材料科学
钝化
量子点
封装(网络)
离子键合
表面改性
纳米技术
光致发光
硅烷
量子产额
化学稳定性
硅氧烷
阳离子聚合
钙钛矿(结构)
化学工程
异质结
光电子学
作者
Yongmin Shin,Somin Park,Junho Jang,Byeong-Soo Bae
标识
DOI:10.1021/acsami.5c22871
摘要
Red-emitting perovskite quantum dots (Red-PQDs) are highly crucial components for achieving full-color PQD-based color-converters. However, red-PQDs are particularly prone to degradation due to their highly ionic bonding nature, phase instability, and insufficient surface passivation. Developing highly stable red-PQDs in diverse environments remains a critical barrier to their practical implementation as light emitters in displays. Here, we report a long-term stable red-PQD through a dual encapsulation strategy involving the introduction of silane-based ligands and a siloxane-based encapsulation matrix. This approach enables the preservation of photoluminescence quantum yield (PLQY) > 60 days in air and water and under continuous blue light irradiation. The silane-based ligands facilitate surface functionalization and passivate cationic defects on the red-PNCs, enabling effective chemical encapsulation within the siloxane hybrid matrix. By optimizing the silane ligand composition, we achieved a high PLQY alongside pure red emission. Furthermore, the underlying mechanism of enhanced stability was elucidated through optical-, chemical-, and molecular-scale analyses. As a proof of concept, we demonstrate red-emitting and white-emitting color-converting films that maintain stability for >60 days in water. These findings underscore the effectiveness of our strategy and highlight the potential of red-PQDs for stable color-converting layers in displays.
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