Excitation Energy Dependence of the Photoluminescence Quantum Yields of Core and Core/Shell Quantum Dots

2013 ◽  
Vol 4 (12) ◽  
pp. 2053-2060 ◽  
Author(s):  
Jessica Hoy ◽  
Paul J. Morrison ◽  
Lindsey K. Steinberg ◽  
William E. Buhro ◽  
Richard A. Loomis
2018 ◽  
Vol 30 (2) ◽  
pp. 465-471 ◽  
Author(s):  
Irina V. Martynenko ◽  
Anvar S. Baimuratov ◽  
Victoria A. Osipova ◽  
Vera A. Kuznetsova ◽  
Finn Purcell-Milton ◽  
...  

2019 ◽  
Author(s):  
Aurelio A. Rossinelli ◽  
Henar Rojo ◽  
Aniket S. Mule ◽  
Marianne Aellen ◽  
Ario Cocina ◽  
...  

<div>Colloidal semiconductor nanoplatelets exhibit exceptionally narrow photoluminescence spectra. This occurs because samples can be synthesized in which all nanoplatelets share the same atomic-scale thickness. As this dimension sets the emission wavelength, inhomogeneous linewidth broadening due to size variation, which is always present in samples of quasi-spherical nanocrystals (quantum dots), is essentially eliminated. Nanoplatelets thus offer improved, spectrally pure emitters for various applications. Unfortunately, due to their non-equilibrium shape, nanoplatelets also suffer from low photo-, chemical, and thermal stability, which limits their use. Moreover, their poor stability hampers the development of efficient synthesis protocols for adding high-quality protective inorganic shells, which are well known to improve the performance of quantum dots. <br></div><div>Herein, we report a general synthesis approach to highly emissive and stable core/shell nanoplatelets with various shell compositions, including CdSe/ZnS, CdSe/CdS/ZnS, CdSe/Cd<sub>x</sub>Zn<sub>1–x</sub>S, and CdSe/ZnSe. Motivated by previous work on quantum dots, we find that slow, high-temperature growth of shells containing a compositional gradient reduces strain-induced crystal defects and minimizes the emission linewidth while maintaining good surface passivation and nanocrystal uniformity. Indeed, our best core/shell nanoplatelets (CdSe/Cd<sub>x</sub>Zn<sub>1–x</sub>S) show photoluminescence quantum yields of 90% with linewidths as low as 56 meV (19.5 nm at 655 nm). To confirm the high quality of our different core/shell nanoplatelets for a specific application, we demonstrate their use as gain media in low-threshold ring lasers. More generally, the ability of our synthesis protocol to engineer high-quality shells can help further improve nanoplatelets for optoelectronic devices.</div>


2020 ◽  
Vol 20 (9) ◽  
pp. 5478-5485
Author(s):  
Cong Xie ◽  
Yubin Zhao ◽  
Yuxiang Song ◽  
Yingjie Liu ◽  
Yaya Wang ◽  
...  

Compared with conventional semiconductor quantum dots, hybrid SiO2 coated CdTe QDs exhibited high stability, long fluorescent lifetime, high photoluminescence quantum yields, and well biocompatibility. In this paper, CdTe QDs with tunable PL from green to red emitting were prepared by an aqueous synthesis. A sol–gel process resulted in CdTe QDs coated with a hybrid SiO2 shell contained CdS-like clusters to obtain red-shifted PL spectra, increased PL efficiency and high stability. The clusters were formed by the reaction of Cd2+ and S2− ions generated via the decomposition of thioglycolic acid. The clusters around CdTe cores created a core–shell structure which is very similar with traditional semiconductor core–shell QDs. After being coated with a hybrid SiO2 shell, the PL of green-emitting naked CdTe QDs was red-shifted largely (~30 nm) while the PL of yellowemitting CdTe QDs revealed a small red-shifted (~20 nm). Furthermore, The PL of red-emitting naked CdTe QDs was red-shifted much small (less than 10 nm). This phenomenon is ascribed to the change of band gap of CdTe cores with sizes. The red-shift of PL spectra is attributed to the CdS-like clusters around the core rather than the thickness of the hybrid SiO2 shell.


Nano Research ◽  
2019 ◽  
Vol 12 (7) ◽  
pp. 1595-1603 ◽  
Author(s):  
Irina V. Martynenko ◽  
Anvar S. Baimuratov ◽  
Florian Weigert ◽  
José X. Soares ◽  
Lorena Dhamo ◽  
...  

