Controlled Steric Hindrance Enables Efficient Ligand Exchange for Stable, Infrared-Bandgap Quantum Dot Inks AITranslate
Abstract AITranslate
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.
KeyWords AITranslate
Basic Information:
DOI:https://doi.org/10.1021/acsenergylett.9b00388
Chinese Library Classification Number:
Citation Information:
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.
quote
| GB/T 7714-2015 | [1] Mengxia Liu, Fanglin Che, Bin Sun, et al. ACS Energy Letters, 2019(4). DOI:10.1021/acsenergylett.9b00388. |
| MLA | [1] Mengxia Liu, et al., ACS Energy Letters, no. 4, 2019, https://doi.org/10.1021/acsenergylett.9b00388. |
| APA | [1] Mengxia Liu, Fanglin Che, Bin Sun, Oleksandr Voznyy, Andrew Proppe, Rahim Munir, Mingyang Wei, Rafael QuinteroBermudez, Lilei Hu, Sjoerd Hoogland, Andreas Mandelis, Aram Amassian, Shana O. Kelley, F. Pelayo García de Arquer, & Edward H. Sargent. (2019). ACS Energy Letters(4). https://doi.org/10.1021/acsenergylett.9b00388 |
| IEEE | [1] Mengxia Liu, Fanglin Che, Bin Sun, Oleksandr Voznyy, Andrew Proppe, Rahim Munir, Mingyang Wei, Rafael QuinteroBermudez, Lilei Hu, Sjoerd Hoogland, Andreas Mandelis, Aram Amassian, Shana O. Kelley, F. Pelayo García de Arquer, and Edward H. Sargent, ACS Energy Letters, no. 4, 2019, doi: 10.1021/acsenergylett.9b00388. |
