A Real-Time In Situ Demonstration of Direct and Indirect Transformation Pathways in CdTe Magic-Size Clusters at Room Temperature

被引:13
|
作者
Luan, Chaoran [1 ]
Shen, Qiu [2 ]
Rowell, Nelson [3 ]
Zhang, Meng [4 ]
Chen, Xiaoqin [2 ]
Huang, Wen [1 ]
Yu, Kui [2 ,4 ]
机构
[1] Sichuan Univ, Lab Ethnopharmacol, Tissueorientated Property Chinese Med Key Lab Sic, West China Sch Med,West China Hosp, Chengdu 610065, Sichuan, Peoples R China
[2] Sichuan Univ, Coll Biomed Engn, Natl Engn Res Ctr Biomat, Chengdu 610065, Sichuan, Peoples R China
[3] Natl Res Council Canada, Metrol Res Ctr, Ottawa, ON K1A 0R6, Canada
[4] Sichuan Univ, Inst Atom & Mol Phys, Chengdu 610065, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
Cadmium Telluride; Cluster Compounds; Colloidal; Magic-Size Clusters; Transformation Pathway; QUANTUM DOTS; SEMICONDUCTOR NANOCRYSTALS; 2-STEP NUCLEATION; GROWTH; CDSE; ISOMERIZATION; MONODISPERSE;
D O I
10.1002/anie.202205784
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The transformations of colloidal semiconductor magic-size clusters (MSCs) are expected to occur with only discrete, step-wise redshifts in optical absorption. Here, we challenge this assumption presenting a novel, conceptually different transformation, for which the redshift is continuous. In the room-temperature transformation from CdTe MSC-448 to MSC-488 (designated by the peak wavelengths in nanometer), the redshift of absorption monitored in situ displays distinctly continuous and/or step-wise behavior. Based on conclusive evidence provided by real-time experiments, the former transformation is apparently direct and intra-cluster with a relatively large energy barrier. The latter transformation is indirect and assisted by MSC precursor compounds (PCs). The former transformation follows the latter often, being predominant at a relatively high temperature. The present findings encourage a reconsideration of the absorption redshift reported previously for transformations of binary II-VI MSCs, together with the pathway associated without the increase of cluster mass.
引用
收藏
页数:9
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