红移
转化(遗传学)
魔术(望远镜)
吸收(声学)
半导体
碲化镉光电
星团(航天器)
化学
化学物理
材料科学
物理
纳米技术
天体物理学
光电子学
光学
计算机科学
生物化学
银河系
基因
程序设计语言
作者
Chaoran Luan,Qiu Shen,N. L. Rowell,Meng Zhang,Xiaoqin Chen,Wen Huang,Kui Yu
标识
DOI:10.1002/ange.202205784
摘要
Abstract 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.
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