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Bright gradient-alloyed CdSe\u2093S\u2081\u208b\u2093 quantum dots exhibiting cyan-blue emission

机译:呈现蓝绿色发射的明亮梯度合金CdSe \ u2093S \ u2081 \ u208b \ u2093量子点

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摘要

Highly emissive alloyed CdSeS quantum dots (QDs) with a gradient structure exhibiting photoluminescence (PL) peaking at 490 nm and an absolute quantum yield (QY) of 79% (in toluene with excitation wavelength of 430 nm) were designed and synthesized. The cyan-blue emitters were synthesized at 180 \ub0C in 1-octadecene (ODE) with cadmium oleate (Cd(OA)2), tri-n-octylphosphine selenide (TOPSe), and tri-n-octylphosphine sulfide (TOPS) as the Cd, Se, and S precursors, respectively; importantly, a commercial secondary phosphine, diphenyl phosphine (DPP or HPPh2), was used as a beneficial additive. Also, our high Cd/(Se + S) feed molar ratio aids in shifting the equilibrium of the chalcogenide exchange, TOPE + HPPh2 \u21d4 TOP + E\u2550PPh2H, to the right. Density functional theory (DFT) calculations suggest that the formation of Se\u2550PPh2H proceeds faster than that of S\u2550PPh2H, which supports our high S/Se feed molar ratio used to synthesize the bright gradient-alloyed CdSeS QDs. Compositional and structural characterization was carried out using powder X-ray diffraction (PXRD), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDX), X-ray photoelectron spectroscopy (XPS), and solid-state nuclear magnetic resonance spectroscopy (NMR). Particularly, our solid-state 113Cd NMR analysis reveals that the highly emissive CdSeS QDs consist of a three-domain structure with a Se-rich inner core region, a Se/S equivalent middle region, and a S-rich outer region. The present study highlights the importance on the use of secondary phosphines together with high cation/anion feed molar ratios in the rational design and synthesis of high-quality metal chalcogenide QDs at relatively low temperature but with high yield and reproducibility.
机译:设计并合成了具有梯度结构的高发射合金CdSeS量子点(QD),该量子点在490 nm处出现光致发光(PL)峰,且绝对量子产率(QY)为79%(在激发波长为430 nm的甲苯中)。在1-十八碳烯(ODE)中,油酸镉(Cd(OA)2),三正辛基膦硒化亚硒酸酯(TOPSe)和三正辛基膦硫醚(TOPS)合成180-ub0C的蓝绿色发射体。 Cd,Se和S前体;重要的是,使用商业化的二级膦,二苯基膦(DPP或HPPh2)作为有益的添加剂。同样,我们高的Cd /(Se + S)进料摩尔比有助于将硫族化物交换的平衡TOPE + HPPh2 TOP + E \ u2550PPh2H向右移动。密度泛函理论(DFT)计算表明,Se \ u2550PPh2H的形成比S \ u2550PPh2H的形成更快,这支持了我们用于合成明亮的梯度合金CdSeS QD的高S / Se进料摩尔比。使用粉末X射线衍射(PXRD),透射电子显微镜(TEM),能量色散X射线光谱(EDX),X射线光电子光谱(XPS)和固态核磁共振进行成分和结构表征光谱(NMR)。特别是,我们的固态113Cd NMR分析表明,高发射CdSeS QD由具有富硒内核区,硒/硫当量中间区和富硫外区的三畴结构组成。本研究强调了在相对较低的温度下合理设计和合成高质量金属硫族化物QD时,在高磷/硫离子进料摩尔比的合理设计和合成中使用二级膦的重要性。

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