Abstract

Ultrafast fluorescence spectroscopy was used to investigate the hole injection in CdxSeyZn1-xS1-y gradient core-shell quantum dot (CSQD) sensitized p-type NiO photocathodes. A series of CSQDs with a wide range of shell thicknesses was studied. Complementary photoelectrochemical cell measurements were carried out to confirm that the hole injection from the active core through the gradient shell to NiO takes place. The hole injection from the valence band of the QDs to NiO depends much less on the shell thickness when compared to the corresponding electron injection to n-type semiconductor (ZnO). We simulate the charge carrier tunneling through the potential barrier due to the gradient shell by numerically solving the Schrödinger equation. The details of the band alignment determining the potential barrier are obtained from X-ray spectroscopy measurements. The observed drastic differences between the hole and electron injection are consistent with a model where the hole effective mass decreases, while the gradient shell thickness increases.

Highlights

  • Colloidal quantum dots (QDs) form an important family of materials for third-generation solar cells

  • The core of our core–shell quantum dot (CSQD) is ternary CdSexS1−x alloy evidenced by energy-dispersive X-ray spectroscopy (EDX) analysis in TEM of our previous work.[19]

  • We have studied the hole injection from gradient CSQD to a common p-type metal oxide (MO), NiO

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Summary

Introduction

Colloidal quantum dots (QDs) form an important family of materials for third-generation solar cells. The hole injection from the valence band of the QDs to NiO depends much less on the shell thickness when compared to the corresponding electron injection to n-type semiconductor (ZnO).

Results
Conclusion
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