TY - JOUR
T1 - Controlled Steric Hindrance Enables Efficient Ligand Exchange for Stable, Infrared-Bandgap Quantum Dot Inks
AU - Liu, Mengxia
AU - Che, Fanglin
AU - Sun, Bin
AU - Voznyy, Oleksandr
AU - Proppe, Andrew
AU - Munir, Rahim
AU - Wei, Mingyang
AU - Quintero-Bermudez, Rafael
AU - Hu, Lilei
AU - Hoogland, Sjoerd
AU - Mandelis, Andreas
AU - Amassian, Aram
AU - Kelley, Shana O.
AU - Garciá De Arquer, F. Pelayo
AU - Sargent, Edward H.
N1 - KAUST Repository Item: Exported on 2020-10-01
Acknowledgements: This publication is based in part on work supported by the Ontario Research Fund Research Excellence Program and by the Natural Sciences and Engineering Research Council (NSERC) of Canada.
PY - 2019/4/30
Y1 - 2019/4/30
N2 - Colloidal quantum dots (CQDs), which benefit from a size-tuned bandgap, are a solution-processed material for infrared energy harvesting. This characteristic enables the fabrication of solar cells that form tandem devices with silicon. Unfortunately, in the case of CQDs having diameters sufficiently large (>4 nm) so that the nanoparticles absorb light well beyond silicon's bandgap, conventional ligand exchanges fail. Here we report a strategy wherein short-chain carboxylates, used as a steric hindrance controller, facilitate the ligand exchange process on small-bandgap CQDs. We demonstrate that the net energy barrier to replace original capping ligands with lead halide anions is decreased when short carboxylates are involved. The approach produces more complete ligand exchange that enables improved packing density and monodispersity. This contributes to a 2-fold reduction in the trap state density compared to the best previously reported exchange. We demonstrate solar cells that achieve a record infrared photon-to-electron conversion efficiency at the excitonic peak.
AB - Colloidal quantum dots (CQDs), which benefit from a size-tuned bandgap, are a solution-processed material for infrared energy harvesting. This characteristic enables the fabrication of solar cells that form tandem devices with silicon. Unfortunately, in the case of CQDs having diameters sufficiently large (>4 nm) so that the nanoparticles absorb light well beyond silicon's bandgap, conventional ligand exchanges fail. Here we report a strategy wherein short-chain carboxylates, used as a steric hindrance controller, facilitate the ligand exchange process on small-bandgap CQDs. We demonstrate that the net energy barrier to replace original capping ligands with lead halide anions is decreased when short carboxylates are involved. The approach produces more complete ligand exchange that enables improved packing density and monodispersity. This contributes to a 2-fold reduction in the trap state density compared to the best previously reported exchange. We demonstrate solar cells that achieve a record infrared photon-to-electron conversion efficiency at the excitonic peak.
UR - http://hdl.handle.net/10754/656427
UR - http://pubs.acs.org/doi/10.1021/acsenergylett.9b00388
UR - http://www.scopus.com/inward/record.url?scp=85066899847&partnerID=8YFLogxK
U2 - 10.1021/acsenergylett.9b00388
DO - 10.1021/acsenergylett.9b00388
M3 - Article
SN - 2380-8195
VL - 4
SP - 1225
EP - 1230
JO - ACS Energy Letters
JF - ACS Energy Letters
IS - 6
ER -