| Literature DB >> 28991386 |
Jea Woong Jo1, Younghoon Kim1, Jongmin Choi1, F Pelayo García de Arquer1, Grant Walters1, Bin Sun1, Olivier Ouellette1, Junghwan Kim1, Andrew H Proppe1, Rafael Quintero-Bermudez1, James Fan1, Jixian Xu1, Chih Shan Tan1, Oleksandr Voznyy1, Edward H Sargent1.
Abstract
The energy disorder that arises from colloidal quantum dot (CQD) polydispersity limits the open-circuit voltage (VOC ) and efficiency of CQD photovoltaics. This energy broadening is significantly deteriorated today during CQD ligand exchange and film assembly. Here, a new solution-phase ligand exchange that, via judicious incorporation of reactivity-engineered additives, provides improved monodispersity in final CQD films is reported. It has been found that increasing the concentration of the less reactive species prevents CQD fusion and etching. As a result, CQD solar cells with a VOC of 0.7 V (vs 0.61 V for the control) for CQD films with exciton peak at 1.28 eV and a power conversion efficiency of 10.9% (vs 10.1% for the control) is achieved.Keywords: colloidal quantum dots; open-circuit voltage; photovoltaics; polydispersity; solution-phase ligand exchange
Year: 2017 PMID: 28991386 DOI: 10.1002/adma.201703627
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849