Understanding the Visible Absorption of Electron Accepting and Donating CNDs
- Autores
- Reva, Yana; Jana, Bikash; Langford, Daniel; Kinzelmann, Marina; Bo, Yifan; Schol, Peter R.; Scharl, Tobias; Zhao, Xinyi; Crisp, Ryan W.; Drewello, Thomas; Clark, Timothy; Cadranel, Alejandro; Guldi, Dirk
- Año de publicación
- 2023
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Carbon nanodots (CNDs) synthesized from citric acid and formyl derivatives, that is, formamide, urea, or N-methylformamide, stand out through their broad-range visible-light absorbance and extraordinary photostability. Despite their potential, their use has thus far been limited to imaging research. This work has now investigated the link between CNDs’ photochemical properties and their chemical structure. Electron-rich, yellow carbon nanodots (yCNDs) are obtained with in situ addition of NaOH during the synthesis, whereas otherwise electron-poor, red carbon nanodots (rCNDs) are obtained. These properties originate from the reduced and oxidized dimer of citrazinic acid within the matrix of yCNDs and rCNDs, respectively. Remarkably, yCNDs deposited on TiO2 give a 30% higher photocurrent density of 0.7 mA cm−2 at +0.3 V versus Ag/AgCl under Xe-lamp irradiation (450 nm long-pass filter, 100 mW cm−2) than rCNDs. The difference in overall photoelectric performance is due to fundamentally different charge-transfer mechanisms. These depend on either the electron-accepting or the electron-donating nature of the CNDs, as is evident from photoelectrochemical tests with TiO2 and NiO and time-resolved spectroscopic measurements.
Fil: Reva, Yana. Universitat Erlangen-Nuremberg; Alemania
Fil: Jana, Bikash. Universitat Erlangen-Nuremberg; Alemania. Technion - Israel Institute of Technology; Israel
Fil: Langford, Daniel. Universitat Erlangen-Nuremberg; Alemania
Fil: Kinzelmann, Marina. Universitat Erlangen-Nuremberg; Alemania
Fil: Bo, Yifan. Universitat Erlangen-Nuremberg; Alemania
Fil: Schol, Peter R.. Universitat Erlangen-Nuremberg; Alemania
Fil: Scharl, Tobias. Universitat Erlangen-Nuremberg; Alemania
Fil: Zhao, Xinyi. Central South University; China. Universitat Erlangen-Nuremberg; Alemania
Fil: Crisp, Ryan W.. Universitat Erlangen-Nuremberg; Alemania
Fil: Drewello, Thomas. Universitat Erlangen-Nuremberg; Alemania
Fil: Clark, Timothy. Universitat Erlangen-Nuremberg; Alemania
Fil: Cadranel, Alejandro. Universitat Erlangen-Nuremberg; Alemania. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Guldi, Dirk. Universitat Erlangen-Nuremberg; Alemania - Materia
-
CARBON NANODOTS
EXCITED STATE
PHOTOELECTROCHEMISTRY
SEMICONDUCTORS
TIME-RESOLVED SPECTROSCOPY - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/228445
Ver los metadatos del registro completo
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CONICET Digital (CONICET) |
spelling |
Understanding the Visible Absorption of Electron Accepting and Donating CNDsReva, YanaJana, BikashLangford, DanielKinzelmann, MarinaBo, YifanSchol, Peter R.Scharl, TobiasZhao, XinyiCrisp, Ryan W.Drewello, ThomasClark, TimothyCadranel, AlejandroGuldi, DirkCARBON NANODOTSEXCITED STATEPHOTOELECTROCHEMISTRYSEMICONDUCTORSTIME-RESOLVED SPECTROSCOPYhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1Carbon nanodots (CNDs) synthesized from citric acid and formyl derivatives, that is, formamide, urea, or N-methylformamide, stand out through their broad-range visible-light absorbance and extraordinary photostability. Despite their potential, their use has thus far been limited to imaging research. This work has now investigated the link between CNDs’ photochemical properties and their chemical structure. Electron-rich, yellow carbon nanodots (yCNDs) are obtained with in situ addition of NaOH during the synthesis, whereas otherwise electron-poor, red carbon nanodots (rCNDs) are obtained. These properties originate from the reduced and oxidized dimer of citrazinic acid within the matrix of yCNDs and rCNDs, respectively. Remarkably, yCNDs deposited on TiO2 give a 30% higher photocurrent density of 0.7 mA cm−2 at +0.3 V versus Ag/AgCl under Xe-lamp irradiation (450 nm long-pass