2009 ◽  
Vol 113 (28) ◽  
pp. 12059-12066 ◽  
Author(s):  
Catherine H. Crouch ◽  
Robert Mohr ◽  
Thomas Emmons ◽  
Siying Wang ◽  
Marija Drndic

2009 ◽  
Vol 60-61 ◽  
pp. 165-169 ◽  
Author(s):  
Shi Chao Xu ◽  
Cui Cui Yao ◽  
Ji Mei Zhang ◽  
Zhao Dai ◽  
Guo Zheng ◽  
...  

Core-shell quantum dots are colloidal particles consisting of a semiconductor core and a shell material as an outer coating layer. It can be utilized to develop sensitive methods for the detection of specific biological entities, such as microbial species, their transcription products, and single genes etc. The goal of current research is to synthesize CdTe and core-shell CdTe/ZnS quantum dots (QDs) with an improved process, and to investigate their properties. Well-dispersed CdTe core was prepared in aqueous phase with using 3-mercaptopropionic acid (MPA) as stabilizer under conditions of pH 9.1, temperature of 100 °C, refluxing for 6h, and mol ratio of Cd2+/Te2-/MPA is 1:0.5:2.4. Average size of 8 nm CdTe core was conformed via transmission electron microscopy (TEM). Core-shell CdTe/ZnS QDs were then synthesized to improve the optical properties and biocompatibility of CdTe core. Various conditions were researched to obtain the core-shell QDs with the best optical properties, such as quantum yields, fluorescence intensity etc. The results indicated that the core-shell qualified CdTe/ZnS was prepared under conditions of pH 9.0, temperature of 45 °C, refluxing for 1h, and mol ratio of CdTe/S2-/Zn2+ is 4/1/1. CdTe/ZnS with average size of 10 nm were achieved and conformed via TEM. Moreover, red shift of a maximum emission wavelength from 547 nm of CdTe to 587 of CdTe/ZnS was observed via fluorescence spectrum (FS), which inferred the growth of QDs and formation of ZnS shells. The achieved ZnS shell make CdTe core less toxic and more biocompatible, it will be useful in biological labeling, diagnostic process and biosensing system based on fluorescence resonance energy transition (FRET).


2019 ◽  
Author(s):  
Aurelio A. Rossinelli ◽  
Henar Rojo ◽  
Aniket S. Mule ◽  
Marianne Aellen ◽  
Ario Cocina ◽  
...  

<div>Colloidal semiconductor nanoplatelets exhibit exceptionally narrow photoluminescence spectra. This occurs because samples can be synthesized in which all nanoplatelets share the same atomic-scale thickness. As this dimension sets the emission wavelength, inhomogeneous linewidth broadening due to size variation, which is always present in samples of quasi-spherical nanocrystals (quantum dots), is essentially eliminated. Nanoplatelets thus offer improved, spectrally pure emitters for various applications. Unfortunately, due to their non-equilibrium shape, nanoplatelets also suffer from low photo-, chemical, and thermal stability, which limits their use. Moreover, their poor stability hampers the development of efficient synthesis protocols for adding high-quality protective inorganic shells, which are well known to improve the performance of quantum dots. <br></div><div>Herein, we report a general synthesis approach to highly emissive and stable core/shell nanoplatelets with various shell compositions, including CdSe/ZnS, CdSe/CdS/ZnS, CdSe/Cd<sub>x</sub>Zn<sub>1–x</sub>S, and CdSe/ZnSe. Motivated by previous work on quantum dots, we find that slow, high-temperature growth of shells containing a compositional gradient reduces strain-induced crystal defects and minimizes the emission linewidth while maintaining good surface passivation and nanocrystal uniformity. Indeed, our best core/shell nanoplatelets (CdSe/Cd<sub>x</sub>Zn<sub>1–x</sub>S) show photoluminescence quantum yields of 90% with linewidths as low as 56 meV (19.5 nm at 655 nm). To confirm the high quality of our different core/shell nanoplatelets for a specific application, we demonstrate their use as gain media in low-threshold ring lasers. More generally, the ability of our synthesis protocol to engineer high-quality shells can help further improve nanoplatelets for optoelectronic devices.</div>


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