TY - JOUR
T1 - Spectroscopic Evidence for the Contribution of Holes to the Bleach of Cd-Chalcogenide Quantum Dots
AU - Grimaldi, Gianluca
AU - Geuchies, Jaco J.
AU - Van Der Stam, Ward
AU - Du Fossé, Indy
AU - Brynjarsson, Baldur
AU - Kirkwood, Nicholas
AU - Kinge, Sachin
AU - Siebbeles, Laurens D.A.
AU - Houtepen, Arjan J.
N1 - Funding Information:
A.J.H., J.J.G., I.D.F., and W.v.d.S. gratefully acknowledge financial support from the European Research Council Horizon 2020 ERC grant agreement no. 678004 (Doping on Demand). G.G. acknowledges financial support from STW (project no. 13903, Stable and Non-Toxic Nanocrystal Solar Cells).
Publisher Copyright:
© 2019 American Chemical Society.
PY - 2019/5/8
Y1 - 2019/5/8
N2 - In transient absorption (TA) measurements on Cd-chalcogenide quantum dots (QDs), the presence of a band-edge (BE) bleach signal is commonly attributed entirely to conduction-band electrons in the 1S(e) state, neglecting contributions from BE holes. While this has been the accepted view for more than 20 years, and has often been used to distinguish electron and hole kinetics, the reason for the absence of a hole contribution to the BE-bleach has remained unclear. Here, we show with three independent experiments that holes do in fact have a significant impact on the BE-bleach of well-passivated Cd-chalcogenide QD samples. Transient absorption experiments on high photoluminescence quantum yield CdSe/CdS/ZnS core-shell-shell QDs clearly show an increase of the band-edge bleach as holes cool down to the band edge. The relative contribution of electron-to-hole bleach is 2:1, as predicted by theory. The same measurements on core-only CdSe QDs with a lower quantum yield do not show a contribution of holes to the band-edge bleach. We assign the lack of hole bleach to the presence of ultrafast hole trapping in samples with insufficient passivation of the QD surface. In addition, we show measurements of optical gain in core-shell-shell QD solutions, providing clear evidence of a significant hole contribution to the BE transient absorption signal. Finally, we present spectroelectrochemical measurements on CdTe QDs films, showing the presence of a BE-bleach for both electron and hole injections. The presence of a contribution of holes to the bleach in passivated Cd-chalcogenides QDs bears important implications for quantitative studies on optical gain as well as for TA determinations of carrier dynamics.
AB - In transient absorption (TA) measurements on Cd-chalcogenide quantum dots (QDs), the presence of a band-edge (BE) bleach signal is commonly attributed entirely to conduction-band electrons in the 1S(e) state, neglecting contributions from BE holes. While this has been the accepted view for more than 20 years, and has often been used to distinguish electron and hole kinetics, the reason for the absence of a hole contribution to the BE-bleach has remained unclear. Here, we show with three independent experiments that holes do in fact have a significant impact on the BE-bleach of well-passivated Cd-chalcogenide QD samples. Transient absorption experiments on high photoluminescence quantum yield CdSe/CdS/ZnS core-shell-shell QDs clearly show an increase of the band-edge bleach as holes cool down to the band edge. The relative contribution of electron-to-hole bleach is 2:1, as predicted by theory. The same measurements on core-only CdSe QDs with a lower quantum yield do not show a contribution of holes to the band-edge bleach. We assign the lack of hole bleach to the presence of ultrafast hole trapping in samples with insufficient passivation of the QD surface. In addition, we show measurements of optical gain in core-shell-shell QD solutions, providing clear evidence of a significant hole contribution to the BE transient absorption signal. Finally, we present spectroelectrochemical measurements on CdTe QDs films, showing the presence of a BE-bleach for both electron and hole injections. The presence of a contribution of holes to the bleach in passivated Cd-chalcogenides QDs bears important implications for quantitative studies on optical gain as well as for TA determinations of carrier dynamics.
KW - Colloidal quantum dots
KW - electronic structure
KW - excited-state dynamics
KW - femto-second transient absorption spectroscopy
UR - http://www.scopus.com/inward/record.url?scp=85065498904&partnerID=8YFLogxK
U2 - 10.1021/acs.nanolett.9b00164
DO - 10.1021/acs.nanolett.9b00164
M3 - Article
C2 - 30938530
AN - SCOPUS:85065498904
SN - 1530-6984
VL - 19
SP - 3002
EP - 3010
JO - Nano Letters
JF - Nano Letters
IS - 5
ER -