filter, 100 mW cm−2) than rCNDs. The difference in overall photoelectric performance is due to fundamentally different charge-transfer mechanisms. These depend on either the electron-accepting or the electron-donating nature of the CNDs, as is evident from photoelectrochemical tests with TiO2 and NiO and time-resolved spectroscopic measurements.Fil: Reva, Yana. Universitat Erlangen-Nuremberg; AlemaniaFil: Jana, Bikash. Universitat Erlangen-Nuremberg; Alemania. Technion - Israel Institute of Technology; IsraelFil: Langford, Daniel. Universitat Erlangen-Nuremberg; AlemaniaFil: Kinzelmann, Marina. Universitat Erlangen-Nuremberg; AlemaniaFil: Bo, Yifan. Universitat Erlangen-Nuremberg; AlemaniaFil: Schol, Peter R.. Universitat Erlangen-Nuremberg; AlemaniaFil: Scharl, Tobias. Universitat Erlangen-Nuremberg; AlemaniaFil: Zhao, Xinyi. Central South University; China. Universitat Erlangen-Nuremberg; AlemaniaFil: Crisp, Ryan W.. Universitat Erlangen-Nuremberg; AlemaniaFil: Drewello, Thomas. Universitat Erlangen-Nuremberg; AlemaniaFil: Clark, Timothy. Universitat Erlangen-Nuremberg; AlemaniaFil: Cadranel, Alejandro. Universitat Erlangen-Nuremberg; Alemania. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Guldi, Dirk. Universitat Erlangen-Nuremberg; AlemaniaWiley VCH Verlag2023-02info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/228445Reva, Yana; Jana, Bikash; Langford, Daniel; Kinzelmann, Marina; Bo, Yifan; et al.; Understanding the Visible Absorption of Electron Accepting and Donating CNDs; Wiley VCH Verlag; Small; 19; 31; 2-2023; 1-101613-6810CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1002/smll.202207238info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/10.1002/smll.202207238info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T10:07:27Zoai:ri.conicet.gov.ar:11336/228445instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 10:07:27.927CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Understanding the Visible Absorption of Electron Accepting and Donating CNDs |
title |
Understanding the Visible Absorption of Electron Accepting and Donating CNDs |
spellingShingle |
Understanding the Visible Absorption of Electron Accepting and Donating CNDs Reva, Yana CARBON NANODOTS EXCITED STATE PHOTOELECTROCHEMISTRY SEMICONDUCTORS TIME-RESOLVED SPECTROSCOPY |
title_short |
Understanding the Visible Absorption of Electron Accepting and Donating CNDs |
title_full |
Understanding the Visible Absorption of Electron Accepting and Donating CNDs |
title_fullStr |
Understanding the Visible Absorption of Electron Accepting and Donating CNDs |
title_full_unstemmed |
Understanding the Visible Absorption of Electron Accepting and Donating CNDs |
title_sort |
Understanding the Visible Absorption of Electron Accepting and Donating CNDs |
dc.creator.none.fl_str_mv |
Reva, Yana Jana, Bikash Langford, Daniel Kinzelmann, Marina Bo, Yifan Schol, Peter R. Scharl, Tobias Zhao, Xinyi Crisp, Ryan W. Drewello, Thomas Clark, Timothy Cadranel, Alejandro Guldi, Dirk |
author |
Reva, Yana |
author_facet |
Reva, Yana Jana, Bikash Langford, Daniel Kinzelmann, Marina Bo, Yifan Schol, Peter R. Scharl, Tobias Zhao, Xinyi Crisp, Ryan W. Drewello, Thomas Clark, Timothy Cadranel, Alejandro Guldi, Dirk |
author_role |
author |
author2 |
Jana, Bikash Langford, Daniel Kinzelmann, Marina Bo, Yifan Schol, Peter R. Scharl, Tobias Zhao, Xinyi Crisp, Ryan W. Drewello, Thomas Clark, Timothy Cadranel, Alejandro Guldi, Dirk |
author2_role |
author author author author author author author author author author author author |
dc.subject.none.fl_str_mv |
CARBON NANODOTS EXCITED STATE PHOTOELECTROCHEMISTRY SEMICONDUCTORS TIME-RESOLVED SPECTROSCOPY |
topic |
CARBON NANODOTS EXCITED STATE PHOTOELECTROCHEMISTRY SEMICONDUCTORS TIME-RESOLVED SPECTROSCOPY |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
