• DocumentCode
    2305240
  • Title

    Observation of biexcitons in the presence of trions generated via sequential absorption of multiple photons in colloidal quantum dot solids

  • Author

    Cihan, Ahmet Fatih ; Martinez, Pedro Ludwig Hernandez ; Kelestemur, Yusuf ; Demir, Hilmi Volkan

  • Author_Institution
    Dept. of Electr. & Electron. Eng., Bilkent Univ., Ankara, Turkey
  • fYear
    2012
  • fDate
    23-27 Sept. 2012
  • Firstpage
    756
  • Lastpage
    757
  • Abstract
    Multi exciton generation (MEG) and multi exciton recombination (MER) in semiconductor quantum dots (QDs) have recently attracted significant scientific interest as a possible means to improve device efficiencies [1-5]. Convenient bandgap tunability, easy colloidal synthesis, and solution-based processability of these QDs make them further attractive for such device applications using MEG and MER. For example, recent theoretical and experimental studies have shown that MEG enables >;100% peak external quantum efficiency where the generated multi excitons (MEs) are collected in a simple QD solar cell structure [1]. Furthermore, MEG has also been shown in QD photodetectors exhibiting substantially increased photocurrent levels [2]. Another promising application for MEs is the use of QDs as an alternative gain medium based on MER for lasers. Although MEG is very promising and supported with quite persuasive reports, there are still some debatable issues that need to be clarified. One of the issues that have generated great debates in the field has been the confusion of MER with the recombination of trions, which takes place in photocharged QDs. To utilize MEG and MER in practical devices such as QD solar cells and QD lasing devices, these phenomena need to be well understood. Here, we showed distinct spectrally-resolved temporal behavior of biexciton (BX), single exciton (X) and trion radiative recombinations in near unity quantum yield (QY) quasi-type II CdSe/CdS core/shell nanocrystal QDs. Upon sequential absorption of multiple photons, the extraction of Xs, BXs, and trions were achieved using time correlated single photon counting (TCSPC) measurements performed on low concentration thin film samples of these QDs at different emission wavelengths. The QDs were embedded in PMMA medium to obtain homogeneous samples and avoid Förster-type nonradiative energy transfer (NRET) between them. Here to extract Xs, BXs, and trions, we devised a new analysis approac- for the time decays of the QDs that allowed us to attribute the physical events to their corresponding time decay terms, which were further verified with their excitation intensity dependencies [6].
  • Keywords
    II-VI semiconductors; biexcitons; cadmium compounds; colloids; nanostructured materials; photodetectors; photoluminescence; photon counting; semiconductor quantum dots; CdSe-CdS; Forster-type nonradiative energy transfer; NRET; QD photodetectors; QD solar cell structure; TCSPC; bandgap tunability; biexcitons; colloidal quantum dot solids; colloidal synthesis; external quantum efficiency; multiexciton generation; multiexciton recombination; nanocrystal QD; quantum yield; radiative recombinations; semiconductor quantum dots; sequential absorption; spectrally resolved temporal behavior; thin film samples; time correlated single photon counting; time decays; trions; Absorption; Excitons; Fitting; Radiative recombination; Trions;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Photonics Conference (IPC), 2012 IEEE
  • Conference_Location
    Burlingame, CA
  • Print_ISBN
    978-1-4577-0731-5
  • Type

    conf

  • DOI
    10.1109/IPCon.2012.6358843
  • Filename
    6358843