Abstract

Colloidal quantum dots are emerging solution-processed materials for large-scale and low-cost photovoltaics. The recent advent of quantum dot inks has overcome the prior need for solid-state exchanges that previously added cost, complexity, and morphological disruption to the quantum dot solid. Unfortunately, these inks remain limited by the photocarrier diffusion length. Here we devise a strategy based on n- and p-type ligands that judiciously shifts the quantum dot band alignment. It leads to ink-based materials that retain the independent surface functionalization of quantum dots, and it creates distinguishable donor and acceptor domains for bulk heterojunctions. Interdot carrier transfer and exciton dissociation studies confirm efficient charge separation at the nanoscale interfaces between the two classes of quantum dots. We fabricate the first mixed-quantum-dot solar cells and achieve a power conversion of 10.4%, which surpasses the performance of previously reported bulk heterojunction quantum dot devices fully two-fold, indicating the potential of the mixed-quantum-dot approach.

Details

Title
Mixed-quantum-dot solar cells
Author
Yang, Zhenyu 1   VIAFID ORCID Logo  ; Fan, James Z 1 ; Proppe, Andrew H 2   VIAFID ORCID Logo  ; F Pelayo García de Arquer 1 ; Rossouw, David 3 ; Voznyy, Oleksandr 1   VIAFID ORCID Logo  ; Lan, Xinzheng 1 ; Liu, Min 1 ; Walters, Grant 1 ; Quintero-Bermudez, Rafael 1 ; Sun, Bin 1 ; Hoogland, Sjoerd 1 ; Botton, Gianluigi A 3 ; Kelley, Shana O 4   VIAFID ORCID Logo  ; Sargent, Edward H 1   VIAFID ORCID Logo 

 Department of Electrical and Computer Engineering, University of Toronto, Toronto, ON, Canada 
 Department of Electrical and Computer Engineering, University of Toronto, Toronto, ON, Canada; Department of Chemistry, University of Toronto, Toronto, ON, Canada 
 Department of Materials Science and Engineering, McMaster University, Hamilton, ON, Canada 
 Department of Chemistry, University of Toronto, Toronto, ON, Canada 
Pages
1-9
Publication year
2017
Publication date
Nov 2017
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
1961026282
Copyright
© 2017. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.