Gain roll-off in cadmium selenide colloidal quantum wells under intense optical excitation

Benjamin T. Diroll*, Alexandra Brumberg, Richard D. Schaller

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

Colloidal quantum wells, or nanoplatelets, show among the lowest thresholds for amplified spontaneous emission and lasing among solution-cast materials and among the highest modal gains of any known materials. Using solution measurements of colloidal quantum wells, this work shows that under photoexcitation, optical gain increases with pump fluence before rolling off due to broad photoinduced absorption at energies lower than the band gap. Despite the common occurrence of gain induced by an electron–hole plasma found in bulk materials and epitaxial quantum wells, under no measurement conditions was the excitonic absorption of the colloidal quantum wells extinguished and gain arising from a plasma observed. Instead, like gain, excitonic absorption reaches a minimum intensity near a photoinduced carrier sheet density of 2 × 1013 cm−2 above which the absorption peak begins to recover. To understand the origins of these saturation and reversal effects, measurements were performed with different excitation energies, which deposit differing amounts of excess energy above the band gap. Across many samples, it was consistently observed that less energetic excitation results in stronger excitonic bleaching and gain for a given carrier density. Transient and static optical measurements at elevated temperatures, as well as transient X-ray diffraction of the samples, suggest that the origin of gain saturation and reversal is a heating and disordering of the colloidal quantum wells which produces sub-gap photoinduced absorption.

Original languageEnglish (US)
Article number8016
JournalScientific reports
Volume12
Issue number1
DOIs
StatePublished - Dec 2022

Funding

Work performed at the Center for Nanoscale Materials, a U.S. Department of Energy Office of Science User Facility, was supported by the U.S. DOE, Office of Basic Energy Sciences, under Contract No. DE-AC02-06CH11357. Transient X-ray diffraction work was supported by the National Science Foundation under Grants Nos. 1629383 and 1808590 and the Graduate Research Fellowship Program under Grant No. DGE-1842165. This research used resources of the Advanced Photon Source, a U.S. Department of Energy (DOE) Office of Science User Facilities operated by Argonne National Laboratory under Contract No. DE-AC02-06CH11357. A.B. gratefully acknowledges support from a 3M Graduate Research Fellowship, the Ryan Fellowship, and the International Institute for Nanotechnology at Northwestern University.

ASJC Scopus subject areas

  • General

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