Carbon nanodots (CNDs) synthesized from citric acid and formyl derivatives, that is, formamide, urea, or N-methylformamide, stand out through their broad-range visible-light absorbance and extraordinary photostability. Despite their potential, their use has thus far been limited to imaging research. This work has now investigated the link between CNDs’ photochemical properties and their chemical structure. Electron-rich, yellow carbon nanodots (yCNDs) are obtained with in situ addition of NaOH during the synthesis, whereas otherwise electron-poor, red carbon nanodots (rCNDs) are obtained. These properties originate from the reduced and oxidized dimer of citrazinic acid within the matrix of yCNDs and rCNDs, respectively. Remarkably, yCNDs deposited on TiO2 give a 30% higher photocurrent density of 0.7 mA cm−2 at +0.3 V versus Ag/AgCl under Xe-lamp irradiation (450 nm long-pass filter, 100 mW cm−2) than rCNDs. The difference in overall photoelectric performance is due to fundamentally different charge-transfer mechanisms. These depend on either the electron-accepting or the electron-donating nature of the CNDs, as is evident from photoelectrochemical tests with TiO2 and NiO and time-resolved spectroscopic measurements. Fil: Reva, Yana. Universitat Erlangen-Nuremberg; Alemania Fil: Jana, Bikash. Universitat Erlangen-Nuremberg; Alemania. Technion - Israel Institute of Technology; Israel Fil: Langford, Daniel. Universitat Erlangen-Nuremberg; Alemania Fil: Kinzelmann, Marina. Universitat Erlangen-Nuremberg; Alemania Fil: Bo, Yifan. Universitat Erlangen-Nuremberg; Alemania Fil: Schol, Peter R.. Universitat Erlangen-Nuremberg; Alemania Fil: Scharl, Tobias. Universitat Erlangen-Nuremberg; Alemania Fil: Zhao, Xinyi. Central South University; China. Universitat Erlangen-Nuremberg; Alemania Fil: Crisp, Ryan W.. Universitat Erlangen-Nuremberg; Alemania Fil: Drewello, Thomas. Universitat Erlangen-Nuremberg; Alemania Fil: Clark, Timothy. Universitat Erlangen-Nuremberg; Alemania Fil: Cadranel, Alejandro. Universitat Erlangen-Nuremberg; Alemania. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Guldi, Dirk. Universitat Erlangen-Nuremberg; Alemania |
description |
Carbon nanodots (CNDs) synthesized from citric acid and formyl derivatives, that is, formamide, urea, or N-methylformamide, stand out through their broad-range visible-light absorbance and extraordinary photostability. Despite their potential, their use has thus far been limited to imaging research. This work has now investigated the link between CNDs’ photochemical properties and their chemical structure. Electron-rich, yellow carbon nanodots (yCNDs) are obtained with in situ addition of NaOH during the synthesis, whereas otherwise electron-poor, red carbon nanodots (rCNDs) are obtained. These properties originate from the reduced and oxidized dimer of citrazinic acid within the matrix of yCNDs and rCNDs, respectively. Remarkably, yCNDs deposited on TiO2 give a 30% higher photocurrent density of 0.7 mA cm−2 at +0.3 V versus Ag/AgCl under Xe-lamp irradiation (450 nm long-pass filter, 100 mW cm−2) than rCNDs. The difference in overall photoelectric performance is due to fundamentally different charge-transfer mechanisms. These depend on either the electron-accepting or the electron-donating nature of the CNDs, as is evident from photoelectrochemical tests with TiO2 and NiO and time-resolved spectroscopic measurements. |
publishDate |
2023 |
dc.date.none.fl_str_mv |
2023-02 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/228445 Reva, Yana; Jana, Bikash; Langford, Daniel; Kinzelmann, Marina; Bo, Yifan; et al.; Understanding the Visible Absorption of Electron Accepting and Donating CNDs; Wiley VCH Verlag; Small; 19; 31; 2-2023; 1-10 1613-6810 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/228445 |
identifier_str_mv |
Reva, Yana; Jana, Bikash; Langford, Daniel; Kinzelmann, Marina; Bo, Yifan; et al.; Understanding the Visible Absorption of Electron Accepting and Donating CNDs; Wiley VCH Verlag; Small; 19; 31; 2-2023; 1-10 1613-6810 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1002/smll.202207238 info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/10.1002/smll.202207238 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Wiley VCH Verlag |
publisher.none.fl_str_mv |
Wiley VCH Verlag |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1842270004826865664 |
score |
13.13397 |