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

Author:

Li Yi1,Zhang Chong1,Tian Jie2,Wu Liang1,Liu Guo-Qiang1,Li Hui-Hui1,Zhang Yu-Zhuo1,Shao Zhen-Chao1,He Zhen1,Yu Shu-Hong1ORCID

Affiliation:

1. Department of Chemistry, Institute of Biomimetic Materials and Chemistry, Anhui Engineering Laboratory of Biomimetic Materials, Division of Nanomaterials and Chemistry, Hefei National Research Center for Physical Sciences at the Microscale, University of Science and Technology of China , Hefei 230026 , China

2. Engineering and Materials Science Experiment Center, University of Science and Technology of China , Hefei 230026 , China

Abstract

Abstract 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 Ag2Se 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 1Se–1Sh 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.

Funder

National Natural Science Foundation of China

Chinese Academy of Sciences

China Postdoctoral Science Foundation

Fundamental Research Funds for the Central Universities

NSF of Anhui Province

Publisher

Oxford University Press (OUP)

Subject

Multidisciplinary

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