Details
Originalsprache | Englisch |
---|---|
Aufsatznummer | 2112621 |
Fachzeitschrift | Advanced functional materials |
Jahrgang | 32 |
Ausgabenummer | 24 |
Frühes Online-Datum | 27 Feb. 2022 |
Publikationsstatus | Veröffentlicht - 8 Juni 2022 |
Abstract
In the large field of research on nanoplatelets (NPLs), their strong tendency to self-assemble into ordered stacks and the resulting changes in their properties are of great interest. The assembly reveals new characteristics such as the charge carrier transport through the NPL assembly or altered optical properties. In particular, a reduced distance should enhance the charge carrier transport due to higher electronic coupling of neighboring NPLs, and therefore, is the focus of this work. To modify the inter-particle distances, the straightforward method of ligand exchange is applied. Various CdSe and CdSe/CdX (hetero-) NPLs serve as building blocks, which not only display different material combinations but also different types of heterostructures. The surface-to-surface distance between the stacked NPLs can be reduced to below 1 nm, thus, to less than the half compared to assemblies of pristine NPLs. Moreover, for certain NPLs stacking is only enabled by the ligand exchange. To characterize the ligand exchanges and to investigate the influences of the reduced distances, photo-electrochemical measurements, fluorescence spectroscopy, energy dispersive X-ray spectroscopy, nuclear magnetic resonance, and X-ray photoelectron spectroscopy are performed. It is possible to show higher photocurrents for smaller distances, indicating enhanced charge transport ability within those stacks.
ASJC Scopus Sachgebiete
- Chemie (insg.)
- Werkstoffwissenschaften (insg.)
- Physik und Astronomie (insg.)
- Physik der kondensierten Materie
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in: Advanced functional materials, Jahrgang 32, Nr. 24, 2112621, 08.06.2022.
Publikation: Beitrag in Fachzeitschrift › Artikel › Forschung › Peer-Review
}
TY - JOUR
T1 - Interparticle Distance Variation in Semiconductor Nanoplatelet Stacks
AU - Graf, Rebecca T.
AU - Schlosser, Anja
AU - Zámbó, Dániel
AU - Schlenkrich, Jakob
AU - Rusch, Pascal
AU - Chatterjee, Atasi
AU - Pfnür, Herbert
AU - Bigall, Nadja C.
N1 - Funding Information: R.T.G. and A.S. contributed equally to this work. N.C.B. thanks the European Research Council (ERC) for financial support under the European Union's Horizon 2020 research and innovation program (grant agreement 714429). Furthermore, this work was supported by the German Research Foundation (Deutsche Forschungsgemeinschaft, DFG) under Germany's excellence strategy within the cluster of excellence PhoenixD (EXC 2122, project ID 390833453). R.T.G. and A.S. thank the Hannover School for Nanotechnology (HSN) for funding. D.Z. acknowledges the program financed by the National Research, Development, and Innovation Office of the Ministry for Innovation and Technology, Hungary (TKP2021‐NKTA‐05). The authors are thankful to the Laboratory of Nano and Quantum Engineering (LNQE) for providing the TEM facilities and Jürgen Caro and Armin Feldhoff for the SEM‐EDX facilities. Additionally, the authors are grateful to Frank Steinbach for the SEM cross‐section measurements. Furthermore, the authors would like to thank Jörg Fohrer and the whole NMR department of the Institute of Organic Chemistry at Leibniz Universität Hannover for the NMR measurements. Funding Information: R.T.G. and A.S. contributed equally to this work. N.C.B. thanks the European Research Council (ERC) for financial support under the European Union's Horizon 2020 research and innovation program (grant agreement 714429). Furthermore, this work was supported by the German Research Foundation (Deutsche Forschungsgemeinschaft, DFG) under Germany's excellence strategy within the cluster of excellence PhoenixD (EXC 2122, project ID 390833453). R.T.G. and A.S. thank the Hannover School for Nanotechnology (HSN) for funding. D.Z. acknowledges the program financed by the National Research, Development, and Innovation Office of the Ministry for Innovation and Technology, Hungary (TKP2021-NKTA-05). The authors are thankful to the Laboratory of Nano and Quantum Engineering (LNQE) for providing the TEM facilities and Jürgen Caro and Armin Feldhoff for the SEM-EDX facilities. Additionally, the authors are grateful to Frank Steinbach for the SEM cross-section measurements. Furthermore, the authors would like to thank Jörg Fohrer and the whole NMR department of the Institute of Organic Chemistry at Leibniz Universität Hannover for the NMR measurements. Open access funding enabled and organized by Projekt DEAL.
PY - 2022/6/8
Y1 - 2022/6/8
N2 - In the large field of research on nanoplatelets (NPLs), their strong tendency to self-assemble into ordered stacks and the resulting changes in their properties are of great interest. The assembly reveals new characteristics such as the charge carrier transport through the NPL assembly or altered optical properties. In particular, a reduced distance should enhance the charge carrier transport due to higher electronic coupling of neighboring NPLs, and therefore, is the focus of this work. To modify the inter-particle distances, the straightforward method of ligand exchange is applied. Various CdSe and CdSe/CdX (hetero-) NPLs serve as building blocks, which not only display different material combinations but also different types of heterostructures. The surface-to-surface distance between the stacked NPLs can be reduced to below 1 nm, thus, to less than the half compared to assemblies of pristine NPLs. Moreover, for certain NPLs stacking is only enabled by the ligand exchange. To characterize the ligand exchanges and to investigate the influences of the reduced distances, photo-electrochemical measurements, fluorescence spectroscopy, energy dispersive X-ray spectroscopy, nuclear magnetic resonance, and X-ray photoelectron spectroscopy are performed. It is possible to show higher photocurrents for smaller distances, indicating enhanced charge transport ability within those stacks.
AB - In the large field of research on nanoplatelets (NPLs), their strong tendency to self-assemble into ordered stacks and the resulting changes in their properties are of great interest. The assembly reveals new characteristics such as the charge carrier transport through the NPL assembly or altered optical properties. In particular, a reduced distance should enhance the charge carrier transport due to higher electronic coupling of neighboring NPLs, and therefore, is the focus of this work. To modify the inter-particle distances, the straightforward method of ligand exchange is applied. Various CdSe and CdSe/CdX (hetero-) NPLs serve as building blocks, which not only display different material combinations but also different types of heterostructures. The surface-to-surface distance between the stacked NPLs can be reduced to below 1 nm, thus, to less than the half compared to assemblies of pristine NPLs. Moreover, for certain NPLs stacking is only enabled by the ligand exchange. To characterize the ligand exchanges and to investigate the influences of the reduced distances, photo-electrochemical measurements, fluorescence spectroscopy, energy dispersive X-ray spectroscopy, nuclear magnetic resonance, and X-ray photoelectron spectroscopy are performed. It is possible to show higher photocurrents for smaller distances, indicating enhanced charge transport ability within those stacks.
KW - charge carrier transport
KW - distance variation
KW - ligand exchange
KW - nanoplatelets
KW - photo-electrochemistry
KW - self-assembly
KW - stacks
UR - http://www.scopus.com/inward/record.url?scp=85125376701&partnerID=8YFLogxK
U2 - 10.1002/adfm.202112621
DO - 10.1002/adfm.202112621
M3 - Article
AN - SCOPUS:85125376701
VL - 32
JO - Advanced functional materials
JF - Advanced functional materials
SN - 1616-301X
IS - 24
M1 - 2112621
ER -