单层
光致发光
钙钛矿(结构)
卤化物
脱质子化
材料科学
成核
光化学
胺气处理
量子产额
质子化
纳米技术
光电子学
无机化学
化学
结晶学
有机化学
光学
荧光
离子
物理
作者
Ye Wu,Yang Liu,Nadesh Fiuza‐Maneiro,Sergio Gómez‐Graña,Muhammad Imran,Lakshminarayana Polavarapu,Andrey L. Rogach,Xiaoming Li,Haibo Zeng
出处
期刊:ACS materials letters
[American Chemical Society]
日期:2024-05-20
卷期号:6 (6): 2425-2433
被引量:1
标识
DOI:10.1021/acsmaterialslett.4c00670
摘要
Ultrathin lead halide perovskite nanoplatelets (NPLs) can enable tunable emission across the entire visible spectrum of light. The band-gap tunability of NPLs does not require halide composition engineering, so halide segregation can be avoided. However, their photoluminescence quantum yield (PLQY) and optoelectronic applications are often hampered due to reversible protonation and deprotonation of conventional amine ligands. Herein, we demonstrate the synthesis of benzenesulfonate-terminated CsPbBr3 NPLs without the use of any amine, and we clarify their nucleation and growth mechanism. The thickness of amine-free NPLs is controlled with monolayer-level precision, and thus, their emission wavelength is tuned between 437 and 504 nm. Amine-free NPLs are solely terminated by a benzenesulfonate group, leading to a Cs-rich surface. The amine-free NPLs exhibit PLQYs up to 80%, and slow charge carrier relaxation. This work offers a comprehensive study of surface chemistry and ligand dynamics of perovskite NPLs.
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