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On-demand synthesis of high-quality, blue-light-active ZnSe colloidal quantum wires

Beyond the state-of-the-art Cd-containing quantum wires (QWs), heavy-metal-free semiconductor QWs, such as ZnSe, are of great interest for next-generation environmental-benign applications. Unfortunately, simultaneous, on-demand manipulation of their radial and axial sizes—that allows strong quantum...

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Detalles Bibliográficos
Autores principales: Li, Yi, Zhang, Chong, Tian, Jie, Wu, Liang, Liu, Guo-Qiang, Li, Hui-Hui, Zhang, Yu-Zhuo, Shao, Zhen-Chao, He, Zhen, Yu, Shu-Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9671665/
https://www.ncbi.nlm.nih.gov/pubmed/36415320
http://dx.doi.org/10.1093/nsr/nwac025
Descripción
Sumario:Beyond the state-of-the-art Cd-containing quantum wires (QWs), heavy-metal-free semiconductor QWs, such as ZnSe, are of great interest for next-generation environmental-benign applications. Unfortunately, simultaneous, on-demand manipulation of their radial and axial sizes—that allows strong quantum confinement in the blue-light region—has so far been challenging. Here we present a two-step catalyzed growth strategy that enables independent, high-precision and wide-range controls over the diameter and length of ZnSe QWs. We find that a new epitaxial orientation between the cubic-phase Ag(2)Se solid catalyst and wurtzite ZnSe QWs kinetically favors the formation of defect-free ultrathin QWs. Thanks to their high uniformity, the resulting blue-light-active, phase-pure ZnSe QWs exhibit well-defined excitonic absorption with the 1S(e)–1S(h) transition linewidth as narrow as sub-13 nm. Combining the transient absorption spectroscopy, we further show that surface electron traps in these ZnSe QWs can be eliminated by thiol passivation, which results in long-lived charge carriers and high-efficiency solar-to-hydrogen conversion.