Abstract
Band bending in colloidal quantum dot (CQD) solids has become important in driving charge carriers through devices. This is typically a result of band alignments at junctions in the device. Whether band bending is intrinsic to CQD solids, i.e. is band bending present at the surface-vacuum interface, has previously been unanswered. Here we use photoemission surface photovoltage measurements to show that depletion regions are present at the surface of n and p-type CQD solids with various ligand treatments (EDT, MPA, PbI2, MAI/PbI2). Using laser-pump photoemission-probe time-resolved measurements, we show that the timescale of carrier dynamics in the surface of CQD solids can vary over at least 6 orders of magnitude, with the fastest dynamics on the order of microseconds in PbS-MAI/PbI2 solids and on the order of seconds for PbS-MPA and PbS-PbI2. By investigating the surface chemistry of the solids, we find a correlation between the carrier dynamics timescales and the presence of oxygen contaminants, which we suggest are responsible for the slower dynamics due to deep trap formation.
| Original language | American English |
|---|---|
| Pages (from-to) | 17793-17806 |
| Number of pages | 14 |
| Journal | Nanoscale |
| Volume | 13 |
| Issue number | 42 |
| DOIs | |
| State | Published - 14 Nov 2021 |
Bibliographical note
Publisher Copyright:© The Royal Society of Chemistry.
NLR Publication Number
- NREL/JA-5K00-81149
Keywords
- band bending
- carriers
- lead sulfide
- ligands
- PbS
- perovskites
- quantum dots
- surface chemistry
- XPS
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