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Engineering the Band Alignment in QD Heterojunction Films via Ligand Exchange
[Image: see text] Colloidal quantum dots (QDs) allow great flexibility in the design of optoelectronic devices, thanks to their size-dependent optical and electronic properties and the possibility to fabricate thin films with solution-based processing. In particular, in QD-based heterojunctions, the...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6913897/ https://www.ncbi.nlm.nih.gov/pubmed/31867087 http://dx.doi.org/10.1021/acs.jpcc.9b09470 |
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author | Grimaldi, Gianluca van den Brom, Mark J. du Fossé, Indy Crisp, Ryan W. Kirkwood, Nicholas Gudjonsdottir, Solrun Geuchies, Jaco J. Kinge, Sachin Siebbeles, Laurens D. A. Houtepen, Arjan J. |
author_facet | Grimaldi, Gianluca van den Brom, Mark J. du Fossé, Indy Crisp, Ryan W. Kirkwood, Nicholas Gudjonsdottir, Solrun Geuchies, Jaco J. Kinge, Sachin Siebbeles, Laurens D. A. Houtepen, Arjan J. |
author_sort | Grimaldi, Gianluca |
collection | PubMed |
description | [Image: see text] Colloidal quantum dots (QDs) allow great flexibility in the design of optoelectronic devices, thanks to their size-dependent optical and electronic properties and the possibility to fabricate thin films with solution-based processing. In particular, in QD-based heterojunctions, the band gap of both components can be controlled by varying the size of the QDs. However, control over the band alignment between the two materials is required to tune the dynamics of carrier transfer across a heterostructure. We demonstrate that ligand exchange strategies can be used to control the band alignment of PbSe and CdSe QDs in a mixed QD solid, shifting it from a type-I to a type-II alignment. The change in alignment is observed in both spectroelectrochemical and transient absorption measurements, leading to a change in the energy of the conduction band edges in the two materials and in the direction of electron transfer upon photoexcitation. Our work demonstrates the possibility to tune the band offset of QD heterostructures via control of the chemical species passivating the QD surface, allowing full control over the energetics of the heterostructure without requiring changes in the QD composition. |
format | Online Article Text |
id | pubmed-6913897 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-69138972019-12-19 Engineering the Band Alignment in QD Heterojunction Films via Ligand Exchange Grimaldi, Gianluca van den Brom, Mark J. du Fossé, Indy Crisp, Ryan W. Kirkwood, Nicholas Gudjonsdottir, Solrun Geuchies, Jaco J. Kinge, Sachin Siebbeles, Laurens D. A. Houtepen, Arjan J. J Phys Chem C Nanomater Interfaces [Image: see text] Colloidal quantum dots (QDs) allow great flexibility in the design of optoelectronic devices, thanks to their size-dependent optical and electronic properties and the possibility to fabricate thin films with solution-based processing. In particular, in QD-based heterojunctions, the band gap of both components can be controlled by varying the size of the QDs. However, control over the band alignment between the two materials is required to tune the dynamics of carrier transfer across a heterostructure. We demonstrate that ligand exchange strategies can be used to control the band alignment of PbSe and CdSe QDs in a mixed QD solid, shifting it from a type-I to a type-II alignment. The change in alignment is observed in both spectroelectrochemical and transient absorption measurements, leading to a change in the energy of the conduction band edges in the two materials and in the direction of electron transfer upon photoexcitation. Our work demonstrates the possibility to tune the band offset of QD heterostructures via control of the chemical species passivating the QD surface, allowing full control over the energetics of the heterostructure without requiring changes in the QD composition. American Chemical Society 2019-11-19 2019-12-12 /pmc/articles/PMC6913897/ /pubmed/31867087 http://dx.doi.org/10.1021/acs.jpcc.9b09470 Text en Copyright © 2019 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | Grimaldi, Gianluca van den Brom, Mark J. du Fossé, Indy Crisp, Ryan W. Kirkwood, Nicholas Gudjonsdottir, Solrun Geuchies, Jaco J. Kinge, Sachin Siebbeles, Laurens D. A. Houtepen, Arjan J. Engineering the Band Alignment in QD Heterojunction Films via Ligand Exchange |
title | Engineering the
Band Alignment in QD Heterojunction
Films via Ligand Exchange |
title_full | Engineering the
Band Alignment in QD Heterojunction
Films via Ligand Exchange |
title_fullStr | Engineering the
Band Alignment in QD Heterojunction
Films via Ligand Exchange |
title_full_unstemmed | Engineering the
Band Alignment in QD Heterojunction
Films via Ligand Exchange |
title_short | Engineering the
Band Alignment in QD Heterojunction
Films via Ligand Exchange |
title_sort | engineering the
band alignment in qd heterojunction
films via ligand exchange |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6913897/ https://www.ncbi.nlm.nih.gov/pubmed/31867087 http://dx.doi.org/10.1021/acs.jpcc.9b09470 |
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