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光学稳健的核/合金壳半导体量子点的超快动力学与超灵敏单粒子光谱学

Ultrafast dynamics and ultrasensitive single particle spectroscopy of optically robust core/alloy shell semiconductor quantum dots.

作者信息

Roy Debjit, De Chayan K, Ghosh Swarnali, Mukherjee Soumen, Mandal Saptarshi, Mandal Prasun K

机构信息

Department of Chemical Sciences, Indian Institute of Science Education and Research (IISER) Kolkata, Mohanpur, West Bengal, 741246, India.

Centre for Advanced Functional Materials, Indian Institute of Science Education and Research (IISER) Kolkata, Mohanpur, West Bengal, 741246, India.

出版信息

Phys Chem Chem Phys. 2022 Apr 13;24(15):8578-8590. doi: 10.1039/d1cp05780d.

Abstract

A "one-pot one-step" synthesis method of Core/Alloy Shell (CAS) quantum dots (QDs) offers the scope of large scale synthesis in a less time consuming, more economical, highly reproducible and high-throughput manner in comparison to "multi-pot multi-step" synthesis for Core/Shell (CS) QDs. Rapid initial nucleation, and smooth & uniform shell growth lead to the formation of a compositionally-gradient alloyed hetero-structure with very significantly reduced interfacial trap density in CAS QDs. Thus, interfacial strain gets reduced in a much smoother manner leading to enhanced confinement for the photo-generated charge carriers in CAS QDs. Convincing proof of alloy-shelling for a CAS QD has been provided from HRTEM images at the single particle level. The band gap could be tuned as a function of composition, temperature, reactivity difference of precursors, and a high PLQY and improved photochemical stability could be achieved for a small sized CAS QD. From the ultrafast exciton dynamics in CdSe and InP CAS QDs, it has been shown that (a) the hot exciton thermalization/relaxation happens in <500 fs, (b) hot electron trapping dynamics occurs within a ∼1 ps time scale, (c) band edge exciton trapping occurs within a 10-25 ps timescale and (d) for CdSe CAS QDs the hot hole gets trapped in about 35 ps. From fast PL decay dynamics, it has been shown that the amplitude of the intermediate time constant can be correlated with the PLQY. A model has been provided to understand these ultrafast to fast exciton dynamical processes. At the ultrasensitive single particle level, unlike CS QDs, CdSe CAS QDs have been shown to exhibit (a) constancy of PL ( no bluing) and (b) constancy of PL intensity ( no bleaching) of the single CAS QDs for continuous irradiation for one hour under an air atmosphere. Thus, CAS QDs hold the promise of being a superior optical probe in comparison to CS QDs both at the ensemble and at the single particle level, leading to enhanced flexibility of the CAS QDs towards designing and developing next generation application devices.

摘要

与核壳(CS)量子点的“多锅多步”合成法相比,核/合金壳(CAS)量子点的“一锅一步”合成法能够以耗时更短、成本更低、高度可重复且高通量的方式进行大规模合成。快速的初始成核以及光滑均匀的壳生长导致形成了一种成分渐变的合金异质结构,使得CAS量子点中的界面陷阱密度显著降低。因此,界面应变以更平滑的方式降低,从而增强了对CAS量子点中光生电荷载流子的限制。通过单粒子水平的高分辨透射电子显微镜(HRTEM)图像,为CAS量子点的合金壳化提供了令人信服的证据。带隙可以根据成分、温度、前驱体的反应性差异进行调节,并且对于小尺寸的CAS量子点可以实现高的光致发光量子产率(PLQY)和改善的光化学稳定性。从CdSe和InP CAS量子点的超快激子动力学研究表明:(a)热激子热化/弛豫发生在<500 fs内;(b)热电子俘获动力学发生在约1 ps的时间尺度内;(c)带边激子俘获发生在10 - 25 ps的时间尺度内;(d)对于CdSe CAS量子点,热空穴在约35 ps内被俘获。从快速光致发光衰减动力学研究表明,中间时间常数的幅度可以与PLQY相关联。已经提供了一个模型来理解这些从超快到快速的激子动力学过程。在超灵敏的单粒子水平上,与CS量子点不同,CdSe CAS量子点已被证明在空气气氛下连续照射一小时时,单个CAS量子点表现出(a)光致发光的稳定性(无蓝移)和(b)光致发光强度的稳定性(无漂白)。因此,无论是在整体水平还是单粒子水平上,与CS量子点相比,CAS量子点都有望成为一种更优异的光学探针,这使得CAS量子点在设计和开发下一代应用器件方面具有更高的灵活性。

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