Abstract
CsPbI3 perovskite quantum dots (PQDs) emerge as promising optoelectronic materials for photovoltaics due to their high photoluminescence quantum yields and solution processability. However, the dynamic binding of long-chain ligands on the PQD surface generally induces numerous surface defects, which severely degrade the optoelectronic properties and stability of PQDs, to a large extent limiting the photovoltaic performance and operational stability of PQD solar cells (PQDSCs). Herein, a complementary dual-ligand reconstruction strategy is proposed to resurface the PQDs, in which the trimethyloxonium tetrafluoroborate and phenylethyl ammonium iodide can form a complementary dual-ligand system on the PQD surface through hydrogen bonds. The results reveal that the complementary dual-ligand system can not only stabilize the surface lattice of PQDs maintaining their good dispersion in the colloidal solution but also largely improve the inter-dot electronic coupling in the PQD solids. As a consequence, the PQDs demonstrate substantially improved optoelectronic properties and environmental stability, as well as a more uniform stacking orientation in the PQD solids, leading to a record high efficiency of up to 17.61% being realized in inorganic PQDSCs. This work provides a new avenue for the surface ligand engineering of PQDs for high-performance optoelectronic devices.
| Original language | English |
|---|---|
| Article number | 2504748 |
| Journal | Small |
| Volume | 21 |
| Issue number | 31 |
| DOIs | |
| State | Published - 7 Aug 2025 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- complementary dual-ligand
- optoelectronic property
- perovskite quantum dot
- solar cell
- surface reconstruction
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