| Literature DB >> 29912564 |
Jea Woong Jo1, Jongmin Choi1, F Pelayo García de Arquer1, Ali Seifitokaldani1, Bin Sun1, Younghoon Kim1, Hyungju Ahn2, James Fan1, Rafael Quintero-Bermudez1, Junghwan Kim1, Min-Jae Choi1, Se-Woong Baek1, Andrew H Proppe1,3, Grant Walters1, Dae-Hyun Nam1, Shana Kelley3,4, Sjoerd Hoogland1, Oleksandr Voznyy1, Edward H Sargent1.
Abstract
Colloidal quantum dots (CQDs) are promising solution-processed infrared-absorbing materials for optoelectronics. In these applications, it is crucial to replace the electrically insulating ligands used in synthesis to form strongly coupled quantum dot solids. Recently, solution-phase ligand-exchange strategies have been reported that minimize the density of defects and the polydispersity of CQDs; however, we find herein that the new ligands exhibit insufficient chemical reactivity to remove original oleic acid ligands completely. This leads to low CQD packing and correspondingly low electronic performance. Here we report an acid-assisted solution-phase ligand-exchange strategy that, by enabling efficient removal of the original ligands, enables the synthesis of densified CQD arrays. Our use of hydroiodic acid simultaneously facilitates high CQD packing via proton donation and CQD passivation through iodine. We demonstrate highly packed CQD films with a 2.5 times increased carrier mobility compared with prior exchanges. The resulting devices achieve the highest infrared photon-to-electron conversion efficiencies (>50%) reported in the spectral range of 0.8 to 1.1 eV.Entities:
Keywords: Colloidal quantum dots; infrared; narrow bandgap; photovoltaics; solution-phase ligand exchange; surface passivation
Year: 2018 PMID: 29912564 DOI: 10.1021/acs.nanolett.8b01470
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189