mei Dan Yang Guilin Zhang Fengxian Xie Wanlu Zhang Ruiqian Guo Surface States Induced Photoluminescence Enhancement of Nitrogen-Doped Carbon Dots Via Post-Treatments Nanoscale Research Letters Carbon dots N-doped Surface states PL enhancement Solvent-dependent effect Reduced-reaction effect |
author_facet |
Xian Wei Shiliang Mei Dan Yang Guilin Zhang Fengxian Xie Wanlu Zhang Ruiqian Guo |
author_sort |
Xian Wei |
title |
Surface States Induced Photoluminescence Enhancement of Nitrogen-Doped Carbon Dots Via Post-Treatments |
title_short |
Surface States Induced Photoluminescence Enhancement of Nitrogen-Doped Carbon Dots Via Post-Treatments |
title_full |
Surface States Induced Photoluminescence Enhancement of Nitrogen-Doped Carbon Dots Via Post-Treatments |
title_fullStr |
Surface States Induced Photoluminescence Enhancement of Nitrogen-Doped Carbon Dots Via Post-Treatments |
title_full_unstemmed |
Surface States Induced Photoluminescence Enhancement of Nitrogen-Doped Carbon Dots Via Post-Treatments |
title_sort |
surface states induced photoluminescence enhancement of nitrogen-doped carbon dots via post-treatments |
publisher |
SpringerOpen |
series |
Nanoscale Research Letters |
issn |
1931-7573 1556-276X |
publishDate |
2019-05-01 |
description |
Abstract The tunable photoluminescence (PL) of nitrogen-doped carbon dots (NCDs) has attracted much attention in recent years while the specific mechanism is still in dispute. Herein, NCDs with yellow emission were successfully synthesized via a facile hydrothermal approach. Three kinds of post-treatment routes were investigated to verify the influence of surface states on the PL emission of NCDs including solvent-dependent, reduced-reaction and metal-enhanced effect. The interaction mechanism was studied by absorption spectrum, structural characterizations, steady-state and time-resolved spectroscopy. When dispersed in different solvents, the as-prepared NCDs show tunable emission and PL enhancement attributed to hydrogen bonding between solvents and NCDs. Besides, the addition of NaBH4 can induce the reduction of the C=O bonds existing in original NCDs to C–O bonds and thus result in the enhancement of the intrinsic (n–π*) emission. Moreover, metal-enhanced fluorescence of NCDs can also be observed when adding Ag+ into initial NCD solution, which might be ascribed to aggregation-induced emission enhancement. These results for post-treated NCDs demonstrate that surface functional groups are responsible for PL emission and provide new possibilities like multi-image sensing and lighting application. |
topic |
Carbon dots N-doped Surface states PL enhancement Solvent-dependent effect Reduced-reaction effect |
url |
http://link.springer.com/article/10.1186/s11671-019-3008-9 |
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