卤化物
钙钛矿(结构)
光致发光
量子点
量子产额
材料科学
电致发光
配体(生物化学)
光电子学
碘化物
光化学
溴化物
激子
离子
发光
产量(工程)
甲脒
离子交换
化学
溴化铵
作者
Sih‐An Chen,Zong‐Liang Tseng,CHIA-CHEN HSU,Robin Khosla,MIAO-TAI YEN,Shun‐Hsyung Chang
标识
DOI:10.1142/s0218625x26410118
摘要
Lead halide perovskite quantum dots (PQDs) exhibit outstanding optoelectronic characteristics, further strengthened by quantum confinement effects that yield higher exciton binding energies, elevated photoluminescence quantum yields (PLQY), and narrow emission bandwidths. Through precise control of halide composition, mixed-halide PQDs can be tuned to emit across the entire visible spectrum. In this work, a ligand-assisted anion exchange approach employing tetraoctyl ammonium bromide (TOAB) is proposed to regulate the halide ratio in FAPbI[Formula: see text]Br x PQDs. The TOAB-mediated post-synthetic treatment enables partial substitution of iodide by bromide, leading to a pronounced blue shift in photoluminescence (PL) from 785[Formula: see text]nm to 536[Formula: see text]nm. Furthermore, TOAB-modified PQDs were incorporated into LED devices, which displayed electroluminescence (EL) emission shifting from 783[Formula: see text]nm to 630[Formula: see text]nm. These findings highlight the effectiveness of TOAB-based ligand modification in tailoring the emission behavior of PQDs, providing a versatile strategy for the design of wavelength-tunable optoelectronic devices.
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