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Little is known about the room-temperature formation of colloidal semiconductor magic-size clusters (MSCs) of II-VI ternary CdE1E2 from ZnE1E2. Here, we report the first synthesis of CdTeSe MSCs from ZnTeSe MSC-340 (displaying a sharp optical absorption peaking at 340 nm) at room temperature. When ZnTeSe MSC-340 and Cd(OAc)2/OLA (made from cadmium acetate and oleylamine) were mixed, the former disappeared, while CdTeSe MSC-422 and/or MSC-399 developed. Based on our experimental data, we propose that the conversion proceeds via the interaction of Cd(OAc)2/OLA and the precursor compound of ZnTeSe MSC-340, PC-340. As such, ZnTeSe MSC-340 first isomerized to PC-340; via cation exchange PC-340 transformed to CdTeSe PCs. In turn, the resultant CdTeSe PC isomerized to CdTeSe MSCs, the process of which was rate-determining. Furthermore, we show that the transformation between CdTeSe MSC-422 and MSC-399 was reversible, providing strong evidence that they are a pair of isomers. Our study introduces a room-temperature avenue towards Cd-based MSCs from Zn-based ones, which follows anionic framework conservation and anionic number conservation.

This is an open access article under the terms of the Creative Commons Attribution 4.0 International License (CC BY 4.0, https://creativecommons.org/licenses/by/4.0/).
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