量子点
材料科学
钙钛矿(结构)
光致发光
光电子学
堆积
纳米技术
配体(生物化学)
光伏
光伏系统
碲化镉光电
化学
结晶学
生物
生物化学
受体
生态学
有机化学
作者
Xinyi Mei,Baoxing Ren,Junming Qiu,Zhimei Sun,Xiaoliang Zhang
出处
期刊:Small
[Wiley]
日期:2025-06-04
卷期号:21 (31): e2504748-e2504748
被引量:6
标识
DOI:10.1002/smll.202504748
摘要
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.
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