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Correction: Surface organic ligand-passivated quantum dots: toward high-performance light-emitting diodes with long lifetimes

Lishuang Wang ab, Ying Lv c, Jie Lin c, Jialong Zhao *b, Xingyuan Liu *c, Ruosheng Zeng b, Xun Wang d and Bingsuo Zou *b
aCollege of Chemistry and Chemical Engineering, Guangxi University, Nanning 530004, China
bMOE Key Lab of New Processing Technology for Nonferrous Metals and Materials and Guangxi Key Lab of Processing for Nonferrous Metals and Featured Materials, School of Physical Science and Technology, Guangxi University, Nanning 530004, China. E-mail: zhaojl@ciomp.ac.cn; zoubs@gxu.edu.cn
cState Key Laboratory of Luminescence and Applications, Changchun Institute of Optics, Fine Mechanics and Physics, Chinese Academy of Sciences, Changchun 130033, Jilin, China. E-mail: liuxy@ciomp.ac.cn
dKey Lab of Organic Optoelectronics and Molecular Engineering, Department of Chemistry, Tsinghua University, Beijing 100084, China

Received 24th January 2022 , Accepted 24th January 2022

First published on 16th February 2022


Abstract

Correction for ‘Surface organic ligand-passivated quantum dots: toward high-performance light-emitting diodes with long lifetimes’ by Lishuang Wang et al., J. Mater. Chem. C, 2021, 9, 2483–2490, DOI: 10.1039/D0TC05391K.


The Synthesis method of the QDs in the Supplementary Information is incorrect. The QDs were not synthesized by the authors and the QDs used in this work were purchased from Mesolight Inc., the commodity IDs of the QDs are 20200914-2 and 20200914-4 for the DDT-QDs and OT-QDs, respectively.

Mesolight Inc. decided to partly provide their synthesis method:

Synthesis method of QDs:

A mixture of CdO (1 mmol), Zn(Ac)2 (20 mmol), oleic acid (50 mmol) and 1-octadecene (150 mmol) was loaded into a 250 mL three-necked flask and heated to 310 °C. A certain amount of Se precursor (Se-TOP, 1.2–1.4 mmol) was added and the reactions were kept at 310 °C for 30 min. The reaction mixture was then kept at 240 °C, 15 mmol of 1-dodecanethiol and 10 mmol of the as-prepared stock solution for the Zn precursor and another 5 mL of the as-prepared stock solution for the S precursor were injected into the flask. The reaction was continued for more than 30 min. Finally, the flask was cooled to room temperature. By comparison, the QDs capped with OT ligands were synthesized by the same procedure during the growth of a ZnS outer shell.

The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.


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